[CITATION][C] Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes
Diabetologia, 2002•Springer
2. Von Muhlendahl KE, Herkenoff H 1995) Long-term course of neonatal diabetes. N Engl J
Med 333: 704±708 3. Temple IK, Gardner RJ, Mackay DJ, Barber JC, Robinson DO, Shield
JP 2000) Transient neonatal diabetes: widening the understanding of the etiopathogenesis
of diabetes. Diabetes 49: 1359±1366 4. Delepine M, Nicolino M, Barrett T, Golamaully M,
Lathrop GM, Julier C 2000) EIF2AK3, encoding translation initiation factor 2-a kinase, is
mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25: 406±409 5. Wildin RS …
Med 333: 704±708 3. Temple IK, Gardner RJ, Mackay DJ, Barber JC, Robinson DO, Shield
JP 2000) Transient neonatal diabetes: widening the understanding of the etiopathogenesis
of diabetes. Diabetes 49: 1359±1366 4. Delepine M, Nicolino M, Barrett T, Golamaully M,
Lathrop GM, Julier C 2000) EIF2AK3, encoding translation initiation factor 2-a kinase, is
mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25: 406±409 5. Wildin RS …
2. Von Muhlendahl KE, Herkenoff H 1995) Long-term course of neonatal diabetes. N Engl J Med 333: 704±708 3. Temple IK, Gardner RJ, Mackay DJ, Barber JC, Robinson DO, Shield JP 2000) Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes. Diabetes 49: 1359±1366 4. Delepine M, Nicolino M, Barrett T, Golamaully M, Lathrop GM, Julier C 2000) EIF2AK3, encoding translation initiation factor 2-a kinase, is mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25: 406±409
5. Wildin RS, Ramsdell F, Peak J et al. 2001) X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nat Genet 27: 18±20 6. Njùlstad PR, Sovik O, Cuesta-Munoz A et al. 2001) Neonatal diabetes mellitus due to complete glucokinase deficiency. N Engl J Med 344: 1588±1592
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