Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: Treatment with sulfonylurea and 40-yr follow-up

Pediatric Diabetes

Volumn 13, Issue 2, 2012, Pages 155-162

  Søvik, Oddmund ^a   Aagenæs, Øystein ^b   Eide, Stig Å ^c   Mackay, Deborah ^d   Temple, Isabel K ^d   Molven, Anders ^a,c   Njølstad, Pål R ^a,c  

^a UNIVERSITY OF BERGEN   (Norway)

^b ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

^c HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^d UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

Author keywords

Chromosome 6; Neonatal diabetes mellitus; Sulfonylurea

Indexed keywords

GLUCOSE; INSULIN; ORAL ANTIDIABETIC AGENT; SULFONYLUREA;

ARTICLE; AUTOSOME; BIRTH WEIGHT; CASE REPORT; CHROMOSOME 6; CHROMOSOME 6Q24; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; DIABETES MELLITUS; DNA METHYLATION; DNA SEQUENCE; FAMILIAL DISEASE; FEMALE; FOLLOW UP; GENE MUTATION; GLUCOSE BLOOD LEVEL; HUMAN; MALE; NEWBORN; NEWBORN DIABETES MELLITUS; PRIORITY JOURNAL; TREATMENT DURATION;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 6; DIABETES MELLITUS; FEMALE; FOLLOW-UP STUDIES; GENE DUPLICATION; HUMANS; HYPOGLYCEMIC AGENTS; INFANT; INSULIN; MALE; METFORMIN; SULFONYLUREA COMPOUNDS; TREATMENT OUTCOME; YOUNG ADULT;

EID: 84857503464     PISSN: 1399543X     EISSN: 13995448     Source Type: Journal    
DOI: 10.1111/j.1399-5448.2011.00776.x     Document Type: Article

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