Acondroplazie (Romanian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acondroplazie" in Romanian language version.

refsWebsite

Global rank Romanian rank

15nih.gov

4^th place

12doi.org

2^nd place

3^rd place

1guinnessworldrecords.com

550^th place

569^th place

1genome.gov

9,308^th place

low place

1marchofdimes.org

low place

1asiaandro.com

low place

1web.archive.org

1^st place

1stevensorenson.com

low place

1zenodo.org

621^st place

1,171^st place

1kidshealth.org

low place

6,822^nd place

1hopkinsmedicine.org

5,712^th place

7,256^th place

1mayoclinic.org

1,610^th place

2,809^th place

1betterhealth.vic.gov.au

low place

1webmd.com

1,169^th place

880^th place

1archive.org

6^th place

23^rd place

1harvard.edu

18^th place

27^th place

1worldcat.org

5^th place

11^th place

1nejm.org

2,374^th place

2,444^th place

archive.org

Willis M.B. (1989). „Inheritance of specific skeletal and structural defects”. În Willis M.B. Genetics of the Dog. Great Britain: Howell Book House. pp. 119–120. ISBN 978-0876055519.

asiaandro.com

„The effects of advanced paternal age on fertility” (PDF). Asian Journal of Andrology. 15 (6): 723–728. 2013. doi:10.1038/aja.2013.92. PMC 3854059 . PMID 23912310.

betterhealth.vic.gov.au

Services, Department of Health & Human. „Dwarfism” (în engleză). Accesat în 26 septembrie 2018.

doi.org

„Achondroplasia: From genotype to phenotype”. Joint Bone Spine. 75 (2): 125–30. 2007. doi:10.1016/j.jbspin.2007.06.007. PMID 17950653.
„Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm”. Proceedings of the National Academy of Sciences of the United States of America. 103 (25): 9601–9606. 2006. doi:10.1073/pnas.0506468103. PMC 1480453 . PMID 16766665.
„The effects of advanced paternal age on fertility” (PDF). Asian Journal of Andrology. 15 (6): 723–728. 2013. doi:10.1038/aja.2013.92. PMC 3854059 . PMID 23912310.
EL-Sobky, TA; Shawky, RM; Sakr, HM; Elsayed, SM; Elsayed, NS; Ragheb, SG; Gamal, R (15 noiembrie 2017). „A systematized approach to radiographic assessment of commonly seen genetic bone diseases in children: A pictorial review”. J Musculoskelet Surg Res. 1 (2): 25. doi:10.4103/jmsr.jmsr_28_17.
„Distraction osteogenesis of the lower extremity in patients that have achondroplasia/hypochondroplasia treated with transplantation of culture-expanded bone marrow cells and platelet-rich plasma”. J Pediatr Orthop. 27 (6): 629–34. 2007. doi:10.1097/BPO.0b013e318093f523. PMID 17717461.
Vajo, Z; Francomano, CA; Wilkin, DJ (2000). „The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans”. Endocrine Reviews. 21 (1): 23–39. doi:10.1210/er.21.1.23. PMID 10696568.
Aviezer, D; Golembo, M; Yayon, A (2003). „Fibroblast growth factor receptor-3 as a therapeutic target for Achondroplasia—genetic short limbed dwarfism”. Current Drug Targets. 4 (5): 353–65. doi:10.2174/1389450033490993. PMID 12816345.
„An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs”. Science. 325 (5943): 995–8. august 2009. Bibcode:2009Sci...325..995P. doi:10.1126/science.1173275. PMC 2748762 . PMID 19608863.
„Morphological studies of the canine intervertebral disc. The assignment of the beagle to the achondroplastic classification”. Res. Vet. Sci. 19 (2): 167–72. septembrie 1975. doi:10.1016/S0034-5288(18)33527-6. PMID 1166121.
„Abnormal growth plate function in pigs carrying a dominant mutation in type X collagen”. Mamm. Genome. 11 (12): 1087–92. decembrie 2000. doi:10.1007/s003350010212. PMID 11130976.
Gidney, Louisa (1019). „Earliest Archaeological Evidence of the Ancon Mutation in Sheep from Leicester, UK”. International Journal of Osteoarchaeology. 15 (27): 318–321. doi:10.1002/oa.872. ISSN 1099-1212.
Savarirayan, Ravi (4 iulie 2019). „C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia”. New England Journal of Medicine. 381 (1): 25–35. doi:10.1056/NEJMoa1813446. PMID 31269546.

genome.gov

„Learning About Achondroplasia”. National Human Genome Research Institute (NHGRI) (în engleză). Accesat în 26 septembrie 2018.

guinnessworldrecords.com

„New world's shortest woman: It's official – Jyoti Amge from India is new record holder”. Guinness World Records. 13 decembrie 2011. Accesat în 12 decembrie 2017.

harvard.edu

adsabs.harvard.edu

„An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs”. Science. 325 (5943): 995–8. august 2009. Bibcode:2009Sci...325..995P. doi:10.1126/science.1173275. PMC 2748762 . PMID 19608863.

