BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 37267430)

  • 21. Autonomic nervous system dysfunction in Prader-Willi syndrome.
    Butler MG; Victor AK; Reiter LT
    Clin Auton Res; 2023 Jun; 33(3):281-286. PubMed ID: 36515769
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.
    Davies JR; Humby T; Dwyer DM; Garfield AS; Furby H; Wilkinson LS; Wells T; Isles AR
    Eur J Neurosci; 2015 Aug; 42(4):2105-13. PubMed ID: 26040449
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities.
    Kimonis VE; Tamura R; Gold JA; Patel N; Surampalli A; Manazir J; Miller JL; Roof E; Dykens E; Butler MG; Driscoll DJ
    Genes (Basel); 2019 Nov; 10(11):. PubMed ID: 31698873
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.
    Zhang K; Liu S; Gu W; Lv Y; Yu H; Gao M; Wang D; Zhao J; Li X; Gai Z; Zhao S; Liu Y; Yuan Y
    Front Genet; 2021; 12():630650. PubMed ID: 34504512
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
    Butler MG; Miller JL; Forster JL
    Curr Pediatr Rev; 2019; 15(4):207-244. PubMed ID: 31333129
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Proteins and proteases of Prader-Willi syndrome: a comprehensive review and perspectives.
    Basak S; Basak A
    Biosci Rep; 2022 Jun; 42(6):. PubMed ID: 35621394
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
    Bittel DC; Butler MG
    Expert Rev Mol Med; 2005 Jul; 7(14):1-20. PubMed ID: 16038620
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
    Hartin SN; Hossain WA; Weisensel N; Butler MG
    Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study.
    Butler MG; Kimonis V; Dykens E; Gold JA; Miller J; Tamura R; Driscoll DJ
    Am J Med Genet A; 2018 Feb; 176(2):368-375. PubMed ID: 29271568
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prader- Willi syndrome: An uptodate on endocrine and metabolic complications.
    Muscogiuri G; Formoso G; Pugliese G; Ruggeri RM; Scarano E; Colao A;
    Rev Endocr Metab Disord; 2019 Jun; 20(2):239-250. PubMed ID: 31065942
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prader-Willi syndrome: an update on obesity and endocrine problems.
    Kim SJ; Cho SY; Jin DK
    Ann Pediatr Endocrinol Metab; 2021 Dec; 26(4):227-236. PubMed ID: 34991300
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Birth seasonality studies in a large Prader-Willi syndrome cohort.
    Butler MG; Kimonis V; Dykens E; Gold JA; Tamura R; Miller JL; Driscoll DJ
    Am J Med Genet A; 2019 Aug; 179(8):1531-1534. PubMed ID: 31225937
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.
    Butler MG
    Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901699
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Alteration of serum leptin and LEP/LEPR promoter methylation in Prader-Willi syndrome.
    Wieting J; Jahn K; Buchholz V; Lichtinghagen R; Deest-Gaubatz S; Bleich S; Eberlein CK; Deest M; Frieling H
    Psychoneuroendocrinology; 2022 Sep; 143():105857. PubMed ID: 35803048
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hypomethylation of the dopamine transporter (DAT) gene promoter is associated with hyperphagia-related behavior in Prader-Willi syndrome: A case-control study.
    Wieting J; Jahn K; Eberlein CK; Bleich S; Frieling H; Deest M
    Behav Brain Res; 2023 Jul; 450():114494. PubMed ID: 37182741
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Increased brain age in adults with Prader-Willi syndrome.
    Azor AM; Cole JH; Holland AJ; Dumba M; Patel MC; Sadlon A; Goldstone AP; Manning KE
    Neuroimage Clin; 2019; 21():101664. PubMed ID: 30658944
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Metabolic syndrome in adult patients with Prader-Willi syndrome.
    Grugni G; Crinò A; Bedogni G; Cappa M; Sartorio A; Corrias A; Di Candia S; Gargantini L; Iughetti L; Pagano C; Ragusa L; Salvatoni A; Spera S; Vettor R; Chiumello G; Brambilla P
    Nutr Metab Cardiovasc Dis; 2013 Nov; 23(11):1134-40. PubMed ID: 23220075
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular genetic diagnostics of Prader-Willi Syndrome: a validation of linkage analysis for the Chinese population.
    Li H; Meng S; Chen Z; Li H; Du M; Ma H; Wei H; Duan H; Zheng H; Wenren Q; Song X
    J Genet Genomics; 2007 Oct; 34(10):885-91. PubMed ID: 17945167
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prader-Willi Syndrome: Obesity due to Genomic Imprinting.
    Butler MG
    Curr Genomics; 2011 May; 12(3):204-15. PubMed ID: 22043168
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.