Microcephaly (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Microcephaly" in English language version.

refsWebsite

Global rank English rank

62nih.gov

4^th place

34doi.org

2^nd place

12web.archive.org

1^st place

12worldcat.org

5^th place

8semanticscholar.org

11^th place

8^th place

4cdc.gov

218^th place

212^th place

4harvard.edu

18^th place

17^th place

4books.google.com

3^rd place

2omim.org

4,380^th place

4,305^th place

2rarediseases.org

5,181^st place

3,260^th place

2orpha.net

3,537^th place

7,177^th place

1clevelandclinic.org

4,925^th place

3,597^th place

1merriam-webster.com

209^th place

191^st place

1archive.org

6^th place

1stanfordchildrens.org

low place

1malacards.org

low place

1rochester.edu

2,691^st place

1,948^th place

1who.int

195^th place

302^nd place

1medlineplus.gov

1,581^st place

1,299^th place

1uptodate.com

3,771^st place

2,605^th place

1mayoclinic.org

1,610^th place

1,279^th place

1mito.org.au

low place

1ajog.org

low place

1jstor.org

26^th place

20^th place

1npr.org

92^nd place

72^nd place

1promedmail.org

low place

1arstechnica.co.uk

low place

1wikiwix.com

194^th place

643^rd place

1city.hiroshima.jp

low place

1thehumanmarvels.com

low place

1zippythepinhead.com

low place

1academia.dk

low place

academia.dk

Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4): 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

ajog.org

Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7 – e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.

archive.org

Behrman, R.E.; Kligman, R. M.; Jensen, H.B. (2000). Nelson's Textbook of Pediatrics (16th ed.). Philadelphia: WB Saunders. ISBN 978-0-7216-7767-5. OCLC 44552900.

arstechnica.co.uk

Beth Mole (2016-01-17). "CDC issues travel advisory for 14 countries with alarming viral outbreaks". Ars Technica. Condé Nast. Archived from the original on 2016-01-18. Retrieved 2016-01-17.

books.google.com

Coley, Brian D. (2013). Caffey's Pediatric Diagnostic Imaging E-Book (12th ed.). Elsevier Health Sciences. ISBN 978-1-4557-5360-4. OCLC 847214216.
Martin, Richard J.; Fanaroff, Avroy A.; Walsh, Michele C. (2014). Fanaroff and Martin's Neonatal-Perinatal Medicine E-Book: Diseases of the Fetus and Infant. Elsevier Health Sciences. ISBN 978-0-323-29537-6. OCLC 909892605.
Kalter, Harold (2010). "Pioneering Studies §Atomic Radiation §Microcephaly and Mental Retardation". Teratology in the Twentieth Century Plus Ten. Springer. p. 21. doi:10.1007/978-90-481-8820-8_2. ISBN 978-90-481-8820-8.
Stories, Wander (4 February 2015). Colosseum in Rome: a travel guide and tour as with the best local guide. WanderStories. ISBN 978-9-949-51606-3.

cdc.gov

"Facts about Microcephaly | Birth Defects | National Center on Birth Defects and Developmental Disabilities". Centers for Disease Control and Prevention. 2016-12-07. Retrieved 2019-07-30.
"Facts about Microcephaly". Centers for Disease Control and Prevention. 2016-12-07. Retrieved 2019-08-02.
"CDC Concludes Zika Causes Microcephaly and Other Birth Defects". CDC. 13 April 2016. Archived from the original on 31 May 2016. Retrieved 1 June 2016.
"CDC issues interim travel guidance related to Zika virus for 14 Countries and Territories in Central and South America and the Caribbean". Centers for Disease Control and Prevention. 2016-01-15. Archived from the original on 2016-01-18. Retrieved 2016-01-17.

city.hiroshima.jp

pcf.city.hiroshima.jp

"Aftereffects". Archived from the original on 2009-05-25.

clevelandclinic.org

my.clevelandclinic.org

"Microcephaly". Health Library: Diseases & Conditions. Cleveland Clinic. April 2023.

