M. Ezabella

Sporadic Medullary Thyroid Carcinoma: Clinical Data From A University Hospital

S. Toledo, R. Toledo, D. Lourenço, 2009, Clinics.

A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma.

J. Krieger, A. Pereira, S. Toledo, 2002, The Journal of clinical endocrinology and metabolism.

Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha.

M. Levine, B. Wajchenberg, R. Salvatori, 2000, European journal of endocrinology.

A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype.

J. Martens, H. Brunner, A. Themmen, 1998, Molecular endocrinology.

Immunohistochemistry of medullary thyroid carcinoma and C‐cell hyperplasia by an affinity‐purified anti‐human calcitonin antiserum

V. Alves, C. Y. Hayashida, S. Toledo, 1993, Cancer.