170 related articles for article (PubMed ID: 24850752)
1. Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases.
Ogata H; Ihara H; Murakami N; Gito M; Kido Y; Nagai T
Am J Med Genet A; 2014 Sep; 164A(9):2180-6. PubMed ID: 24850752
[TBL] [Abstract][Full Text] [Related]
2. Gender Differences in the Behavioral Symptom Severity of Prader-Willi Syndrome.
Gito M; Ihara H; Ogata H; Sayama M; Murakami N; Nagai T; Ayabe T; Oto Y; Shimoda K
Behav Neurol; 2015; 2015():294127. PubMed ID: 26633919
[TBL] [Abstract][Full Text] [Related]
3. QOL in caregivers of Japanese patients with Prader-Willi syndrome with reference to age and genotype.
Ihara H; Ogata H; Sayama M; Kato A; Gito M; Murakami N; Kido Y; Nagai T
Am J Med Genet A; 2014 Sep; 164A(9):2226-31. PubMed ID: 24953026
[TBL] [Abstract][Full Text] [Related]
4. Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
Veltman MW; Thompson RJ; Roberts SE; Thomas NS; Whittington J; Bolton PF
Eur Child Adolesc Psychiatry; 2004 Feb; 13(1):42-50. PubMed ID: 14991431
[TBL] [Abstract][Full Text] [Related]
5. Aberrant White Matter Microstructure in Children and Adolescents With the Subtype of Prader-Willi Syndrome at High Risk for Psychosis.
Lukoshe A; van den Bosch GE; van der Lugt A; Kushner SA; Hokken-Koelega AC; White T
Schizophr Bull; 2017 Sep; 43(5):1090-1099. PubMed ID: 28510708
[TBL] [Abstract][Full Text] [Related]
6. Brain-stem serotonin transporter availability in maternal uniparental disomy and deletion Prader-Willi syndrome.
Krishnadas R; Cooper SA; Nicol A; Pimlott S; Soni S; Holland AJ; McArthur L; Cavanagh J
Br J Psychiatry; 2018 Jan; 212(1):57-58. PubMed ID: 29433608
[TBL] [Abstract][Full Text] [Related]
7. Autistic, Aberrant, and Food-Related Behaviors in Adolescents and Young Adults with Prader-Willi Syndrome: The Effects of Age and Genotype.
Ishii A; Ihara H; Ogata H; Sayama M; Gito M; Murakami N; Ayabe T; Oto Y; Takahashi A; Nagai T
Behav Neurol; 2017; 2017():4615451. PubMed ID: 29440778
[TBL] [Abstract][Full Text] [Related]
8. Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
Milner KM; Craig EE; Thompson RJ; Veltman MW; Thomas NS; Roberts S; Bellamy M; Curran SR; Sporikou CM; Bolton PF
J Child Psychol Psychiatry; 2005 Oct; 46(10):1089-96. PubMed ID: 16178933
[TBL] [Abstract][Full Text] [Related]
9. Social responsiveness and competence in Prader-Willi syndrome: direct comparison to autism spectrum disorder.
Dimitropoulos A; Ho A; Feldman B
J Autism Dev Disord; 2013 Jan; 43(1):103-13. PubMed ID: 22576167
[TBL] [Abstract][Full Text] [Related]
10. Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD).
Heseding H; Jahn K; Brändl B; Haase A; Shum IO; Kohrn T; Bleich S; Frieling H; Martin U; Müller FJ; Wunderlich S; Deest M
Stem Cell Res; 2023 Sep; 71():103143. PubMed ID: 37343429
[TBL] [Abstract][Full Text] [Related]
11. Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study.
Bennett JA; Hodgetts S; Mackenzie ML; Haqq AM; Zwaigenbaum L
Int J Mol Sci; 2017 Feb; 18(3):. PubMed ID: 28264487
[TBL] [Abstract][Full Text] [Related]
12. Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature.
Rosenberg AGW; Wellink CM; Tellez Garcia JM; Pellikaan K; Van Abswoude DH; Davidse K; Van Zutven LJCM; Brüggenwirth HT; Resnick JL; Van der Lely AJ; De Graaff LCG
J Clin Med; 2022 Jul; 11(14):. PubMed ID: 35887798
[TBL] [Abstract][Full Text] [Related]
13. Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients.
Promkan M; Teingtat S; Stheinkijkarnchai A; Wasant P; Patmasiriwat P
Clin Chem Lab Med; 2007; 45(8):972-80. PubMed ID: 17867985
[TBL] [Abstract][Full Text] [Related]
14. Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.
Dimitropoulos A; Ferranti A; Lemler M
J Commun Disord; 2013; 46(2):193-201. PubMed ID: 23295077
[TBL] [Abstract][Full Text] [Related]
15. Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
Bennett JA; Germani T; Haqq AM; Zwaigenbaum L
Am J Med Genet A; 2015 Dec; 167A(12):2936-44. PubMed ID: 26331980
[TBL] [Abstract][Full Text] [Related]
16. Impaired theory of mind and symptoms of Autism Spectrum Disorder in children with Prader-Willi syndrome.
Lo ST; Siemensma E; Collin P; Hokken-Koelega A
Res Dev Disabil; 2013 Sep; 34(9):2764-73. PubMed ID: 23792373
[TBL] [Abstract][Full Text] [Related]
17. Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Veltman MW; Craig EE; Bolton PF
Psychiatr Genet; 2005 Dec; 15(4):243-54. PubMed ID: 16314754
[TBL] [Abstract][Full Text] [Related]
18. Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.
Yang L; Zhan GD; Ding JJ; Wang HJ; Ma D; Huang GY; Zhou WH
PLoS One; 2013; 8(8):e72640. PubMed ID: 23967326
[TBL] [Abstract][Full Text] [Related]
19. Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controls.
Descheemaeker MJ; Govers V; Vermeulen P; Fryns JP
Am J Med Genet A; 2006 Jun; 140(11):1136-42. PubMed ID: 16646032
[TBL] [Abstract][Full Text] [Related]
20. Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
Whittington JE; Butler JV; Holland AJ
Eur J Hum Genet; 2007 Jan; 15(1):127-30. PubMed ID: 16957680
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]