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Page 1
Did you mean maciaszek j[Author] (78 results)?
[CADASIL: genetics and physiopathology].
Joutel A, François A, Chabriat H, Vahedi K, Andreux F, Domenga V, Cecillon M, Maciazek J, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: maciazek j. Bull Acad Natl Med. 2000;184(7):1535-42; discussion 1542-4. Bull Acad Natl Med. 2000. PMID: 11261257 Review. French.
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: maciazek j. Ann N Y Acad Sci. 1997 Sep 26;826:213-7. doi: 10.1111/j.1749-6632.1997.tb48472.x. Ann N Y Acad Sci. 1997. PMID: 9329692 Review.
A gene for familial hemiplegic migraine maps to chromosome 19.
Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al. Joutel A, et al. Among authors: maciazek j. Nat Genet. 1993 Sep;5(1):40-5. doi: 10.1038/ng0993-40. Nat Genet. 1993. PMID: 8220421
ATP1A2 mutations in 11 families with familial hemiplegic migraine.
Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E. Riant F, et al. Among authors: maciazek j. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Hum Mutat. 2005. PMID: 16088919
Mutations within the MGC4607 gene cause cerebral cavernous malformations.
Denier C, Goutagny S, Labauge P, Krivosic V, Arnoult M, Cousin A, Benabid AL, Comoy J, Frerebeau P, Gilbert B, Houtteville JP, Jan M, Lapierre F, Loiseau H, Menei P, Mercier P, Moreau JJ, Nivelon-Chevallier A, Parker F, Redondo AM, Scarabin JM, Tremoulet M, Zerah M, Maciazek J, Tournier-Lasserve E; Société Française de Neurochirurgie. Denier C, et al. Among authors: maciazek j. Am J Hum Genet. 2004 Feb;74(2):326-37. doi: 10.1086/381718. Epub 2004 Jan 22. Am J Hum Genet. 2004. PMID: 14740320 Free PMC article.
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, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: maciazek j. Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0. Nature. 1996. PMID: 8878478
Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E; Sociéte Française de Neurochirgurgie; Sociéte de Neurochirurgie de Langue Française. Denier C, et al. Among authors: maciazek j. Ann Neurol. 2004 Feb;55(2):213-20. doi: 10.1002/ana.10804. Ann Neurol. 2004. PMID: 14755725
A novel hereditary small vessel disease of the brain.
Verreault S, Joutel A, Riant F, Neves G, Rui Silva M, Maciazek J, Tournier-Lasserve E, Bousser MG, Chabriat H. Verreault S, et al. Among authors: maciazek j. Ann Neurol. 2006 Feb;59(2):353-7. doi: 10.1002/ana.20775. Ann Neurol. 2006. PMID: 16404745
20 results