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Refinado por: autor: Nishi, M remover
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1
Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort
Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort

Andria C. V. Lido Marcela M França; Fernanda A Correa; Aline P Otto; Luciani R Carvalho; Elisangela P. S Quedas; Mirian Y Nishi; Berenice B Mendonça; Ivo J. P Arnhold; Alexander A. L Jorge

Growth Hormone and IGF Research London v. 24, n. 5, p. 180-186, 2014

London 2014

Localização: FM - Fac. Medicina    (BCSEP 450 2014 )(Acessar)

2
Combined pituitary hormone deficiency caused by PROP1 mutations update 20 years post-discovery
Combined pituitary hormone deficiency caused by PROP1 mutations update 20 years post-discovery
Material Type:
Artigo 		Adicionar ao Meu Espaço

Combined pituitary hormone deficiency caused by PROP1 mutations update 20 years post-discovery

Fernanda A Correa Marilena Nakaguma; Joao L. O Madeira; Mirian Y Nishi; Milena G Abrao; Alexander Augusto de Lima Jorge; Luciani R Carvalho; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça

Archives of endocrinology metabolism v. 63, n. 2, p. 167-174, 2019

Rio De Janeiro, Rj 2019

Acesso online. A biblioteca também possui exemplares impressos.

3
Absent or late adrenarche and pubarche and cortisol deficiency in patients with combined pituitary hormone deficiency (CPHD) due to PROP1 mutations
Absent or late adrenarche and pubarche and cortisol deficiency in patients with combined pituitary hormone deficiency (CPHD) due to PROP1 mutations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Absent or late adrenarche and pubarche and cortisol deficiency in patients with combined pituitary hormone deficiency (CPHD) due to PROP1 mutations

Frederico G. Marchisotti M. Y Nishi; Karina Berger; Luciani R. S Carvalho; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça; Annual Meeting of the Endocrine Society's (88. 2006 Boston)

Program & Abstracts Boston, 2006

Boston 2006

Localização: FM - Fac. Medicina    (FM BCSEP 245 2006 ) e outros locais(Acessar)

4
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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)

5
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)

6
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)

7
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)

8
Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors
Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors

Maria Helena Soares Costa Ana Claudia Latronico; Regina Matsunaga Martin; Angela S Barbosa; Madson Q Almeida; Claudimara Ferini Pacicco Lotfi; Helena P. Lima Valassi; Mirian Yumie Nishi; Antônio Marmo Lucon; Sheila Aparecida Siqueira; Maria Cláudia Nogueira Zerbini; Luciani Renata Carvalho; Berenice Bilharinho de Mendonça; Maria Candida Barisson Villares Fragoso

Journal of Endocrinology London v. 200, n. 2, p. 167-175, 2009

London 2009

Item não circula. Consulte sua biblioteca.(Acessar)

9
Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors
Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors

Maria Helena Soares Costa Ana Claudia Latronico; Regina Matsunaga Martin; Angela S Barbosa; Madson Q Almeida; Claudimara Ferini Pacicco Lotfi; Helena P. Lima Valassi; Mirian Yumie Nishi; Antônio Marmo Lucon; Sheila Aparecida Siqueira; Maria Cláudia Nogueira Zerbini; Luciani Renata Carvalho; Berenice Bilharinho de Mendonça; Maria Candida Barisson Villares Fragoso

Journal of Endocrinology London v. 200, n. 2, p. 167-175, 2009

London 2009

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Mendonça, B
  2. Nishi, M
  3. Carvalho, L
  4. Costa, E
  5. Domenice, S

Neste Assunto:

  1. Mutação Genética
  2. Transtornos Gonadais
  3. Peso-Estatura
  4. Gonadotrofina Coriônica (Análise)
  5. Genes

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

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