doi.org

Faheem, Muhammad; Naseer, Muhammad Imran; Rasool, Mahmood; Chaudhary, Adeel G; Kumosani, Taha A; Ilyas, Asad Muhammad; Pushparaj, Peter Natesan; Ahmed, Farid; Algahtani, Hussain A; Al-Qahtani, Mohammad H; Saleh Jamal, Hasan (2015). "Molecular genetics of human primary microcephaly: an overview". BMC Medical Genomics. 8 (Suppl 1): S4. doi:10.1186/1755-8794-8-S1-S4. PMC 4315316. PMID 25951892.
Leviton, A.; Holmes, L.B.; Allred, E.N.; Vargas, J. (2002). "Methodologic issues in epidemiologic studies of congenital microcephaly". Early Hum Dev. 69 (1): 91–105. doi:10.1016/S0378-3782(02)00065-8. PMID 12324187.
Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–8. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Ashwal, S.; Michelson, D.; Plawner, L.; Dobyns, W. B. (2009). "Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review)". Neurology. 73 (11): 887–897. doi:10.1212/WNL.0b013e3181b783f7. PMC 2744281. PMID 19752457.
Opladen T, López-Laso E, Cortès-Saladelafont E, Pearson TS, Sivri HS, Yildiz Y, Assmann B, Kurian MA, Leuzzi V, Heales S, Pope S, Porta F, García-Cazorla A, Honzík T, Pons R, Regal L, Goez H, Artuch R, Hoffmann GF, Horvath G, Thöny B, Scholl-Bürgi S, Burlina A, Verbeek MM, Mastrangelo M, Friedman J, Wassenberg T, Jeltsch K, Kulhánek J, Kuseyri Hübschmann O (May 2020). "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies". Orphanet Journal of Rare Diseases. 15 (1): 126. doi:10.1186/s13023-020-01379-8. PMC 7251883. PMID 32456656.
Szczepanski, Sandra; Hussain, MuhammadSajid; Sur, Ilknur; Altmüller, Janine; Thiele, Holger; Abdullah, Uzma; Waseem, SyedaSeema; Moawia, Abubakar; Nürnberg, Gudrun; Noegel, Angelika Anna; Baig, Shahid Mahmood; Nürnberg, Peter (30 November 2015). "A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family". Human Genetics. 135 (2): 157–170. doi:10.1007/s00439-015-1619-5. PMID 26621532. S2CID 2295608.
Emily E. Petersen; Erin Staples; Dana Meaney-Delman; Marc Fischer; Sascha R. Ellington; William M. Callaghan; Denise J. Jamieson (January 22, 2016). "Interim Guidelines for Pregnant Women During a Zika Virus Outbreak — United States, 2016". Morbidity and Mortality Weekly Report. 65 (2): 30–33. doi:10.15585/mmwr.mm6502e1. PMID 26796813.
Reddy, Nihaal; Calloni, Sonia F.; Vernon, Hilary J.; Boltshauser, Eugen; Huisman, Thierry A. G. M.; Soares, Bruno P. (2018-05-01). "Neuroimaging Findings of Organic Acidemias and Aminoacidopathies". RadioGraphics. 38 (3): 912–931. doi:10.1148/rg.2018170042. ISSN 0271-5333. PMID 29757724.
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Tibussek, Daniel; Sinclair, Adriane; Yau, Ivanna; Teatero, Sarah; Fittipaldi, Nahuel; Richardson, Susan E.; Mayatepek, Ertan; Jahn, Peter; Askalan, Rand (2015). "Late-Onset Group B Streptococcal Meningitis Has Cerebrovascular Complications". The Journal of Pediatrics. 166 (5): 1187–92.e1. doi:10.1016/j.jpeds.2015.02.014. PMID 25919727.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7 – e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.
Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–41. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–382. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–8. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Rasmussen, Sonja A.; Jamieson, Denise J.; Honein, Margaret A.; Petersen, Lyle R. (13 April 2016). "Zika Virus and Birth Defects — Reviewing the Evidence for Causality". New England Journal of Medicine. 374 (20): 1981–7. doi:10.1056/NEJMsr1604338. PMID 27074377. S2CID 20675635.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–8. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
