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Endocrine|October 15, 2009
RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crestEliska Vaclavikova, Sarka Dvorakova, Vlasta Sykorova, et al.
Clinical Chemistry and Laboratory Medicine|May 9, 2007
Prevalence of insulin resistance and prediction of glucose intolerance and type 2 diabetes mellitus in women with polycystic ovary syndromeJana Vrbikova, Katerina Dvorakova, Tereza Grimmichova, et al.
International Journal of Endocrinology|August 19, 2014
MTNR1B Genetic Variability Is Associated with Gestational Diabetes in Czech WomenDaniela Vejrazkova, Petra Lukasova, Marketa Vankova, et al.
European Journal of Heart Failure|June 15, 2012
Availability of energetic substrates and exercise performance in heart failure with or without diabetesVojtech Melenovsky, Martin Kotrc, Jan Polak, et al.
Frontiers in Endocrinology|June 23, 2022
The rs10830963 Polymorphism of the MTNR1B Gene: Association With Abnormal Glucose, Insulin and C-peptide KineticsDaniela Vejrazkova, Marketa Vankova, Josef Vcelak, et al.
Frontiers in Endocrinology|December 10, 2021
Recurrence of Graves' Disease: What Genetics of HLA and <i>PTPN22</i> Can Tell UsDaniela Vejrazkova, Josef Vcelak, Eliska Vaclavikova, et al.
Thyroid : Official Journal of the American Thyroid Association|June 5, 2020
<i>RET</i>, <i>NTRK</i>, <i>ALK</i>, <i>BRAF</i>, and <i>MET</i> Fusions in a Large Cohort of Pediatric Papillary Thyroid CarcinomasBarbora Pekova, Vlasta Sykorova, Sarka Dvorakova, et al.
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