Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2008-11-21
pubmed:abstractText
Knowing the molecular background of monogenic diabetes in affected individuals influences the clinical practice. Mutations in the HNF1A gene are the most frequent cause of MODY. The aim of the present study was to identify the genetic and clinical characteristics of HNF1A MODY in a Polish population, and the prevalence of diabetic complications and renal malformations.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1262-3636
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
524-8
pubmed:meshHeading
pubmed-meshheading:18838325-Abdomen, pubmed-meshheading:18838325-Adult, pubmed-meshheading:18838325-Blood Glucose, pubmed-meshheading:18838325-C-Peptide, pubmed-meshheading:18838325-Cholesterol, pubmed-meshheading:18838325-Cholesterol, HDL, pubmed-meshheading:18838325-Cholesterol, LDL, pubmed-meshheading:18838325-Diabetes Mellitus, Type 2, pubmed-meshheading:18838325-Female, pubmed-meshheading:18838325-Hemoglobin A, Glycosylated, pubmed-meshheading:18838325-Hepatocyte Nuclear Factor 1-alpha, pubmed-meshheading:18838325-Humans, pubmed-meshheading:18838325-Kidney, pubmed-meshheading:18838325-Male, pubmed-meshheading:18838325-Middle Aged, pubmed-meshheading:18838325-Mutation, pubmed-meshheading:18838325-Poland, pubmed-meshheading:18838325-Quantitative Trait Loci, pubmed-meshheading:18838325-Reference Values, pubmed-meshheading:18838325-Triglycerides
pubmed:year
2008
pubmed:articleTitle
Molecular background and clinical characteristics of HNF1A MODY in a Polish population.
pubmed:affiliation
Department of Metabolic Diseases, Jagiellonian University, Medical College, 15, Kopernika Street, 31-501 Krakow, Poland.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't