143 related articles for article (PubMed ID: 9642645)
1. Non-insulin dependent diabetes mellitus in a prepubertal child with Prader-Willi syndrome.
Sills IN; Rapaport R
J Pediatr Endocrinol Metab; 1998; 11(2):281-2. PubMed ID: 9642645
[TBL] [Abstract][Full Text] [Related]
2. Metabolic syndrome in adult patients with Prader-Willi syndrome.
Grugni G; Crinò A; Bedogni G; Cappa M; Sartorio A; Corrias A; Di Candia S; Gargantini L; Iughetti L; Pagano C; Ragusa L; Salvatoni A; Spera S; Vettor R; Chiumello G; Brambilla P
Nutr Metab Cardiovasc Dis; 2013 Nov; 23(11):1134-40. PubMed ID: 23220075
[TBL] [Abstract][Full Text] [Related]
3. Membranoproliferative glomerulonephritis in a child with Prader-Willi syndrome.
Robson WL; Leung AK
Am J Med Genet; 1992 Jul; 43(5):858-9. PubMed ID: 1642276
[TBL] [Abstract][Full Text] [Related]
4. Prader-Willi syndrome and mosaic Turner's syndrome.
Monzavi R; Fefferman RA; Pitukcheewanont P
J Pediatr Endocrinol Metab; 2005 Jul; 18(7):711-7. PubMed ID: 16128248
[TBL] [Abstract][Full Text] [Related]
5. Glucose homeostasis in Prader-Willi syndrome and potential implications of growth hormone therapy.
Zipf WB
Acta Paediatr Suppl; 1999 Dec; 88(433):115-7. PubMed ID: 10626560
[TBL] [Abstract][Full Text] [Related]
6. [Self-induced cutaneous lesions in Prader-Willi syndrome].
Plantin P; Milochau P; Broussine L; Blondin G
Ann Dermatol Venereol; 1997; 124(5):390-2. PubMed ID: 9739896
[TBL] [Abstract][Full Text] [Related]
7. Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13).
Bassali R; Hoffman WH; Chen H; Tuck-Muller CM
Am J Med Genet; 1997 Aug; 71(3):267-70. PubMed ID: 9268093
[TBL] [Abstract][Full Text] [Related]
8. [Neonatal hypotonia in Prader-Willi syndrome due to t(15;16)].
Fernández-Novoa MC; Vargas MT; Santano MR; Moya J; Garnacho MC
Rev Neurol; 2000 Sep 1-15; 31(5):499-500. PubMed ID: 11027108
[No Abstract] [Full Text] [Related]
9. Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.
Hwu WL; Tsai WY; Lee JS; Wang PJ; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1991; 32(2):105-11. PubMed ID: 2063683
[TBL] [Abstract][Full Text] [Related]
10. Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype.
Stagi S; Lapi E; Pantaleo M; Chiarelli F; Seminara S; de Martino M
BMC Med Genet; 2014 Jan; 15():16. PubMed ID: 24479866
[TBL] [Abstract][Full Text] [Related]
11. Hormonal change in an adult with Prader-Willi syndrome: report of a case.
Shiah CJ; Lee LS; Hwang JY; Liao ST; Hsu CH; Lin WY
J Formos Med Assoc; 1994 Apr; 93(4):324-7. PubMed ID: 7914775
[TBL] [Abstract][Full Text] [Related]
12. Severe neonatal-onset panniculitis in a female infant with Prader-Willi syndrome.
Sakthivel M; Hughes SM; Riley P; Arkwright PD; Mukherjee A; Ramsden S; Urquhart J; Crow YJ
Am J Med Genet A; 2011 Dec; 155A(12):3087-9. PubMed ID: 22052851
[TBL] [Abstract][Full Text] [Related]
13. Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).
Chen H; Aiello F
Am J Med Genet; 1993 Feb; 45(3):335-9. PubMed ID: 8434620
[TBL] [Abstract][Full Text] [Related]
14. Prader-Willi syndrome with del(15)(q11,q13) associated with hepatoblastoma.
Hashizume K; Nakajo T; Kawarasaki H; Iwanaka T; Kanamori Y; Tanaka K; Utuki T; Mishina J; Watanabe T
Acta Paediatr Jpn; 1991 Dec; 33(6):718-22. PubMed ID: 1666244
[TBL] [Abstract][Full Text] [Related]
15. Confirmation of a clinical diagnosis of Prader-Willi syndrome by fluorescence in situ hybridization (FISH).
Joseph A; Martin ES; McCormack BJ; Storlazzi JJ; Bean SC; Borgaonkar DS
Del Med J; 1995 Dec; 67(12):620-2. PubMed ID: 8557163
[No Abstract] [Full Text] [Related]
16. Recurrent brief depression in Prader-Willi syndrome: a case report.
Watanabe H; Ohmori O; Abe K
Psychiatr Genet; 1997; 7(1):41-4. PubMed ID: 9264138
[TBL] [Abstract][Full Text] [Related]
17. A further case of coincidental Prader-Willi and Klinefelter syndromes.
Schneider M; Forrester S; Crain V; Kimonis V
Am J Med Genet A; 2004 Apr; 126A(2):213-4. PubMed ID: 15057989
[No Abstract] [Full Text] [Related]
18. Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
Buiting K; Neumann M; Lüdecke HJ; Senger G; Claussen U; Antich J; Passarge E; Horsthemke B
Genomics; 1990 Mar; 6(3):521-7. PubMed ID: 2328991
[TBL] [Abstract][Full Text] [Related]
19. Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.
Fernandez F; Berry C; Mutton D
Arch Dis Child; 1987 Aug; 62(8):841-3. PubMed ID: 3662590
[TBL] [Abstract][Full Text] [Related]
20. A case of Prader Willi syndrome with del 15 (q11-->q13).
Tunçman G; Tükün A; Yalaz K; Bökesoy I
Turk J Pediatr; 1993; 35(4):333-6. PubMed ID: 8160287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
