De Toffol B - Search Results

1

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees.

Praline J, Guennoc AM, Vourc'h P, De Toffol B, Corcia P. Praline J, et al. Among authors: de toffol b. Amyotroph Lateral Scler. 2010;11(1-2):154-6. doi: 10.3109/17482960802483038. Amyotroph Lateral Scler. 2010. PMID: 20184517

2

ALS and mercury intoxication: a relationship?

Praline J, Guennoc AM, Limousin N, Hallak H, de Toffol B, Corcia P. Praline J, et al. Among authors: de toffol b. Clin Neurol Neurosurg. 2007 Dec;109(10):880-3. doi: 10.1016/j.clineuro.2007.07.008. Epub 2007 Aug 23. Clin Neurol Neurosurg. 2007. PMID: 17719172

3

Pure bulbar motor neuron involvement linked to an abnormal CAG repeat expansion in the androgen receptor gene.

Praline J, Guennoc AM, Malinge MC, de Toffol B, Corcia P. Praline J, et al. Among authors: de toffol b. Amyotroph Lateral Scler. 2008 Feb;9(1):40-2. doi: 10.1080/17482960701553915. Amyotroph Lateral Scler. 2008. PMID: 17852020

4

Occurrence of eye movement disorders in motor neuron disease.

Beaufils E, Corcia P, de Toffol B, Praline J. Beaufils E, et al. Among authors: de toffol b. Amyotroph Lateral Scler. 2012 Jan;13(1):84-6. doi: 10.3109/17482968.2011.580848. Epub 2011 Nov 25. Amyotroph Lateral Scler. 2012. PMID: 22117133

5

[Primary lateral sclerosis with breast cancer, a potential paraneoplastic neurological syndrome].

Corcia P, Honnorat J, Guennoc AM, de Toffol B, Autret A. Corcia P, et al. Among authors: de toffol b. Rev Neurol (Paris). 2000 Nov;156(11):1020-2. Rev Neurol (Paris). 2000. PMID: 11119056 French.

6

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.

Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Among authors: de toffol b. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.

7

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Among authors: de toffol b. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

8

Association of a paraneoplastic motor neuron disease with anti-Ri antibodies and a novel SOD1 I18del mutation.

Diard-Detoeuf C, Dangoumau A, Limousin N, Biberon J, Vourc'h P, Andres CR, de Toffol B, Praline J. Diard-Detoeuf C, et al. Among authors: de toffol b. J Neurol Sci. 2014 Feb 15;337(1-2):212-4. doi: 10.1016/j.jns.2013.11.025. Epub 2013 Nov 27. J Neurol Sci. 2014. PMID: 24296360

9

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.

Corcia P, Khoris J, Couratier P, Mayeux-Portas V, Bieth E, De Toffol B, Autret A, Müh JP, Andres C, Camu W. Corcia P, et al. Among authors: de toffol b. Neurology. 2002 Nov 12;59(9):1464-6. doi: 10.1212/01.wnl.0000032500.73621.c5. Neurology. 2002. PMID: 12427909

10

[Acute motor axonal neuropathy, enterovirus and Amyotrophic lateral sclerosis: can there be a link?].

Corcia P, Giraud P, Guennoc AM, de Toffol B, Autret A. Corcia P, et al. Among authors: de toffol b. Rev Neurol (Paris). 2003 Jan;159(1):80-2. Rev Neurol (Paris). 2003. PMID: 12618659 French.

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