Angelman syndrome (English Wikipedia)

Urraca N, Reiter L (2013). "Angelman syndrome". Comprehensive Developmental Neuroscience: Neural Circuit Development and Function in the Heathy and Diseased Brain. Elsevier Inc. Chapter 32. ISBN 9780128063415. Retrieved April 15, 2022 – via Google Books.
Wilson GN, Cooley WC (2000). Preventive Management of Children with Congenital Anomalies and Syndromes. Cambridge University Press. p. 193. ISBN 9780521776738. Archived from the original on 2017-11-05.
Kumar V, Abbas AK, Aster JC (2013). "Genetic and Pediatric Diseases". Robbins Basic Pathology. Elsevier Health Sciences. p. 244. ISBN 978-1437717815. Archived from the original on 2017-11-05. Retrieved 2022-04-15 – via Google Books.

cureangelman.org.au

"Common Misdiagnoses". Foundation For Angelman Syndrome Therapeutics. 2 August 2019. Retrieved 10 March 2024.

doi.org

Angelman H (1965). "'Puppet' Children: A report of three cases". Developmental Medicine & Child Neurology. 7 (6): 681–688. doi:10.1111/j.1469-8749.1965.tb07844.x. S2CID 53730099.
Khan N (8 April 2019). "Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study". Molecular Genetics & Genomic Medicine. 7 (7): 3. doi:10.1002/mgg3.734. PMC 6625091. PMID 31090212.
Weeber E, Levenson J, Sweatt J (2002). "Molecular genetics of human cognition". Molecular Interventions. 2 (6): 376–91, 339. doi:10.1124/mi.2.6.376. PMID 14993414.
Wang, Yiyang, et al. (2017). "Identifying the ubiquitination targets of E6AP by orthogonal ubiquitin transfer". Nature Communications. 8 (1): 2232. Bibcode:2017NatCo...8.2232W. doi:10.1038/s41467-017-01974-7. PMC 5738348. PMID 29263404.
Mabb AM, Judson MC, Zylka MJ, Philpot BD (May 2011). "Angelman Syndrome: Insights into Genomic Imprinting and Neurodevelopmental Phenotypes". Trends Neurosci. 34 (6): 293–303. doi:10.1016/j.tins.2011.04.001. PMC 3116240. PMID 21592595.
Cassidy SB, Dykens E (2000). "Prader–Willi and Angelman syndromes: sister imprinted disorders". Am J Med Genet. 97 (2): 136–146. doi:10.1002/1096-8628(200022)97:2<136::aid-ajmg5>3.0.co;2-v. PMID 11180221. S2CID 20832857.
White HE, Durston VJ, Harvey JF, Cross NC (2006). "Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader–Willi syndrome and Angelman syndrome". Clin. Chem. 52 (6): 1005–13. doi:10.1373/clinchem.2005.065086. PMID 16574761.
Laan LA, Vein AA (2005). "Angelman syndrome: is there a characteristic EEG?". Brain and Development. 27 (2): 80–87. doi:10.1016/j.braindev.2003.09.013. ISSN 0387-7604. PMID 15668045. S2CID 5912.
Sidorov MS, Deck GM, Dolatshahi M, Thibert RL, Bird LM, Chu CJ, Philpot BD (2017-05-08). "Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis". Journal of Neurodevelopmental Disorders. 9: 17. doi:10.1186/s11689-017-9195-8. ISSN 1866-1955. PMC 5422949. PMID 28503211.
Williams CA, Angelman H, Clayton-Smith J, et al. (1995). "Angelman syndrome: consensus for diagnostic criteria. Angelman syndrome Foundation". Am. J. Med. Genet. 56 (2): 237–8. doi:10.1002/ajmg.1320560224. PMID 7625452.
Williams CA, Beaudet AL, Clayton-Smith J, et al. (2006). "Angelman syndrome 2005: updated consensus for diagnostic criteria". Am. J. Med. Genet. A. 140 (5): 413–8. doi:10.1002/ajmg.a.31074. PMID 16470747. S2CID 2449346.
Buntinx IM, Hennekam RC, Brouwer OF, et al. (March 1995). "Clinical profile of Angelman syndrome at different ages". American Journal of Medical Genetics. 56 (2): 176–83. doi:10.1002/ajmg.1320560213. PMID 7625442.
