Gilberto K. Furuzawa

The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome

Anamaria A. Camargo, Helena P. B. Samaia, Emmanuel Dias‐Neto et al. · Proceedings of the National Academy of Sciences · 2001 · 139 citations · Full text

DUOX2 Mutations Are Associated With Congenital Hypothyroidism With Ectopic Thyroid Gland

Marina M. L. Kizys, Ruy A. Louzada, Miguel Mitne‐Neto et al. · The Journal of Clinical Endocrinology & Metabolism · 2017 · 59 citations · Full text

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Ca_v1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Magnus R. Dias‐da‐Silva, Janete M. Cerutti, Célia Harumi Tengan et al. · Clinical Endocrinology · 2002 · 50 citations · Full text

Low prevalence of MODY2 and MODY3 mutations in Brazilian individuals with clinical MODY phenotype

Gilberto K. Furuzawa, Fernando M. A. Giuffrida, Carolina S.V. Oliveira et al. · Diabetes Research and Clinical Practice · 2008 · 34 citations

Mendelian Disorder, Genetic Disorder, Genetics +10

M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds

M. Cecilia Martins-Costa, Lucas Leite Cunha, Susan C. Lindsey et al. · Endocrine Related Cancer · 2016 · 24 citations · Full text

Affected Kindreds, M918v Mtc, Genetic Disorder +12