BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 18184946)

  • 1. 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]  

  • 2. [Prader-Willi syndrome in 22-year-old man--case study].
    Kardas P; Adamiak-Kardas M
    Wiad Lek; 2001; 54(11-12):709-14. PubMed ID: 11928560
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
    Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
    Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
    Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
    Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I
    Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
    Varela MC; Simões-Sato AY; Kim CA; Bertola DR; De Castro CI; Koiffmann CP
    Eur J Med Genet; 2006; 49(4):298-305. PubMed ID: 16829351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. The Prader-Willi phenotype of fragile X syndrome.
    Nowicki ST; Tassone F; Ono MY; Ferranti J; Croquette MF; Goodlin-Jones B; Hagerman RJ
    J Dev Behav Pediatr; 2007 Apr; 28(2):133-8. PubMed ID: 17435464
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hormonal, metabolic and skeletal phenotype of Schaaf-Yang syndrome: a comparison to Prader-Willi syndrome.
    McCarthy JM; McCann-Crosby BM; Rech ME; Yin J; Chen CA; Ali MA; Nguyen HN; Miller JL; Schaaf CP
    J Med Genet; 2018 May; 55(5):307-315. PubMed ID: 29496979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Severe infantile hypotonia with ethylmalonic aciduria: case report.
    Okuyaz C; Ezgü FS; Biberoglu G; Zeviani M; Tiranti V; Yilgör E
    J Child Neurol; 2008 Jun; 23(6):703-5. PubMed ID: 18539996
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [To know more about the Prader-Willi syndrome. Diagnosis].
    Midro AT; Olchowik B; Lebiedzińska A; Midro H
    Psychiatr Pol; 2009; 43(2):135-49. PubMed ID: 19697784
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis].
    Scommegna S; Zollino M; Paolone G
    Pediatr Med Chir; 2001; 23(3-4):191-6. PubMed ID: 11723857
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The paradox of Prader-Willi syndrome: a genetic model of starvation.
    Holland A; Whittington J; Hinton E
    Lancet; 2003 Sep; 362(9388):989-91. PubMed ID: 14511934
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.