These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 2737375)

  • 21. The neonatal presentation of Prader-Willi syndrome revisited.
    Miller SP; Riley P; Shevell MI
    J Pediatr; 1999 Feb; 134(2):226-8. PubMed ID: 9931534
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prader-Willi and Klinefelter syndrome: a coincidence or not?
    Vasudevan PC; Quarrell OWJ
    Clin Dysmorphol; 2007 Apr; 16(2):127-129. PubMed ID: 17351360
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Syndromes and disorders associated with mental retardation.
    Greydanus DE; Pratt HD
    Indian J Pediatr; 2005 Oct; 72(10):859-64. PubMed ID: 16272659
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Prader-Willi syndrome: consensus diagnostic criteria.
    Holm VA; Cassidy SB; Butler MG; Hanchett JM; Greenswag LR; Whitman BY; Greenberg F
    Pediatrics; 1993 Feb; 91(2):398-402. PubMed ID: 8424017
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A fetus with Prader-Willi syndrome showing normal diurnal rhythm and abnormal ultradian rhythm on heart rate monitoring.
    Hiroi H; Kozuma S; Hayashi N; Unno N; Fujii T; Tsutsumi O; Okai T; Taketani Y
    Fetal Diagn Ther; 2000; 15(5):304-7. PubMed ID: 10971085
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prader-Willi syndrome and scoliosis.
    Holm VA; Laurnen EL
    Dev Med Child Neurol; 1981 Apr; 23(2):192-201. PubMed ID: 7215706
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Bilateral opercular syndrome caused by perinatal difficulties.
    Yamamoto T; Koeda T; Maegaki Y; Tanaka C; Takeshita K
    Eur J Paediatr Neurol; 1997; 1(2-3):73-7. PubMed ID: 10728199
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
    de Vries BB; Fryns JP; Butler MG; Canziani F; Wesby-van Swaay E; van Hemel JO; Oostra BA; Halley DJ; Niermeijer MF
    J Med Genet; 1993 Sep; 30(9):761-6. PubMed ID: 8411072
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome].
    Tamminga S; Stalman SE; Kamp GA; Hendriks YM; Knegt AC; Elting MW
    Ned Tijdschr Geneeskd; 2015; 159():A8240. PubMed ID: 25898865
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Neonatal subdural and extradural haemorrhage in Prader-Willi syndrome.
    Klinge L; Scott RC; de Sousa C
    Neuropediatrics; 2001 Aug; 32(4):221-2. PubMed ID: 11571706
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. [Neuropsychiatric aspects of Prader-Willi syndrome – a review].
    Briegel W
    Z Kinder Jugendpsychiatr Psychother; 2018 May; 46(3):238-246. PubMed ID: 28613110
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Systematic follow-up of newborns with idiopathic respiratory distress syndrome. Results in 197 patients born 1971 to 1976.
    Nars PS; Schubarth L; Kindler R; Werthemann U; Stalder G
    Helv Paediatr Acta; 1981 Nov; 36(5):389-404. PubMed ID: 7031020
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical and Molecular Characterization of Prader-Willi Syndrome.
    Sanjeeva GN; Maganthi M; Kodishala H; Marol RKR; Kulshreshtha PS; Lorenzetto E; Kadandale JS; Hladnik U; Raghupathy P; Bhat M
    Indian J Pediatr; 2017 Nov; 84(11):815-821. PubMed ID: 28660389
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prader-Willi syndrome: clinical and molecular cytogenetic investigations.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Jun; 95(6):474-9. PubMed ID: 8772055
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Morbid obesity in an adolescent with Prader-Willi syndrome.
    Santos VM; Henrique de Paula F; Osterne EM; Nery NS; Turra TZ
    Rev Med Chil; 2009 Feb; 137(2):264-8. PubMed ID: 19543650
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Prader-Willi syndrome in New Zealand: a survey of 36 affected people.
    Thornton L; Dawson KP
    N Z Med J; 1990 Mar; 103(885):97-8. PubMed ID: 2314743
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.