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 *

175 related articles for article (PubMed ID: 36796507)

  • 1. Consensus recommendations on altered sensory functioning in Phelan-McDermid syndrome.
    Walinga M; Jesse S; Alhambra N; ; Van Buggenhout G
    Eur J Med Genet; 2023 May; 66(5):104726. PubMed ID: 36796507
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASD.
    Tavassoli T; Layton C; Levy T; Rowe M; George-Jones J; Zweifach J; Lurie S; Buxbaum JD; Kolevzon A; Siper PM
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34206779
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gait Abnormalities in Children with Phelan-McDermid Syndrome.
    Frank Y; Levy T; Lozano R; Friedman K; Underwood S; Kostic A; Walker H; Kolevzon A
    J Child Neurol; 2023 Dec; 38(13-14):665-671. PubMed ID: 37849292
    [No Abstract]   [Full Text] [Related]  

  • 4. Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.
    Cammarata-Scalisi F; Callea M; Martinelli D; Willoughby CE; Tadich AC; Araya Castillo M; Lacruz-Rengel MA; Medina M; Grimaldi P; Bertini E; Nevado J
    Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328058
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Sensory processing and adaptive behavior in Phelan-McDermid syndrome: a cross-sectional study.
    Serrada-Tejeda S; Cuadrado ML; Martínez-Piédrola RM; Máximo-Bocanegra N; Sánchez-Herrera-Baeza P; Camacho-Montaño LR; Pérez-de-Heredia-Torres M
    Eur J Pediatr; 2022 Aug; 181(8):3141-3152. PubMed ID: 35840778
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Brief Report: Sensory Reactivity in Children with Phelan-McDermid Syndrome.
    Mieses AM; Tavassoli T; Li E; Soorya L; Lurie S; Wang AT; Siper PM; Kolevzon A
    J Autism Dev Disord; 2016 Jul; 46(7):2508-13. PubMed ID: 26914612
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22.
    Koza SA; Tabet AC; Bonaglia MC; Andres S; Anderlid BM; Aten E; Stiefsohn D; ; Evans DG; van Ravenswaaij-Arts CMA; Kant SG
    Eur J Med Genet; 2023 Jul; 66(7):104773. PubMed ID: 37120077
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey.
    Landlust AM; Koza SA; Carbin M; Walinga M; Robert S; Cooke J; Vyshka K; ; van Balkom IDC; van Ravenswaaij-Arts C
    Eur J Med Genet; 2023 Jul; 66(7):104771. PubMed ID: 37120079
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome.
    Schön M; Lapunzina P; Nevado J; Mattina T; Gunnarsson C; Hadzsiev K; Verpelli C; Bourgeron T; Jesse S; van Ravenswaaij-Arts CMA; ; Hennekam RC
    Eur J Med Genet; 2023 Jul; 66(7):104754. PubMed ID: 37003575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations.
    Oberman LM; Boccuto L; Cascio L; Sarasua S; Kaufmann WE
    Orphanet J Rare Dis; 2015 Aug; 10():105. PubMed ID: 26306707
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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; 38(9):917-920. PubMed ID: 34487544
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Consensus recommendations on Epilepsy in Phelan-McDermid syndrome.
    de Coo IFM; Jesse S; Le TL; Sala C;
    Eur J Med Genet; 2023 Jun; 66(6):104746. PubMed ID: 36967043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phelan-McDermid Syndrome and SHANK3: Implications for Treatment.
    Costales JL; Kolevzon A
    Neurotherapeutics; 2015 Jul; 12(3):620-30. PubMed ID: 25894671
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome.
    van Eeghen AM; Stemkens D; Fernández-Fructuoso JR; Maruani A; Hadzsiev K; ; ; van Balkom IDC
    Eur J Med Genet; 2023 Jul; 66(7):104747. PubMed ID: 37003574
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Consensus recommendations on mental health issues in Phelan-McDermid syndrome.
    van Balkom IDC; Burdeus-Olavarrieta M; Cooke J; de Cuba AG; Turner A; ; Vogels A; Maruani A
    Eur J Med Genet; 2023 Jun; 66(6):104770. PubMed ID: 37085014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Phelan-McDermid syndrome: a classification system after 30 years of experience.
    Phelan K; Boccuto L; Powell CM; Boeckers TM; van Ravenswaaij-Arts C; Rogers RC; Sala C; Verpelli C; Thurm A; Bennett WE; Winrow CJ; Garrison SR; Toro R; Bourgeron T
    Orphanet J Rare Dis; 2022 Jan; 17(1):27. PubMed ID: 35093143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Behavioral Phenotyping of an Improved Mouse Model of Phelan-McDermid Syndrome with a Complete Deletion of the
    Drapeau E; Riad M; Kajiwara Y; Buxbaum JD
    eNeuro; 2018; 5(3):. PubMed ID: 30302388
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.