Leung HT, Ring H (January 2013). "Epilepsy in four genetically determined syndromes of intellectual disability". Journal of Intellectual Disability Research. 57 (1): 3–20. doi:10.1111/j.1365-2788.2011.01505.x. PMID 22142420.
Pearson E, Wilde L, Heald M, Royston R, Oliver C (November 2019). "Communication in Angelman syndrome: a scoping review". Developmental Medicine & Child Neurology. 61 (11): 1266–1274. doi:10.1111/dmcn.14257. ISSN 0012-1622. PMID 31074506. S2CID 149445749.
Walz NC, Baranek GT (2006-07-01). "Sensory Processing Patterns in Persons With Angelman Syndrome". American Journal of Occupational Therapy. 60 (4): 472–479. doi:10.5014/ajot.60.4.472. ISSN 0272-9490. PMID 16915878.
Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.
>Didden R, Sigafoos J, Korzilius H, Baas A, Lancioni GE, O'Reilly MF, Curfs LM (2009). "Form and Function of Communicative Behaviors in Individuals with Angelman Syndrome". Journal of Applied Research in Intellectual Disabilities. 22 (6): 526–537. doi:10.1111/j.1468-3148.2009.00520.x. hdl:2066/77094.
Key AP, Roth S, Jones D, Hunt-Hawkins H (2023). "Typical and atypical neural mechanisms support spoken word processing in Angelman syndrome". Brain and Language. 236. doi:10.1016/j.bandl.2022.105215. PMC 9839587. PMID 36502770.
Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y (2023). "Cortical and subcortical morphological alteration in Angelman syndrome". Journal of Neurodevelopmental Disorders. 15 (1): 7. doi:10.1186/s11689-022-09469-3. ISSN 1866-1955. PMC 9930225. PMID 36788499.
Key AP, Roth S, Venker C (11 October 2022). "Spoken language comprehension in children and adults with Angelman Syndrome". Journal of Communication Disorders. 100. doi:10.1016/j.jcomdis.2022.106272. PMC 9994640. PMID 36244082.
Lossie A, Driscoll D (1999). "Transmission of Angelman syndrome by an affected mother". Genet Med. 1 (6): 262–6. doi:10.1097/00125817-199909000-00004. PMID 11258627.
Laan LA, den Boer AT, Hennekam RC, Renier WO, Brouwer OF (1996). "Angelman syndrome in adulthood". Am. J. Med. Genet. 66 (3): 356–60. doi:10.1002/(SICI)1096-8628(19961218)66:3<356::AID-AJMG21>3.0.CO;2-K. hdl:2066/22929. PMID 9072912.
Coppus AM (2013). "People with intellectual disability: What do we know about adulthood and life expectancy?". Developmental Disabilities Research Reviews. 18 (1): 6–16. doi:10.1002/ddrr.1123. PMID 23949824.
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M (1996). "Autism in Angelman syndrome: a population-based study". Pediatr. Neurol. 14 (2): 131–6. doi:10.1016/0887-8994(96)00011-2. PMID 8703225.
Petersen MB, Brøndum-Nielsen K, Hansen LK, Wulff K (1995). "Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county; the disorder predominantly affects Anglo-Saxons". Am. J. Med. Genet. 60 (3): 261–2. doi:10.1002/ajmg.1320600317. PMID 7573182.
Galassi FM, Armocida E, Rühli FJ (September 2016). "Angelman Syndrome in the Portrait of a Child With a Drawing by Giovanni F. Caroto" (PDF). JAMA Pediatrics. 170 (9): 831. doi:10.1001/jamapediatrics.2016.0581. PMID 27380555.
Dooley JM, Berg JM, Pakula Z, MacGregor DL. (1981). "The puppet-like syndrome of Angelman". Am J Dis Child. 135 (7): 621–4. doi:10.1001/archpedi.1981.02130310027010. PMID 7246489.
Williams CA, Frias JL (1982). "The Angelman ("happy puppet") syndrome". Am J Med Genet. 11 (4): 453–60. doi:10.1002/ajmg.1320110411. PMID 7091188.
Magenis RE, Brown MG, Lacy DA, Budden S, LaFranchi S. (1987). "Is Angelman syndrome an alternate result of del(15)(q11q13)?". Am J Med Genet. 28 (4): 829–38. doi:10.1002/ajmg.1320280407. PMID 3688021.

glpbio.com

"Alogabat". www.glpbio.com (in German). Retrieved 2024-09-20.

