Neglected-Noncompliant Type 1 Diabetes Mellitus with Complications
AbstrakDiabetes mellitus (DM) tipe 1 merupakan kelainan sistemik akibat terjadinya gangguan metabolisme glukosayang ditandai oleh hiperglikemia kronis.
Afdal ., Eka Agustia Rini
doaj
The purpose of the study was to evaluate the severity of changes in the values of markers-candidates for the differential diagnosis of anemia of chronic diseases in patients with type 1 and type 2 diabetes mellitus.
N. N. Musina +3 more
doaj +1 more source
Fulminant type 1 diabetes: A distinct subtype of type 1 diabetes mellitus
Jiao Fu, Bing-Yin Shi
doaj +1 more source
PHARMACOLOGICAL NEUROPROTECTION OF TYPE 1 DIABETES MELLITUS
Type 1 diabetes mellitus (DM) - one of the most common diseases of modern endocrinology. The growing number of sick children, emergence of chronic diseases and high percentage of disability determine the severity of the problem. Diabetic neuropathy (DN),
O. Fitsner, M. Khaitovych
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Association of RPS26 gene polymorphism with different types of diabetes in Chinese individuals
Aims/Introduction Different types of diabetes show distinct genetic characteristics, but the specific genetic susceptibility factors remain unclear. Our study aimed to explore the associations between the ribosomal protein S26 (RPS26) gene rs1131017 ...
Rong Song +12 more
doaj +1 more source
Bioleptin as a useful marker of metabolic status in children with diabetes mellitus type 1. [PDF]
Jakubek-Kipa K +6 more
europepmc +1 more source
Hepatic insulin synthesis increases in rat models of diabetes mellitus type 1 and 2 differently. [PDF]
Abidov M +8 more
europepmc +1 more source
Déficits de autocuidado vivenciados por familias de crianças e adolescentes com diabetes mellitus tipo 1 [PDF]
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde. Programa de Pós-graduação em EnfermagemEste estudo constitui-se de uma pesquisa qualitativa do tipo convergente assistencial, realizada com oito famílias de ...
Mello, Maria Berra de
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Genes and type 2 diabetes: polymorphisms of the EIF2AK3 gene and its relationship to type 2 diabetes mellitus [PDF]
MDAims/ Hypothesis: Wolcott- Rallison syndrome (WRS) is a rare autosomal recessively inherited Mendelian disorder. It is characterised by a short trunk compared to arm span, multiple epiphyseal dysplasia, multiple fractures, hepatosplenomegaly and renal ...
Sudagani, Jaidev
core +1 more source
Incidence of insulin-treated diabetes in Australia 2000-2011 [PDF]
Australia\u27s rate of incidence of insulin-treated diabetes has remained stable over the last decade, with between 10 and 12 new cases per 100,000 population per year.
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