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Glibenclamide unresponsiveness in a Brazilian child with permanent neonatal diabetes mellitus and DEND syndrome due to a C166Y mutation in KCNJ11 (Kir6.2) gene
(Sociedade Brasileira de Endocrinologia e Metabologia, 2008)
Heterozygous activating mutations of KCNJ11 (Kir6.2) are the most common cause of permanent neonatal diabetes mellitus (PNDM) and several cases have been successfully treated with oral sulfonylureas. We report on the ...
Glibenclamide unresponsiveness in a Brazilian child with permanent neonatal diabetes mellitus and DEND syndrome due to a C166Y mutation in KCNJ11 (Kir6.2) gene
(Sociedade Brasileira de Endocrinologia e Metabologia, 2008-11-01)
Heterozygous activating mutations of KCNJ11 (Kir6.2) are the most common cause of permanent neonatal diabetes mellitus (PNDM) and several cases have been successfully treated with oral sulfonylureas. We report on the ...
Filogenia e bioprospecção de mutações no gene ERG11 de isolados clínicos do gênero Candida
(Universidade Federal da Grande DouradosBrasilFaculdade de Ciências Biológicas e AmbientaisPrograma de pós-graduação em Biologia Geral/BioprospecçãoUFGD, 2019)
Preliminary Safety Assessment Of C-8 Xylitol Monoester And Xylitol Phosphate Esters
(Blackwell Publishing Ltd, 2016)