handle.net

hdl.handle.net

Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.
>Didden R, Sigafoos J, Korzilius H, Baas A, Lancioni GE, O'Reilly MF, Curfs LM (2009). "Form and Function of Communicative Behaviors in Individuals with Angelman Syndrome". Journal of Applied Research in Intellectual Disabilities. 22 (6): 526–537. doi:10.1111/j.1468-3148.2009.00520.x. hdl:2066/77094.
Laan LA, den Boer AT, Hennekam RC, Renier WO, Brouwer OF (1996). "Angelman syndrome in adulthood". Am. J. Med. Genet. 66 (3): 356–60. doi:10.1002/(SICI)1096-8628(19961218)66:3<356::AID-AJMG21>3.0.CO;2-K. hdl:2066/22929. PMID 9072912.

harvard.edu

ui.adsabs.harvard.edu

Wang, Yiyang, et al. (2017). "Identifying the ubiquitination targets of E6AP by orthogonal ubiquitin transfer". Nature Communications. 8 (1): 2232. Bibcode:2017NatCo...8.2232W. doi:10.1038/s41467-017-01974-7. PMC 5738348. PMID 29263404.

independent.ie

"Superstar Colin tells of 'blessed' life with special needs child". Irish Independent. 15 October 2007. Archived from the original on 17 October 2007. Retrieved 15 October 2007.

lexico.com

"Angelman syndrome". Oxford English Dictionary. Archived from the original on June 17, 2020 – via Lexico.com.

merriam-webster.com

"Angelman syndrome". Merriam-Webster Medical Dictionary. Merriam-Webster. Retrieved April 15, 2022 – via Merriam-Webster.com.

