Limpar
4 resultados

Acesso aberto

Tipo do recurso

Ano de criação

Produção nacional

Revisado por pares

Áreas

Idioma

Editores

Artigo Acesso aberto Revisado por pares

F. Bouldjennet, Anette P. Gjesing, Malha Azzouz, Samir Ait Abderrahman, A. El Guecier, Said M. Ali, Brahim Oudjit, Farida Mennadi-Lacete, Lyèce Yargui, A. Boudiba, A. Chibane, Chafia Touil–Boukoffa, Torben Hansen, Rachida Raache,

To investigate the prevalence of variants within selected maturity-onset diabetes of the young (MODY)-genes among Algerian patients initially diagnosed with type 1 diabetes (T1D) or type 2 diabetes (T2D), yet presenting with a MODY-like phenotype.Eight unrelated patients with early-onset diabetes (before 30 years) and six relatives with diabetes were examined by targeted re-sequencing for variants in genes known to be involved in MODY (HNF1A, GCK, HNF4A, HNF1B, INS, ABCC8, KCNJ1). Clinical data for probands ...

Tópico(s): Genetics and Neurodevelopmental Disorders

2020 - Dove Medical Press | Diabetes Metabolic Syndrome and Obesity

Artigo Revisado por pares

K. Hireche, F. Lacete, H. Benkhedda, A. Lebied,

Tópico(s): Urological Disorders and Treatments

1999 - Elsevier BV | Archives de Pédiatrie