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Items: 1 to 20 of 186

1.

Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis.

Al-Chalabi A, Scheffler MD, Smith BN, Parton MJ, Cudkowicz ME, Andersen PM, Hayden DL, Hansen VK, Turner MR, Shaw CE, Leigh PN, Brown RH Jr.

Ann Neurol. 2003 Jul;54(1):130-4.

PMID:
12838531
2.

Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis.

Van Vught PW, Van Wijk J, Bradley TE, Plasmans D, Jakobs ME, Veldink JH, de Jong JM, Van den Berg LH, Baas F.

Neuromuscul Disord. 2007 Dec;17(11-12):964-7. Epub 2007 Jul 24.

PMID:
17651970
3.
4.

Investigation of a null mutation of the CNTF gene in familial amyotrophic lateral sclerosis.

Orrell RW, King AW, Lane RJ, de Belleroche JS.

J Neurol Sci. 1995 Oct;132(2):126-8.

PMID:
8543936
5.
6.

Association of a null mutation in the CNTF gene with early onset of multiple sclerosis.

Giess R, Mäurer M, Linker R, Gold R, Warmuth-Metz M, Toyka KV, Sendtner M, Rieckmann P.

Arch Neurol. 2002 Mar;59(3):407-9.

PMID:
11890844
7.

[Survival in amyotrophic lateral sclerosis].

Alcaz S, Jarebinski M, Pekmezović T, Marinković Z, Apostolski S.

Srp Arh Celok Lek. 1997 Jan-Feb;125(1-2):19-23. Serbian.

PMID:
17974351
8.

Decrease in the ciliary neurotrophic factor of the spinal cord in amyotrophic lateral sclerosis.

Ono S, Imai T, Igarashi A, Shimizu N, Nakagawa H, Hu J.

Eur Neurol. 1999;42(3):163-8.

PMID:
10529543
9.

Increased serum CNTF level in patients with amyotrophic lateral sclerosis.

Iłzecka J.

Eur Cytokine Netw. 2003 Jul-Sep;14(3):192-4.

10.

Progranulin genetic variability contributes to amyotrophic lateral sclerosis.

Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P, van Vught PW, van der Zee J, Serneels S, De Pooter T, Van den Broeck M, Cruts M, Schymkowitz J, De Jonghe P, Rousseau F, van den Berg LH, Robberecht W, Van Broeckhoven C.

Neurology. 2008 Jul 22;71(4):253-9. doi: 10.1212/01.wnl.0000289191.54852.75. Epub 2008 Jan 9.

PMID:
18184915
11.

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.

Giess R, Holtmann B, Braga M, Grimm T, Müller-Myhsok B, Toyka KV, Sendtner M.

Am J Hum Genet. 2002 May;70(5):1277-86. Epub 2002 Apr 9.

12.
13.

Potential implications of a ciliary neurotrophic factor gene mutation in a German population of patients with motor neuron disease.

Giess R, Goetz R, Schrank B, Ochs G, Sendtner M, Toyka K.

Muscle Nerve. 1998 Feb;21(2):236-8.

PMID:
9466600
14.

Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments.

de Belleroche J, Orrell R, King A.

J Med Genet. 1995 Nov;32(11):841-7. Review. No abstract available.

15.

Association of monoamine oxidase B alleles with age at onset in amyotrophic lateral sclerosis.

Orrù S, Mascia V, Casula M, Giuressi E, Loizedda A, Carcassi C, Giagheddu M, Contu L.

Neuromuscul Disord. 1999 Dec;9(8):593-7.

PMID:
10619718
16.

Natural history of young-adult amyotrophic lateral sclerosis.

Sabatelli M, Madia F, Conte A, Luigetti M, Zollino M, Mancuso I, Lo Monaco M, Lippi G, Tonali P.

Neurology. 2008 Sep 16;71(12):876-81. doi: 10.1212/01.wnl.0000312378.94737.45. Epub 2008 Jul 2.

PMID:
18596241
17.

Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.

Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G.

Neurosci Lett. 2007 Jun 13;420(2):163-8. Epub 2007 May 5.

PMID:
17531381
18.

Survival rate of patients with amyotrophic lateral sclerosis in Wakayama Prefecture, Japan, 1966 to 2005.

Kihira T, Yoshida S, Okamoto K, Kazimoto Y, Ookawa M, Hama K, Miwa H, Kondo T.

J Neurol Sci. 2008 May 15;268(1-2):95-101. doi: 10.1016/j.jns.2007.11.011. Epub 2007 Dec 31.

PMID:
18164728
19.

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