skip to main content
Idioma:
Resultados 1 2 3 next page
Mostrar Somente
Refinado por: assunto: Medical Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
2
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2435-2440 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

Texto completo disponível

Citações Citado por
3
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

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.

Clinical endocrinology (Oxford), 2000-05, Vol.52 (5), p.601-607 [Periódico revisado por pares]

Oxford BSL: Blackwell Science Ltd

Texto completo disponível

Citações Citado por
4
Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR
Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Journal of Clinical Microbiology, 1998-05, Vol.36 (5), p.1453-1455 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

Texto completo disponível

Citações Citado por
5
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

The journal of clinical endocrinology and metabolism, 1998-12, Vol.83 (12), p.4416-4419 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

Texto completo disponível

Citações Citado por
6
A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency
A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2870-2872 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

Texto completo disponível

Citações Citado por
7
A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

DOMENICE, S ; NISHI, M. Y ; BILHARINHO MENDONCA, B ; CORREIA BILLERBECK, A. E ; LATRONICO, A. C ; MEDEIROS, M. A ; RUSSELL, A. J ; VASS, K ; CARVALHO, F. M ; COSTA FRADE, E. M ; PRADO ARNHOLD, I. J

Human genetics, 1998-02, Vol.102 (2), p.213-215 [Periódico revisado por pares]

Heidelberg: Springer

Texto completo disponível

Citações Citado por
8
Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

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.

Human heredity, 1999-01, Vol.49 (1), p.9-14 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

Texto completo disponível

Citações Citado por
9
Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome
Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome

DAMIANI, D ; BILLERBECK, A. E. C ; GOLDBERG, A. C. K ; SETIAN, N ; FELLOUS, M ; KALIL, J

Human genetics, 1990, Vol.85 (1), p.85-88 [Periódico revisado por pares]

Berlin: Springer

Texto completo disponível

Citações Citado por
10
HIV therapy by a combination of broadly neutralizing antibodies in humanized mice
HIV therapy by a combination of broadly neutralizing antibodies in humanized mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

HIV therapy by a combination of broadly neutralizing antibodies in humanized mice

KLEIN, Florian ; HALPER-STROMBERG, Ariel ; ZANG, Trinity ; DORNER, Marcus ; BILLERBECK, Eva ; LABITT, Rachael N ; GAEBLER, Christian ; MARCOVECCHIO, Paola M ; INCESU, Reha-Baris ; EISENREICH, Thomas R ; BIENIASZ, Paul D ; SEAMAN, Michael S ; HORWITZ, Joshua A ; BJORKMAN, Pamela J ; RAVETCH, Jeffrey V ; PLOSS, Alexander ; NUSSENZWEIG, Michel C ; GRUELL, Henning ; SCHEID, Johannes F ; BOURNAZOS, Stylianos ; MOUQUET, Hugo ; SPATZ, Linda A ; DISKIN, Ron ; ABADIR, Alexander

Nature (London), 2012-12, Vol.492 (7427), p.118-122 [Periódico revisado por pares]

London: Nature Publishing Group

Texto completo disponível

Citações Citado por
Resultados 1 2 3 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (26)

Data de Publicação 

De até
Refinar
  1. Antes de1999  (6)
  2. 1999Até2001  (4)
  3. 2002Até2004  (6)
  4. 2005Até2008  (6)
  5. Após 2008  (6)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.