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1
Role of GLI2 in hypopituitarism phenotype
Role of GLI2 in hypopituitarism phenotype
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Artigo 		Adicionar ao Meu Espaço

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
Analysis of Craniofacial and Extremity Growth in Patients with Growth Hormone Deficiency during Growth Hormone Therapy
Analysis of Craniofacial and Extremity Growth in Patients with Growth Hormone Deficiency during Growth Hormone Therapy
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Analysis of Craniofacial and Extremity Growth in Patients with Growth Hormone Deficiency during Growth Hormone Therapy

Maria Estela Justamante de Faria Luciani R Carvalho; Shirley M Rossetto; Terezinha Sampaio Amaral; Karina Berger; Ivo Jorge Arnhold Prado; Berenice Bilharinho Mendonca

Hormone research in paediatrics Basel v. 71, n. 3, p. 173-177, 2009

Basel 2009

Acesso online. A biblioteca também possui exemplares impressos.

3
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
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An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles

Viviani De-Marco Luciani R Carvalho; Mariana F Guzzo; Paulo S. L Oliveira; Larissa G Gomes; Berenice B Mendonca

Clinics São Paulo v. 72, n. 9, p. 575-581, 2017

São Paulo 2017

Localização: FM - Fac. Medicina    (BCSEP 004 2017 )(Acessar)

4
Absence of HEXS1 gene mutations in patients with growth hormone deficiency (GHD) associated to cerebral and/or facial midline defects (MLD)
Absence of HEXS1 gene mutations in patients with growth hormone deficiency (GHD) associated to cerebral and/or facial midline defects (MLD)
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Artigo de Congresso 		Adicionar ao Meu Espaço

Absence of HEXS1 gene mutations in patients with growth hormone deficiency (GHD) associated to cerebral and/or facial midline defects (MLD)

Luciani R. S. Carvalho Berenice Bilharinho de Mendonca; Veronica Mericq; Jose A. M Marcondes; Teresa C. A Vieira; Mirta Knoepfelmacher; Fernando Kok; Ivo J. P Arnhold; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)

Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 33A res. P2-194, 2001

Philadelphia 2001

Item não circula. Consulte sua biblioteca.(Acessar)

5
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
Material Type:
Artigo 		Adicionar ao Meu Espaço

An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles

De-Marco, Viviani; Carvalho, Luciani R.; Guzzo, Mariana F.; Oliveira, Paulo S.L.; Gomes, Larissa G.; Mendonca, Berenice B.

Clinics; v. 72 n. 9 (2017); 575-581

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo 2017-10-01

Acesso online

6
PROP1 overexpression in corticotrophinomas evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
PROP1 overexpression in corticotrophinomas evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
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PROP1 overexpression in corticotrophinomas evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

Ricardo V. Araujo Claudia V Chang; Valter A. S Cescato; Maria Candida B. V Fragoso; Marcello D Bronstein; Berenice B Mendonca; Ivo J. P Arnhold; Luciani R. S Carvalho

Clinics São Paulo v. 68, n. 6, p. 887-891, 2013

São Paulo 2013

Localização: FM - Fac. Medicina    (BCSEP 045 2013 )(Acessar)

7
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly
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Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly

Marcela M. França Alexander A. L Jorge; Luciani R. S Carvalho; Everlayny F Costalonga; Aline P Otto; Fernanda A Correa; Berenice B Mendonca; Ivo J. P Arnhold

Clinical endocrinology Oxford v. 78, n. 4, p. 551-557, 2013

Oxford 2013

Localização: FM - Fac. Medicina    (BECEP 091 2013 )(Acessar)

8
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency a long term follow-up of patients from a single center
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency a long term follow-up of patients from a single center
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Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency a long term follow-up of patients from a single center

Aline P. Otto Marcela M França; Fernanda A Correa; Everlayny F Costalonga; Claudia C Leite; Berenice B Mendonca; Ivo J. P Arnhold; Luciani R. S Carvalho; Alexander A. L Jorge

Pituitary Norwell, MA v. 18, n. 4, p. 561-567, 2015

Norwell, MA 2015

Localização: FM - Fac. Medicina    (BCSEP 314 2015 )(Acessar)

9
PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
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PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

Araujo, Ricardo V.; Chang, Claudia V.; Cescato, Valter A. S.; Fragoso, Maria Candida B. V.; Bronstein, Marcello D.; Mendonca, Berenice B.; Arnhold, Ivo J. P.; Carvalho, Luciani R. S.

Clinics; v. 68 n. 6 (2013); 887-891

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo 2013-06-01

Acesso online

10
Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma
Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma
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Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma

Claudia Veiga Chang Ricardo Vieira Araujo; Cinthya Santos Cirqueira; Carolina Maria Gomes Cani; Hamilton Matushita; Valter Angelo Sperling Cescato; Maria Candida Barisson Villares Fragoso; Marcello Delano Bronstein; Maria Claudia Nogueira Zerbini; Berenice Bilharinho Mendonca; Luciani Renata Carvalho

Neuroendocrinology Basel v. 104, p. 183-193, 2017

Basel 2017

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Mendonca, B
  2. Carvalho, L
  3. Arnhold, I
  4. Araujo, R
  5. Jorge, A

Neste Assunto:

  1. Glândula Pituitária
  2. Mutação Genética
  3. Biomarcadores
  4. Adenoma
  5. Hiperadrenocorticismo

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

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