nih.gov

pubmed.ncbi.nlm.nih.gov

Khan N (8 April 2019). "Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study". Molecular Genetics & Genomic Medicine. 7 (7): 3. doi:10.1002/mgg3.734. PMC 6625091. PMID 31090212.
Weeber E, Levenson J, Sweatt J (2002). "Molecular genetics of human cognition". Molecular Interventions. 2 (6): 376–91, 339. doi:10.1124/mi.2.6.376. PMID 14993414.
Wang, Yiyang, et al. (2017). "Identifying the ubiquitination targets of E6AP by orthogonal ubiquitin transfer". Nature Communications. 8 (1): 2232. Bibcode:2017NatCo...8.2232W. doi:10.1038/s41467-017-01974-7. PMC 5738348. PMID 29263404.
Dagli AI, Mathews J, Williams CA (22 April 2021). Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE (eds.). "Angelman Syndrome". GeneReviews. Seattle: University of Washington, Seattle. PMID 20301323. Retrieved 28 August 2022.
Mabb AM, Judson MC, Zylka MJ, Philpot BD (May 2011). "Angelman Syndrome: Insights into Genomic Imprinting and Neurodevelopmental Phenotypes". Trends Neurosci. 34 (6): 293–303. doi:10.1016/j.tins.2011.04.001. PMC 3116240. PMID 21592595.
Cassidy SB, Dykens E (2000). "Prader–Willi and Angelman syndromes: sister imprinted disorders". Am J Med Genet. 97 (2): 136–146. doi:10.1002/1096-8628(200022)97:2<136::aid-ajmg5>3.0.co;2-v. PMID 11180221. S2CID 20832857.
White HE, Durston VJ, Harvey JF, Cross NC (2006). "Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader–Willi syndrome and Angelman syndrome". Clin. Chem. 52 (6): 1005–13. doi:10.1373/clinchem.2005.065086. PMID 16574761.
Laan LA, Vein AA (2005). "Angelman syndrome: is there a characteristic EEG?". Brain and Development. 27 (2): 80–87. doi:10.1016/j.braindev.2003.09.013. ISSN 0387-7604. PMID 15668045. S2CID 5912.
Sidorov MS, Deck GM, Dolatshahi M, Thibert RL, Bird LM, Chu CJ, Philpot BD (2017-05-08). "Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis". Journal of Neurodevelopmental Disorders. 9: 17. doi:10.1186/s11689-017-9195-8. ISSN 1866-1955. PMC 5422949. PMID 28503211.
Williams CA, Angelman H, Clayton-Smith J, et al. (1995). "Angelman syndrome: consensus for diagnostic criteria. Angelman syndrome Foundation". Am. J. Med. Genet. 56 (2): 237–8. doi:10.1002/ajmg.1320560224. PMID 7625452.
Williams CA, Beaudet AL, Clayton-Smith J, et al. (2006). "Angelman syndrome 2005: updated consensus for diagnostic criteria". Am. J. Med. Genet. A. 140 (5): 413–8. doi:10.1002/ajmg.a.31074. PMID 16470747. S2CID 2449346.
Buntinx IM, Hennekam RC, Brouwer OF, et al. (March 1995). "Clinical profile of Angelman syndrome at different ages". American Journal of Medical Genetics. 56 (2): 176–83. doi:10.1002/ajmg.1320560213. PMID 7625442.
Leung HT, Ring H (January 2013). "Epilepsy in four genetically determined syndromes of intellectual disability". Journal of Intellectual Disability Research. 57 (1): 3–20. doi:10.1111/j.1365-2788.2011.01505.x. PMID 22142420.
Pearson E, Wilde L, Heald M, Royston R, Oliver C (November 2019). "Communication in Angelman syndrome: a scoping review". Developmental Medicine & Child Neurology. 61 (11): 1266–1274. doi:10.1111/dmcn.14257. ISSN 0012-1622. PMID 31074506. S2CID 149445749.
Walz NC, Baranek GT (2006-07-01). "Sensory Processing Patterns in Persons With Angelman Syndrome". American Journal of Occupational Therapy. 60 (4): 472–479. doi:10.5014/ajot.60.4.472. ISSN 0272-9490. PMID 16915878.
Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.
Key AP, Roth S, Jones D, Hunt-Hawkins H (2023). "Typical and atypical neural mechanisms support spoken word processing in Angelman syndrome". Brain and Language. 236. doi:10.1016/j.bandl.2022.105215. PMC 9839587. PMID 36502770.
Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y (2023). "Cortical and subcortical morphological alteration in Angelman syndrome". Journal of Neurodevelopmental Disorders. 15 (1): 7. doi:10.1186/s11689-022-09469-3. ISSN 1866-1955. PMC 9930225. PMID 36788499.
Key AP, Roth S, Venker C (11 October 2022). "Spoken language comprehension in children and adults with Angelman Syndrome". Journal of Communication Disorders. 100. doi:10.1016/j.jcomdis.2022.106272. PMC 9994640. PMID 36244082.
Lossie A, Driscoll D (1999). "Transmission of Angelman syndrome by an affected mother". Genet Med. 1 (6): 262–6. doi:10.1097/00125817-199909000-00004. PMID 11258627.
Laan LA, den Boer AT, Hennekam RC, Renier WO, Brouwer OF (1996). "Angelman syndrome in adulthood". Am. J. Med. Genet. 66 (3): 356–60. doi:10.1002/(SICI)1096-8628(19961218)66:3<356::AID-AJMG21>3.0.CO;2-K. hdl:2066/22929. PMID 9072912.
Coppus AM (2013). "People with intellectual disability: What do we know about adulthood and life expectancy?". Developmental Disabilities Research Reviews. 18 (1): 6–16. doi:10.1002/ddrr.1123. PMID 23949824.
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M (1996). "Autism in Angelman syndrome: a population-based study". Pediatr. Neurol. 14 (2): 131–6. doi:10.1016/0887-8994(96)00011-2. PMID 8703225.
Petersen MB, Brøndum-Nielsen K, Hansen LK, Wulff K (1995). "Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county; the disorder predominantly affects Anglo-Saxons". Am. J. Med. Genet. 60 (3): 261–2. doi:10.1002/ajmg.1320600317. PMID 7573182.
Galassi FM, Armocida E, Rühli FJ (September 2016). "Angelman Syndrome in the Portrait of a Child With a Drawing by Giovanni F. Caroto" (PDF). JAMA Pediatrics. 170 (9): 831. doi:10.1001/jamapediatrics.2016.0581. PMID 27380555.
Dooley JM, Berg JM, Pakula Z, MacGregor DL. (1981). "The puppet-like syndrome of Angelman". Am J Dis Child. 135 (7): 621–4. doi:10.1001/archpedi.1981.02130310027010. PMID 7246489.
Williams CA, Frias JL (1982). "The Angelman ("happy puppet") syndrome". Am J Med Genet. 11 (4): 453–60. doi:10.1002/ajmg.1320110411. PMID 7091188.
Magenis RE, Brown MG, Lacy DA, Budden S, LaFranchi S. (1987). "Is Angelman syndrome an alternate result of del(15)(q11q13)?". Am J Med Genet. 28 (4): 829–38. doi:10.1002/ajmg.1320280407. PMID 3688021.

