1149 related articles for article (PubMed ID: 26062517)
1. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
Angulo MA; Butler MG; Cataletto ME
J Endocrinol Invest; 2015 Dec; 38(12):1249-63. PubMed ID: 26062517
[TBL] [Abstract][Full Text] [Related]
2. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
[TBL] [Abstract][Full Text] [Related]
3. Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.
Butler MG; Manzardo AM; Forster JL
Curr Pediatr Rev; 2016; 12(2):136-66. PubMed ID: 26592417
[TBL] [Abstract][Full Text] [Related]
4. Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.
Muscogiuri G; Barrea L; Faggiano F; Maiorino MI; Parrillo M; Pugliese G; Ruggeri RM; Scarano E; Savastano S; Colao A;
J Endocrinol Invest; 2021 Oct; 44(10):2057-2070. PubMed ID: 33891302
[TBL] [Abstract][Full Text] [Related]
5. Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Butler MG; Miller JL; Forster JL
Curr Pediatr Rev; 2019; 15(4):207-244. PubMed ID: 31333129
[TBL] [Abstract][Full Text] [Related]
6. Hypogonadism in Patients with Prader Willi Syndrome: A Narrative Review.
Napolitano L; Barone B; Morra S; Celentano G; La Rocca R; Capece M; Morgera V; Turco C; Caputo VF; Spena G; Romano L; De Luca L; Califano G; CollĂ Ruvolo C; Mangiapia F; Mirone V; Longo N; Creta M
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33671467
[TBL] [Abstract][Full Text] [Related]
7. Prader- Willi syndrome: An uptodate on endocrine and metabolic complications.
Muscogiuri G; Formoso G; Pugliese G; Ruggeri RM; Scarano E; Colao A;
Rev Endocr Metab Disord; 2019 Jun; 20(2):239-250. PubMed ID: 31065942
[TBL] [Abstract][Full Text] [Related]
8. Endocrine manifestations and management of Prader-Willi syndrome.
Emerick JE; Vogt KS
Int J Pediatr Endocrinol; 2013 Aug; 2013(1):14. PubMed ID: 23962041
[TBL] [Abstract][Full Text] [Related]
9. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
Hartin SN; Hossain WA; Weisensel N; Butler MG
Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
[TBL] [Abstract][Full Text] [Related]
10. Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.
Jin DK
Korean J Pediatr; 2011 Feb; 54(2):55-63. PubMed ID: 21503198
[TBL] [Abstract][Full Text] [Related]
11. Prader-Willi syndrome.
Cassidy SB; Driscoll DJ
Eur J Hum Genet; 2009 Jan; 17(1):3-13. PubMed ID: 18781185
[TBL] [Abstract][Full Text] [Related]
12. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
Hassan M; Butler MG
Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
[TBL] [Abstract][Full Text] [Related]
13. Proteins and proteases of Prader-Willi syndrome: a comprehensive review and perspectives.
Basak S; Basak A
Biosci Rep; 2022 Jun; 42(6):. PubMed ID: 35621394
[TBL] [Abstract][Full Text] [Related]
14. Prader-Willi Syndrome: Obesity due to Genomic Imprinting.
Butler MG
Curr Genomics; 2011 May; 12(3):204-15. PubMed ID: 22043168
[TBL] [Abstract][Full Text] [Related]
15. Prader-Willi syndrome.
Cassidy SB; Schwartz S; Miller JL; Driscoll DJ
Genet Med; 2012 Jan; 14(1):10-26. PubMed ID: 22237428
[TBL] [Abstract][Full Text] [Related]
16. Prader-Willi syndrome: an update on obesity and endocrine problems.
Kim SJ; Cho SY; Jin DK
Ann Pediatr Endocrinol Metab; 2021 Dec; 26(4):227-236. PubMed ID: 34991300
[TBL] [Abstract][Full Text] [Related]
17. Relationship of thyroid function with genetic subtypes and treatment with growth hormone in Prader-Willi syndrome.
Schmok T; Surampalli A; Khare M; Zandihaghighi S; Baghbaninogourani R; Patolia B; Gold JA; Naidu A; Cassidy SB; Kimonis VE
Am J Med Genet A; 2024 Jun; ():e63724. PubMed ID: 38837660
[TBL] [Abstract][Full Text] [Related]
18. Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.
Rocha CF; Paiva CL
Genet Mol Res; 2014 Mar; 13(1):2290-8. PubMed ID: 24737477
[TBL] [Abstract][Full Text] [Related]
19. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
Bittel DC; Kibiryeva N; Butler MG
Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]