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 *

164 related articles for article (PubMed ID: 28494825)

  • 1. Prader-Willi Syndrome: Background and Management.
    Abdilla Y; Andria Barbara M; Calleja-Agius J
    Neonatal Netw; 2017 May; 36(3):134-141. PubMed ID: 28494825
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular analysis in Prader-Willi syndrome diagnosis].
    Szpecht-Potocka A
    Med Wieku Rozwoj; 1999; 3(3):407-19. PubMed ID: 10910667
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prader Willi and Angelman syndromes: exemplars of genomic imprinting.
    Prows CA; Hopkin RJ
    J Perinat Neonatal Nurs; 1999 Sep; 13(2):76-89. PubMed ID: 10818855
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.
    Raca G; Buiting K; Das S
    Genet Test; 2004; 8(4):387-94. PubMed ID: 15684868
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Attitudes toward prenatal genetic testing and therapeutic termination of pregnancy among parents of offspring with Prader-Willi syndrome.
    Even-Zohar Gross N; Geva-Eldar T; Pollak Y; Hirsch HJ; Gross I; Gross-Tsur V
    Eur J Med Genet; 2017 Apr; 60(4):205-211. PubMed ID: 28119110
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. [Prader-Willi syndrome in 2015].
    Tauber M; Thuilleaux D; Bieth É
    Med Sci (Paris); 2015 Oct; 31(10):853-60. PubMed ID: 26481024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling].
    Klosowski S; Delobel B; Morisot C; Kongolo G; Biancalana V; Thelliez P; Djebara A; Croquette MF; Deroubaix P
    Arch Pediatr; 1998 Aug; 5(8):934-5. PubMed ID: 9759307
    [No Abstract]   [Full Text] [Related]  

  • 11. The genetics, diagnosis, and management of Prader-Willi syndrome.
    Nativio DG
    J Pediatr Health Care; 2002; 16(6):298-303. PubMed ID: 12436099
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical report—health supervision for children with Prader-Willi syndrome.
    McCandless SE;
    Pediatrics; 2011 Jan; 127(1):195-204. PubMed ID: 21187304
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Case report: neonatal Prader-Willi syndrome].
    Yan G; He X
    Zhonghua Er Ke Za Zhi; 2014 Jan; 52(1):57-8. PubMed ID: 24680410
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Prader-Willi syndrome.
    Couper RT; Couper JJ
    Lancet; 2000 Aug; 356(9230):673-5. PubMed ID: 10968453
    [No Abstract]   [Full Text] [Related]  

  • 16. [Care continuity for patients with Prader-Willi syndrome during transition from childhood to adulthood].
    Saitoh S
    Nihon Rinsho; 2010 Jan; 68(1):141-4. PubMed ID: 20077807
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Prader-Willi syndrome].
    Fujieda K
    Nihon Rinsho; 2006 Jun; Suppl 2():229-33. PubMed ID: 16817390
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Prader-Willi Syndrome: A Case Study and Parent Perspective.
    Glaspy E; Foge J
    Adv Neonatal Care; 2015 Aug; 15(4):290-8. PubMed ID: 26225598
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.