13 results for author:"Vahedi K." in Literature citations
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| Clinical spectrum of type IV collagen (COL4A1) mutations: a novel genetic multisystem disease. Vahedi K., Alamowitch S. Curr. Opin. Neurol. 24:63-68(2011) · Mapped (5) |
| Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation. Malpas T.J., Riant F., Tournier-Lasserve E., Vahedi K., Neville B.G. Dev Med Child Neurol 52:103-104(2010) · Mapped (8) |
| Identification of CACNA1A large deletions in four patients with episodic ataxia. Riant F., Lescoat C., Vahedi K., Kaphan E., Toutain A., Soisson T., Wiener-Vacher S.R., Tournier-Lasserve E. Neurogenetics 11:101-106(2010) · Mapped (8) |
| Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. Vahedi K., Depienne C., Le Fort D., Riant F., Chaine P., Trouillard O., Gaudric A., Morris M.A., LeGuern E., Tournier-Lasserve E. et al. |
| Clinical and brain MRI follow-up study of a family with COL4A1 mutation. Vahedi K., Boukobza M., Massin P., Gould D.B., Tournier-Lasserve E., Bousser M.G. Neurology 69:1564-1568(2007) · Mapped (5) |
| COL4A1 mutation in a patient with sporadic, recurrent intracerebral hemorrhage. Vahedi K., Kubis N., Boukobza M., Arnoult M., Massin P., Tournier-Lasserve E., Bousser M.G. Stroke 38:1461-1464(2007) · UniProtKB (1) |
| Role of COL4A1 in small-vessel disease and hemorrhagic stroke. Gould D.B., Phalan F.C., van Mil S.E., Sundberg J.P., Vahedi K., Massin P., Bousser M.G., Heutink P., Miner J.H., Tournier-Lasserve E. et al. N. Engl. J. Med. 354:1489-1496(2006) · UniProtKB (1) · Mapped (7) |
| Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis. Joutel A., Favrole P., Labauge P., Chabriat H., Lescoat C., Andreux F., Domenga V., Cecillon M., Vahedi K., Ducros A. et al. Lancet 358:2049-2051(2001) · UniProtKB (1) |
| The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. Ducros A., Denier C., Joutel A., Cecillon M., Lescoat C., Vahedi K., Darcel F., Vicaut E., Bousser M.G., Tournier-Lasserve E. N. Engl. J. Med. 345:17-24(2001) · UniProtKB (1) |
| Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL. Joutel A., Chabriat H., Vahedi K., Domenga V., Vayssiere C., Ruchoux M.M., Lucas C., Leys D., Bousser M.-G., Tournier-Lasserve E. Neurology 54:1874-1875(2000) · UniProtKB (1) |
| Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Joutel A., Vahedi K., Corpechot C., Troesch A., Chabriat H., Vayssiere C., Cruaud C., Maciazek J., Weissenbach J., Bousser M.-G. et al. Lancet 350:1511-1515(1997) · UniProtKB (1) |
| A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region. Joutel A., Ducros A., Alamowitch S., Cruaud C., Domenga V., Marechal E., Vahedi K., Chabriat H., Bousser M.G., Tournier-Lasserve E. Genomics 38:192-198(1996) · UniProtKB (1) |
| Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Joutel A., Corpechot C., Ducros A., Vahedi K., Chabriat H., Mouton P., Alamowitch S., Domenga V., Cecillion M., Marechal E. et al. |