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1
Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism
Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism

Karina Berger Ana Elisa Correia Billerbeck; Elaine Maria Frade Costa; Luciani Silveira Carvalho; Ivo Jorge Prado Arnhold; Berenice Bilharinho de Mendonça

Clinics São Paulo v. 60, n. 6, p. 461-464, december, 2005

São Paulo 2005

Localização: FM - Fac. Medicina    (FM BCBIB )(Acessar)

2
Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism
Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism

Karina Berger Ana Elisa Correia Billerbeck; Elaine Maria Frade Costa; Luciani Silveira Carvalho; Ivo Jorge Prado Arnhold; Berenice Bilharinho de Mendonça

Clinics São Paulo v. 60, n. 6, p. 461-464, december, 2005

São Paulo 2005

Localização: FM - Fac. Medicina    (FM BCBIB )(Acessar)

3
Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage
Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage
Material Type:
Artigo 		Adicionar ao Meu Espaço

Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage

Mirian Yumie Nishi Rafaela Vieira Correa; Elaine Maria Frade Costa; Ana Elisa Correia Billerbreck; André Luis Cruzes; Sorahia Domenice; Luciani Renata Carvalho; Berenice Bilharinho de Mendonça

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1282-1287, 2008

Rio de Janeiro 2008

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

4
A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome
A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome

Rafael Loch Batista Andresa di Santi Rodrigues; Miriam Yumie Nishi; Nathalia Lisboa Gomes; José Antonio Diniz Faria Junior; Daniela Rodrigues Moraes; Luciani Renata Carvalho; Elaine Maria Frede Costa; Sorahia Domenice; Berenice Bilharinho de Mendonça

The Journal of Steroid Biochemistry and Molecular Biology Oxford v. 174, p. 14-16, 2017

Oxford 2017

Localização: FM - Fac. Medicina    (BCSEP 0161 2017 )(Acessar)

5
Androgen receptor mRNA analysis from whole blood [Carta] a low-cost strategy for detection of androgen receptor gene splicing defects
Androgen receptor mRNA analysis from whole blood [Carta] a low-cost strategy for detection of androgen receptor gene splicing defects
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Androgen receptor mRNA analysis from whole blood [Carta] a low-cost strategy for detection of androgen receptor gene splicing defects

Juliana M Silva Berenice Bilharinho de Mendonça; Rafael Loch Batista; Andresa de Santi Rodrigues; Mirian Y Nishi; Elaine M. F Costa; Sorahia Domenice; Luciani R. S Carvalho

Clinical genetics v. 94, n. 5, p. 489-490, 2018

Hoboken 2018

Localização: FM - Fac. Medicina    (OPI 29372 2018 )(Acessar)

6
Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage
Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage
Material Type:
Artigo 		Adicionar ao Meu Espaço

Tall stature and poor breast development after estrogen replacement in a hypergonoadotrophic hypogonadic patient with a 45,X/46,X,der (X) karyotype with SHOX gene overdosage

Mirian Yumie Nishi Rafaela Vieira Correa; Elaine Maria Frade Costa; Ana Elisa Correia Billerbreck; André Luis Cruzes; Sorahia Domenice; Luciani Renata Carvalho; Berenice Bilharinho de Mendonça

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1282-1287, 2008

Rio de Janeiro 2008

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

7
Ausência de mutações no gene HESX1 em pacientes portadores de deficiência do hormônio de crescimento (DGH) associada a defeitos de linha média (DLM) cerebral e ou facial
Ausência de mutações no gene HESX1 em pacientes portadores de deficiência do hormônio de crescimento (DGH) associada a defeitos de linha média (DLM) cerebral e ou facial
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Ausência de mutações no gene HESX1 em pacientes portadores de deficiência do hormônio de crescimento (DGH) associada a defeitos de linha média (DLM) cerebral e ou facial

Luciani R. S. Carvalho Suemi Marui; Vivian Estefan; Cláudia da Costa Leite; Berenice Bilharinho de Mendonça; Congresso Paulista de Endocrinologia e Metabologia (4. 2001 São Paulo)

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 45, n. 2, supl. 02, p. S199 res. PO11, 2001

São Paulo 2001

Localização: FM - Fac. Medicina    (BCSEP 2001 039 ) e outros locais(Acessar)

8
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes

Fernanda A Corrêa Alexander AL Jorge; Marilena Nakaguma; Ana PM Canton; Sílvia S Costa; Mariana F Funari; Antonio M Lerario; Marcela M Franca; Luciani R Carvalho; Ana Cristina Victorino Krepischi; Ivo JP Arnhold; Carla Rosenberg; Berenice B Mendonça

Clinical Endocrinology West Sussex online, p. 1-7, Dec. 2017

West Sussex 2017

Item não circula. Consulte sua biblioteca.(Acessar)

9
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)

10
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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Deste Autor:

  1. Mendonça, B
  2. Carvalho, L
  3. Arnhold, I
  4. Costa, E
  5. Nishi, M

Neste Assunto:

  1. Genes
  2. Hipogonadismo
  3. Transtornos Gonadais
  4. Peso-Estatura
  5. Hormônio

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

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