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Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.
Inappropriately elevated insulin secretion is the hallmark of persistent hyperinsulinemic hypoglycemia of infancy (PHHI), also denoted congenital hyperinsulinism. Causal mutations have been uncovered… Expand
Bone mass in non-insulin-dependent diabetes mellitus.
- U. Rishaug, K. Birkeland, J. Falch, S. Vaaler
- Scandinavian journal of clinical and laboratory…
- 1 May 1995
In view of the contradictory results of earlier reports regarding bone mass in patients with non-insulin-dependent diabetes, we measured bone mass using dual X-ray absorptiometry and ultrasound… Expand
NIDDM: a rapid progressive disease Results from a long-term, randomised, comparative study of insulin or sulphonylurea treatment
Summary The objective of the present study was to assess the relative efficacy of insulin or glibenclamide treatment for non-insulin-dependent diabetes mellitus (NIDDM) over 42 months. We performed a… Expand
Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.
- A. Molven, U. Rishaug, G. Matre, P. Njølstad, O. Søvik
- Biology, Medicine
- American journal of medical genetics
- 15 November 2002
Hypoglycemia is a dreaded complication in diabetes mellitus patients treated with insulin, but is also a symptom that is observed in many disorders. In some metabolic diseases of early infancy, low… Expand