Neonatal diabetes mellitus

Pediatric Diabetes

Volumn 3, Issue 2, 2002, Pages 109-112

  Shield, J P H ^a   Temple, I K ^a  

^a BRISTOL ROYAL HOSPITAL FOR CHILDREN   (United Kingdom)

Author keywords

Imprinting; Neonatal diabetes mellitus; UPD 6

Indexed keywords

GLUCOKINASE; HOMEODOMAIN PROTEIN; INSULIN;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DIABETES MELLITUS; DISEASE CLASSIFICATION; ENTEROPATHY; ENZYME DEFICIENCY; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC DISORDER; HUMAN; IMMUNOPATHOLOGY; INSULIN TREATMENT; NEWBORN; NEWBORN DISEASE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

EID: 0036045722     PISSN: 1399543X     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-5448.2002.30208.x     Document Type: Article

References (26)

1. Neonatal diabetes: A study of its aetiopathology and genetic basis
2. Long-term course of neonatal diabetes
3. Transient neonatal diabetes mellitus: Widening our understanding of the aetiopathogenesis of diabetes
4. An imprinted gene(s) for diabetes?
5. Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-23
6. The cell cycle control gene ZAC/PLAGL1 is imprinted - A strong candidate gene for transient neonatal diabetes
7. Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus
8. An imprinted locus associated with transient neonatal diabetes mellitus
9. Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus
10. A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
11. Pancreatic agenesis attributable to a single nucleotide deletion in human IPF-1 coding region
12. Insulin promoter factor-1 gene mutation linked to early onset type 2 diabetes mellitus directs expression of dominant negative isoprotein
13. Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset 2 diabetes mellitus
14. Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia
15. EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome
16. X-linked immune dysregulation, neonatal insulin dependent diabetes, and intractable diarrhoea
17. Treatment of the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) by allogeneic bone marrow transplantation
18. Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
19. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
20. Molecular and biochemical analysis of the MODY syndromes
21. Permanent neonatal diabetes mellitus due to glucokinase deficiency: An inborn error of the glucose/insulin signalling pathway
22. Complete gluco-kinase deficiency is not a common cause of permanent neonatal diabetes in European cases of neonatal diabetes
23. Distinct neurological syndrome in two brothers with hyperuricaemia
24. Neonatal diabetes mellitus and cerebellar hypoplasia/agenesis: Report of an association in three members of a consanguineous family
25. Expression of neuronal traits in pancreatic beta cells
26. Maturity onset diabetes of the young (MODY) and early onset type 2 diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locus