Cavallin, Mara; Rujano, Maria A.; Bednarek, Nathalie; Medina-Cano, Daniel; Bernabe Gelot, Antoinette; Drunat, Severine; Maillard, Camille; Garfa-Traore, Meriem; Bole, Christine (2017-10-01). "WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells". Brain. 140 (10): 2597–2609. doi:10.1093/brain/awx218. ISSN 1460-2156. PMID 28969387.
Kalter, Harold (2010). "Pioneering Studies §Atomic Radiation §Microcephaly and Mental Retardation". Teratology in the Twentieth Century Plus Ten. Springer. p. 21. doi:10.1007/978-90-481-8820-8_2. ISBN 978-90-481-8820-8.
Adams, Hieab H. H.; Hibar, Derrek P.; Chouraki, Vincent; Stein, Jason L.; Nyquist, Paul A.; Rentería, Miguel E.; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha (2016). "Novel genetic loci underlying human intracranial volume identified through genome-wide association". Nature Neuroscience. 19 (12): 1569–82. doi:10.1038/nn.4398. PMC 5227112. PMID 27694991.
Jamuar, SS; Walsh, CA (June 2015). "Genomic variants and variations in malformations of cortical development". Pediatric Clinics of North America. 62 (3): 571–85. doi:10.1016/j.pcl.2015.03.002. PMC 4449454. PMID 26022163.
Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
Shen, J; Gilmore, EC; Marshall, CA; Haddadin, M; Reynolds, JJ; Eyaid, W; Bodell, A; Barry, B; Gleason, D; Allen, K; Ganesh, VS; Chang, BS; Grix, A; Hill, RS; Topcu, M; Caldecott, KW; Barkovich, AJ; Walsh, CA (March 2010). "Mutations in PNKP cause microcephaly, seizures and defects in DNA repair". Nature Genetics. 42 (3): 245–9. doi:10.1038/ng.526. PMC 2835984. PMID 20118933.
Alkuraya, FS; Cai, X; Emery, C; Mochida, GH; Al-Dosari, MS; Felie, JM; Hill, RS; Barry, BJ; Partlow, JN; Gascon, GG; Kentab, A; Jan, M; Shaheen, R; Feng, Y; Walsh, CA (13 May 2011). "Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]". American Journal of Human Genetics. 88 (5): 536–47. doi:10.1016/j.ajhg.2011.04.003. PMC 3146728. PMID 21529751.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–5. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. PMC 6095461. PMID 29643508.
Nowakowski, TJ; Pollen, AA; Di Lullo, E; Sandoval-Espinosa, C; Bershteyn, M; Kriegstein, AR (5 May 2016). "Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells". Cell Stem Cell. 18 (5): 591–6. doi:10.1016/j.stem.2016.03.012. PMC 4860115. PMID 27038591.
Li, C; Xu, D; Ye, Q; Hong, S; Jiang, Y; Liu, X; Zhang, N; Shi, L; Qin, CF; Xu, Z (7 July 2016). "Zika Virus Disrupts Neural Progenitor Development and Leads to Microcephaly in Mice". Cell Stem Cell. 19 (1): 120–6. doi:10.1016/j.stem.2016.04.017. PMID 27179424.
O'Driscoll M, Jeggo PA (July 2008). "The role of the DNA damage response pathways in brain development and microcephaly: insight from human disorders". DNA Repair (Amst). 7 (7): 1039–50. doi:10.1016/j.dnarep.2008.03.018. PMID 18458003.
Ribeiro JH, Altinisik N, Rajan N, Verslegers M, Baatout S, Gopalakrishnan J, Quintens R (2023). "DNA damage and repair: underlying mechanisms leading to microcephaly". Front Cell Dev Biol. 11: 1268565. doi:10.3389/fcell.2023.1268565. PMC 10597653. PMID 37881689.
de Koning, T. J. (2006). "Treatment with amino acids in serine deficiency disorders". Journal of Inherited Metabolic Disease. 29 (2–3): 347–351. doi:10.1007/s10545-006-0269-0. ISSN 0141-8955. PMID 16763900. S2CID 35908740.
Mateen, F.J.; Boes, C.J. (2010). "'Pinheads': the exhibition of neurologic disorders at 'The Greatest Show on Earth'". Neurology. 75 (22): 2028–32. doi:10.1212/WNL.0b013e3181ff9636. PMID 21115959. S2CID 207118420.
Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4): 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

