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Page 1
Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome.
Srivastava S, Scherrer B, Prohl AK, Filip-Dhima R, Kapur K, Kolevzon A, Buxbaum JD, Berry-Kravis E, Soorya L, Thurm A, Powell CM, Bernstein JA, Warfield SK, Sahin M; Developmental Synaptopathies Consortium. Srivastava S, et al. Among authors: kolevzon a. Pediatr Neurol. 2019 Jan;90:37-43. doi: 10.1016/j.pediatrneurol.2018.09.008. Epub 2018 Sep 21. Pediatr Neurol. 2019. PMID: 30396833 Free PMC article.
Familial symptom domains in monozygotic siblings with autism.
Kolevzon A, Smith CJ, Schmeidler J, Buxbaum JD, Silverman JM. Kolevzon A, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):76-81. doi: 10.1002/ajmg.b.30011. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274045
Advancing paternal age and simplex autism.
Puleo CM, Schmeidler J, Reichenberg A, Kolevzon A, Soorya LV, Buxbaum JD, Silverman JM. Puleo CM, et al. Among authors: kolevzon a. Autism. 2012 Jul;16(4):367-80. doi: 10.1177/1362361311427154. Epub 2011 Dec 16. Autism. 2012. PMID: 22180389
Functional deficits of the attentional networks in autism.
Fan J, Bernardi S, Van Dam NT, Anagnostou E, Gu X, Martin L, Park Y, Liu X, Kolevzon A, Soorya L, Grodberg D, Hollander E, Hof PR. Fan J, et al. Among authors: kolevzon a. Brain Behav. 2012 Sep;2(5):647-60. doi: 10.1002/brb3.90. Epub 2012 Aug 27. Brain Behav. 2012. PMID: 23139910 Free PMC article.
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Soorya L, Kolevzon A, Zweifach J, Lim T, Dobry Y, Schwartz L, Frank Y, Wang AT, Cai G, Parkhomenko E, Halpern D, Grodberg D, Angarita B, Willner JP, Yang A, Canitano R, Chaplin W, Betancur C, Buxbaum JD. Soorya L, et al. Among authors: kolevzon a. Mol Autism. 2013 Jun 11;4(1):18. doi: 10.1186/2040-2392-4-18. Mol Autism. 2013. PMID: 23758760 Free PMC article.
141 results