Hamilton Cabral de Menezes Filho

Severe Hypercalcemia in a 9-Year-Old Brazilian Girl Due to a Novel Inactivating Mutation of the Calcium-Sensing Receptor

Kozue Miyashiro, Ilda S. Kunii, Thaís Della Manna et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 28 citations · Full text

Medicine, Endocrinology, Genetics +17

Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities

Hamilton Cabral de Menezes Filho, Suemi Marui, Thaís Della Manna et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 2011 · 24 citations · Full text

Medicine, Endocrinology, Genetics +17

The recurrent homozygous translation start site variant in <scp><i>CCDC134</i></scp> in an individual with severe osteogenesis imperfecta of <scp>non‐Morrocan</scp> ancestry

Taccyanna Mikulski Ali, Bianca Domit Werner Linnenkamp, Guilherme Lopes Yamamoto et al. · American Journal of Medical Genetics Part A · 2022 · 17 citations

Medicine, Genetics, Orthopaedic Surgery +17

A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism

Claudilene Battistin, Hamilton Cabral de Menezes Filho, Sorahia Domenice et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 2012 · 12 citations · Full text

Medicine, Endocrinology, Pediatrics +17