Blasco H - Search Results

1

Treatment of hereditary amyotrophic lateral sclerosis.

Corcia P, Blasco H, Beltran S, Piegay AS, Vourc'h P. Corcia P, et al. Among authors: blasco h. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):54-60. doi: 10.1016/j.neurol.2022.09.001. Epub 2022 Nov 3. Rev Neurol (Paris). 2023. PMID: 36336493 Review.

2

[Chronic demyelinating polyneuropathy and B6 hypervitaminosis].

Castagnet S, Blasco H, Vourc'h P, Andres CR, Praline J. Castagnet S, et al. Among authors: blasco h. Rev Med Interne. 2010 Dec;31(12):e1-3. doi: 10.1016/j.revmed.2010.03.457. Epub 2010 Jun 2. Rev Med Interne. 2010. PMID: 20627481 French.

3

Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS.

Limousin N, Blasco H, Corcia P, Gordon PH, De Toffol B, Andres C, Praline J. Limousin N, et al. Among authors: blasco h. J Neurol Sci. 2010 Oct 15;297(1-2):36-9. doi: 10.1016/j.jns.2010.06.028. Epub 2010 Jul 31. J Neurol Sci. 2010. PMID: 20673675

4

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.

Blasco H, Corcia P, Veyrat-Durebex C, Coutadeur C, Fournier C, Camu W, Gordon P, Praline J, Andres CR, Vourc'h P; French ALS Study Group. Blasco H, et al. Amyotroph Lateral Scler. 2011 May;12(3):210-4. doi: 10.3109/17482968.2010.522587. Epub 2010 Oct 11. Amyotroph Lateral Scler. 2011. PMID: 20932227

5

1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosis.

Blasco H, Corcia P, Moreau C, Veau S, Fournier C, Vourc'h P, Emond P, Gordon P, Pradat PF, Praline J, Devos D, Nadal-Desbarats L, Andres CR. Blasco H, et al. PLoS One. 2010 Oct 8;5(10):e13223. doi: 10.1371/journal.pone.0013223. PLoS One. 2010. PMID: 20949041 Free PMC article.

6

APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in men.

Praline J, Blasco H, Vourc'h P, Garrigue MA, Gordon PH, Camu W, Corcia P, Andres CR; French ALS Study Group. Praline J, et al. Among authors: blasco h. Eur J Neurol. 2011 Aug;18(8):1046-52. doi: 10.1111/j.1468-1331.2010.03330.x. Epub 2011 Jan 20. Eur J Neurol. 2011. PMID: 21251163

7

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis.

Blasco H, Vourc'h P, Nadjar Y, Ribourtout B, Gordon PH, Guettard YO, Camu W, Praline J, Meininger V, Andres CR, Corcia P; French ALS study group. Blasco H, et al. J Neurol Sci. 2011 Apr 15;303(1-2):124-7. doi: 10.1016/j.jns.2010.12.018. Epub 2011 Jan 26. J Neurol Sci. 2011. PMID: 21276595

8

The high frequency of restless legs syndrome in patients with amyotrophic lateral sclerosis.

Limousin N, Blasco H, Corcia P, Arnulf I, Praline J. Limousin N, et al. Among authors: blasco h. Amyotroph Lateral Scler. 2011 Jul;12(4):303-6. doi: 10.3109/17482968.2011.557736. Epub 2011 Feb 11. Amyotroph Lateral Scler. 2011. PMID: 21314298

9

Predictive value of motor evoked potentials in clinically isolated syndrome.

Pallix-Guyot M, Guennoc AM, Blasco H, de Toffol B, Corcia P, Praline J. Pallix-Guyot M, et al. Among authors: blasco h. Acta Neurol Scand. 2011 Dec;124(6):410-6. doi: 10.1111/j.1600-0404.2011.01498.x. Epub 2011 Mar 1. Acta Neurol Scand. 2011. PMID: 21355856

10

Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma.

Corcia P, Praline J, Guennoc AM, Thépault RA, Gordon PH, Blasco H, Andres CR, Vourc'h P. Corcia P, et al. Among authors: blasco h. J Neurol Sci. 2011 Oct 15;309(1-2):16-7. doi: 10.1016/j.jns.2011.07.044. Epub 2011 Aug 17. J Neurol Sci. 2011. PMID: 21851955

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