452 related articles for article (PubMed ID: 17435464)
1. The Prader-Willi phenotype of fragile X syndrome.
Nowicki ST; Tassone F; Ono MY; Ferranti J; Croquette MF; Goodlin-Jones B; Hagerman RJ
J Dev Behav Pediatr; 2007 Apr; 28(2):133-8. PubMed ID: 17435464
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
de Vries BB; Fryns JP; Butler MG; Canziani F; Wesby-van Swaay E; van Hemel JO; Oostra BA; Halley DJ; Niermeijer MF
J Med Genet; 1993 Sep; 30(9):761-6. PubMed ID: 8411072
[TBL] [Abstract][Full Text] [Related]
3. [Hair root fragile X mental retardation protein assay for the diagnosis of fragile X syndrome].
Luo XF; Zhong JM; Zhang XZ; Zou Y; Chen Y; Wu HP; Yu XY
Zhongguo Dang Dai Er Ke Za Zhi; 2009 Oct; 11(10):817-20. PubMed ID: 19849940
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Nishimura Y; Martin CL; Vazquez-Lopez A; Spence SJ; Alvarez-Retuerto AI; Sigman M; Steindler C; Pellegrini S; Schanen NC; Warren ST; Geschwind DH
Hum Mol Genet; 2007 Jul; 16(14):1682-98. PubMed ID: 17519220
[TBL] [Abstract][Full Text] [Related]
5. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
[TBL] [Abstract][Full Text] [Related]
6. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
[TBL] [Abstract][Full Text] [Related]
7. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
Wiriyaukaradecha S; Patmasiriwat P; Wasant P; Tantiniti P
Southeast Asian J Trop Med Public Health; 2003 Dec; 34(4):881-6. PubMed ID: 15115105
[TBL] [Abstract][Full Text] [Related]
8. Neonatal diagnosis of Prader-Willi syndrome and its implications.
Greenberg F; Elder FF; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):845-56. PubMed ID: 3688023
[TBL] [Abstract][Full Text] [Related]
9. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
Varela MC; Simões-Sato AY; Kim CA; Bertola DR; De Castro CI; Koiffmann CP
Eur J Med Genet; 2006; 49(4):298-305. PubMed ID: 16829351
[TBL] [Abstract][Full Text] [Related]
10. Neonatal presentation of Prader Willi sindrome. Personal records.
Maggio MC; Corsello M; Piccione M; Piro E; Giuffrè M; Liotta A
Minerva Pediatr; 2007 Dec; 59(6):817-23. PubMed ID: 17978792
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. Water intake and risk of hyponatraemia in Prader-Willi syndrome.
Akefeldt A
J Intellect Disabil Res; 2009 Jun; 53(6):521-8. PubMed ID: 19302470
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
14. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
[TBL] [Abstract][Full Text] [Related]
15. Altered expression of Autism-associated genes in the brain of Fragile X mouse model.
Zhang A; Shen CH; Ma SY; Ke Y; El Idrissi A
Biochem Biophys Res Commun; 2009 Feb; 379(4):920-3. PubMed ID: 19138667
[TBL] [Abstract][Full Text] [Related]
16. [Prader-Willi syndrome in 22-year-old man--case study].
Kardas P; Adamiak-Kardas M
Wiad Lek; 2001; 54(11-12):709-14. PubMed ID: 11928560
[TBL] [Abstract][Full Text] [Related]
17. Molecular diagnosis of Prader-Willi syndrome.
Pangkanon S
J Med Assoc Thai; 2003 Aug; 86 Suppl 3():S510-6. PubMed ID: 14700141
[TBL] [Abstract][Full Text] [Related]
18. Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
Baker EK; Arpone M; Aliaga SM; Bretherton L; Kraan CM; Bui M; Slater HR; Ling L; Francis D; Hunter MF; Elliott J; Rogers C; Field M; Cohen J; Cornish K; Santa Maria L; Faundes V; Curotto B; Morales P; Trigo C; Salas I; Alliende AM; Amor DJ; Godler DE
Mol Autism; 2019; 10():21. PubMed ID: 31073396
[TBL] [Abstract][Full Text] [Related]
19. The fragile X syndrome: exploring its molecular basis and seeking a treatment.
Bardoni B; Davidovic L; Bensaid M; Khandjian EW
Expert Rev Mol Med; 2006 Apr; 8(8):1-16. PubMed ID: 16626504
[TBL] [Abstract][Full Text] [Related]
20. Social behavior phenotypes in fragile X syndrome, autism, and the Fmr1 knockout mouse: theoretical comment on McNaughton et al. (2008).
Brodkin ES
Behav Neurosci; 2008 Apr; 122(2):483-9. PubMed ID: 18410188
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]