ncbi.nlm.nih.gov

Khan N (8 April 2019). "Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study". Molecular Genetics & Genomic Medicine. 7 (7): 3. doi:10.1002/mgg3.734. PMC 6625091. PMID 31090212.
Wang, Yiyang, et al. (2017). "Identifying the ubiquitination targets of E6AP by orthogonal ubiquitin transfer". Nature Communications. 8 (1): 2232. Bibcode:2017NatCo...8.2232W. doi:10.1038/s41467-017-01974-7. PMC 5738348. PMID 29263404.
Dagli AI, Mathews J, Williams CA (22 April 2021). Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE (eds.). "Angelman Syndrome". GeneReviews. Seattle: University of Washington, Seattle. PMID 20301323. Retrieved 28 August 2022.
Mabb AM, Judson MC, Zylka MJ, Philpot BD (May 2011). "Angelman Syndrome: Insights into Genomic Imprinting and Neurodevelopmental Phenotypes". Trends Neurosci. 34 (6): 293–303. doi:10.1016/j.tins.2011.04.001. PMC 3116240. PMID 21592595.
Sidorov MS, Deck GM, Dolatshahi M, Thibert RL, Bird LM, Chu CJ, Philpot BD (2017-05-08). "Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis". Journal of Neurodevelopmental Disorders. 9: 17. doi:10.1186/s11689-017-9195-8. ISSN 1866-1955. PMC 5422949. PMID 28503211.
Key AP, Roth S, Jones D, Hunt-Hawkins H (2023). "Typical and atypical neural mechanisms support spoken word processing in Angelman syndrome". Brain and Language. 236. doi:10.1016/j.bandl.2022.105215. PMC 9839587. PMID 36502770.
Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y (2023). "Cortical and subcortical morphological alteration in Angelman syndrome". Journal of Neurodevelopmental Disorders. 15 (1): 7. doi:10.1186/s11689-022-09469-3. ISSN 1866-1955. PMC 9930225. PMID 36788499.
Key AP, Roth S, Venker C (11 October 2022). "Spoken language comprehension in children and adults with Angelman Syndrome". Journal of Communication Disorders. 100. doi:10.1016/j.jcomdis.2022.106272. PMC 9994640. PMID 36244082.

ghr.nlm.nih.gov

"Angelman syndrome". ghr.nlm.nih.gov. Genetics Home Reference, US National Institutes of Health. May 2015. Archived from the original on 27 August 2016. Retrieved 28 April 2017.

patents.google.com

WO2018104419A1, Buettelmann, Bernd; Cecere, Giuseppe & FASCHING, Bernhard et al., "New isoxazolyl ether derivatives as gaba a alpha5 pam", issued 2018-06-14

rarediseases.org

"Angelman Syndrome". rarediseases.org. National Organization for Rare Disorders (NORD). 2015. Archived from the original on 13 November 2016. Retrieved 28 April 2017.

semanticscholar.org

api.semanticscholar.org

Angelman H (1965). "'Puppet' Children: A report of three cases". Developmental Medicine & Child Neurology. 7 (6): 681–688. doi:10.1111/j.1469-8749.1965.tb07844.x. S2CID 53730099.
Cassidy SB, Dykens E (2000). "Prader–Willi and Angelman syndromes: sister imprinted disorders". Am J Med Genet. 97 (2): 136–146. doi:10.1002/1096-8628(200022)97:2<136::aid-ajmg5>3.0.co;2-v. PMID 11180221. S2CID 20832857.
Laan LA, Vein AA (2005). "Angelman syndrome: is there a characteristic EEG?". Brain and Development. 27 (2): 80–87. doi:10.1016/j.braindev.2003.09.013. ISSN 0387-7604. PMID 15668045. S2CID 5912.
Williams CA, Beaudet AL, Clayton-Smith J, et al. (2006). "Angelman syndrome 2005: updated consensus for diagnostic criteria". Am. J. Med. Genet. A. 140 (5): 413–8. doi:10.1002/ajmg.a.31074. PMID 16470747. S2CID 2449346.
Pearson E, Wilde L, Heald M, Royston R, Oliver C (November 2019). "Communication in Angelman syndrome: a scoping review". Developmental Medicine & Child Neurology. 61 (11): 1266–1274. doi:10.1111/dmcn.14257. ISSN 0012-1622. PMID 31074506. S2CID 149445749.
Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.

