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Journal Abstract Search

215 related items for PubMed ID: 35093163

  • 21. Phelan-McDermid Syndrome and SHANK3: Implications for Treatment.
    Costales JL, Kolevzon A.
    Neurotherapeutics; 2015 Jul; 12(3):620-30. PubMed ID: 25894671
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  • 22. Psychiatric illness and regression in individuals with Phelan-McDermid syndrome.
    Kohlenberg TM, Trelles MP, McLarney B, Betancur C, Thurm A, Kolevzon A.
    J Neurodev Disord; 2020 Feb 12; 12(1):7. PubMed ID: 32050889
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  • 26. Evidence for common mechanisms of pathology between SHANK3 and other genes of Phelan-McDermid syndrome.
    Mitz AR, Boccuto L, Thurm A.
    Clin Genet; 2024 May 12; 105(5):459-469. PubMed ID: 38414139
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  • 28. Stratification of a Phelan-McDermid Syndrome Population Based on Their Response to Human Growth Hormone and Insulin-like Growth Factor.
    Moffitt BA, Sarasua SM, Ivankovic D, Ward LD, Valentine K, Bennett WE, Rogers C, Phelan K, Boccuto L.
    Genes (Basel); 2023 Feb 15; 14(2):. PubMed ID: 36833418
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  • 30. [Advance of research on Phelan-McDermid syndrome].
    Li S, Xi K, Liu T, Zhang Y, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Sep 10; 38(9):917-920. PubMed ID: 34487544
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  • 31. Psychometric Study of the Social Responsiveness Scale in Phelan-McDermid Syndrome.
    Gergoudis K, Weinberg A, Templin J, Farmer C, Durkin A, Weissman J, Siper P, Foss-Feig J, Del Pilar Trelles M, Bernstein JA, Buxbaum JD, Berry-Kravis E, Powell CM, Sahin M, Soorya L, Thurm A, Kolevzon A, Developmental Synaptopathies ConsortiumDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA..
    Autism Res; 2020 Aug 10; 13(8):1383-1396. PubMed ID: 32406614
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  • 32. Transcriptional signatures of participant-derived neural progenitor cells and neurons implicate altered Wnt signaling in Phelan-McDermid syndrome and autism.
    Breen MS, Browne A, Hoffman GE, Stathopoulos S, Brennand K, Buxbaum JD, Drapeau E.
    Mol Autism; 2020 Jun 19; 11(1):53. PubMed ID: 32560742
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  • 39. Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes.
    Ricciardello A, Tomaiuolo P, Persico AM.
    Am J Med Genet A; 2021 Jul 19; 185(7):2211-2233. PubMed ID: 33949759
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