harvard.edu

ui.adsabs.harvard.edu

Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–41. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–8. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–5. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. PMC 6095461. PMID 29643508.

jstor.org

Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–8. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.

malacards.org

"Microcephaly with Spastic Quadriplegia disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 2019-08-02.

mayoclinic.org

"Microcephaly - Symptoms and causes". Mayo Clinic. Retrieved 2019-07-30.

medlineplus.gov

"Trisomy 18: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 2020-10-29.

merriam-webster.com

"Microcephaly - Definition of Microcephaly by Merriam-Webster". Archived from the original on 2014-09-14.

mito.org.au

"Mito Info". Mito Foundation. Retrieved 2019-08-01.

nih.gov

pubmed.ncbi.nlm.nih.gov

Faheem, Muhammad; Naseer, Muhammad Imran; Rasool, Mahmood; Chaudhary, Adeel G; Kumosani, Taha A; Ilyas, Asad Muhammad; Pushparaj, Peter Natesan; Ahmed, Farid; Algahtani, Hussain A; Al-Qahtani, Mohammad H; Saleh Jamal, Hasan (2015). "Molecular genetics of human primary microcephaly: an overview". BMC Medical Genomics. 8 (Suppl 1): S4. doi:10.1186/1755-8794-8-S1-S4. PMC 4315316. PMID 25951892.
Leviton, A.; Holmes, L.B.; Allred, E.N.; Vargas, J. (2002). "Methodologic issues in epidemiologic studies of congenital microcephaly". Early Hum Dev. 69 (1): 91–105. doi:10.1016/S0378-3782(02)00065-8. PMID 12324187.
Opitz, J. M.; Holt, M. C. (1990). "Microcephaly: general considerations and aids to nosology". Journal of Craniofacial Genetics and Developmental Biology. 10 (2): 75–204. PMID 2211965.
Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–8. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Ashwal, S.; Michelson, D.; Plawner, L.; Dobyns, W. B. (2009). "Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review)". Neurology. 73 (11): 887–897. doi:10.1212/WNL.0b013e3181b783f7. PMC 2744281. PMID 19752457.
Opladen T, López-Laso E, Cortès-Saladelafont E, Pearson TS, Sivri HS, Yildiz Y, Assmann B, Kurian MA, Leuzzi V, Heales S, Pope S, Porta F, García-Cazorla A, Honzík T, Pons R, Regal L, Goez H, Artuch R, Hoffmann GF, Horvath G, Thöny B, Scholl-Bürgi S, Burlina A, Verbeek MM, Mastrangelo M, Friedman J, Wassenberg T, Jeltsch K, Kulhánek J, Kuseyri Hübschmann O (May 2020). "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies". Orphanet Journal of Rare Diseases. 15 (1): 126. doi:10.1186/s13023-020-01379-8. PMC 7251883. PMID 32456656.
Szczepanski, Sandra; Hussain, MuhammadSajid; Sur, Ilknur; Altmüller, Janine; Thiele, Holger; Abdullah, Uzma; Waseem, SyedaSeema; Moawia, Abubakar; Nürnberg, Gudrun; Noegel, Angelika Anna; Baig, Shahid Mahmood; Nürnberg, Peter (30 November 2015). "A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family". Human Genetics. 135 (2): 157–170. doi:10.1007/s00439-015-1619-5. PMID 26621532. S2CID 2295608.
Emily E. Petersen; Erin Staples; Dana Meaney-Delman; Marc Fischer; Sascha R. Ellington; William M. Callaghan; Denise J. Jamieson (January 22, 2016). "Interim Guidelines for Pregnant Women During a Zika Virus Outbreak — United States, 2016". Morbidity and Mortality Weekly Report. 65 (2): 30–33. doi:10.15585/mmwr.mm6502e1. PMID 26796813.
Reddy, Nihaal; Calloni, Sonia F.; Vernon, Hilary J.; Boltshauser, Eugen; Huisman, Thierry A. G. M.; Soares, Bruno P. (2018-05-01). "Neuroimaging Findings of Organic Acidemias and Aminoacidopathies". RadioGraphics. 38 (3): 912–931. doi:10.1148/rg.2018170042. ISSN 0271-5333. PMID 29757724.
Joyce, Tina; Huecker, Martin R. (2019), "Pediatric Abusive Head Trauma (Shaken Baby Syndrome)", National Center for Biotechnology Information, AU.S. National Library of Medicine, PMID 29763011, retrieved 2019-07-30
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Tibussek, Daniel; Sinclair, Adriane; Yau, Ivanna; Teatero, Sarah; Fittipaldi, Nahuel; Richardson, Susan E.; Mayatepek, Ertan; Jahn, Peter; Askalan, Rand (2015). "Late-Onset Group B Streptococcal Meningitis Has Cerebrovascular Complications". The Journal of Pediatrics. 166 (5): 1187–92.e1. doi:10.1016/j.jpeds.2015.02.014. PMID 25919727.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7 – e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.
Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–41. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–382. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–8. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Rasmussen, Sonja A.; Jamieson, Denise J.; Honein, Margaret A.; Petersen, Lyle R. (13 April 2016). "Zika Virus and Birth Defects — Reviewing the Evidence for Causality". New England Journal of Medicine. 374 (20): 1981–7. doi:10.1056/NEJMsr1604338. PMID 27074377. S2CID 20675635.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–8. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
Cavallin, Mara; Rujano, Maria A.; Bednarek, Nathalie; Medina-Cano, Daniel; Bernabe Gelot, Antoinette; Drunat, Severine; Maillard, Camille; Garfa-Traore, Meriem; Bole, Christine (2017-10-01). "WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells". Brain. 140 (10): 2597–2609. doi:10.1093/brain/awx218. ISSN 1460-2156. PMID 28969387.
Burrow, Gerard N.; Hamilton, Howard B.; Hrubec, Zdenek (June 1964). "Study of Adolescents Exposed in Utero to the Atomic Bomb, Nagasaki, Japan". Yale Journal of Biology and Medicine. 36 (6): 430–444. PMC 2604646. PMID 14173443.
Adams, Hieab H. H.; Hibar, Derrek P.; Chouraki, Vincent; Stein, Jason L.; Nyquist, Paul A.; Rentería, Miguel E.; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha (2016). "Novel genetic loci underlying human intracranial volume identified through genome-wide association". Nature Neuroscience. 19 (12): 1569–82. doi:10.1038/nn.4398. PMC 5227112. PMID 27694991.
Jamuar, SS; Walsh, CA (June 2015). "Genomic variants and variations in malformations of cortical development". Pediatric Clinics of North America. 62 (3): 571–85. doi:10.1016/j.pcl.2015.03.002. PMC 4449454. PMID 26022163.
Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
Shen, J; Gilmore, EC; Marshall, CA; Haddadin, M; Reynolds, JJ; Eyaid, W; Bodell, A; Barry, B; Gleason, D; Allen, K; Ganesh, VS; Chang, BS; Grix, A; Hill, RS; Topcu, M; Caldecott, KW; Barkovich, AJ; Walsh, CA (March 2010). "Mutations in PNKP cause microcephaly, seizures and defects in DNA repair". Nature Genetics. 42 (3): 245–9. doi:10.1038/ng.526. PMC 2835984. PMID 20118933.
Alkuraya, FS; Cai, X; Emery, C; Mochida, GH; Al-Dosari, MS; Felie, JM; Hill, RS; Barry, BJ; Partlow, JN; Gascon, GG; Kentab, A; Jan, M; Shaheen, R; Feng, Y; Walsh, CA (13 May 2011). "Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]". American Journal of Human Genetics. 88 (5): 536–47. doi:10.1016/j.ajhg.2011.04.003. PMC 3146728. PMID 21529751.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–5. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. PMC 6095461. PMID 29643508.
Nowakowski, TJ; Pollen, AA; Di Lullo, E; Sandoval-Espinosa, C; Bershteyn, M; Kriegstein, AR (5 May 2016). "Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells". Cell Stem Cell. 18 (5): 591–6. doi:10.1016/j.stem.2016.03.012. PMC 4860115. PMID 27038591.
Li, C; Xu, D; Ye, Q; Hong, S; Jiang, Y; Liu, X; Zhang, N; Shi, L; Qin, CF; Xu, Z (7 July 2016). "Zika Virus Disrupts Neural Progenitor Development and Leads to Microcephaly in Mice". Cell Stem Cell. 19 (1): 120–6. doi:10.1016/j.stem.2016.04.017. PMID 27179424.
O'Driscoll M, Jeggo PA (July 2008). "The role of the DNA damage response pathways in brain development and microcephaly: insight from human disorders". DNA Repair (Amst). 7 (7): 1039–50. doi:10.1016/j.dnarep.2008.03.018. PMID 18458003.
Ribeiro JH, Altinisik N, Rajan N, Verslegers M, Baatout S, Gopalakrishnan J, Quintens R (2023). "DNA damage and repair: underlying mechanisms leading to microcephaly". Front Cell Dev Biol. 11: 1268565. doi:10.3389/fcell.2023.1268565. PMC 10597653. PMID 37881689.
de Koning, T. J. (2006). "Treatment with amino acids in serine deficiency disorders". Journal of Inherited Metabolic Disease. 29 (2–3): 347–351. doi:10.1007/s10545-006-0269-0. ISSN 0141-8955. PMID 16763900. S2CID 35908740.
Mateen, F.J.; Boes, C.J. (2010). "'Pinheads': the exhibition of neurologic disorders at 'The Greatest Show on Earth'". Neurology. 75 (22): 2028–32. doi:10.1212/WNL.0b013e3181ff9636. PMID 21115959. S2CID 207118420.
Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4): 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

