(Q40335643)

19 September 2017

title

Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents (English)

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19 September 2017

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4

Lebl J

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19 September 2017

Feigerlová E

1

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19 September 2017

Pruhová S

2

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19 September 2017

Dittertová L

3

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19 September 2017

Pinterová D

5

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19 September 2017

Kolostová K

6

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19 September 2017

Cerná M

7

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19 September 2017

Pedersen O

8

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19 September 2017

Hansen T

9

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19 September 2017

language of work or name

English

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publication date

7 April 2006

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European Journal of Pediatrics

19 September 2017

published in

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19 September 2017

volume

165

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19 September 2017

issue

7

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19 September 2017

page(s)

446-452

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Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

19 September 2017

cites work

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12 December 2020

Type 2 diabetes mellitus is becoming the most common type of diabetes in school children

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12 December 2020

Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young

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12 December 2020

Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes

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12 December 2020

Prediction of type 1 diabetes mellitus in first degree Czech relatives of diabetic patients

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12 December 2020

A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.

1 reference

12 December 2020

Pre-type I diabetes. Linear loss of beta cell response to intravenous glucose.

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12 December 2020

beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations

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12 December 2020

Immunogenetic determinants and prediction of IDDM in French schoolchildren

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12 December 2020

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha

1 reference

12 December 2020

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

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12 December 2020

Standardization of IVGTT to predict IDDM

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12 December 2020

Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM

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12 December 2020

[MODY in clinical practice. When and why to consider it?]

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12 December 2020

Neonatal diabetes: new insights into aetiology and implications

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12 December 2020

Maturity-onset diabetes of the young (MODY): genetic and clinical characteristics

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12 December 2020

Stability of autoantibodies and their relation to genetic and metabolic markers of Type I diabetes in initially unaffected schoolchildren.

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12 December 2020

Newly defined genetic diabetes syndromes: maturity onset diabetes of the young

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12 December 2020

First-phase insulin response in young healthy children at genetic and immunological risk for Type I diabetes.

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12 December 2020

Diagnosis and classification of diabetes mellitus

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12 December 2020

Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: how effective are the techniques of DHPLC and direct sequencing used in combination?

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12 December 2020

10.1007/S00431-006-0106-3

Identifiers

DOI

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19 September 2017

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