Gil R - Search Results

1

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.

Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O. Saugier-Veber P, et al. Among authors: gil r. Nat Genet. 1994 Mar;6(3):257-62. doi: 10.1038/ng0394-257. Nat Genet. 1994. PMID: 8012387

2

X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.

Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M. Bonneau D, et al. Among authors: gil r. J Med Genet. 1993 May;30(5):381-4. doi: 10.1136/jmg.30.5.381. J Med Genet. 1993. PMID: 8320699 Free PMC article.

3

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.

Dürr A, Camuzat A, Colin E, Tallaksen C, Hannequin D, Coutinho P, Fontaine B, Rossi A, Gil R, Rousselle C, Ruberg M, Stevanin G, Brice A. Dürr A, et al. Among authors: gil r. Arch Neurol. 2004 Dec;61(12):1867-72. doi: 10.1001/archneur.61.12.1867. Arch Neurol. 2004. PMID: 15596607

4

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

Tassin J, Dürr A, Bonnet AM, Gil R, Vidailhet M, Lücking CB, Goas JY, Durif F, Abada M, Echenne B, Motte J, Lagueny A, Lacomblez L, Jedynak P, Bartholomé B, Agid Y, Brice A. Tassin J, et al. Among authors: gil r. Brain. 2000 Jun;123 ( Pt 6):1112-21. doi: 10.1093/brain/123.6.1112. Brain. 2000. PMID: 10825351

5

[Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders].

Mettey R, Hoppeler A, Gil R. Mettey R, et al. Among authors: gil r. J Genet Hum. 1981 Sep;29(3):227-34. J Genet Hum. 1981. PMID: 7334346 French. No abstract available.

6

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.

Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A; French Dystonia Network. Clot F, et al. Among authors: gil r. Brain. 2009 Jul;132(Pt 7):1753-63. doi: 10.1093/brain/awp084. Epub 2009 Jun 2. Brain. 2009. PMID: 19491146

7

Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study.

Bensimon G, Ludolph A, Agid Y, Vidailhet M, Payan C, Leigh PN; NNIPPS Study Group. Bensimon G, et al. Brain. 2009 Jan;132(Pt 1):156-71. doi: 10.1093/brain/awn291. Epub 2008 Nov 23. Brain. 2009. PMID: 19029129 Free PMC article. Clinical Trial.

8

Event-related auditory evoked potentials and amyotrophic lateral sclerosis.

Gil R, Neau JP, Dary-Auriol M, Agbo C, Tantot AM, Ingrand P. Gil R, et al. Arch Neurol. 1995 Sep;52(9):890-6. doi: 10.1001/archneur.1995.00540330068017. Arch Neurol. 1995. PMID: 7661727

9

Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale.

Payan CA, Viallet F, Landwehrmeyer BG, Bonnet AM, Borg M, Durif F, Lacomblez L, Bloch F, Verny M, Fermanian J, Agid Y, Ludolph AC, Leigh PN, Bensimon G; NNIPPS Study Group. Payan CA, et al. PLoS One. 2011;6(8):e22293. doi: 10.1371/journal.pone.0022293. Epub 2011 Aug 4. PLoS One. 2011. PMID: 21829612 Free PMC article.

10

Recurrent intracerebral hemorrhage.

Neau JP, Ingrand P, Couderq C, Rosier MP, Bailbe M, Dumas P, Vandermarcq P, Gil R. Neau JP, et al. Among authors: gil r. Neurology. 1997 Jul;49(1):106-13. doi: 10.1212/wnl.49.1.106. Neurology. 1997. PMID: 9222177

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