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1
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)

2
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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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)

3
Análise molecular dos genes NEUROD4, FGFR1 e PROKR2 em pacientes com hipopituitarismo congênito
Análise molecular dos genes NEUROD4, FGFR1 e PROKR2 em pacientes com hipopituitarismo congênito
Material Type:
Tese de Doutorado 		Adicionar ao Meu Espaço

Análise molecular dos genes NEUROD4, FGFR1 e PROKR2 em pacientes com hipopituitarismo congênito

Correa, Fernanda De Azevedo

Biblioteca Digital de Teses e Dissertações da USP; Universidade de São Paulo; Faculdade de Medicina 2015-05-28

Acesso online. A biblioteca também possui exemplares impressos.

4
Possibly damaging FGFR1 variants in Brazilian patients with Severe Congenital Hypopituitarism
Possibly damaging FGFR1 variants in Brazilian patients with Severe Congenital Hypopituitarism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Possibly damaging FGFR1 variants in Brazilian patients with Severe Congenital Hypopituitarism

Fernanda A Correa; Erika B Trarbach; Ana Latroníco; Luciani Carvalho; Marcela França; Aline Otto; Everlayny F Costalonga; Vinivius N Brito; Mirian Y Nishi; Ivo J. P Arnhold; Berenice B Mendonça; Annual meeting of the european (50. 2011 Basel)

Basel v. 46, suppl. 2, 2011

Basel 2011

Acesso online. A biblioteca também possui exemplares impressos.

5
TRH-stimulated TSH and PRL levels in patients with PRQP1 mutations: model for exclusive congenital pituitary deficiency
TRH-stimulated TSH and PRL levels in patients with PRQP1 mutations: model for exclusive congenital pituitary deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

TRH-stimulated TSH and PRL levels in patients with PRQP1 mutations: model for exclusive congenital pituitary deficiency

F A Correa L R Carvalho; V N Brito; M Y Nishi; I J P Arnhold; Berenice Bilharinho de Mendonça; M C B V Fragoso; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S62, res. 72, 2010

São Paulo 2010

Localização: FM - Fac. Medicina    (BCBIB 2010 ) e outros locais(Acessar)

6
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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Artigo 		Adicionar ao Meu Espaço

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)

7
Growth hormone deficiency with advanced bone age phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
Growth hormone deficiency with advanced bone age phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
Material Type:
Artigo 		Adicionar ao Meu Espaço

Growth hormone deficiency with advanced bone age phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

Fernanda A. Correa Marcela M França; Qing Fang; Qianyi Ma; Tânia Aparecida Sartori Sanchez Bachega; Andresa Rodrigues; Bilge A Ozel; Jun Z Li; Berenice Bilharinho de Mendonça; Alexander Augusto de Lima Jorge; Luciani R Carvalho; Sally A Camper; Ivo J Arnhold

Archives of endocrinology metabolism v. 61, n. 6, p. 633-636, 2017

Rio De Janeiro, Rj 2017

Localização: FM - Fac. Medicina    (BCSEP 250 2017 )(Acessar)

8
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.

9
Copy number variants in Brazilian patients with congenital hypopituirarism
Copy number variants in Brazilian patients with congenital hypopituirarism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Copy number variants in Brazilian patients with congenital hypopituirarism

Fernanda A. Correa Marcela M Franca; Ana P. M Canton; Aline p Otto; Everlayne F Costalonga; Vinicius N Brito; Luciani R Carvalho; Silvia Costa; Ivo J. P Arnhold; Alexander Augusto de Lima Jorge; Carla Rosenberg; Berenice Bilharinho de Mendonça; European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting (9. 2013 Milan, Italy)

Hormone Research in Paediatrics Basel v. 80, suppl. 1, p. 161, res. P1-d1-506, 2013

Basel 2013

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

10
sucessful pregnancies and live births after adequate hormone replacement and ovarian stimulation in four patients with congenital hypopituitarism
sucessful pregnancies and live births after adequate hormone replacement and ovarian stimulation in four patients with congenital hypopituitarism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

sucessful pregnancies and live births after adequate hormone replacement and ovarian stimulation in four patients with congenital hypopituitarism

P. H. M. Bianchi P. C Serafini; R. J. M Rodrigues; L. R. S Carvalho; F. A Correa; E. C Baracat; Annual Meeting of the American Society for Reproductive Medicine Hawai) 2014 (70.

Fertility and Sterility New York v. 102, n. 3, Supl. p. e254, res. P-349, 2014

New York 2014

Localização: FM - Fac. Medicina    (BCSEP 228 2014 )(Acessar)

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