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genetic syndrome associated with obesity 相关文献:
An obesity genetic risk score is associated with metabolic syndrome in Chinese children.
PMID:
Genetic Rodent Models of Obesity-Associated Ovarian Dysfunction and Subfertility: Insights into Polycystic Ovary Syndrome.
PMID:
Obesity-associated genetic variants in young Asian Indians with the metabolic syndrome and myocardial infarction.
PMID:
Current Treatments for Patients with Genetic Obesity.
Faccioli N, Poitou C, Clément K, Dubern B.
J Clin Res Pediatr Endocrinol. 2023 May 29;15(2):108-119. doi: 10.4274/jcrpe.galenos.2023.2023-3-2. Epub 2023 May 16.
PMID:37191347
Obesity and female infertility: potential mediators of obesity's impact.
Broughton DE, Moley KH.
Fertil Steril. 2017 Apr;107(4):840-847. doi: 10.1016/j.fertnstert.2017.01.017. Epub 2017 Mar 11.
PMID:28292619
Prader-Willi syndrome.
Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.
Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26.
PMID:22237428
Hypothalamic syndrome.
Müller HL, Tauber M, Lawson EA, Özyurt J, Bison B, Martinez-Barbera JP, Puget S, Merchant TE, van Santen HM.
Nat Rev Dis Primers. 2022 Apr 21;8(1):24. doi: 10.1038/s41572-022-00351-z.
PMID:35449162
Setmelanotide: First Approval.
Markham A.
Drugs. 2021 Feb;81(3):397-403. doi: 10.1007/s40265-021-01470-9.
PMID:33638809
Microbial Medicine: Prebiotic and Probiotic Functional Foods to Target Obesity and Metabolic Syndrome.
Green M, Arora K, Prakash S.
Int J Mol Sci. 2020 Apr 21;21(8):2890. doi: 10.3390/ijms21082890.
PMID:32326175
The role of diet in hyperuricemia and gout.
Yokose C, McCormick N, Choi HK.
Curr Opin Rheumatol. 2021 Mar 1;33(2):135-144. doi: 10.1097/BOR.0000000000000779.
PMID:33399399
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. doi: 10.1007/s40618-015-0312-9. Epub 2015 Jun 11.
PMID:26062517
Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alstrom syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period.
Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J.
Lancet Diabetes Endocrinol. 2022 Dec;10(12):859-868. doi: 10.1016/S2213-8587(22)00277-7. Epub 2022 Nov 7.
PMID:36356613
Special Issue: Genetics of Prader-Willi Syndrome.
Godler DE, Butler MG.
Genes (Basel). 2021 Sep 16;12(9):1429. doi: 10.3390/genes12091429.
PMID:34573411
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