M T M Baptista

Inhibition of CYP21A2 Enzyme Activity Caused by Novel Missense Mutations Identified in Brazilian and Scandinavian Patients

Fernanda Caroline Soardi, Michela Barbaro, Ivy F. Lau et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 67 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism

Milena Gurgel Teles, Ericka Barbosa Trarbach, Sekoni D. Noel et al. · European Journal of Endocrinology · 2010 · 59 citations · Full text

Medicine, Endocrinology, Genetics +15

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients

Ericka Barbosa Trarbach, M T M Baptista, Heraldo Mendes Garmes et al. · Journal of Endocrinology · 2005 · 45 citations · Full text

Medicine, Endocrinology, Genetics +16

Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patients

Aline Maria Garcia Costa, Sofia Helena Valente de Lemos‐Marini, M T M Baptista et al. · Journal of Bone and Mineral Metabolism · 2002 · 38 citations

Medicine, Endocrinology, Orthopedic Surgery +16

Turner's Syndrome and Thyroid Disease: A Transverse Study of Pediatric Patients in Brazil

Carla Campos Muniz Medeiros, M T M Baptista, Guillermo Guerra et al. · Journal of Pediatric Endocrinology and Metabolism · 2000 · 37 citations

Life Sciences, Endocrinology, Pediatrics +17