hopkinsmedicine.org

Kieffer, Sara. „Achondroplasia | Johns Hopkins Pediatric Neurosurgery” (în engleză). Accesat în 26 septembrie 2018.

kidshealth.org

„Dwarfism”. kidshealth.org (în engleză). Accesat în 26 septembrie 2018.

marchofdimes.org

„Achondroplasia” (în engleză). Accesat în 26 septembrie 2018.

mayoclinic.org

„Hydrocephalus - Diagnosis and treatment - Mayo Clinic”. www.mayoclinic.org (în engleză). Accesat în 26 septembrie 2018.

nejm.org

Savarirayan, Ravi (4 iulie 2019). „C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia”. New England Journal of Medicine. 381 (1): 25–35. doi:10.1056/NEJMoa1813446. PMID 31269546.

nih.gov

ncbi.nlm.nih.gov

Pauli, RM; Adam, MP; Ardinger, HH; Pagon, RA; Wallace, SE; Bean, LJH; Mefford, HC; Stephens, K; Amemiya, A (2012). „Achondroplasia”. GeneReviews. PMID 20301331.
„Achondroplasia: From genotype to phenotype”. Joint Bone Spine. 75 (2): 125–30. 2007. doi:10.1016/j.jbspin.2007.06.007. PMID 17950653.
„Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm”. Proceedings of the National Academy of Sciences of the United States of America. 103 (25): 9601–9606. 2006. doi:10.1073/pnas.0506468103. PMC 1480453 . PMID 16766665.
„The effects of advanced paternal age on fertility” (PDF). Asian Journal of Andrology. 15 (6): 723–728. 2013. doi:10.1038/aja.2013.92. PMC 3854059 . PMID 23912310.
„Distraction osteogenesis of the lower extremity in patients that have achondroplasia/hypochondroplasia treated with transplantation of culture-expanded bone marrow cells and platelet-rich plasma”. J Pediatr Orthop. 27 (6): 629–34. 2007. doi:10.1097/BPO.0b013e318093f523. PMID 17717461.
Vajo, Z; Francomano, CA; Wilkin, DJ (2000). „The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans”. Endocrine Reviews. 21 (1): 23–39. doi:10.1210/er.21.1.23. PMID 10696568.
Aviezer, D; Golembo, M; Yayon, A (2003). „Fibroblast growth factor receptor-3 as a therapeutic target for Achondroplasia—genetic short limbed dwarfism”. Current Drug Targets. 4 (5): 353–65. doi:10.2174/1389450033490993. PMID 12816345.
„An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs”. Science. 325 (5943): 995–8. august 2009. Bibcode:2009Sci...325..995P. doi:10.1126/science.1173275. PMC 2748762 . PMID 19608863.
„Morphological studies of the canine intervertebral disc. The assignment of the beagle to the achondroplastic classification”. Res. Vet. Sci. 19 (2): 167–72. septembrie 1975. doi:10.1016/S0034-5288(18)33527-6. PMID 1166121.
„Abnormal growth plate function in pigs carrying a dominant mutation in type X collagen”. Mamm. Genome. 11 (12): 1087–92. decembrie 2000. doi:10.1007/s003350010212. PMID 11130976.
Savarirayan, Ravi (4 iulie 2019). „C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia”. New England Journal of Medicine. 381 (1): 25–35. doi:10.1056/NEJMoa1813446. PMID 31269546.

ghr.nlm.nih.gov

„Achondroplasia”. Genetics Home Reference (în engleză). mai 2012. Accesat în 12 decembrie 2017.
Reference, Genetics Home. „FGFR3 gene”. Genetics Home Reference (în engleză). Accesat în 26 septembrie 2018.

rarediseases.info.nih.gov

„Achondroplasia”. Genetic and Rare Diseases Information Center (GARD) – an NCATS Program (în engleză). 2016. Accesat în 12 decembrie 2017.
„Achondroplasia | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”. rarediseases.info.nih.gov (în engleză). Accesat în 26 septembrie 2018.

stevensorenson.com

„Achondroplasia Pelvis”. Arhivat din original la 22 octombrie 2007. Accesat în 28 noiembrie 2007.

web.archive.org

„Achondroplasia Pelvis”. Arhivat din original la 22 octombrie 2007. Accesat în 28 noiembrie 2007.

webmd.com

pets.webmd.com

„WebMD”.

worldcat.org

Gidney, Louisa (1019). „Earliest Archaeological Evidence of the Ancon Mutation in Sheep from Leicester, UK”. International Journal of Osteoarchaeology. 15 (27): 318–321. doi:10.1002/oa.872. ISSN 1099-1212.

zenodo.org

Vajo, Z; Francomano, CA; Wilkin, DJ (2000). „The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans”. Endocrine Reviews. 21 (1): 23–39. doi:10.1210/er.21.1.23. PMID 10696568.