Reproductive Outcome of Women with 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia
Moran, C, Azziz, R, Weintrob, N, Witchel, S. F, Rohmer, V, Dewailly, D, Marcondes, J. A. M, Pugeat, M, Speiser, P. W, Pignatelli, D, Mendonca, B. B, Bachega, T. A. S, Escobar-Morreale, H. F, Carmina, E, Fruzzetti, F, Kelestimur, F
Published in The journal of clinical endocrinology and metabolism (01.09.2006)
Published in The journal of clinical endocrinology and metabolism (01.09.2006)
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CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia
Moura-Massari, V O, Bugano, D D G, Marcondes, J A M, Gomes, L G, Mendonca, B B, Bachega, T A S S
Published in Hormone and metabolic research (01.04.2013)
Published in Hormone and metabolic research (01.04.2013)
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Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: Further characterization of classic and non-classic patients and heterozygote carriers
Costa-Barbosa, F. A., Carvalho, V. M., Nakamura, O. H., Bachega, T. A. S. S., Vieira, J. G. H., Kater, C. E.
Published in Journal of endocrinological investigation (01.09.2011)
Published in Journal of endocrinological investigation (01.09.2011)
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Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia
Silveira, EL, Elnecave, RH, Dos Santos, EP, Moura, V, Pinto, EM, Van Der Linden Nader, I, Mendonca, BB, Bachega, TASS
Published in Clinical genetics (01.12.2009)
Published in Clinical genetics (01.12.2009)
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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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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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Adrenal Steroids Synthesis During Acute Infectious Diseases in Infants
Longui, C.A., Zlochevsky, E.R.M., Bachega, T.A.S.S., Monte, O.
Published in Journal of Pediatric Endocrinology and Metabolism (01.11.2002)
Published in Journal of Pediatric Endocrinology and Metabolism (01.11.2002)
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Growth Potential in Congenital Adrenal Hyperplasia(Cah) Due To 21-Hydroxylase Deficiency Treated With Cortisone Acetate(Ca) and Fludrohidrocortisone(Fh)
Madureira, G, Bachega, T A S S, Arnhold, I J P, Bloise, W, Mendonça, B B
Published in Pediatric research (01.02.1997)
Published in Pediatric research (01.02.1997)
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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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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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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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