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M A Giuffrida

Showing results (31-40 of 40) with videos related to

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Cardiovascular Diabetology|November 13, 2024
Low-frequency variants in genes involved in glutamic acid metabolism and γ-glutamyl cycle and risk of coronary artery disease in type 2 diabetesFernando M A Giuffrida, Sharan K Rai, Yaling Tang, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|August 6, 2008
Relationship between GH response and glycemic fluctuations in the glucagon stimulation testFernando M A Giuffrida, Karina Berger, Lia Monte, et al.
Journal of Diabetes and Its Complications|March 31, 2012
Association of ADIPOQ variants, total and high molecular weight adiponectin levels with coronary artery disease in diabetic and non-diabetic Brazilian subjectsCarolina S V Oliveira, Pedro Saddi-Rosa, Felipe Crispim, et al.
Archives of Endocrinology and Metabolism|February 8, 2018
More than kin, less than kind: one family and the many faces of diabetes in youthLuciana F Franco, Renata Peixoto-Barbosa, Renata P Dotto, et al.
Diabetes Research and Clinical Practice|February 26, 2013
A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian familiesFernando M A Giuffrida, Luis Eduardo Calliari, Thais Della Manna, et al.
Diabetes Research and Clinical Practice|June 21, 2016
Unexpected finding of a whole HNF1B gene deletion during the screening of rare MODY types in a series of Brazilian patients negative for GCK and HNF1A mutationsRenata P Dotto, Fernando M A Giuffrida, Luciana Franco, et al.
Cardiovascular Diabetology|December 29, 2012
Heterogeneous behavior of lipids according to HbA1c levels undermines the plausibility of metabolic syndrome in type 1 diabetes: data from a nationwide multicenter surveyFernando M A Giuffrida, Alexis D Guedes, Eloa R Rocco, et al.
Diabetes Research and Clinical Practice|September 2, 2014
Three unreported glucokinase (GCK) missense mutations detected in the screening of thirty-two Brazilian kindreds for GCK and HNF1A-MODYLetícia S Weinert, Sandra P Silveiro, Fernando M A Giuffrida, et al.
Archives of Endocrinology and Metabolism|May 9, 2019
Searching for mutations in the HNF1B gene in a Brazilian cohort with renal cysts and hyperglycemiaRenata P Dotto, Lucas Santos de Santana, Susan C Lindsey, et al.
Diabetes Research and Clinical Practice|December 25, 2016
Maturity-onset diabetes of the young (MODY) in Brazil: Establishment of a national registry and appraisal of available genetic and clinical dataFernando M A Giuffrida, Regina S Moises, Leticia S Weinert, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Cardiovascular Diabetology|November 13, 2024
Low-frequency variants in genes involved in glutamic acid metabolism and γ-glutamyl cycle and risk of coronary artery disease in type 2 diabetesFernando M A Giuffrida, Sharan K Rai, Yaling Tang, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|August 6, 2008
Relationship between GH response and glycemic fluctuations in the glucagon stimulation testFernando M A Giuffrida, Karina Berger, Lia Monte, et al.
Journal of Diabetes and Its Complications|March 31, 2012
Association of ADIPOQ variants, total and high molecular weight adiponectin levels with coronary artery disease in diabetic and non-diabetic Brazilian subjectsCarolina S V Oliveira, Pedro Saddi-Rosa, Felipe Crispim, et al.
Archives of Endocrinology and Metabolism|February 8, 2018
More than kin, less than kind: one family and the many faces of diabetes in youthLuciana F Franco, Renata Peixoto-Barbosa, Renata P Dotto, et al.
Diabetes Research and Clinical Practice|February 26, 2013
A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian familiesFernando M A Giuffrida, Luis Eduardo Calliari, Thais Della Manna, et al.
Diabetes Research and Clinical Practice|June 21, 2016
Unexpected finding of a whole HNF1B gene deletion during the screening of rare MODY types in a series of Brazilian patients negative for GCK and HNF1A mutationsRenata P Dotto, Fernando M A Giuffrida, Luciana Franco, et al.
Cardiovascular Diabetology|December 29, 2012
Heterogeneous behavior of lipids according to HbA1c levels undermines the plausibility of metabolic syndrome in type 1 diabetes: data from a nationwide multicenter surveyFernando M A Giuffrida, Alexis D Guedes, Eloa R Rocco, et al.
Diabetes Research and Clinical Practice|September 2, 2014
Three unreported glucokinase (GCK) missense mutations detected in the screening of thirty-two Brazilian kindreds for GCK and HNF1A-MODYLetícia S Weinert, Sandra P Silveiro, Fernando M A Giuffrida, et al.
Archives of Endocrinology and Metabolism|May 9, 2019
Searching for mutations in the HNF1B gene in a Brazilian cohort with renal cysts and hyperglycemiaRenata P Dotto, Lucas Santos de Santana, Susan C Lindsey, et al.
Diabetes Research and Clinical Practice|December 25, 2016
Maturity-onset diabetes of the young (MODY) in Brazil: Establishment of a national registry and appraisal of available genetic and clinical dataFernando M A Giuffrida, Regina S Moises, Leticia S Weinert, et al.
Pageof 4