ncbi.nlm.nih.gov

Faheem, Muhammad; Naseer, Muhammad Imran; Rasool, Mahmood; Chaudhary, Adeel G; Kumosani, Taha A; Ilyas, Asad Muhammad; Pushparaj, Peter Natesan; Ahmed, Farid; Algahtani, Hussain A; Al-Qahtani, Mohammad H; Saleh Jamal, Hasan (2015). "Molecular genetics of human primary microcephaly: an overview". BMC Medical Genomics. 8 (Suppl 1): S4. doi:10.1186/1755-8794-8-S1-S4. PMC 4315316. PMID 25951892.
Ashwal, S.; Michelson, D.; Plawner, L.; Dobyns, W. B. (2009). "Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review)". Neurology. 73 (11): 887–897. doi:10.1212/WNL.0b013e3181b783f7. PMC 2744281. PMID 19752457.
Opladen T, López-Laso E, Cortès-Saladelafont E, Pearson TS, Sivri HS, Yildiz Y, Assmann B, Kurian MA, Leuzzi V, Heales S, Pope S, Porta F, García-Cazorla A, Honzík T, Pons R, Regal L, Goez H, Artuch R, Hoffmann GF, Horvath G, Thöny B, Scholl-Bürgi S, Burlina A, Verbeek MM, Mastrangelo M, Friedman J, Wassenberg T, Jeltsch K, Kulhánek J, Kuseyri Hübschmann O (May 2020). "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies". Orphanet Journal of Rare Diseases. 15 (1): 126. doi:10.1186/s13023-020-01379-8. PMC 7251883. PMID 32456656.
Joyce, Tina; Huecker, Martin R. (2019), "Pediatric Abusive Head Trauma (Shaken Baby Syndrome)", National Center for Biotechnology Information, AU.S. National Library of Medicine, PMID 29763011, retrieved 2019-07-30
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Crespi, B.; Stead, P.; Elliot, M. (January 2010). "Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (Suppl 1): 1736–41. Bibcode:2010PNAS..107.1736C. doi:10.1073/pnas.0906080106. PMC 2868282. PMID 19955444.
Stone, Jennifer L.; O'Donovan, Michael C.; Gurling, Hugh; Kirov, George K.; Blackwood, Douglas H. R.; Corvin, Aiden; et al. (September 2008). "Rare chromosomal deletions and duplications increase risk of schizophrenia". Nature. 455 (7210): 237–241. Bibcode:2008Natur.455..237S. doi:10.1038/nature07239. PMC 3912847. PMID 18668038.
Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–382. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Rimol, Lars M.; Agartz, Ingrid; Djurovic, Srdjan; Brown, Andrew A.; Roddey, J. Cooper; Kahler, Anna K.; et al. (2010). "Sex-dependent association of common variants of microcephaly genes with brain structure". Proceedings of the National Academy of Sciences. 107 (1): 384–8. Bibcode:2010PNAS..107..384R. doi:10.1073/pnas.0908454107. JSTOR 40536283. PMC 2806758. PMID 20080800.
Burrow, Gerard N.; Hamilton, Howard B.; Hrubec, Zdenek (June 1964). "Study of Adolescents Exposed in Utero to the Atomic Bomb, Nagasaki, Japan". Yale Journal of Biology and Medicine. 36 (6): 430–444. PMC 2604646. PMID 14173443.
Adams, Hieab H. H.; Hibar, Derrek P.; Chouraki, Vincent; Stein, Jason L.; Nyquist, Paul A.; Rentería, Miguel E.; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha (2016). "Novel genetic loci underlying human intracranial volume identified through genome-wide association". Nature Neuroscience. 19 (12): 1569–82. doi:10.1038/nn.4398. PMC 5227112. PMID 27694991.
Jamuar, SS; Walsh, CA (June 2015). "Genomic variants and variations in malformations of cortical development". Pediatric Clinics of North America. 62 (3): 571–85. doi:10.1016/j.pcl.2015.03.002. PMC 4449454. PMID 26022163.
Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
Shen, J; Gilmore, EC; Marshall, CA; Haddadin, M; Reynolds, JJ; Eyaid, W; Bodell, A; Barry, B; Gleason, D; Allen, K; Ganesh, VS; Chang, BS; Grix, A; Hill, RS; Topcu, M; Caldecott, KW; Barkovich, AJ; Walsh, CA (March 2010). "Mutations in PNKP cause microcephaly, seizures and defects in DNA repair". Nature Genetics. 42 (3): 245–9. doi:10.1038/ng.526. PMC 2835984. PMID 20118933.
Alkuraya, FS; Cai, X; Emery, C; Mochida, GH; Al-Dosari, MS; Felie, JM; Hill, RS; Barry, BJ; Partlow, JN; Gascon, GG; Kentab, A; Jan, M; Shaheen, R; Feng, Y; Walsh, CA (13 May 2011). "Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]". American Journal of Human Genetics. 88 (5): 536–47. doi:10.1016/j.ajhg.2011.04.003. PMC 3146728. PMID 21529751.
Johnson, Matthew B.; Sun, Xingshen; Kodani, Andrew; Borges-Monroy, Rebeca; Girskis, Kelly M.; Ryu, Steven C.; Wang, Peter P.; Patel, Komal; Gonzalez, Dilenny M.; Woo, Yu Mi; Yan, Ziying; Liang, Bo; Smith, Richard S.; Chatterjee, Manavi; Coman, Daniel; Papademetris, Xenophon; Staib, Lawrence H.; Hyder, Fahmeed; Mandeville, Joseph B.; Grant, P. Ellen; Im, Kiho; Kwak, Hojoong; Engelhardt, John F.; Walsh, Christopher A.; Bae, Byoung-Il (2018). "Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size". Nature. 556 (7701): 370–5. Bibcode:2018Natur.556..370J. doi:10.1038/s41586-018-0035-0. PMC 6095461. PMID 29643508.
Nowakowski, TJ; Pollen, AA; Di Lullo, E; Sandoval-Espinosa, C; Bershteyn, M; Kriegstein, AR (5 May 2016). "Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells". Cell Stem Cell. 18 (5): 591–6. doi:10.1016/j.stem.2016.03.012. PMC 4860115. PMID 27038591.
Ribeiro JH, Altinisik N, Rajan N, Verslegers M, Baatout S, Gopalakrishnan J, Quintens R (2023). "DNA damage and repair: underlying mechanisms leading to microcephaly". Front Cell Dev Biol. 11: 1268565. doi:10.3389/fcell.2023.1268565. PMC 10597653. PMID 37881689.

rarediseases.info.nih.gov

"Microcephaly autosomal dominant". Genetic and Rare Diseases Information Center. Archived from the original on 2020-09-21. Retrieved 2019-07-30.
"Poland syndrome". Genetic and Rare Diseases Information Center. Retrieved 2019-07-30.
"Trisomy 13 | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2020-10-29.

ninds.nih.gov

"NINDS Microcephaly Information Page". NINDS. June 30, 2015. Archived from the original on 2016-03-11. Retrieved 11 March 2016.
"Cephalic Disorders Fact Sheet". National Institute of Neurological Disorders and Stroke. Archived from the original on 2019-07-27. Retrieved 2019-08-02.

ghr.nlm.nih.gov

Reference, Genetics Home. "GLUT1 deficiency syndrome". Genetics Home Reference. Retrieved 2019-08-01.
Reference, Genetics Home. "Fanconi anemia". Genetics Home Reference. Retrieved 2019-08-02.

