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Arquivos Brasileiros De Endocrinologia E Metabologia
|
July 8, 2008
[Molecular aspects of pituitary tumorigenesis]
Emilia M Pinto, Marcello D Bronstein
Best Practice & Research. Clinical Endocrinology & Metabolism
|
September 14, 2010
Familial predisposition to adrenocortical tumors: clinical and biological features and management strategies
Raul C Ribeiro, Emilia M Pinto, Gerard P Zambetti
Acta Neuropathologica
|
August 31, 2019
An update on the central nervous system manifestations of Li-Fraumeni syndrome
Brent A Orr, Michael R Clay, Emilia M Pinto, et al.
Genes & Cancer
|
July 23, 2011
TP53-Associated Pediatric Malignancies
Emilia M Pinto, Raul C Ribeiro, Bonald C Figueiredo, et al.
Molecular and Cellular Endocrinology
|
November 2, 2011
The International Pediatric Adrenocortical Tumor Registry initiative: contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors
Raul C Ribeiro, Emilia M Pinto, Gerard P Zambetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 2021
Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma
Michael R Clay, Emilia M Pinto, Lauren Fishbein, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 3, 2005
Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg337His mutation of the p53 tumor suppressor protein
Emilia M Pinto, Ana Elisa C Billerbeck, Maria Candida B Villares Fragoso, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia
|
March 12, 2005
Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors
Emilia M Pinto, Ana Elisa C Billerbeck, Maria Candida B F Villares, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
May 21, 2010
Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of β cells
Silvana M Lovisolo, Berenice B Mendonça, Emilia M Pinto, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect
Ana Elisa C Billerbeck, Berenice B Mendonca, Emilia M Pinto, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Arquivos Brasileiros De Endocrinologia E Metabologia
|
July 8, 2008
[Molecular aspects of pituitary tumorigenesis]
Emilia M Pinto, Marcello D Bronstein
Best Practice & Research. Clinical Endocrinology & Metabolism
|
September 14, 2010
Familial predisposition to adrenocortical tumors: clinical and biological features and management strategies
Raul C Ribeiro, Emilia M Pinto, Gerard P Zambetti
Acta Neuropathologica
|
August 31, 2019
An update on the central nervous system manifestations of Li-Fraumeni syndrome
Brent A Orr, Michael R Clay, Emilia M Pinto, et al.
Genes & Cancer
|
July 23, 2011
TP53-Associated Pediatric Malignancies
Emilia M Pinto, Raul C Ribeiro, Bonald C Figueiredo, et al.
Molecular and Cellular Endocrinology
|
November 2, 2011
The International Pediatric Adrenocortical Tumor Registry initiative: contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors
Raul C Ribeiro, Emilia M Pinto, Gerard P Zambetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 2021
Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma
Michael R Clay, Emilia M Pinto, Lauren Fishbein, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 3, 2005
Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg337His mutation of the p53 tumor suppressor protein
Emilia M Pinto, Ana Elisa C Billerbeck, Maria Candida B Villares Fragoso, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia
|
March 12, 2005
Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors
Emilia M Pinto, Ana Elisa C Billerbeck, Maria Candida B F Villares, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
May 21, 2010
Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of β cells
Silvana M Lovisolo, Berenice B Mendonça, Emilia M Pinto, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect
Ana Elisa C Billerbeck, Berenice B Mendonca, Emilia M Pinto, et al.
Page
of 4