132 related articles for article (PubMed ID: 23329756)
1. Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy.
Ma Y; Wu T; Liu Y; Wang Q; Song J; Song F; Yang Y
J Pediatr Endocrinol Metab; 2012; 25(11-12):1103-9. PubMed ID: 23329756
[TBL] [Abstract][Full Text] [Related]
2. [Clinical aspects and genetics of Prader-Willi syndrome].
Rittinger O
Klin Padiatr; 2001; 213(3):91-8. PubMed ID: 11417368
[TBL] [Abstract][Full Text] [Related]
3. [Prader-Labhart-Willi syndrome in infants].
Schmeling H; Gillessen-Kaesbach G; Schulte-Mattler U; Burdach S; Horneff G
Klin Padiatr; 2002; 214(2):51-3. PubMed ID: 11972309
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. The Prader-Willi syndrome: a study of 40 patients and a review of the literature.
Bray GA; Dahms WT; Swerdloff RS; Fiser RH; Atkinson RL; Carrel RE
Medicine (Baltimore); 1983 Mar; 62(2):59-80. PubMed ID: 6338343
[TBL] [Abstract][Full Text] [Related]
6. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
Lukusa T; Fryns JP
Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663
[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. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
Giurgiutiu DV; Espinoza LM; Wood TC; DuPont BR; Holden KR
J Child Neurol; 2008 Jan; 23(1):112-7. PubMed ID: 18184946
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Body growth in the early diagnosis of Prader-Labhart-Willi syndrome].
Cabezuelo-Huerta G; Frontera-Izquierdo P
An Esp Pediatr; 1983 Jan; 18(1):33-8. PubMed ID: 6870076
[TBL] [Abstract][Full Text] [Related]
11. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA
Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Early diagnosis and multidisciplinary care reduce the hospitalization time and duration of tube feeding and prevent early obesity in PWS infants.
Bacheré N; Diene G; Delagnes V; Molinas C; Moulin P; Tauber M
Horm Res; 2008; 69(1):45-52. PubMed ID: 18059083
[TBL] [Abstract][Full Text] [Related]
14. Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader-Willi syndrome.
Festen DA; Wevers M; Lindgren AC; Böhm B; Otten BJ; Wit JM; Duivenvoorden HJ; Hokken-Koelega AC
Clin Endocrinol (Oxf); 2008 Jun; 68(6):919-25. PubMed ID: 18031326
[TBL] [Abstract][Full Text] [Related]
15. [Cytogenetic detection of Prader-Willi syndrome in infancy].
Götz J; Krüger G; Westphal BC; Pelz L
Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122
[TBL] [Abstract][Full Text] [Related]
16. Prader-Willi syndrome in neonates: twenty cases and review of the literature in Southern China.
Wang P; Zhou W; Yuan W; Huang L; Zhao N; Chen X
BMC Pediatr; 2016 Aug; 16():124. PubMed ID: 27506196
[TBL] [Abstract][Full Text] [Related]
17. Prader-Willi syndrome.
Cassidy SB; Ledbetter DH
Neurol Clin; 1989 Feb; 7(1):37-54. PubMed ID: 2646521
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]