187 related articles for article (PubMed ID: 34569897)
1. Neuropsychological and ASD phenotypes in rare genetic syndromes: A critical review of the literature.
Bush L; Scott MN
Clin Neuropsychol; 2022 Jul; 36(5):993-1027. PubMed ID: 34569897
[TBL] [Abstract][Full Text] [Related]
2. Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison.
Lubbers K; Stijl EM; Dierckx B; Hagenaar DA; Ten Hoopen LW; Legerstee JS; de Nijs PFA; Rietman AB; Greaves-Lord K; Hillegers MHJ; Dieleman GC; Mous SE;
Front Psychiatry; 2022; 13():852208. PubMed ID: 35651825
[TBL] [Abstract][Full Text] [Related]
3. Autism Spectrum Disorder Symptoms in Infants with Fragile X Syndrome: A Prospective Case Series.
Hogan AL; Caravella KE; Ezell J; Rague L; Hills K; Roberts JE
J Autism Dev Disord; 2017 Jun; 47(6):1628-1644. PubMed ID: 28281129
[TBL] [Abstract][Full Text] [Related]
4. Melatonin as a Novel Interventional Candidate for Fragile X Syndrome with Autism Spectrum Disorder in Humans.
Won J; Jin Y; Choi J; Park S; Lee TH; Lee SR; Chang KT; Hong Y
Int J Mol Sci; 2017 Jun; 18(6):. PubMed ID: 28632163
[TBL] [Abstract][Full Text] [Related]
5. Double Genetic Hit: Fragile X Syndrome and Partial Deletion of Protein Patched Homolog 1 Antisense as Cause of Severe Autism Spectrum Disorder.
Saldarriaga W; Payán-Gómez C; González-Teshima LY; Rosa L; Tassone F; Hagerman RJ
J Dev Behav Pediatr; 2020 Dec; 41(9):724-728. PubMed ID: 32947579
[TBL] [Abstract][Full Text] [Related]
6. Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
Baker EK; Arpone M; Vera SA; Bretherton L; Ure A; Kraan CM; Bui M; Ling L; Francis D; Hunter MF; Elliott J; Rogers C; Field MJ; Cohen J; Maria LS; Faundes V; Curotto B; Morales P; Trigo C; Salas I; Alliende AM; Amor DJ; Godler DE
J Neurodev Disord; 2019 Dec; 11(1):41. PubMed ID: 31878865
[TBL] [Abstract][Full Text] [Related]
7. A cross-syndrome cohort comparison of sleep disturbance in children with Smith-Magenis syndrome, Angelman syndrome, autism spectrum disorder and tuberous sclerosis complex.
Trickett J; Heald M; Oliver C; Richards C
J Neurodev Disord; 2018 Mar; 10(1):9. PubMed ID: 29490614
[TBL] [Abstract][Full Text] [Related]
8. Autism Symptoms in Fragile X Syndrome.
Niu M; Han Y; Dy ABC; Du J; Jin H; Qin J; Zhang J; Li Q; Hagerman RJ
J Child Neurol; 2017 Sep; 32(10):903-909. PubMed ID: 28617074
[TBL] [Abstract][Full Text] [Related]
9. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Pollak RM; Murphy MM; Epstein MP; Zwick ME; Klaiman C; Saulnier CA; ; Mulle JG
Mol Autism; 2019; 10():30. PubMed ID: 31346402
[TBL] [Abstract][Full Text] [Related]
10. Predictors, Parental Views, and Concordance Across Diagnostic Sources of Autism in Male Youth with Fragile X Syndrome: Clinical Best Estimate and Community Diagnoses.
Klusek J; Will E; Moser C; Hills K; Thurman AJ; Abbeduto L; Roberts JE
Res Child Adolesc Psychopathol; 2023 Jul; 51(7):989-1004. PubMed ID: 36867382
[TBL] [Abstract][Full Text] [Related]
11. Recurrent missense variant in the nuclear export signal of FMR1 associated with FXS-like phenotype including intellectual disability, ASD, facial abnormalities.
Mangano GD; Fontana A; Salpietro V; Antona V; Mangano GR; Nardello R
Eur J Med Genet; 2022 Mar; 65(3):104441. PubMed ID: 35091116
[TBL] [Abstract][Full Text] [Related]
12. Gaze avoidance and perseverative language in fragile X syndrome and autism spectrum disorder: brief report.
Friedman L; Sterling A; Barton-Hulsey A
Dev Neurorehabil; 2018 Feb; 21(2):137-140. PubMed ID: 29333915
[TBL] [Abstract][Full Text] [Related]
13. Atypical language characteristics and trajectories in children with 22q11.2 deletion syndrome.
Van Den Heuvel E; Manders E; Swillen A; Zink I
J Commun Disord; 2018; 75():37-56. PubMed ID: 30005318
[TBL] [Abstract][Full Text] [Related]
14. Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach.
Bozhilova N; Welham A; Adams D; Bissell S; Bruining H; Crawford H; Eden K; Nelson L; Oliver C; Powis L; Richards C; Waite J; Watson P; Rhys H; Wilde L; Woodcock K; Moss J
Mol Autism; 2023 Jan; 14(1):3. PubMed ID: 36639821
[TBL] [Abstract][Full Text] [Related]
15. The use of demonstratives and personal pronouns in fragile X syndrome and autism spectrum disorder.
Friedman L; Lorang E; Sterling A
Clin Linguist Phon; 2019; 33(5):420-436. PubMed ID: 30346853
[TBL] [Abstract][Full Text] [Related]
16. Prospective study of autism phenomenology and the behavioural phenotype of Phelan-McDermid syndrome: comparison to fragile X syndrome, Down syndrome and idiopathic autism spectrum disorder.
Richards C; Powis L; Moss J; Stinton C; Nelson L; Oliver C
J Neurodev Disord; 2017 Nov; 9(1):37. PubMed ID: 29126394
[TBL] [Abstract][Full Text] [Related]
17. Autism spectrum disorders in genetic syndromes: implications for diagnosis, intervention and understanding the wider autism spectrum disorder population.
Moss J; Howlin P
J Intellect Disabil Res; 2009 Oct; 53(10):852-73. PubMed ID: 19708861
[TBL] [Abstract][Full Text] [Related]
18. Systematic Review: Emotion Dysregulation in Syndromic Causes of Intellectual and Developmental Disabilities.
Shaffer RC; Reisinger DL; Schmitt LM; Lamy M; Dominick KC; Smith EG; Coffman MC; Esbensen AJ
J Am Acad Child Adolesc Psychiatry; 2023 May; 62(5):518-557. PubMed ID: 36007813
[TBL] [Abstract][Full Text] [Related]
19. Cholesterol alterations in fragile X syndrome, autism spectrum disorders and other neurodevelopmental disorders.
Benachenhou S; Laroui A; Dionne O; Rojas D; Toupin A; Çaku A
Int Rev Neurobiol; 2023; 173():115-139. PubMed ID: 37993175
[TBL] [Abstract][Full Text] [Related]
20. Epilepsy in four genetically determined syndromes of intellectual disability.
Leung HT; Ring H
J Intellect Disabil Res; 2013 Jan; 57(1):3-20. PubMed ID: 22142420
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
