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Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
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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.

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.294-300 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Effects of Cymbopogon nardus (L.) W. Watson essential oil on the growth and morphogenesis of Aspergillus niger
Effects of Cymbopogon nardus (L.) W. Watson essential oil on the growth and morphogenesis of Aspergillus niger
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Effects of Cymbopogon nardus (L.) W. Watson essential oil on the growth and morphogenesis of Aspergillus niger

Billerbeck, V.G. de ; Roques, C.G ; Bessiere, J.M ; Fonvieille, J.L ; Dargent, R

Canadian journal of microbiology, 2001, Vol.47 (1), p.9-17 [Periódico revisado por pares]

Ottawa, ON: National Research Council of Canada

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3
A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency
A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency
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A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency

Correa, Rafaela V ; Domenice, Sorahia ; Bingham, Nathan C ; Billerbeck, Ana Elisa C ; Rainey, William E ; Parker, Keith L ; Mendonca, Berenice B

The journal of clinical endocrinology and metabolism, 2004-04, Vol.89 (4), p.1767-1772 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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4
SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability
SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability
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SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability

Jorge, Alexander A. L. ; Souza, Silvia C. ; Nishi, Miriam Y. ; Billerbeck, Ana E. ; Libório, Débora C. C. ; Kim, Chong A. ; Arnhold, Ivo J. P. ; Mendonca, Berenice B.

Clinical endocrinology (Oxford), 2007-01, Vol.66 (1), p.130-135 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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5
Differential Antigen Specificity of Hepatitis C Virus-Specific Interleukin 17-and Interferon γ-Producing CD8⁺ T Cells During Chronic Infection
Differential Antigen Specificity of Hepatitis C Virus-Specific Interleukin 17-and Interferon γ-Producing CD8⁺ T Cells During Chronic Infection
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Differential Antigen Specificity of Hepatitis C Virus-Specific Interleukin 17-and Interferon γ-Producing CD8⁺ T Cells During Chronic Infection

Grafmueller, Stefanie ; Billerbeck, Eva ; Blum, Hubert E. ; Neumann-Haefelin, Christoph ; Thimme, Robert

The Journal of infectious diseases, 2012-04, Vol.205 (7), p.1142-1146 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency
Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency
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Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency

Araújo, Rogério S ; Mendonca, Berenice B ; Barbosa, Ângela S ; Lin, Chin J ; Marcondes, José A. M ; Billerbeck, Ana Elisa C ; Bachega, Tânia A. S. S

The journal of clinical endocrinology and metabolism, 2007-10, Vol.92 (10), p.4028-4034 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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7
Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein
Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein
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Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein

Pinto, Emilia M ; Billerbeck, Ana Elisa C ; Fragoso, Maria Candida B. Villares ; Mendonca, Berenice B ; Latronico, Ana Claudia

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2976-2981 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation
Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation
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Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation

Araujo, Rogério S. ; Billerbeck, Ana Elisa C. ; Madureira, Guiomar ; Mendonca, Berenice B. ; Bachega, Tânia A. S. S.

Clinical endocrinology (Oxford), 2005-02, Vol.62 (2), p.132-136 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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9
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene
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The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

Rocha, Rosana O. ; Billerbeck, Ana Elisa C. ; Pinto, Emília M. ; Melo, Karla F. S. ; Lin, Chin J. ; Longui, Carlos A. ; Mendonca, Berenice B. ; Bachega, Tânia A. S. S.

Clinical endocrinology (Oxford), 2008-02, Vol.68 (2), p.226-232 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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