thefreedictionary.com

encyclopedia2.thefreedictionary.com

"Angelman syndrome". McGraw-Hill Dictionary of Scientific & Technical Terms. The McGraw-Hill Companies, Inc. 2003. Retrieved April 15, 2022 – via thefreedictionary.com.

medical-dictionary.thefreedictionary.com

"Angelman syndrome". American Heritage Medical Dictionary (2007 ed.). Houghton Mifflin Company. 2004. Retrieved April 15, 2022 – via thefreedictionary.com.

uzh.ch

zora.uzh.ch

Galassi FM, Armocida E, Rühli FJ (September 2016). "Angelman Syndrome in the Portrait of a Child With a Drawing by Giovanni F. Caroto" (PDF). JAMA Pediatrics. 170 (9): 831. doi:10.1001/jamapediatrics.2016.0581. PMID 27380555.

web.archive.org

"Angelman syndrome". Oxford English Dictionary. Archived from the original on June 17, 2020 – via Lexico.com.
"Angelman syndrome". ghr.nlm.nih.gov. Genetics Home Reference, US National Institutes of Health. May 2015. Archived from the original on 27 August 2016. Retrieved 28 April 2017.
"Angelman Syndrome". rarediseases.org. National Organization for Rare Disorders (NORD). 2015. Archived from the original on 13 November 2016. Retrieved 28 April 2017.
Wilson GN, Cooley WC (2000). Preventive Management of Children with Congenital Anomalies and Syndromes. Cambridge University Press. p. 193. ISBN 9780521776738. Archived from the original on 2017-11-05.
Kumar V, Abbas AK, Aster JC (2013). "Genetic and Pediatric Diseases". Robbins Basic Pathology. Elsevier Health Sciences. p. 244. ISBN 978-1437717815. Archived from the original on 2017-11-05. Retrieved 2022-04-15 – via Google Books.
"Facts about Angelman syndrome" (PDF). US: Angelman Syndrome Foundation. Archived from the original (PDF) on 2013-05-27. Retrieved 2012-09-29.
Williams C. "Harry Angelman and the History of AS". Stay informed. US: Angelman Syndrome Foundation. Archived from the original on 2011-02-06. Retrieved 2011-07-01.
"Superstar Colin tells of 'blessed' life with special needs child". Irish Independent. 15 October 2007. Archived from the original on 17 October 2007. Retrieved 15 October 2007.

wiley.com

onlinelibrary.wiley.com

Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.
>Didden R, Sigafoos J, Korzilius H, Baas A, Lancioni GE, O'Reilly MF, Curfs LM (2009). "Form and Function of Communicative Behaviors in Individuals with Angelman Syndrome". Journal of Applied Research in Intellectual Disabilities. 22 (6): 526–537. doi:10.1111/j.1468-3148.2009.00520.x. hdl:2066/77094.

worldcat.org

search.worldcat.org

Laan LA, Vein AA (2005). "Angelman syndrome: is there a characteristic EEG?". Brain and Development. 27 (2): 80–87. doi:10.1016/j.braindev.2003.09.013. ISSN 0387-7604. PMID 15668045. S2CID 5912.
Sidorov MS, Deck GM, Dolatshahi M, Thibert RL, Bird LM, Chu CJ, Philpot BD (2017-05-08). "Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis". Journal of Neurodevelopmental Disorders. 9: 17. doi:10.1186/s11689-017-9195-8. ISSN 1866-1955. PMC 5422949. PMID 28503211.
Pearson E, Wilde L, Heald M, Royston R, Oliver C (November 2019). "Communication in Angelman syndrome: a scoping review". Developmental Medicine & Child Neurology. 61 (11): 1266–1274. doi:10.1111/dmcn.14257. ISSN 0012-1622. PMID 31074506. S2CID 149445749.
Walz NC, Baranek GT (2006-07-01). "Sensory Processing Patterns in Persons With Angelman Syndrome". American Journal of Occupational Therapy. 60 (4): 472–479. doi:10.5014/ajot.60.4.472. ISSN 0272-9490. PMID 16915878.
Heald M, Adams D, Oliver C (2020). "Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes". Journal of Intellectual Disability Research. 64 (2): 117–130. doi:10.1111/jir.12702. hdl:10072/396330. ISSN 1365-2788. PMID 31828905. S2CID 209329797.
Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y (2023). "Cortical and subcortical morphological alteration in Angelman syndrome". Journal of Neurodevelopmental Disorders. 15 (1): 7. doi:10.1186/s11689-022-09469-3. ISSN 1866-1955. PMC 9930225. PMID 36788499.