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1
Nova mutação no gene AVP-NPII em uma família com diabetes insipidus central
Nova mutação no gene AVP-NPII em uma família com diabetes insipidus central
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Nova mutação no gene AVP-NPII em uma família com diabetes insipidus central

M. E. Melo S Marui Mendonça B. B.; M Knoepfelmacher; Congresso Brasileiro de Endocrinologia e Metabologia (26. 2004 Florianópolis)

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 48, n. 5, supl. 1, p. S599, res. TLP 355, 2004

São Paulo Sociedade Brasileira de Endocrinologia e Metabologia - SBEM 2004

Item não circula. Consulte sua biblioteca.(Acessar)

2
A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus
A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus

M. E. Melo S Marui; B. B Mendonca; M Knoepfelmacher; International Congress of Endocrinology (12. 2004 Lisboa)

Program and Abstracts Lisboa: International Society of Endocrinology, 2004

Lisboa International Society of Endocrinology 2004

Localização: FM - Fac. Medicina    (BCSEP 357 2004 )(Acessar)

3
Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations
Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations

M. E. Melo S Marui; C. C Leite; B. B Mendonca; M knoepfelmacher; International Congress of Endocrinology (12. 2004 Lisboa)

Program and Abstracts Lisboa: International Society of Endocrinology, 2004

Lisboa International Society of Endocrinology 2004

Localização: FM - Fac. Medicina    (BCSEP 357 2004 )(Acessar)

4
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family

Maria Edna de Melo Suemi Marui; Vinícius Nahime de Brito; Marcio Corrêa Mancini; Berenice Bilharinho de Mendonça; Mirta Knoepfelmacher

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1272-1276, 2008

Rio de Janeiro 2008

Item não circula. Consulte sua biblioteca.(Acessar)

5
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family

Maria Edna de Melo Suemi Marui; Vinícius Nahime de Brito; Marcio Corrêa Mancini; Berenice B Mendonca; Mirta Knoepfelmacher

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 52, n. 8, p. 1272-1276, 2008

São Paulo 2008

Localização: FM - Fac. Medicina    (BCSEP 126 2008 )(Acessar)

6
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family

Maria Edna de Melo Suemi Marui; Vinícius Nahime de Brito; Marcio Corrêa Mancini; Berenice Bilharinho de Mendonça; Mirta Knoepfelmacher

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1272-1276, 2008

Rio de Janeiro 2008

Item não circula. Consulte sua biblioteca.(Acessar)

7
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe

Maria Edna Melo Suemi Marui; Luciani Renata Carvalho; Ivo Jorge Arnhold; Claudia da Costa Leite; Berenice Bilharinho Mendonça; Mirta Knoepfelmacher

Clinical Endocrinology Oxford v. 66, p. 95-102, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (FM BCSEP 001 2007 ) e outros locais(Acessar)

8
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe

Maria Edna Melo Suemi Marui; Luciani Renata Carvalho; Ivo Jorge Arnhold; Claudia da Costa Leite; Berenice Bilharinho Mendonça; Mirta Knoepfelmacher

Clinical Endocrinology Oxford v. 66, p. 95-102, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (FM BCSEP 001 2007 ) e outros locais(Acessar)

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