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762 results

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Page 1
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.
Ducros A, Nagy T, Alamowitch S, Nibbio A, Joutel A, Vahedi K, Chabriat H, Iba-Zizen MT, Julien J, Davous P, Goas JY, Lyon-Caen O, Dubois B, Ducrocq X, Salsa F, Ragno M, Burkhard P, Bassetti C, Hutchinson M, Vérin M, Viader F, Chapon F, Levasseur M, Mas JL, Delrieu O, et al. Ducros A, et al. Among authors: julien j. Am J Hum Genet. 1996 Jan;58(1):171-81. Am J Hum Genet. 1996. PMID: 8554054 Free PMC article.
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Among authors: julien j. Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192. Am J Hum Genet. 1999. PMID: 9915947 Free PMC article.
[Autosomal dominant centronuclear myopathy].
Ferrer X, Vital C, Coquet M, Deleplanque B, Ellie E, Lagueny A, Julien J. Ferrer X, et al. Among authors: julien j. Rev Neurol (Paris). 1992;148(10):622-30. Rev Neurol (Paris). 1992. PMID: 1295057 Review. French.
[Multiple sclerosis: current problems].
Julien J, Ferrer X. Julien J, et al. Ann Med Interne (Paris). 1988;139(3):206-12. Ann Med Interne (Paris). 1988. PMID: 3059905 Review. French. No abstract available.
[Limb-girdle syndrome. A study of 46 cases].
Ferrer X, Larrivière M, Coquet M, Ellie E, Lagueny A, Julien J. Ferrer X, et al. Among authors: julien j. Rev Neurol (Paris). 1993;149(12):788-93. Rev Neurol (Paris). 1993. PMID: 7997739 Review. French.
[Paraneoplastic cerebral venous thrombosis].
Ellie E, Becouarn Y, Brunet R, Gonday G, Julien J. Ellie E, et al. Among authors: julien j. Rev Neurol (Paris). 1993;149(4):297-9. Rev Neurol (Paris). 1993. PMID: 8235231 French.
762 results