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Refinado por: Nome da Publicação: Journal of Clinical Endocrinology and Metabolism remover nível superior: Disponível na Biblioteca remover
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1
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment
Material Type:
Artigo 		Adicionar ao Meu Espaço

Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment

Debora C. Coutinho Berenice B Mendonça; Rocio R. D Coletta; Elaine M. F Costa; Paulo R Pachi; Margaret C. S Boguszewski; Durval Damiani; Ivo J. P Arnhold; Alexander A. L Jorge

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 92, n. 12, p. 4889-4892, 2007

Philadelphia 2007

Localização: FM - Fac. Medicina    (BCSEP 166 2007 )(Acessar)

2
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency

Marcela M. França Alexander A. L Jorge; Kyriaki S Alatzoglou; Luciani R. S Carvalho; Berenice Bilharinho Mendonça; Laura Audi; Antonio Carrascosa; Mehul T Dattani; Ivo J. P Arnhold

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 96, n. 9, p. E1457-1460, 2011

Philadelphia 2011

Acesso online. A biblioteca também possui exemplares impressos.

3
Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly

Marcela M. França Alexander A. L Jorge; Luciani R. S Carvalho; Everlany F Costalonga; Gabriela A Vasques; Cláudia da Costa Leite; Berenice Bilharinho de Mendonça; Ivo J. P Arnhold

Journal of Clinical Endocrinology and Metabolism Springfield v. 95, n. 11, p. E384-E391, 2010

Springfield 2010

Acesso online. A biblioteca também possui exemplares impressos.

4
Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly

Marcela M. França Alexander A. L Jorge; Luciani R. S Carvalho; Everlany F Costalonga; Gabriela A Vasques; Cláudia da Costa Leite; Berenice Bilharinho de Mendonça; Ivo J. P Arnhold

Journal of Clinical Endocrinology and Metabolism Springfield v. 95, n. 11, p. E384-E391, 2010

Springfield 2010

Acesso online. A biblioteca também possui exemplares impressos.

5
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment
Material Type:
Artigo 		Adicionar ao Meu Espaço

Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment

Debora C. Coutinho Berenice B Mendonça; Rocio R. D Coletta; Elaine M. F Costa; Paulo R Pachi; Margaret C. S Boguszewski; Durval Damiani; Ivo J. P Arnhold; Alexander A. L Jorge

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 92, n. 12, p. 4889-4892, 2007

Philadelphia 2007

Localização: FM - Fac. Medicina    (BCSEP 166 2007 )(Acessar)

6
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency

Marcela M. França Alexander A. L Jorge; Kyriaki S Alatzoglou; Luciani R. S Carvalho; Berenice Bilharinho Mendonça; Laura Audi; Antonio Carrascosa; Mehul T Dattani; Ivo J. P Arnhold

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 96, n. 9, p. E1457-1460, 2011

Philadelphia 2011

Acesso online. A biblioteca também possui exemplares impressos.

7
Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults
Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults
Material Type:
Artigo 		Adicionar ao Meu Espaço

Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults

Madson Q. Almeida Ibere Cauduro Soares; Tamaya C Ribeiro; Maria Candida B. V Fragoso; Lidiane V Marins; Alda Wakamatsu; Rodrigo A Ressio; Mirian Y Nishi; Alexander A. L Jorge; Antonio M Lerario; Venancio A. F Alves; B. B Mendonca; A. C Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 3, p. 1458-1462, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

8
Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults
Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults
Material Type:
Artigo 		Adicionar ao Meu Espaço

Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults

Madson Q. Almeida Ibere Cauduro Soares; Tamaya C Ribeiro; Maria Candida B. V Fragoso; Lidiane V Marins; Alda Wakamatsu; Rodrigo A Ressio; Mirian Y Nishi; Alexander A. L Jorge; Antonio M Lerario; Venancio A. F Alves; B. B Mendonca; A. C Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 3, p. 1458-1462, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

9
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations

Alexandra Gkourogianni Melissa Andrew; Leah Tyzinski; Melissa Crocker; Jessica Douglas; Nancy Dunbar; Jan Fairchild; Mariana F. A Funari; Karen E Heath; Alexander A. L Jorge; Tracey Kurtzman; Stephen LaFranchi; Seema Lalani; Jan Lebl; Yuezhen Lin; Evan Los; Dorothee Newbern; Catherine Nowak; Micah Olson; Jadranka Popovic; Štěpánka Průhová; Lenka Elblova; Jose Bernardo Quintos; Emma Segerlund; Lucia Sentchordi; Marwan Shinawi; Eva-Lena Stattin; Jonathan Swartz; Ariadna González del Angel; Sinhué Diaz Cuéllar; Hidekazu Hosono; Pedro A Sanchez-Lara; Vivian Hwa; Jeffrey Baron; Ola Nilsson; Andrew Dauber

Journal of clinical endocrinology and metabolism Springfield v. 102, n. 2, p. 460-469, 2017

Springfield 2017

Localização: FM - Fac. Medicina    (BCSEP 130 2017 )(Acessar)

10
Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome the influence of a SOCS2 polymorphism
Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome the influence of a SOCS2 polymorphism
Material Type:
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Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome the influence of a SOCS2 polymorphism

Adriana F. Braz Everlayny F Costalonga; Ericka B Trarbach; Renata C Scalco; Alexsandra C Malaquias; Gil Guerra-Junior; Sonir Roberto Rauber Antonini; Berenice Bilharinho de Mendonça; Ivo J. P Arnhold; Alexander Augusto de Lima Jorge

Journal of clinical endocrinology and metabolism Springfield v. 99, n. 9, p. E1808-E1813, 2014

Springfield 2014

Localização: FM - Fac. Medicina    (BCSEP 023 2014 ) e outros locais(Acessar)

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Deste Autor:

  1. Jorge, A
  2. Mendonça, B
  3. Arnhold, I
  4. Latronico, A
  5. Almeida, M

Neste Assunto:

  1. Polimorfismo
  2. Crianças
  3. Mutação Genética
  4. Anatomia
  5. Jovens

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

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