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Administration of nitric oxide synthase inhibitors does not alter disease course of amyotrophic lateral sclerosis SOD1 mutant transgenic mice.
Ann Neurol. 1999 Mar;45(3):413-4. doi: 10.1002/1531-8249(199903)45:3<413::aid-ana24>3.0.co;2-5.
Ann Neurol. 1999.
PMID: 10072062
No abstract available.
Basic fibroblast growth factor does not prolong survival in a transgenic model of familial amyotrophic lateral sclerosis.
Upton-Rice MN, Cudkowicz ME, Warren L, Mathew RK, Ren JM, Finklestein SP, Brown RH Jr.
Upton-Rice MN, et al.
Ann Neurol. 1999 Dec;46(6):934. doi: 10.1002/1531-8249(199912)46:6<934::aid-ana21>3.0.co;2-0.
Ann Neurol. 1999.
PMID: 10589551
No abstract available.
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Effect of neurophilin ligands on motor units in mice with SOD1 ALS mutations.
Shefner JM, Brown RH Jr, Cole D, Chaturvedi P, Schoenfeld D, Pastuszak K, Matthews R, Upton-Rice M, Cudkowicz ME.
Shefner JM, et al.
Neurology. 2001 Nov 27;57(10):1857-61. doi: 10.1212/wnl.57.10.1857.
Neurology. 2001.
PMID: 11723276
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Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy.
Shefner JM, Reaume AG, Flood DG, Scott RW, Kowall NW, Ferrante RJ, Siwek DF, Upton-Rice M, Brown RH Jr.
Shefner JM, et al.
Neurology. 1999 Oct 12;53(6):1239-46. doi: 10.1212/wnl.53.6.1239.
Neurology. 1999.
PMID: 10522879
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