Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes.

Porta, Massimo; Toppila, Iiro; Sandholm, Niina; Hosseini, S Mohsen; Forsblom, Carol; Hietala, Kustaa; Borio, Lorenzo; Harjutsalo, Valma; Klein, Barbara E; Klein, Ronald; Paterson, Andrew D; Groop, Per-Henrik

Porta, Massimo; Toppila, Iiro; Sandholm, Niina; Hosseini, S Mohsen; Forsblom, Carol; Hietala, Kustaa; Borio, Lorenzo; Harjutsalo, Valma; Klein, Barbara E; Klein, Ronald; Paterson, Andrew D; Groop, Per-Henrik.

Afiliação

Porta M; Department of Medical Sciences, University of Turin, Turin, Italy.
Toppila I; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Abdominal Center Nephrology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland Diabetes and Obesity Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Sandholm N; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Abdominal Center Nephrology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland Diabetes and Obesity Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Hosseini SM; Genetics and Genome Biology Program, Hospital for Sick Children, Toronto, Canada.
Forsblom C; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Abdominal Center Nephrology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland Diabetes and Obesity Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Hietala K; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Department of Ophthalmology, Helsinki University Central Hospital, Helsinki, Finland.
Borio L; Department of Medical Sciences, University of Turin, Turin, Italy.
Harjutsalo V; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Abdominal Center Nephrology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland Diabetes and Obesity Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland National In
Klein BE; Department Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI.
Klein R; Department Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI.
Paterson AD; Genetics and Genome Biology Program, Hospital for Sick Children, Toronto, Canada.
Groop PH; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland Abdominal Center Nephrology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland Diabetes and Obesity Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland Baker IDI H

Diabetes ; 65(4): 1022-30, 2016 04.

Article em En | MEDLINE | ID: mdl-26718501

Assuntos

Diabetes Mellitus Tipo 1/complicações; Diabetes Mellitus Tipo 1/genética; Angiopatias Diabéticas/genética; Proteínas de Membrana Transportadoras/genética; Polimorfismo de Nucleotídeo Único; Adulto; Estudos de Casos e Controles; Citoproteção/genética; Nefropatias Diabéticas/genética; Retinopatia Diabética/genética; Feminino; Predisposição Genética para Doença; Estudo de Associação Genômica Ampla; Humanos; Masculino; Metanálise como Assunto; Pessoa de Meia-Idade

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Polimorfismo de Nucleotídeo Único / Diabetes Mellitus Tipo 1 / Angiopatias Diabéticas Tipo de estudo: Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália

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