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Page 1
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: billard c. Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192. Am J Hum Genet. 1999. PMID: 9915947 Free PMC article.
[Oral and written language].
Billard C, Gillet P, Barthez MA. Billard C, et al. Arch Pediatr. 1999;6 Suppl 2:387s-388s. doi: 10.1016/s0929-693x(99)80477-1. Arch Pediatr. 1999. PMID: 10370545 French. No abstract available.
[A very strange seizure].
Barthez MA, Autret E, Billard C, Santini JJ. Barthez MA, et al. Among authors: billard c. Arch Fr Pediatr. 1987 Oct;44(8):622. Arch Fr Pediatr. 1987. PMID: 2964812 French. No abstract available.
[Facial paralyses a frigore misdiagnosed].
Barthez MA, Billard C, Santini JJ, Maheut J. Barthez MA, et al. Among authors: billard c. Ann Pediatr (Paris). 1987 Jun;34(6):449-50. Ann Pediatr (Paris). 1987. PMID: 3619315 French. No abstract available.
193 results