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 *

318 related articles for article (PubMed ID: 33647242)

  • 1. Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction.
    Tauber M; Hoybye C
    Lancet Diabetes Endocrinol; 2021 Apr; 9(4):235-246. PubMed ID: 33647242
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prader-Willi syndrome: Hormone therapies.
    Tauber M; Diene G
    Handb Clin Neurol; 2021; 181():351-367. PubMed ID: 34238470
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
    Goldstone AP
    Trends Endocrinol Metab; 2004; 15(1):12-20. PubMed ID: 14693421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
    Angulo MA; Butler MG; Cataletto ME
    J Endocrinol Invest; 2015 Dec; 38(12):1249-63. PubMed ID: 26062517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypogonadism and endocrine metabolic disorders in Prader-Willi syndrome.
    Müller J
    Acta Paediatr Suppl; 1997 Nov; 423():58-9. PubMed ID: 9401541
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.
    Wang XY; Sun R; Gao YQ
    Yi Chuan; 2022 Oct; 44(10):899-912. PubMed ID: 36384726
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
    Madeo SF; Zagaroli L; Vandelli S; Calcaterra V; Crinò A; De Sanctis L; Faienza MF; Fintini D; Guazzarotti L; Licenziati MR; Mozzillo E; Pajno R; Scarano E; Street ME; Wasniewska M; Bocchini S; Bucolo C; Buganza R; Chiarito M; Corica D; Di Candia F; Francavilla R; Fratangeli N; Improda N; Morabito LA; Mozzato C; Rossi V; Schiavariello C; Farello G; Iughetti L; Salpietro V; Salvatoni A; Giordano M; Grugni G; Delvecchio M
    Front Endocrinol (Lausanne); 2024; 15():1382583. PubMed ID: 38737552
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome.
    Correa-da-Silva F; Fliers E; Swaab DF; Yi CX
    J Neuroendocrinol; 2021 Jul; 33(7):e12994. PubMed ID: 34156126
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH.
    Burman P; Ritzén EM; Lindgren AC
    Endocr Rev; 2001 Dec; 22(6):787-99. PubMed ID: 11739333
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prader-Willi syndrome: endocrine manifestations and management.
    Alves C; Franco RR
    Arch Endocrinol Metab; 2020; 64(3):223-234. PubMed ID: 32555988
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prader-Willi syndrome: A model for understanding the ghrelin system.
    Tauber M; Coupaye M; Diene G; Molinas C; Valette M; Beauloye V
    J Neuroendocrinol; 2019 Jul; 31(7):e12728. PubMed ID: 31046160
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gonadal Hormone Substitution in People with Prader-Labhart-Willi Syndrome: An International Prader-Willi Syndrome Organisation Survey.
    Eiholzer U; Stephan A; Fritz C; Katschnig C; Noordam C;
    Horm Res Paediatr; 2021; 94(5-6):176-185. PubMed ID: 34348303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; Butler MG
    Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prader-Willi Syndrome and Hypogonadism: A Review Article.
    Noordam C; Höybye C; Eiholzer U
    Int J Mol Sci; 2021 Mar; 22(5):. PubMed ID: 33800122
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A 14-year-old male patient with diagnosis of Prader-Willi syndrome in Ethiopia: a case report.
    Belay KE; Ayalew BL; Amogne MT; Alemneh TA; Geletew TK
    J Med Case Rep; 2023 Dec; 17(1):530. PubMed ID: 38143282
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypogonadism in Patients with Prader Willi Syndrome: A Narrative Review.
    Napolitano L; Barone B; Morra S; Celentano G; La Rocca R; Capece M; Morgera V; Turco C; Caputo VF; Spena G; Romano L; De Luca L; Califano G; Collà Ruvolo C; Mangiapia F; Mirone V; Longo N; Creta M
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33671467
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center.
    Passone CGB; Aragão LFF; Franco RR; Leite JES; Gonzalez MAB; Schil PSA; Ybarra M; Damiani D; Kerkhof GF; Montenegro Junior RM; Silva CA
    Front Endocrinol (Lausanne); 2024; 15():1403470. PubMed ID: 38966214
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.