DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins (Q84061922)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19521719%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

title

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins (English)

1 reference

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31 January 2020

2

1 reference

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31 January 2020

Karen Temple

series ordinal

3

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31 January 2020

5

Oddmund Søvik

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31 January 2020

6

Pål Rasmus Njølstad

1 reference

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31 January 2020

4

Anders Molven

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31 January 2020

author name string

Lene Bjerke Laborie

series ordinal

1

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31 January 2020

publication date

13 June 2009

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European Journal of Pediatrics

31 January 2020

published in

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31 January 2020

volume

169

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31 January 2020

issue

2

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31 January 2020

page(s)

207-213

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https://scigraph.springernature.com/pub.10.1007/s00431-009-1008-y

31 January 2020

exact match

0 references

cites work

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

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Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.

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Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

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Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes

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Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

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Prune-belly syndrome in two children and review of the literature

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Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

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Prune belly syndrome: clinicopathologic study of 29 cases

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Patterns of inheritance in familial prune belly syndrome

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Whole gene deletion of the hepatocyte nuclear factor-1beta gene in a patient with the prune-belly syndrome

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

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Neonatal diabetes: new insights into aetiology and implications

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The prune belly syndrome: a review of its etiology, defects, treatment and prognosis

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An imprinted gene(s) for diabetes?

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Epigenetics in development

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Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

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Aetiopathology and genetic basis of neonatal diabetes

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Concordant prune belly syndrome in monozygotic twins

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12 December 2020

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

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Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

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Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region.

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Permanent diabetes mellitus in the first year of life

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Refinement of the 6q chromosomal region implicated in transient neonatal diabetes

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Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23

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12 December 2020