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6. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized? Kim HJ; Cho HJ; Jin DK; Kwon EK; Ki CS; Kim JW; Kim SH Clin Genet; 2004 Oct; 66(4):368-72. PubMed ID: 15355442 [No Abstract] [Full Text] [Related]
7. Scoliosis associated with Prader-Willi syndrome. Yamada K; Miyamoto K; Hosoe H; Mizutani M; Shimizu K Spine J; 2007; 7(3):345-8. PubMed ID: 17482119 [TBL] [Abstract][Full Text] [Related]
8. Brain developmental abnormalities in Prader-Willi syndrome detected by diffusion tensor imaging. Yamada K; Matsuzawa H; Uchiyama M; Kwee IL; Nakada T Pediatrics; 2006 Aug; 118(2):e442-8. PubMed ID: 16882785 [TBL] [Abstract][Full Text] [Related]
9. Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders. Vogels A; Van Den Ende J; Keymolen K; Mortier G; Devriendt K; Legius E; Fryns JP Eur J Hum Genet; 2004 Mar; 12(3):238-40. PubMed ID: 14679397 [TBL] [Abstract][Full Text] [Related]
12. A photographic study: the natural history of Prader-Willi syndrome. Char F J Clin Dysmorphol; 1984; 2(1):2-4. PubMed ID: 6587012 [No Abstract] [Full Text] [Related]
13. Diversion tactics. Lowenstein L Nurs Times; 1996 May 22-28; 92(21):42-3. PubMed ID: 8716286 [No Abstract] [Full Text] [Related]
14. The genetics, diagnosis, and management of Prader-Willi syndrome. Nativio DG J Pediatr Health Care; 2002; 16(6):298-303. PubMed ID: 12436099 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Expressive language in persons with Prader-Willi syndrome. Van Borsel J; Defloor T; Curfs LM Genet Couns; 2007; 18(1):17-28. PubMed ID: 17515298 [TBL] [Abstract][Full Text] [Related]
17. Dietary intervention in the first four years prevents abnormal weight gain but negatively affects height development in Prader-Willi syndrome. Schmidt H; Schwarz HP; Enders A Acta Paediatr; 2001 Apr; 90(4):468-9. PubMed ID: 11332946 [No Abstract] [Full Text] [Related]
18. Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation. Alliende A; Curotto B; Santa Maria L; Cortés F; Aracena M Am J Med Genet; 2002 Dec; 113(3):307-8. PubMed ID: 12439903 [No Abstract] [Full Text] [Related]
19. 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]
20. Quality of life assessment in a sample of patients affected by Prader-Willi syndrome. Caliandro P; Grugni G; Padua L; Kodra Y; Tonali P; Gargantini L; Ragusa L; Crinò A; Taruscio D J Paediatr Child Health; 2007 Dec; 43(12):826-30. PubMed ID: 17803668 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]