BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 18831731)

  • 1. French database of children and adolescents with Prader-Willi syndrome.
    Molinas C; Cazals L; Diene G; Glattard M; Arnaud C; Tauber M;
    BMC Med Genet; 2008 Oct; 9():89. PubMed ID: 18831731
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Endocrine disorders in children with Prader-Willi syndrome--data from 142 children of the French database.
    Diene G; Mimoun E; Feigerlova E; Caula S; Molinas C; Grandjean H; Tauber M;
    Horm Res Paediatr; 2010; 74(2):121-8. PubMed ID: 20395666
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.
    Dudley O; McManus B; Vogels A; Whittington J; Muscatelli F
    J Intellect Disabil Res; 2008 May; 52(Pt 5):426-36. PubMed ID: 18298478
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France.
    Laurier V; Lapeyrade A; Copet P; Demeer G; Silvie M; Bieth E; Coupaye M; Poitou C; Lorenzini F; Labrousse F; Molinas C; Tauber M; Thuilleaux D; Jauregi J
    J Intellect Disabil Res; 2015 May; 59(5):411-21. PubMed ID: 24947991
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The impact of Prader-Willi syndrome on the family's quality of life and caregiving, and the unaffected siblings' psychosocial adjustment.
    Mazaheri MM; Rae-Seebach RD; Preston HE; Schmidt M; Kountz-Edwards S; Field N; Cassidy S; Packman W
    J Intellect Disabil Res; 2013 Sep; 57(9):861-73. PubMed ID: 23057501
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Causes of death in Prader-Willi syndrome: lessons from 11 years' experience of a national reference center.
    Pacoricona Alfaro DL; Lemoine P; Ehlinger V; Molinas C; Diene G; Valette M; Pinto G; Coupaye M; Poitou-Bernert C; Thuilleaux D; Arnaud C; Tauber M
    Orphanet J Rare Dis; 2019 Nov; 14(1):238. PubMed ID: 31684997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder.
    Holland A; Whittington J; Cohen O; Curfs L; Delahaye F; Dudley O; Horsthemke B; Lindgren AC; Nourissier C; Sharma N; Vogels A
    J Intellect Disabil Res; 2009 Jun; 53(6):538-47. PubMed ID: 19457156
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Economic burden and health-related quality of life associated with Prader-Willi syndrome in France.
    Chevreul K; Berg Brigham K; Clément MC; Poitou C; Tauber M;
    J Intellect Disabil Res; 2016 Sep; 60(9):879-90. PubMed ID: 27174598
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia.
    Thomson AK; Glasson EJ; Bittles AH
    J Intellect Disabil Res; 2006 Jan; 50(Pt 1):69-78. PubMed ID: 16316432
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prader-Willi Syndrome in children: Quality of life and caregiver burden.
    Meade C; Martin R; McCrann A; Lyons J; Meehan J; Hoey H; Roche E
    Acta Paediatr; 2021 May; 110(5):1665-1670. PubMed ID: 33378107
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome.
    Borghgraef M; Fryns JP; Van Den Berghe H
    Genet Couns; 1990; 1(2):141-50. PubMed ID: 1706926
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Quality of life in children with Prader Willi Syndrome: Parent and child reports.
    Wilson KS; Wiersma LD; Rubin DA
    Res Dev Disabil; 2016 Oct; 57():149-57. PubMed ID: 27433979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.
    Copet P; Jauregi J; Laurier V; Ehlinger V; Arnaud C; Cobo AM; Molinas C; Tauber M; Thuilleaux D
    J Intellect Disabil Res; 2010 Mar; 54(3):204-15. PubMed ID: 20136683
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prader-Willi syndrome in Taiwan.
    Lin HY; Lin SP; Yen JL; Lee YJ; Huang CY; Hung HY; Hsu CH; Kao HA; Chang JH; Chiu NC; Ho CS; Chao MC; Niu DM; Tsai LP; Kuo PL
    Pediatr Int; 2007 Jun; 49(3):375-9. PubMed ID: 17532839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Global Prader-Willi Syndrome Registry: Development, Launch, and Early Demographics.
    Bohonowych J; Miller J; McCandless SE; Strong TV
    Genes (Basel); 2019 Sep; 10(9):. PubMed ID: 31540108
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sexual dichotomy of gonadal function in Prader-Willi syndrome from early infancy through the fourth decade.
    Hirsch HJ; Eldar-Geva T; Bennaroch F; Pollak Y; Gross-Tsur V
    Hum Reprod; 2015 Nov; 30(11):2587-96. PubMed ID: 26345685
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prader-Willi Syndrome - nutritional management in children, adolescents and adults].
    Krasińska A; Skowrońska B
    Pediatr Endocrinol Diabetes Metab; 2017; 23(2):101-106. PubMed ID: 29073293
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.
    Roux-Levy PH; Bournez M; Masurel A; Jean N; Chancenotte S; Bordes M; Debomy F; Minot D; Schmitt E; Vinault S; Gautier E; Lacombe D; Odent S; Mikaty M; Manouvrier S; Ghoumid J; Geneviève D; Lehman N; Philip N; Edery P; Cornaton J; Gallard J; Héron D; Rastel C; Huet F; Thauvin-Robinet C; Verloes A; Binquet C; Tauber M; Lejeune C; Faivre L
    Eur J Med Genet; 2020 Dec; 63(12):104064. PubMed ID: 32998064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.