Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and CYP3A4[original query] |
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Risk of acute promyelocytic leukemia in multiple sclerosis: coding variants of DNA repair genes. Neurology 2011 Mar 76 (12): 1059-65. Hasan S K, Buttari F, Ottone T, Voso M T, Hohaus S, Marasco E, Mantovani V, Garagnani P, Sanz M A, Cicconi L, Bernardi G, Centonze D, Lo-Coco |
A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information. PloS one 2017 12 (1): e0169214. Silva-Alves Mariana S, Secolin Rodrigo, Carvalho Benilton S, Yasuda Clarissa L, Bilevicius Elizabeth, Alvim Marina K M, Santos Renato O, Maurer-Morelli Claudia V, Cendes Fernando, Lopes-Cendes Isc |
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
Retrospective pharmacogenetic study in a cohort of pediatric tuberous sclerosis complex patients using everolimus. Pharmacogenomics 2023 10 . Julia Concha, Estela Sangüesa, Jose Luis Peña, María Pilar Ribate, Cristina Belén Garc |
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