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 unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty
LATRONICO, A. C, ABELL, A. N, ARNHOLD, I. J. P, LIU, X, LINS, T. S. S, BRITO, V. N, BILLERBECK, A. E, SEGALOFF, D. L, MENDONCA, B. B
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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
A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome
Melo, Karla F.S., Latronico, Ana Claudia, Costa, Elaine M.F., Billerbeck, Ana Elisa C., Mendonca, Berenice B., Arnhold, Ivo J.P.
Published in Human mutation (01.10.1999)
Published in Human mutation (01.10.1999)
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Journal Article
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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Journal Article
Post-mortem forensic identity testing: application of PCR to the identification of fire victim
Soares-Vieira, J A, Billerbeck, A E, Iwamura, E S, Cardoso, L d, Romero Muñoz, D
Published in São Paulo medical journal (04.05.2000)
Published in São Paulo medical journal (04.05.2000)
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Journal Article
Nongenetic Male Pseudohermaphroditism and Reduced Prenatal Growth
de Zegher, Francis, Mendonca, Berenice B, Billerbeck, Ana Elisa C
Published in The New England journal of medicine (11.10.2001)
Published in The New England journal of medicine (11.10.2001)
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Journal Article
Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reaction
Domenice, S, Billerbeck, A E, Rocha, R O, Nishi, M Y, Medeiros, M A, Bachega, T A, Budunki, V, Mendonca, B B
Published in Revista do Hospital das Clinicás (01.03.1998)
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Published in Revista do Hospital das Clinicás (01.03.1998)
Journal Article
Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue
Domenice, S, Nishi, M Y, Billerbeck, A E, Carvalho, F M, Frade, E M, Latronico, A C, Arnhold, I J, Mendonca, B B
Published in Medical science monitor (01.03.2001)
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Published in Medical science monitor (01.03.2001)
Journal Article
A Unique Constitutively Activating Mutation in Third Transmembrane Helix of Luteinizing Hormone Receptor Causes Sporadic Male Gonadotropin-Independent Precocious Puberty1
Latronico, A. C, Abell, A. N, Arnhold, I. J. P, Liu, X, Lins, T. S. S, Brito, V. N, Billerbeck, A. E, Segaloff, D. L, Mendonca, B. B
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
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Journal Article
A Unique Constitutively Activating Mutation in Third Transmembrane Helix of Luteinizing Hormone Receptor Causes Sporadic Male Gonadotropin-Independent Precocious Puberty 1
Latronico, A. C., Abell, A. N., Arnhold, I. J. P., Liu, X., Lins, T. S. S., Brito, V. N., Billerbeck, A. E., Segaloff, D. L., Mendonca, B. B.
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
Published in The journal of clinical endocrinology and metabolism (01.07.1998)
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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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