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83 results
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X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies.
Cambi F, Tartaglino L, Lublin F, McCarren D. Cambi F, et al. Arch Neurol. 1995 Jul;52(7):665-9. doi: 10.1001/archneur.1995.00540310035013. Arch Neurol. 1995. PMID: 7619021
Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M. Starling A, et al. Among authors: cambi f. Am J Med Genet. 2002 Aug 1;111(2):152-6. doi: 10.1002/ajmg.10551. Am J Med Genet. 2002. PMID: 12210342
Association of metabolic syndrome and change in Unified Parkinson's Disease Rating Scale scores.
Leehey M, Luo S, Sharma S, Wills AA, Bainbridge JL, Wong PS, Simon DK, Schneider J, Zhang Y, Pérez A, Dhall R, Christine CW, Singer C, Cambi F, Boyd JT. Leehey M, et al. Among authors: cambi f. Neurology. 2017 Oct 24;89(17):1789-1794. doi: 10.1212/WNL.0000000000004572. Epub 2017 Sep 29. Neurology. 2017. PMID: 28972194 Free PMC article. Clinical Trial.
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases.
Espay AJ, Vizcarra JA, Marsili L, Lang AE, Simon DK, Merola A, Josephs KA, Fasano A, Morgante F, Savica R, Greenamyre JT, Cambi F, Yamasaki TR, Tanner CM, Gan-Or Z, Litvan I, Mata IF, Zabetian CP, Brundin P, Fernandez HH, Standaert DG, Kauffman MA, Schwarzschild MA, Sardi SP, Sherer T, Perry G, Leverenz JB. Espay AJ, et al. Among authors: cambi f. Neurology. 2019 Feb 12;92(7):329-337. doi: 10.1212/WNL.0000000000006926. Neurology. 2019. PMID: 30745444 Free PMC article. Review.
The molecular pathogenesis of Pelizaeus-Merzbacher disease.
Garbern J, Cambi F, Shy M, Kamholz J. Garbern J, et al. Among authors: cambi f. Arch Neurol. 1999 Oct;56(10):1210-4. doi: 10.1001/archneur.56.10.1210. Arch Neurol. 1999. PMID: 10520936 Review.
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia.
Cambi F, Tang XM, Cordray P, Fain PR, Keppen LD, Barker DF. Cambi F, et al. Neurology. 1996 Apr;46(4):1112-7. doi: 10.1212/wnl.46.4.1112. Neurology. 1996. PMID: 8780101
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T. Fink JK, et al. Among authors: cambi f. Neurology. 1996 Jun;46(6):1507-14. doi: 10.1212/wnl.46.6.1507. Neurology. 1996. PMID: 8649538 Review.
Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study.
Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, Prakash R, Williamson S, Berg CJ, Sun M, Goldwurm S, Pezzoli G, Racette BA, Perlmutter JS, Parsian A, Baker KB, Giroux ML, Litvan I, Pramstaller PP, Nicholson G, Burn DJ, Chinnery PF, Vieregge P, Slevin JT, Cambi F, MacDonald ME, Gusella JF, Myers RH, Golbe LI. Wilk JB, et al. Among authors: cambi f. Neurology. 2006 Dec 26;67(12):2206-10. doi: 10.1212/01.wnl.0000249149.22407.d1. Neurology. 2006. PMID: 17190945
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Among authors: cambi f. Neurology. 2000 Nov 14;55(9):1388-90. doi: 10.1212/wnl.55.9.1388. Neurology. 2000. PMID: 11087788
Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1B.
Sabet A, Li J, Ghandour K, Pu Q, Wu X, Kamholz J, Shy ME, Cambi F. Sabet A, et al. Among authors: cambi f. Neurology. 2006 Oct 10;67(7):1141-6. doi: 10.1212/01.wnl.0000238499.37764.b1. Neurology. 2006. PMID: 17030746
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