Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
Abrão, M. G., Leite, M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., Martin, R. M., Arnhold, I. J. P., Mendonca, B. B.
Published in Clinical endocrinology (Oxford) (01.09.2006)
Published in Clinical endocrinology (Oxford) (01.09.2006)
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A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency
BILLERBECK, A. E. C, BACHEGA, T. A. S. S, FRAZZATTO, E. T, NISHI, M. Y, GOLDBERG, A. C, MARIN, M. L. C, MADUREIRA, G, MONTE, O, ARNHOLD, I. J. P, MENDONCA, B. B
Published in The journal of clinical endocrinology and metabolism (01.08.1999)
Published in The journal of clinical endocrinology and metabolism (01.08.1999)
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Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency
Mangklabruks, A, Billerbeck, A E, Wajchenberg, B, Knobel, M, Cox, N J, DeGroot, L J, Medeiros-Neto, G
Published in The journal of clinical endocrinology and metabolism (01.02.1991)
Published in The journal of clinical endocrinology and metabolism (01.02.1991)
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Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
BACHEGA, T. A. S. S, BILLERBECK, A. E. C, MADUREIRA, G, MARCONDES, J. A. M, LONGUI, C. A, LEITE, M. V, ARNHOLD, I. J. P, MENDONCA, B. B
Published in The journal of clinical endocrinology and metabolism (01.12.1998)
Published in The journal of clinical endocrinology and metabolism (01.12.1998)
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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Bachega, Tânia A. S. S., Billerbeck, Ana E. C., Marcondes, José A. M., Madureira, Guiomar, Arnhold, Ivo J. P., Mendonca, Berenice B.
Published in Clinical endocrinology (Oxford) (01.05.2000)
Published in Clinical endocrinology (Oxford) (01.05.2000)
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Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR
ROMERO, E. C, BILLERBECK, A. E. C, LANDO, V. S, CAMARGO, E. D, SOUZA, C. C, YASUDA, P. H
Published in Journal of Clinical Microbiology (01.05.1998)
Published in Journal of Clinical Microbiology (01.05.1998)
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A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
Targovnik, H M, Vono, J, Billerbeck, A E, Cerrone, G E, Varela, V, Mendive, F, Wajchenberg, B L, Medeiros-Neto, G
Published in The journal of clinical endocrinology and metabolism (01.11.1995)
Published in The journal of clinical endocrinology and metabolism (01.11.1995)
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Journal Article
Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Bachega, Tânia A.S.S., Billerbeck, Ana Elisa C., Madureira, Guiomar, Arnhold, Ivo J.P., Medeiros, Maria A., Marcondes, José A.M., Longui, Carlos A., Nicolau, Willian, Bloise, Walter, Mendonca, Berenice B.
Published in Human heredity (01.01.1999)
Published in Human heredity (01.01.1999)
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Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31
Bachega, T AS, Billerbeck, A E C, Madureira, G, Amhold, I J P, Marcondes, J A M, Longui, C A, Medeiros, M A, Bloise, W, Nicolau, W, Mendonça, B B
Published in Pediatric research (01.02.1998)
Published in Pediatric research (01.02.1998)
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Gene and genotype frequencies for HLA-DQA1 in Caucasians and Mulattoes in Brazil
Soares-Vieira, J A, Billerbeck, A E, Iwamura, E S, Otto, P A, Muñoz, D R
Published in Journal of forensic sciences (01.09.1999)
Published in Journal of forensic sciences (01.09.1999)
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Frequency of Deletions and Gene Conversions in Brazilian Patients With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency
Bachega, T A S, Billerbeck, A E C, Madureira, G, Amhold, I J P, New, M I, Nicolau, W, Marcondes, J A M, Longui, C A, Medeiros, M A, Bloise, W, Villares, S M F, Bianco, A C, Mendonça, B B
Published in Pediatric research (01.02.1997)
Published in Pediatric research (01.02.1997)
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