Tournier-Lasserve E - Search Results

1

Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K. Damak M, et al. J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615. J Neurol Neurosurg Psychiatry. 2009. PMID: 19372292

2

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.

Vahedi K, Joutel A, Van Bogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Ann Neurol. 1995 Mar;37(3):289-93. doi: 10.1002/ana.410370304. Ann Neurol. 1995. PMID: 7695228

3

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.

Vahedi K, Denier C, Ducros A, Bousson V, Levy C, Chabriat H, Haguenau M, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Neurology. 2000 Oct 10;55(7):1040-2. doi: 10.1212/wnl.55.7.1040. Neurology. 2000. PMID: 11061267

4

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.

Vahedi K, Massin P, Guichard JP, Miocque S, Polivka M, Goutières F, Dress D, Chapon F, Ruchoux MM, Riant F, Joutel A, Gaudric A, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Neurology. 2003 Jan 14;60(1):57-63. doi: 10.1212/wnl.60.1.57. Neurology. 2003. PMID: 12525718

5

Clinical and brain MRI follow-up study of a family with COL4A1 mutation.

Vahedi K, Boukobza M, Massin P, Gould DB, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Neurology. 2007 Oct 16;69(16):1564-8. doi: 10.1212/01.wnl.0000295994.46586.e7. Neurology. 2007. PMID: 17938367

6

Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood.

Bertholon P, Chabrier S, Riant F, Tournier-Lasserve E, Peyron R. Bertholon P, et al. J Neurol Neurosurg Psychiatry. 2009 Nov;80(11):1289-92. doi: 10.1136/jnnp.2008.159103. J Neurol Neurosurg Psychiatry. 2009. PMID: 19864665

7

[Hereditary episodic ataxia].

Riant F, Vahedi K, Tournier-Lasserve E. Riant F, et al. Rev Neurol (Paris). 2011 May;167(5):401-7. doi: 10.1016/j.neurol.2010.10.016. Epub 2011 Apr 13. Rev Neurol (Paris). 2011. PMID: 21492892 Review. French.

8

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. Ann Neurol. 2006 Feb;59(2):353-7. doi: 10.1002/ana.20775. Ann Neurol. 2006. PMID: 16404745

9

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus.

Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A, et al. Chabriat H, et al. Neurology. 1995 Jun;45(6):1086-91. doi: 10.1212/wnl.45.6.1086. Neurology. 1995. PMID: 7783868

10

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. J Mal Vasc. 1996;21(5):277-82. J Mal Vasc. 1996. PMID: 9026542 Review. French.

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