These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 35603006)

  • 1. Case study: organizing outpatient pharmacological treatment of bipolar disorder in autism, intellectual disability and Phelan-McDermid syndrome (22q13.3 deletion syndrome).
    Rysstad AL; Kildahl AN; Skavhaug JO; Dønnum MS; Helverschou SB
    Int J Dev Disabil; 2022; 68(3):378-387. PubMed ID: 35603006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder.
    Görker I; Gürkan H; Demir Ulusal S; Atlı E; Ikbal Atlı E
    Balkan J Med Genet; 2016 Dec; 19(2):85-90. PubMed ID: 28289594
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case.
    Samogy-Costa CI; Varella-Branco E; Monfardini F; Ferraz H; Fock RA; Barbosa RHA; Pessoa ALS; Perez ABA; Lourenço N; Vibranovski M; Krepischi A; Rosenberg C; Passos-Bueno MR
    J Neurodev Disord; 2019 Jul; 11(1):13. PubMed ID: 31319798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.
    Xu N; Lv H; Yang T; Du X; Sun Y; Xiao B; Fan Y; Luo X; Zhan Y; Wang L; Li F; Yu Y
    Orphanet J Rare Dis; 2020 Nov; 15(1):335. PubMed ID: 33256793
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report.
    Khalifa Y; Hassan HY; Weise A; Liehr T; Alkhayyat H
    Mol Cytogenet; 2022 Dec; 15(1):52. PubMed ID: 36528601
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterisation of the clinical phenotype in Phelan-McDermid syndrome.
    Burdeus-Olavarrieta M; San José-Cáceres A; García-Alcón A; González-Peñas J; Hernández-Jusdado P; Parellada-Redondo M
    J Neurodev Disord; 2021 Jul; 13(1):26. PubMed ID: 34246244
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype?
    Verhoeven WM; Egger JI; Willemsen MH; de Leijer GJ; Kleefstra T
    Neuropsychiatr Dis Treat; 2012; 8():175-9. PubMed ID: 22570549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phelan McDermid Syndrome: From Genetic Discoveries to Animal Models and Treatment.
    Harony-Nicolas H; De Rubeis S; Kolevzon A; Buxbaum JD
    J Child Neurol; 2015 Dec; 30(14):1861-70. PubMed ID: 26350728
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
    Kolevzon A; Angarita B; Bush L; Wang AT; Frank Y; Yang A; Rapaport R; Saland J; Srivastava S; Farrell C; Edelmann LJ; Buxbaum JD
    J Neurodev Disord; 2014; 6(1):39. PubMed ID: 25784960
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome.
    Droogmans G; Swillen A; Van Buggenhout G
    Mol Syndromol; 2020 Jan; 10(6):294-305. PubMed ID: 32021603
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion syndrome 22q13: what the dentist should know to manage children with Phelan-McDermid syndrome effectively.
    Ivanoff C; Ivanoff AE
    J Tenn Dent Assoc; 2014; 94(1):15-8; quiz 19-20. PubMed ID: 25241497
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phelan-McDermid syndrome: clinical report of a 70-year-old woman.
    Verhoeven WM; Egger JI; Cohen-Snuijf R; Kant SG; de Leeuw N
    Am J Med Genet A; 2013 Jan; 161A(1):158-61. PubMed ID: 23166010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Co-occurrence of Metachromatic Leukodystrophy in Phelan-McDermid Syndrome.
    Mingbunjerdsuk D; Wong M; Bozarth X; Sun A
    J Child Neurol; 2021 Feb; 36(2):148-151. PubMed ID: 32991243
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genomic evaluation of a Chinese patient with a novel deletion associated with Phelan-McDermid syndrome.
    Lei D; Li S; Banerjee S; Zhang H; Li C; Hou S; Chen D; Yan H; Li H; Peng HH; Liu S; Zhang X; Peng Z; Wang J; Yang H; Huang H; Wu J
    Oncotarget; 2016 Dec; 7(49):80327-80335. PubMed ID: 27741506
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype.
    Ponson L; Gomot M; Blanc R; Barthelemy C; Roux S; Munnich A; Romana S; Aguillon-Hernandez N; Malan V; Bonnet-Brilhault F
    Transl Psychiatry; 2018 Aug; 8(1):146. PubMed ID: 30089781
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study.
    Guillory SB; Baskett VZ; Grosman HE; McLaughlin CS; Isenstein EL; Wilkinson E; Weissman J; Britvan B; Trelles MP; Halpern DB; Buxbaum JD; Siper PM; Wang AT; Kolevzon A; Foss-Feig JH
    J Neurodev Disord; 2021 Dec; 13(1):58. PubMed ID: 34863106
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Efficacy and Safety of Q10 Ubiquinol With Vitamins B and E in Neurodevelopmental Disorders: A Retrospective Chart Review.
    Cucinotta F; Ricciardello A; Turriziani L; Mancini A; Keller R; Sacco R; Persico AM
    Front Psychiatry; 2022; 13():829516. PubMed ID: 35308885
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and
    Cooke J; Molloy CJ; Cáceres ASJ; Dinneen T; Bourgeron T; Murphy D; Gallagher L; Loth E
    Front Neurosci; 2022; 16():806990. PubMed ID: 35250452
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Zinc deficiency and supplementation in autism spectrum disorder and Phelan-McDermid syndrome.
    Alsufiani HM; Alkhanbashi AS; Laswad NAB; Bakhadher KK; Alghamdi SA; Tayeb HO; Tarazi FI
    J Neurosci Res; 2022 Apr; 100(4):970-978. PubMed ID: 35114017
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 185(7):2211-2233. PubMed ID: 33949759
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.