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26. [Report of case of Prader-Willi syndrome]. Visco G; Ughi M; Trevenzoli G Pediatr Med Chir; 1999; 21(3):149-50. PubMed ID: 10687166 [TBL] [Abstract][Full Text] [Related]
28. [Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis]. Scommegna S; Zollino M; Paolone G Pediatr Med Chir; 2001; 23(3-4):191-6. PubMed ID: 11723857 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. [Retinopapillary alterations during a neuro-endocrine syndrome of the Willi-Prader-Labardt type]. Bonn G; Dollfus MA; Polliot L; Richard M Bull Soc Ophtalmol Fr; 1971; 71(9):847-51. PubMed ID: 5151027 [No Abstract] [Full Text] [Related]
34. Body mass index in children with Prader-Willi Syndrome during human growth hormone therapy: a real world situation. Dewan T; Chanoine JP J Pediatr; 2009 May; 154(5):777-8; author reply 779. PubMed ID: 19364570 [No Abstract] [Full Text] [Related]
35. [Studies of palm and finger dermatoglyphics in the Prader-Labhardt-Willi syndrome]. Dziuba P Pediatr Pol; 1972 Jul; 47(7):879-82. PubMed ID: 5054577 [No Abstract] [Full Text] [Related]
36. [Torsion of the large omentum in Prader-Willi syndrome]. Bassetti S; Donati D; Buetti L Schweiz Med Wochenschr; 1995 Jun; 125(22):1089-91. PubMed ID: 7784871 [TBL] [Abstract][Full Text] [Related]
37. [Prader-Willi syndrome. Treatment with growth hormone in 2 cases]. Youlton R Rev Med Chil; 2001 Oct; 129(10):1186-90. PubMed ID: 11775347 [TBL] [Abstract][Full Text] [Related]
38. Focal segmental glomerulosclerosis in a patient with Prader-Willi syndrome. Mochizuki H; Joh K; Matsuyama N; Imadachi A; Usui N; Eto Y Clin Nephrol; 2000 Mar; 53(3):212-5. PubMed ID: 10749301 [TBL] [Abstract][Full Text] [Related]
39. Prader-Willi syndrome phenotype in X chromosome anomalies: evidence for a distinct syndrome. Stratakis CA Am J Med Genet; 1998 Nov; 80(3):294-5, 300-1. PubMed ID: 9843058 [No Abstract] [Full Text] [Related]
40. Prader-Willi Syndrome: clinical concerns for the orthopaedic surgeon. Kroonen LT; Herman M; Pizzutillo PD; Macewen GD J Pediatr Orthop; 2006; 26(5):673-9. PubMed ID: 16932110 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]