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1
Role of GLI2 in hypopituitarism phenotype
Role of GLI2 in hypopituitarism phenotype
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Role of GLI2 in hypopituitarism phenotype

Ivo J. P. Arnhold Marcela M França; Luciani R Carvalho; Berenice B Mendonca; Alexander A. L Jorge

Journal of Molecular Endocrinology Bristol v. 54, n. 3, p. R141-R150, 2015

Bristol 2015

Acesso online. A biblioteca também possui exemplares impressos.

2
Growth hormone (GH) pharmacogenetics
Growth hormone (GH) pharmacogenetics
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Artigo 		Adicionar ao Meu Espaço

Growth hormone (GH) pharmacogenetics

Alexander A. L. Jorge Frederico G Marchisotti; Luciana R Montenegro; Luciani R Carvalho; Ivo J. P Arnhold; Berenice Bilharinho Mendonça

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 91, n. 3, p. 1076-1080, 2006

Philadelphia 2006

Localização: FM - Fac. Medicina    (FM BCSEP 103 2006 )(Acessar)

3
Growth hormone (GH) pharmacogenetics
Growth hormone (GH) pharmacogenetics
Material Type:
Artigo 		Adicionar ao Meu Espaço

Growth hormone (GH) pharmacogenetics

Alexander A. L. Jorge Frederico G Marchisotti; Luciana R Montenegro; Luciani R Carvalho; Ivo J. P Arnhold; Berenice Bilharinho Mendonça

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 91, n. 3, p. 1076-1080, 2006

Philadelphia 2006

Localização: FM - Fac. Medicina    (FM BCSEP 103 2006 )(Acessar)

4
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy
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Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy

Luciani R. Carvalho Maria Estela Justamante de Faria; Maria Geralda Farah Osorio; Vivian Estefan; Alexander Augusto Lima Jorge; Ivo Jorge P Arnhold; Berenice B Mendonça

Clinical Endocrinology 2003 v. 59, p. 788-792, 2003

Oxford 2003

Localização: FM - Fac. Medicina    (BCSEP 2003 214 )(Acessar)

5
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy

Luciani R. Carvalho Maria Estela Justamante de Faria; Maria Geralda Farah Osorio; Vivian Estefan; Alexander Augusto Lima Jorge; Ivo Jorge P Arnhold; Berenice B Mendonça

Clinical Endocrinology 2003 v. 59, p. 788-792, 2003

Oxford 2003

Localização: FM - Fac. Medicina    (BCSEP 2003 214 )(Acessar)

6
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
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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)

7
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
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Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients

Andria C. V. Lido Marcela M França; Aline P Otto; Luciani R Carvalho; Berenice Bilharinho de Mendonça; Ivo J.P Arnhold; Alexander Augusto de Lima Jorge; European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting (9. 2013 Milan, Italy)

Hormone Research in Paediatrics Basel v. 80, suppl. 1, p. 295, res. P2-d1-952, 2013

Basel 2013

Localização: FM - Fac. Medicina    (BCSEP 418 2013 )(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
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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
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
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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.

10
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD)
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD)
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A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD)

João L. O. Madeira Alexander Augusto de Lima Jorge; Regina M Martin; Luciana Ribeiro Montenegro; Marcela M Franca; Everlayny F Costalong; Fernanda A Correa; Aline P Otto; Ivo J. P Arnhold; Helayne S Freitas; Ubiratan Fabres Machado; Berenice Bilharinho de Mendonça; Luciani R Carvalho

European journal of endocrinology Oslo v. 175, n. 02, p. K7-K15, 2016

Oslo 2016

Acesso online

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