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MeSH Review

Wolfram Syndrome

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Disease relevance of Wolfram Syndrome


High impact information on Wolfram Syndrome


Biological context of Wolfram Syndrome


Gene context of Wolfram Syndrome


  1. Ophthalmologic findings in fifteen patients with Wolfram syndrome. Al-Till, M., Jarrah, N.S., Ajlouni, K.M. European journal of ophthalmology. (2002) [Pubmed]
  2. Mitochondrial DNA studies in Wolfram (DIDMOAD) syndrome. Seyrantepe, V., Topaloglu, H., Simsek, E., Ozguc, M., Yordam, N. Lancet (1996) [Pubmed]
  3. Adult-onset type 1 diabetes with DIDMOAD syndrome-like manifestations. Fukui, M., Kitagawa, Y., Nakamura, N., Yoshikawa, T. Arch. Intern. Med. (2001) [Pubmed]
  4. Treatment of DIDMOAD syndrome with thiamine. Schwingshandl, J., Borkenstein, M. J. Pediatr. (1989) [Pubmed]
  5. Wolfram syndrome: identification of a phenotypic and genotypic variant from Jordan. Ajlouni, K., Jarrah, N., El-Khateeb, M., El-Zaheri, M., El Shanti, H., Lidral, A. Am. J. Med. Genet. (2002) [Pubmed]
  6. Molecular characterization of WFS1 in patients with Wolfram syndrome. van ven Ouweland, J.M., Cryns, K., Pennings, R.J., Walraven, I., Janssen, G.M., Maassen, J.A., Veldhuijzen, B.F., Arntzenius, A.B., Lindhout, D., Cremers, C.W., Van Camp, G., Dikkeschei, L.D. The Journal of molecular diagnostics : JMD. (2003) [Pubmed]
  7. Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family. Ohata, T., Koizumi, A., Kayo, T., Shoji, Y., Watanabe, A., Monoh, K., Higashi, K., Ito, S., Ogawa, O., Wada, Y., Takada, G. Hum. Genet. (1998) [Pubmed]
  8. Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis. Awata, T., Inoue, K., Kurihara, S., Ohkubo, T., Inoue, I., Abe, T., Takino, H., Kanazawa, Y., Katayama, S. Biochem. Biophys. Res. Commun. (2000) [Pubmed]
  9. A DIDMOAD syndrome family with juvenile glaucoma and myopia findings. Bekir, N.A., Güngör, K., Güran, S. Acta ophthalmologica Scandinavica. (2000) [Pubmed]
  10. Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study. Soliman, A.T., Bappal, B., Darwish, A., Rajab, A., Asfour, M. Arch. Dis. Child. (1995) [Pubmed]
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