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PUBMED FOR HANDHELDS

Journal Abstract Search


331 related items for PubMed ID: 25597928

  • 1. The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views.
    Reilly C, Murtagh L, Senior J.
    J Genet Couns; 2015 Oct; 24(5):851-61. PubMed ID: 25597928
    [Abstract] [Full Text] [Related]

  • 2. A comparative study of educational provision for children with neurogenetic syndromes: parent and teacher survey.
    Reilly C, Senior J, Murtagh L.
    J Intellect Disabil Res; 2015 Dec; 59(12):1094-107. PubMed ID: 26780264
    [Abstract] [Full Text] [Related]

  • 3. Stress, locus of control, and family cohesion and adaptability in parents of children with Down, Williams, Fragile X, and Prader-Willi syndromes.
    Lanfranchi S, Vianello R.
    Am J Intellect Dev Disabil; 2012 May; 117(3):207-24. PubMed ID: 22716263
    [Abstract] [Full Text] [Related]

  • 4. The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader-Willi Syndromes.
    Royston R, Oliver C, Howlin P, Dosse A, Armitage P, Moss J, Waite J.
    J Autism Dev Disord; 2020 Mar; 50(3):893-903. PubMed ID: 31802317
    [Abstract] [Full Text] [Related]

  • 5. ASD, ADHD, mental health conditions and psychopharmacology in neurogenetic syndromes: parent survey.
    Reilly C, Senior J, Murtagh L.
    J Intellect Disabil Res; 2015 Apr; 59(4):307-18. PubMed ID: 24965264
    [Abstract] [Full Text] [Related]

  • 6. Children with Prader-Willi syndrome vs. Williams syndrome: indirect effects on parents during a jigsaw puzzle task.
    Ly TM, Hodapp RM.
    J Intellect Disabil Res; 2005 Dec; 49(Pt 12):929-39. PubMed ID: 16287481
    [Abstract] [Full Text] [Related]

  • 7. Cognitive and behavioral heterogeneity in genetic syndromes.
    Pegoraro LF, Steiner CE, Celeri EH, Banzato CE, Dalgalarrondo P.
    J Pediatr (Rio J); 2014 Dec; 90(2):155-60. PubMed ID: 24184301
    [Abstract] [Full Text] [Related]

  • 8. Behavioural phenotypes and special educational needs: is aetiology important in the classroom?
    Reilly C.
    J Intellect Disabil Res; 2012 Oct; 56(10):929-46. PubMed ID: 22471356
    [Abstract] [Full Text] [Related]

  • 9. [Social cognition in children with neurogenetic syndromes: A literature review].
    Morel A, Demily C.
    Arch Pediatr; 2017 Aug; 24(8):757-765. PubMed ID: 28668215
    [Abstract] [Full Text] [Related]

  • 10. Elimination disorders in persons with Prader-Willi and Fragile-X syndromes.
    Equit M, Piro-Hussong A, Niemczyk J, Curfs L, von Gontard A.
    Neurourol Urodyn; 2013 Sep; 32(7):986-92. PubMed ID: 23239431
    [Abstract] [Full Text] [Related]

  • 11. Social-sexual education in adolescents with behavioral neurogenetic syndromes.
    Plaks M, Argaman R, Stawski M, Qwiat T, Polak D, Gothelf D.
    Isr J Psychiatry Relat Sci; 2010 Sep; 47(2):118-24. PubMed ID: 20733254
    [Abstract] [Full Text] [Related]

  • 12. The impact of Prader-Willi syndrome on the family's quality of life and caregiving, and the unaffected siblings' psychosocial adjustment.
    Mazaheri MM, Rae-Seebach RD, Preston HE, Schmidt M, Kountz-Edwards S, Field N, Cassidy S, Packman W.
    J Intellect Disabil Res; 2013 Sep; 57(9):861-73. PubMed ID: 23057501
    [Abstract] [Full Text] [Related]

  • 13. Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome.
    van Lieshout CF, De Meyer RE, Curfs LM, Fryns JP.
    J Child Psychol Psychiatry; 1998 Jul; 39(5):699-710. PubMed ID: 9690933
    [Abstract] [Full Text] [Related]

  • 14. A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.
    Goodwin J, Schoch K, Shashi V, Hooper SR, Morad O, Zalevsky M, Gothelf D, Campbell LE.
    J Intellect Disabil Res; 2015 May; 59(5):474-86. PubMed ID: 25059276
    [Abstract] [Full Text] [Related]

  • 15. Parent training education program: a pilot study, involving families of children with Prader-Willi syndrome.
    Kodra Y, Kondili LA, Ferraroni A, Serra MA, Caretto F, Ricci MA, Taruscio D.
    Ann Ist Super Sanita; 2016 May; 52(3):428-433. PubMed ID: 27698302
    [Abstract] [Full Text] [Related]

  • 16. Evaluating the challenges and needs of parents caring for children with Williams syndrome: A preliminary study from Poland.
    Domaradzki J, Walkowiak D.
    Res Dev Disabil; 2024 Feb; 145():104669. PubMed ID: 38215502
    [Abstract] [Full Text] [Related]

  • 17. Personality profiles of youngsters with velo-cardio-facial syndrome.
    Prinzie P, Swillen A, Vogels A, Kockuyt V, Curfs L, Haselager G, Hellinckx W, Devriendt K, Onghena P, Van Lieshout CF, Fryns JP.
    Genet Couns; 2002 Feb; 13(3):265-80. PubMed ID: 12416634
    [Abstract] [Full Text] [Related]

  • 18. Behavioral phenotypes of genetic syndromes with intellectual disability: comparison of adaptive profiles.
    Di Nuovo S, Buono S.
    Psychiatry Res; 2011 Oct 30; 189(3):440-5. PubMed ID: 21507490
    [Abstract] [Full Text] [Related]

  • 19. The developmental trajectory of disruptive behavior in Down syndrome, fragile X syndrome, Prader-Willi syndrome and Williams syndrome.
    Rice LJ, Gray KM, Howlin P, Taffe J, Tonge BJ, Einfeld SL.
    Am J Med Genet C Semin Med Genet; 2015 Jun 30; 169(2):182-7. PubMed ID: 25983069
    [Abstract] [Full Text] [Related]

  • 20. Brief Report: Challenging Behaviors in Toddlers and Preschoolers with Angelman, Prader-Willi, and Williams Syndromes.
    Neo WS, Tonnsen BL.
    J Autism Dev Disord; 2019 Apr 30; 49(4):1717-1726. PubMed ID: 30542941
    [Abstract] [Full Text] [Related]


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