Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Metabolic Syndrome X and HFE[original query] |
---|
Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia. The Journal of clinical endocrinology and metabolism 2009 Nov 94 (11): 4391-7. Solanas-Barca María, Mateo-Gallego Rocío, Calmarza Pilar, Jarauta Estíbaliz, Bea Ana M, Cenarro Ana, Civeira Fernan |
Liver steatosis correlates with iron overload but not with HFE gene mutations in chronic hepatitis C. Hepatobiliary & pancreatic diseases international : HBPD INT 2013 Aug 12 (4): 377-84. Sikorska Katarzyna, Stalke Piotr, Romanowski Tomasz, Rzepko Robert, Bielawski Krzysztof Pio |
Serum ferritin, insulin resistance, and metabolic syndrome: clinical and laboratory associations in 769 non-hispanic whites without diabetes mellitus in the HEIRS study. Metabolic syndrome and related disorders 2015 Mar 13 (2): 57-63. Acton Ronald T, Barton J Clayborn, Barton James |
Insulin Resistance and Metabolic Syndrome: Clinical and Laboratory Associations in African Americans Without Diabetes in the Hemochromatosis and Iron Overload Screening Study. Metabolic syndrome and related disorders 2018 6 16 (6): 267-273. Barton James C, Barton Jackson Clayborn, Acton Ronald |
Hepcidin is a useful biomarker to evaluate hyperferritinemia associated with metabolic syndrome. Anais da Academia Brasileira de Ciencias 2019 5 91 (2): e20180286. Rauber Mariana R, Pilger Diogo A, Cecconello Daiane K, Falcetta Frederico S, Marcondes Natália A, Faulhaber Gustavo A |
- Page last reviewed:Feb 1, 2024
- Content source: