Additional Distinct Findings in Three Cases with Wolfram Syndrome

Turk J Med Sci 2005; 35(1): 51-55. Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.1.
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Additional Distinct Findings in Three Cases with Wolfram Syndrome

Turk J Med Sci 2005; 35(1): 51-55. Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.1.
Keywords:

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  • 1. Wolfram D, Wagener HP, Diabetes mellitus and simple optic atrophy among siblings: report of four cases. Maya Clin 13: 715- 718, 1938.
  • 2. Barrett TG, Bundey SE, Macleod AF. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome. Lancet 346: 1458-1463, 1995.
  • 3. Kinsley BT, Swift M, Dumont RH, et al. Morbidity and mortality in the Wolfram syndrome. Diabetes Care 18: 1566-1570, 1995. 4. Fraser FC, Gunn T. Diabetes mellitus, diabetes insipidus and optic atrophy. An autosomal recessive syndome? J Med Genet 14: 190- 193, 1997.
  • 5. Osman AA, Saito M, Makepeace C et al. Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium. J Biol Chem 26: 52755-52762, 2003.
  • 6. Gunn T, Bortolussi R, Little JM et al. Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness and diabtees insipidus - a syndrome. J Pediatre 89: 565-570, 1976.
  • 7. Polymeropoulos MH, Seift M, Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4. Nat Genet 8: 95-97, 1994.
  • 8. Jackson MJ, Bindoff LA, Weber K et al. Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabates mellitus, optic atrophy and deafness. Diabetes Care 7: 728-33, 1994.
  • 9. Swift RG, Polymeropoulos MH, Torres R et al. Predisposition of Wolfram syndrome heterozygotes to psychiatric illness. Mol. Psychiat 3: 86-91, 1998.
  • 10. Genis D, Davalos A, Molins A et al. Wolfram syndrome: a neuropathological study: Acta Neuropathol 9: 426-429, 1997. 11. Barrett TG, Bundey SE. Wolfram (DIDMOAD) syndrome J Med Genet 34: 838-841, 1997.
  • 12. Strom TM, Hörtnagel K, Hofmann S et al. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (D‹DMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Human Molecular Genetics 13: 2021- 2028, 1998.
  • 13. Sequeira A, Kim C, Seguin M et al. Wolfram syndrome and suicide: Evidence for a role of WFS1 in suicidal and impulsive behavior. Am J Med Genet 15: 108-13, 2003.
  • 14. Delbello MP, Strakowski SM, Zimmerman ME et al. MRI analysis of the cerebellum in bipolar disorder: a pilot study. Neuropsychopharmacology 21: 63-8, 1999.
Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
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