Lista de obras -

A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.

artículo científico publicado en 2010

A new method for body fat evaluation, body adiposity index, is useful in women with familial partial lipodystrophy

artículo científico publicado en 2011

Adiponectin complexes composition in Japanese-Brazilians regarding their glucose tolerance status

artículo científico publicado en 2013

Association of fat mass and obesity-associated (FTO) gene rs9939609 with obesity-related traits and glucose intolerance in an indigenous population, the Xavante

artículo científico publicado en 2022

Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese Brazilians

artículo científico publicado en 2009

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation

artículo científico publicado en 2008

Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation

artículo científico publicado en 2007

Comparison of Body Composition Study by Dual-Energy X-Ray Absorptiometry (DEXA) in Familial Partial Lipodystrophies and Control Subjects

article

Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation

artículo científico publicado en 2007

Dual-energy X-ray absorptiometry study of body composition in patients with lipodystrophy

artículo científico publicado en 2007

Erratum: Body composition study by dual-energy x-ray absorptiometry in familial partial lipodystrophy: finding new tools for an objective evaluation.

artículo científico publicado en 2015

Evaluation of body adiposity index (BAI) to estimate percent body fat in an indigenous population

artículo científico publicado en 2013

Evidence for a direct effect of captopril on early steps of insulin action in BC3H-1 myocytes.

artículo científico publicado en 2003

Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture

artículo científico publicado en 2012

High prevalence of type 2 diabetes mellitus in Xavante Indians from Mato Grosso, Brazil

artículo científico publicado en 2014

Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation

artículo científico publicado en 2010

Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.

artículo científico publicado en 2008

Influence of the polymorphisms Tpr64Arg in the beta 3-adrenergic receptor gene and Pro12Ala in the PPAR gamma 2 gene on metabolic syndrome-related phenotypes in an indigenous population of the Brazilian Amazon.

artículo científico publicado en 2004

Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene

artículo científico publicado en 2010

Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism

artículo científico publicado en 2012

Maturity-onset diabetes of the young (MODY) in Brazil: Establishment of a national registry and appraisal of available genetic and clinical data.

artículo científico publicado en 2016

Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10

scientific article published on 25 October 2005

Neonatal diabetes mellitus

artículo científico publicado en 2008

Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians

artículo científico publicado en 2008

Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene

artículo científico publicado en 2017

Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations

scientific article published on 14 June 2012

Plasma adiponectin levels and incident glucose intolerance in Japanese-Brazilians: a seven-year follow-up study.

artículo científico publicado en 2006

Role of the Gly40Ser mutation in the glucagon receptor gene in Brazilian patients with type 2 diabetes mellitus

artículo científico publicado en 2002

Serum 25-hydroxyvitamin D concentration and its association with glucose intolerance in an indigenous population

artículo científico publicado en 2020

Serum retinol binding protein 4 in patients with familial partial lipodystrophy

artículo científico publicado en 2009

Special issue on molecular genetics in endocrinology

artículo científico publicado en 2012

Sulfonylrea treatment in permanent neonatal diabetes due to G53D mutation in the KCNJ11 gene: improvement in glycemic control and neurological function

artículo científico publicado en 2007

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.

artículo científico publicado en 2008

[The mother factor in the transmission of DM type 2: environment or inheritance?]

artículo científico publicado en 2006

[Wolfram syndrome: from definition to molecular bases]

scientific article published on 01 October 2006

Lista de obras de

A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.

A new method for body fat evaluation, body adiposity index, is useful in women with familial partial lipodystrophy

Adiponectin complexes composition in Japanese-Brazilians regarding their glucose tolerance status

Association of fat mass and obesity-associated (FTO) gene rs9939609 with obesity-related traits and glucose intolerance in an indigenous population, the Xavante

Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese Brazilians

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation

Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation

Comparison of Body Composition Study by Dual-Energy X-Ray Absorptiometry (DEXA) in Familial Partial Lipodystrophies and Control Subjects

Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation

Dual-energy X-ray absorptiometry study of body composition in patients with lipodystrophy

Erratum: Body composition study by dual-energy x-ray absorptiometry in familial partial lipodystrophy: finding new tools for an objective evaluation.

Evaluation of body adiposity index (BAI) to estimate percent body fat in an indigenous population

Evidence for a direct effect of captopril on early steps of insulin action in BC3H-1 myocytes.

Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture

High prevalence of type 2 diabetes mellitus in Xavante Indians from Mato Grosso, Brazil

Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation

Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.

Influence of the polymorphisms Tpr64Arg in the beta 3-adrenergic receptor gene and Pro12Ala in the PPAR gamma 2 gene on metabolic syndrome-related phenotypes in an indigenous population of the Brazilian Amazon.

Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene

Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism

Maturity-onset diabetes of the young (MODY) in Brazil: Establishment of a national registry and appraisal of available genetic and clinical data.

Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10

Neonatal diabetes mellitus

Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians

Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene

Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations

Plasma adiponectin levels and incident glucose intolerance in Japanese-Brazilians: a seven-year follow-up study.

Role of the Gly40Ser mutation in the glucagon receptor gene in Brazilian patients with type 2 diabetes mellitus

Serum 25-hydroxyvitamin D concentration and its association with glucose intolerance in an indigenous population

Serum retinol binding protein 4 in patients with familial partial lipodystrophy

Special issue on molecular genetics in endocrinology

Sulfonylrea treatment in permanent neonatal diabetes due to G53D mutation in the KCNJ11 gene: improvement in glycemic control and neurological function

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.

[The mother factor in the transmission of DM type 2: environment or inheritance?]

[Wolfram syndrome: from definition to molecular bases]