Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: HADHA[original query] |
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A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in Poland. Journal of inherited metabolic disease 2010 Dec 33 Suppl 3 S373-7. Piekutowska-Abramczuk Dorota, Olsen Rikke K J, Wierzba Jolanta, Popowska Ewa, Jurkiewicz Dorota, Ciara El?bieta, O?tarzewski Mariusz, Gradowska Wanda, Sykut-Cegielska Jolanta, Krajewska-Walasek Ma?gorzata, Andresen Brage S, Gregersen Niels, Pronicka E |
Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease. PloS one 2011 6 (1): e16542. Banasik Karina, Justesen Johanne M, Hornbak Malene, Krarup Nikolaj T, Gjesing Anette P, Sandholt Camilla H, Jensen Thomas S, Grarup Niels, Andersson Asa, Jørgensen Torben, Witte Daniel R, Sandbæk Annelli, Lauritzen Torsten, Thorens Bernard, Brunak Søren, Sørensen Thorkild I A, Pedersen Oluf, Hansen Torb |
Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia. JIMD reports 2012 2 79-85. Joost K, Ounap K, Zordania R, Uudelepp M-L, Olsen R K, Kall K, Kilk K, Soomets U, Kahre |
High prevalence of carriers of variant c.1528G>C of HADHA gene causing long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) in the population of adult Kashubians from North Poland. PloS one 2017 11 12 (11): e0187365. Nedoszytko Bogus?aw, Siemi?ska Alicja, Strapagiel Dominik, D?browski S?awomir, S?omka Marcin, Sobalska-Kwapis Marta, Marciniak B?a?ej, Wierzba Jolanta, Skokowski Jaros?aw, Fija?kowski Marcin, Nowicki Roman, Kalinowski Lesz |
Prevalence of the most common pathogenic variants in three genes for inborn errors of metabolism associated with sudden unexpected death in infancy: a population-based study in south Brazil. Genetics and molecular biology 2020 7 43 (3): 20190298. Randon Dévora N, Sperb-Ludwig Fernanda, Vianna Fernanda S L, Becker Ana P P, Vargas Carmen R, Sitta Angela, Sant'Ana Alexia N, Schwartz Ida V D, Bitencourt Fernanda H |
Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic. Orphanet journal of rare diseases 2022 9 17 (1): 360. Ambrose Anastasia, Sheehan Melissa, Bahl Shalini, Athey Taryn, Ghai-Jain Shailly, Chan Alicia, Mercimek-Andrews Saad |
Gene Variants Related to Cardiovascular and Pulmonary Diseases May Correlate with Severe Outcome of COVID-19. International journal of molecular sciences 2022 8 23 (15): . Sypniewski Mateusz, Król Zbigniew J, Szyda Joanna, Kaja El?bieta, Mroczek Magdalena, Suchocki Tomasz, Lejman Adrian, St?pie? Maria, Topolski Piotr, D?browski Maciej, Kotlarz Krzysztof, Aplas Angelika, Wasiak Micha?, Wojtaszewska Marzena, Zawadzki Pawe?, Pawlak Agnieszka, Gil Robert, Dobosz Paula, Stojak Joan |
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