Recent Publications on Wolfram Syndrome: |  |
Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.
OBJECTIVE: Wolfram syndrome is an autosomal recessive neurodegenerative...
Direct Link | 19th November, 2008
| Pediatric Clinic, University of Genoa, G. Gaslini Institute, Genoa, Italy.
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| [The rare syndromic forms of monogenic diabetes in childhood]
| 17th October, 2008
| Kliniki Chorob Dzieci l Katedry Pediatrii UM w Lodzi.
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| Wolfram syndrome.
| 11th October, 2008
| M.V. Hospital for Diabetes and Diabetes Research Centre, Chennai.
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Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system.
Wolfram syndrome (OMIM 222300) is a neurodegenerative disorder defined by...
Direct Link | 1st October, 2008
| Laboratory for Neuroanatomy, Department of Neurology, Kagoshima University
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| Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations.
| 25th September, 2008
| Department of Genetics, Conde de Valenciana, Mexico City, Mexico.
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WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
Most cases of juvenile-onset diabetes (JOD) are diagnosed as type 1...
Direct Link | 23rd September, 2008
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Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.
Most familial cases of autosomal dominant low frequency sensorineural...
Direct Link | 16th September, 2008
| Department of Otolaryngology, Head and Neck Surgery, University of Iowa,
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| Hearing impairment in genotyped Wolfram syndrome patients.
| 13th September, 2008
| Department of Otorhinolaryngology, Radboud University Nijmegen Medical
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Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome.
Mutations in the coding region of the WFS1 gene cause Wolfram syndrome, a...
Direct Link | 21st August, 2008
| Department of Physiology, University of Tartu, Tartu 50411, Estonia.
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Dissecting the Nutrigenomics, Diabetes, and Gastrointestinal Disease Interface: From Risk Assessment to Health Intervention.
Abstract The promise of nutrigenomics is of personalized nutrition that...
Direct Link | 20th August, 2008
| The University of Auckland, Auckland, New Zealand.
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In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.
OBJECTIVES: To evaluate the auditory, vestibular, and retinal...
Direct Link | 1st August, 2008
| V. M. Bloedel Hearing Research Center, Otolaryngology-HNS Department,
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Behavioral and gene expression analyses of Wfs1 knockout mice as a possible animal model of mood disorder.
Wolfram disease is a rare genetic disorder frequently accompanying...
Direct Link | 30th July, 2008
| Laboratory for Molecular Dynamics of Mental Disorders, RIKEN Brain Science
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ATF4-mediated induction of 4E-BP1 contributes to pancreatic beta cell survival under endoplasmic reticulum stress.
Endoplasmic reticulum (ER) stress-mediated apoptosis may play a crucial...
Direct Link | 30th April, 2008
| Division of Molecular Metabolism and Diabetes, Tohoku University Graduate
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| Gene symbol: WFS1. Disease: Wolfram syndrome.
| 26th April, 2008
| Research Centre for Medical Genetics, Laboratory of Inborn Errors of
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| [Wolfram syndrome: four case reports]
| 2nd April, 2008
| Service d'Ophtalmologie A- Hopital des Specialites Rabat, Maroc.
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