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161 results
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Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
Gleeson JG, Minnerath SR, Fox JW, Allen KM, Luo RF, Hong SE, Berg MJ, Kuzniecky R, Reitnauer PJ, Borgatti R, Mira AP, Guerrini R, Holmes GL, Rooney CM, Berkovic S, Scheffer I, Cooper EC, Ricci S, Cusmai R, Crawford TO, Leroy R, Andermann E, Wheless JW, Dobyns WB, Walsh CA, et al. Gleeson JG, et al. Among authors: crawford to. Ann Neurol. 1999 Feb;45(2):146-53. doi: 10.1002/1531-8249(199902)45:2<146::aid-ana3>3.0.co;2-n. Ann Neurol. 1999. PMID: 9989615
Perspectives on clinical trials in spinal muscular atrophy.
Swoboda KJ, Kissel JT, Crawford TO, Bromberg MB, Acsadi G, D'Anjou G, Krosschell KJ, Reyna SP, Schroth MK, Scott CB, Simard LR. Swoboda KJ, et al. Among authors: crawford to. J Child Neurol. 2007 Aug;22(8):957-66. doi: 10.1177/0883073807305665. J Child Neurol. 2007. PMID: 17761650 Free PMC article. Review.
Localization of the giant axonal neuropathy gene to chromosome 16q24.
Flanigan KM, Crawford TO, Griffin JW, Goebel HH, Kohlschütter A, Ranells J, Camfield PR, Ptácek LJ. Flanigan KM, et al. Among authors: crawford to. Ann Neurol. 1998 Jan;43(1):143-8. doi: 10.1002/ana.410430126. Ann Neurol. 1998. PMID: 9450783
Toxic neuropathy in patients with pre-existing neuropathy.
Chaudhry V, Chaudhry M, Crawford TO, Simmons-O'Brien E, Griffin JW. Chaudhry V, et al. Among authors: crawford to. Neurology. 2003 Jan 28;60(2):337-40. doi: 10.1212/01.wnl.0000043691.53710.53. Neurology. 2003. PMID: 12552058
Pentobarbital for status.
Crawford TO, Mitchell WG, Snodgrass RS. Crawford TO, et al. Neurology. 1994 Apr;44(4):782-3. doi: 10.1212/wnl.44.4.782-c. Neurology. 1994. PMID: 8164854 No abstract available.
Intraventricular alpha 2b interferon for SSPE.
Mitchell WG, Crawford TO. Mitchell WG, et al. Among authors: crawford to. Neurology. 1987 Dec;37(12):1884. doi: 10.1212/wnl.37.12.1884. Neurology. 1987. PMID: 3683883 No abstract available.
161 results