대한내분비학회

번호	카테고리	제목	저자	저널명	출판년도/월
73	기타	Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome.-21(3):126-135	Cheon Chong Kun	Ann Pediatr Endocrinol Metab	2016/09
72	기타	Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.	Lee Ji-Eun	Orphanet J Rare Dis	2016/08
71	기타	MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome.	Yoo Han-Wook	Mol Genet Metab Rep	2016/08
70	기타	Molecular circadian rhythm shift due to bright light exposure before bedtime is related to subthreshold bipolarity.	Gi Hoon Son	Sci Rep	2016/08
69	기타	The Orphan Nuclear Receptor ERRgamma Regulates Hepatic CB1 Receptor-Mediated Fibroblast Growth Factor 21 Gene Expression.	In-Kyu Lee	PLoS One	2016/07
68	기타	Hypothalamic TLR2 triggers sickness behavior via a microglia-neuronal axis.	Lee Byung-Ju	Sci Rep	2016/07
67	기타	Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma.	Ji Hyun Lee, Jung Hee Kim	BMC Med Genet	2016/07
66	기타	Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency.	Cheon Chong Kun, Yoo Han-Wook	Ann Clin Lab Sci	2016/07

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