npr.org

"Mosquitos kill more people than any other creature, the CDC warns". NPR.org. NPR Morning Edition. 8 July 2024. Retrieved 6 October 2024.

omim.org

orpha.net

"Zellweger syndrome". Orphanet. Retrieved 2019-08-01.
"Maternal phenylketonuria". Orphanet. Retrieved 2019-08-01.

promedmail.org

"Zika virus - Brazil: confirmed Archive Number: 20150519.3370768". Pro-MED-mail. International Society for Infectious Diseases. Archived from the original on 2016-01-30.

rarediseases.org

"Congenital Disorders of Glycosylation". NORD (National Organization for Rare Disorders). Retrieved 2019-08-01.
"Galloway-Mowat Syndrome". NORD (National Organization for Rare Disorders). Archived from the original on 2021-03-11. Retrieved 2019-08-02.

rochester.edu

urmc.rochester.edu

"Microcephaly in Children". Health Encyclopedia. University of Rochester Medical Center. Retrieved 2019-07-30.

semanticscholar.org

api.semanticscholar.org

Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–8. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Szczepanski, Sandra; Hussain, MuhammadSajid; Sur, Ilknur; Altmüller, Janine; Thiele, Holger; Abdullah, Uzma; Waseem, SyedaSeema; Moawia, Abubakar; Nürnberg, Gudrun; Noegel, Angelika Anna; Baig, Shahid Mahmood; Nürnberg, Peter (30 November 2015). "A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family". Human Genetics. 135 (2): 157–170. doi:10.1007/s00439-015-1619-5. PMID 26621532. S2CID 2295608.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Rasmussen, Sonja A.; Jamieson, Denise J.; Honein, Margaret A.; Petersen, Lyle R. (13 April 2016). "Zika Virus and Birth Defects — Reviewing the Evidence for Causality". New England Journal of Medicine. 374 (20): 1981–7. doi:10.1056/NEJMsr1604338. PMID 27074377. S2CID 20675635.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–8. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
de Koning, T. J. (2006). "Treatment with amino acids in serine deficiency disorders". Journal of Inherited Metabolic Disease. 29 (2–3): 347–351. doi:10.1007/s10545-006-0269-0. ISSN 0141-8955. PMID 16763900. S2CID 35908740.
Mateen, F.J.; Boes, C.J. (2010). "'Pinheads': the exhibition of neurologic disorders at 'The Greatest Show on Earth'". Neurology. 75 (22): 2028–32. doi:10.1212/WNL.0b013e3181ff9636. PMID 21115959. S2CID 207118420.
Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4): 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

stanfordchildrens.org

"Microcephaly". Stanford Children's Health. Retrieved 2 August 2019.

thehumanmarvels.com

"Zip the Pinhead: What is it?". The Human Marvels. 16 October 2010. Archived from the original on 14 April 2016.

uptodate.com

"Microcephaly in infants and children: Etiology and evaluation". UpToDate. Retrieved 2019-08-02.

web.archive.org

"Microcephaly - Definition of Microcephaly by Merriam-Webster". Archived from the original on 2014-09-14.
"NINDS Microcephaly Information Page". NINDS. June 30, 2015. Archived from the original on 2016-03-11. Retrieved 11 March 2016.
"Cephalic Disorders Fact Sheet". National Institute of Neurological Disorders and Stroke. Archived from the original on 2019-07-27. Retrieved 2019-08-02.
"Microcephaly autosomal dominant". Genetic and Rare Diseases Information Center. Archived from the original on 2020-09-21. Retrieved 2019-07-30.
"Galloway-Mowat Syndrome". NORD (National Organization for Rare Disorders). Archived from the original on 2021-03-11. Retrieved 2019-08-02.
"Zika virus - Brazil: confirmed Archive Number: 20150519.3370768". Pro-MED-mail. International Society for Infectious Diseases. Archived from the original on 2016-01-30.
"CDC Concludes Zika Causes Microcephaly and Other Birth Defects". CDC. 13 April 2016. Archived from the original on 31 May 2016. Retrieved 1 June 2016.
"CDC issues interim travel guidance related to Zika virus for 14 Countries and Territories in Central and South America and the Caribbean". Centers for Disease Control and Prevention. 2016-01-15. Archived from the original on 2016-01-18. Retrieved 2016-01-17.
"Aftereffects". Archived from the original on 2009-05-25.
"Zip the Pinhead: What is it?". The Human Marvels. 16 October 2010. Archived from the original on 14 April 2016.
"Interview with Bill Griffith". ZippythePinhead.com. Goblin Magazine. 1995. Archived from the original on 31 January 2012. Retrieved 13 February 2013.
Kozma, Chahira (10 October 2005). "Historical Review - Dwarfs in Ancient Egypt" (PDF). American Journal of Medical Genetics. 140 (4): 303–311. doi:10.1002/ajmg.a.31068. PMID 16380966. S2CID 797288. Archived (PDF) from the original on 17 May 2017. Retrieved 17 February 2018.

who.int

"Microcephaly". World Health Organization. Retrieved 2019-07-30.

