Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.
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Undiagnosed MODY: Time for ActionOpposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene.Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing.Identification and functional characterisation of novel glucokinase mutations causing maturity-onset diabetes of the young in Slovakia.Glucokinase (GCK) mutations and their characterization in MODY2 children of southern Italy.MODY: history, genetics, pathophysiology, and clinical decision making.Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.Adolescent non-adherence reveals a genetic cause for diabetesCharacteristics of maturity onset diabetes of the young in a large diabetes center.Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).When is it MODY? Challenges in the Interpretation of Sequence Variants in MODY Genes.GCK-MODY in the US National Monogenic Diabetes Registry: frequently misdiagnosed and unnecessarily treated.GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2.GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.Insight into the biochemical characteristics of a novel glucokinase gene mutation.Glucokinase mutations in pediatric patients with impaired fasting glucose.Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY).Incidental mild hyperglycemia in children: two MODY 2 families identified in Brazilian subjects.The glucokinase mutation p.T206P is common among MODY patients of Jewish Ashkenazi descent.Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic population.Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations.Genetic and bioinformatics analysis of four novel GCK missense variants detected in Caucasian families with GCK-MODY phenotype.Onset of type 1 diabetes mellitus in two patients with maturity onset diabetes of the youngThe diagnosis and management of monogenic diabetes in children and adolescentsMODY type 2 P59S GCK mutant: founder effect in South of ItalySubstantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme
P2860
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P2860
Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.
description
article científic
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article scientifique
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articolo scientifico
@it
artigo científico
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bilimsel makale
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scientific article published on 29 June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
Maturity-onset diabetes of the ...... Italian study of 172 families.
@en
Maturity-onset diabetes of the ...... Italian study of 172 families.
@nl
type
label
Maturity-onset diabetes of the ...... Italian study of 172 families.
@en
Maturity-onset diabetes of the ...... Italian study of 172 families.
@nl
prefLabel
Maturity-onset diabetes of the ...... Italian study of 172 families.
@en
Maturity-onset diabetes of the ...... Italian study of 172 families.
@nl
P2093
P2860
P356
P1433
P1476
Maturity-onset diabetes of the ...... Italian study of 172 families.
@en
P2093
Anna Paola Frongia
Christine Bellannè-Chantelot
Dario Iafusco
Franco Cerutti
Franco Meschi
Giuseppe d'Annunzio
Italian Society of Pediatric Endocrinology and Diabetology (ISPED) Study Group
Nicola Minuto
Ornella Massa
Renata Lorini
P2860
P304
P356
10.2337/DC08-2018
P407
P577
2009-06-29T00:00:00Z