wikiwix.com

archive.wikiwix.com

Beth Mole (2016-01-17). "CDC issues travel advisory for 14 countries with alarming viral outbreaks". Ars Technica. Condé Nast. Archived from the original on 2016-01-18. Retrieved 2016-01-17.

worldcat.org

search.worldcat.org

Behrman, R.E.; Kligman, R. M.; Jensen, H.B. (2000). Nelson's Textbook of Pediatrics (16th ed.). Philadelphia: WB Saunders. ISBN 978-0-7216-7767-5. OCLC 44552900.
Stoler-Poria, S.; Lev, D.; Schweiger, A.; Lerman-Sagie, T.; Malinger, G. (2010-01-12). "Developmental outcome of isolated fetal microcephaly". Ultrasound in Obstetrics and Gynecology. 36 (2). Wiley: 154–8. doi:10.1002/uog.7556. ISSN 0960-7692. PMID 20069548. S2CID 30379486.
Reddy, Nihaal; Calloni, Sonia F.; Vernon, Hilary J.; Boltshauser, Eugen; Huisman, Thierry A. G. M.; Soares, Bruno P. (2018-05-01). "Neuroimaging Findings of Organic Acidemias and Aminoacidopathies". RadioGraphics. 38 (3): 912–931. doi:10.1148/rg.2018170042. ISSN 0271-5333. PMID 29757724.
Donald, Kirsten A.; Walker, Kathleen G.; Kilborn, Tracy; Carrara, Henri; Langerak, Nelleke G; Eley, Brian; Wilmshurst, Jo M (2015). "HIV Encephalopathy: pediatric case series description and insights from the clinic coalface". AIDS Research and Therapy. 12 (1): 2. doi:10.1186/s12981-014-0042-7. ISSN 1742-6405. PMC 4297380. PMID 25598835.
Ramos, Regina; Viana, Rafaela; Brainer-Lima, Alessandra; Florêncio, Telma; Carvalho, Maria Durce; van Der Linden, Vanessa; Amorim, Antonio; Rocha, Maria Ângela; Medeiros, Fabíola (2017). "Perinatal Chikungunya Virus-Associated Encephalitis Leading to Postnatal-Onset Microcephaly and Optic Atrophy". The Pediatric Infectious Disease Journal. 37 (1): 94–95. doi:10.1097/INF.0000000000001690. ISSN 0891-3668. PMID 28737626. S2CID 31790738.
Kurian, Manju A; Jungbluth, Heinz (July 2014). "Genetic disorders of thyroid metabolism and brain development". Developmental Medicine and Child Neurology. 56 (7): 627–634. doi:10.1111/dmcn.12445. ISSN 0012-1622. PMC 4231219. PMID 24665922.
Damlich, Jennifer; Qato, Roa; Cruz, Meredith; Colon, Maria; Wilkins, Isabelle (2009-07-01). "Discussion: 'Microcephaly associated with congenital heart defect' by Barbu et al". American Journal of Obstetrics & Gynecology. 201 (1): e7 – e12. doi:10.1016/j.ajog.2009.05.042. ISSN 0002-9378. PMID 19576365.
Mlakar, Jernej; Korva, Misa; Tul, Nataša; Popović, Mara; Poljšak-Prijatelj, Mateja; Mraz, Jerica; Kolenc, Marko; Resman Rus, Katarina; Vesnaver Vipotnik, Tina (2016-03-10). "Zika Virus Associated with Microcephaly". New England Journal of Medicine. 374 (10): 951–8. doi:10.1056/NEJMoa1600651. ISSN 0028-4793. PMID 26862926. S2CID 205099844.
Cavallin, Mara; Rujano, Maria A.; Bednarek, Nathalie; Medina-Cano, Daniel; Bernabe Gelot, Antoinette; Drunat, Severine; Maillard, Camille; Garfa-Traore, Meriem; Bole, Christine (2017-10-01). "WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells". Brain. 140 (10): 2597–2609. doi:10.1093/brain/awx218. ISSN 1460-2156. PMID 28969387.
Coley, Brian D. (2013). Caffey's Pediatric Diagnostic Imaging E-Book (12th ed.). Elsevier Health Sciences. ISBN 978-1-4557-5360-4. OCLC 847214216.
Martin, Richard J.; Fanaroff, Avroy A.; Walsh, Michele C. (2014). Fanaroff and Martin's Neonatal-Perinatal Medicine E-Book: Diseases of the Fetus and Infant. Elsevier Health Sciences. ISBN 978-0-323-29537-6. OCLC 909892605.
de Koning, T. J. (2006). "Treatment with amino acids in serine deficiency disorders". Journal of Inherited Metabolic Disease. 29 (2–3): 347–351. doi:10.1007/s10545-006-0269-0. ISSN 0141-8955. PMID 16763900. S2CID 35908740.

zippythepinhead.com

"Interview with Bill Griffith". ZippythePinhead.com. Goblin Magazine. 1995. Archived from the original on 31 January 2012. Retrieved 13 February 2013.