-
1
-
-
0038281572
-
Degenerative diseases of the nervous system
-
Adams RD, Victor M, eds. New York: McGrall-Hill
-
Adams RD, Victor M. Degenerative diseases of the nervous system. In: Adams RD, Victor M, eds. Principles of neurology. New York: McGrall-Hill, 1989:953-956
-
(1989)
Principles of Neurology
, pp. 953-956
-
-
Adams, R.D.1
Victor, M.2
-
2
-
-
0017182853
-
Familial motor neuron disease: Evidence for at least three different types
-
Horton WA, Eldridge R, Brody JA. Familial motor neuron disease: evidence for at least three different types. Neurology 1976:26:460-465
-
(1976)
Neurology
, vol.26
, pp. 460-465
-
-
Horton, W.A.1
Eldridge, R.2
Brody, J.A.3
-
3
-
-
0028986461
-
Neurodegenerative disease and risk factors: A literature review
-
Emard JF, Thouez JP, Gauvreau D, Neurodegenerative disease and risk factors: a literature review. Soc Sci Med 1995;40:847-858
-
(1995)
Soc Sci Med
, vol.40
, pp. 847-858
-
-
Emard, J.F.1
Thouez, J.P.2
Gauvreau, D.3
-
4
-
-
0008787510
-
The epidemiology of neurologic disease
-
Joynt R, ed. Philadelphia: JB Lippincott
-
Kurtzke JF, Kurland LT. The epidemiology of neurologic disease. In: Joynt R, ed. Clinical neurology. Philadelphia: JB Lippincott, 1983:1-43
-
(1983)
Clinical Neurology
, pp. 1-43
-
-
Kurtzke, J.F.1
Kurland, L.T.2
-
5
-
-
0025869916
-
Incidence and prevalence of amyotrophic lateral sclerosis in Harris County, Texas, 1985-1988
-
Annegers JF, Appel S, Lee JF, Perkins P. Incidence and prevalence of amyotrophic lateral sclerosis in Harris County, Texas, 1985-1988. Arch Neurol 1988:48:589-593
-
(1988)
Arch Neurol
, vol.48
, pp. 589-593
-
-
Annegers, J.F.1
Appel, S.2
Lee, J.F.3
Perkins, P.4
-
7
-
-
0022443737
-
Familial adult motor neuron disease: Amyotrophic lateral sclerosis
-
Mulder DW, Kurland LT, Offord KP, Beard CM. Familial adult motor neuron disease: amyotrophic lateral sclerosis. Neurology 1986;36:511-517
-
(1986)
Neurology
, vol.36
, pp. 511-517
-
-
Mulder, D.W.1
Kurland, L.T.2
Offord, K.P.3
Beard, C.M.4
-
8
-
-
0027401203
-
Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen DR, Siddique T, Patterson D, et al. Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993;362:59-62
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
Siddique, T.2
Patterson, D.3
-
9
-
-
0343973682
-
Sclerose laterale amyotrophique familiale
-
Swerts L, VanDenBerg P. Sclerose laterale amyotrophique familiale. J Genet 1976;24:147-155
-
(1976)
J Genet
, vol.24
, pp. 147-155
-
-
Swerts, L.1
Van Den Berg, P.2
-
10
-
-
0026009673
-
Risk factors in amyotrophic lateral sclerosis
-
Kurtzke JF. Risk factors in amyotrophic lateral sclerosis. Adv Neurol 1991:56:245-270
-
(1991)
Adv Neurol
, vol.56
, pp. 245-270
-
-
Kurtzke, J.F.1
-
11
-
-
0005925788
-
Adult motor neuron disease
-
Rowland LP, ed. Philadelphia: Lea & Febiger
-
Munsat TL. Adult motor neuron disease. In: Rowland LP, ed. Merritt's textbook of neurology. Philadelphia: Lea & Febiger, 1989:682-687
-
(1989)
Merritt's Textbook of Neurology
, pp. 682-687
-
-
Munsat, T.L.1
-
12
-
-
0025022757
-
Amyotrophic lateral sclerosis: A case-control study following detection of a cluster in a small Wisconsin community
-
Sienko DG, Davis JP, Taylor JA, Brooks B. Amyotrophic lateral sclerosis: a case-control study following detection of a cluster in a small Wisconsin community. Arch Neurol 1990;47:38-41
-
(1990)
Arch Neurol
, vol.47
, pp. 38-41
-
-
Sienko, D.G.1
Davis, J.P.2
Taylor, J.A.3
Brooks, B.4
-
13
-
-
0023195073
-
A rating scale for amyotrophic lateral sclerosis: Description and preliminary experience
-
Appel V, Stewart SS, Smith G, Appel SH. A rating scale for amyotrophic lateral sclerosis: description and preliminary experience. Ann Neurol 1987:22:328-333
-
(1987)
Ann Neurol
, vol.22
, pp. 328-333
-
-
Appel, V.1
Stewart, S.S.2
Smith, G.3
Appel, S.H.4
-
14
-
-
0042406384
-
The natural history of motorneuron loss in ALS
-
Munsat TL, Andres PL, Finison L, et al. The natural history of motorneuron loss in ALS. Neurology 1988;38:452-458
-
(1988)
Neurology
, vol.38
, pp. 452-458
-
-
Munsat, T.L.1
Andres, P.L.2
Finison, L.3
-
15
-
-
0029037348
-
Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction
-
Haverkamp LJ, Appel V, Appel SH. Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. Brain 1995;118:707-719
-
(1995)
Brain
, vol.118
, pp. 707-719
-
-
Haverkamp, L.J.1
Appel, V.2
Appel, S.H.3
-
16
-
-
0027327087
-
Onset, natural history and outcome in idiopathic adult motor neuron disease
-
Norris F, Shepherd R, Denys E, et al. Onset, natural history and outcome in idiopathic adult motor neuron disease. J Neurol Sci 1993;118:48-55
-
(1993)
J Neurol Sci
, vol.118
, pp. 48-55
-
-
Norris, F.1
Shepherd, R.2
Denys, E.3
-
17
-
-
0024433154
-
Survival prediction in amyotrophic lateral sclerosis
-
Jablecki CK, Berry C, Leach J. Survival prediction in amyotrophic lateral sclerosis. Muscle Nerve 1989;12:833-841
-
(1989)
Muscle Nerve
, vol.12
, pp. 833-841
-
-
Jablecki, C.K.1
Berry, C.2
Leach, J.3
-
18
-
-
0021927646
-
Amyotrophic lateral sclerosis: A study of its presentation and prognosis
-
Gubbay SS, Kahana E, Zilber N, et al. Amyotrophic lateral sclerosis: a study of its presentation and prognosis. J Neurol 1985;232:295-300
-
(1985)
J Neurol
, vol.232
, pp. 295-300
-
-
Gubbay, S.S.1
Kahana, E.2
Zilber, N.3
-
19
-
-
0027454681
-
Duration of amyotrophic lateral sclerosis is age dependent
-
Eisen A, Schulzer M, MacNeil M, et al. Duration of amyotrophic lateral sclerosis is age dependent. Muscle Nerve 1993:16:27-32
-
(1993)
Muscle Nerve
, vol.16
, pp. 27-32
-
-
Eisen, A.1
Schulzer, M.2
MacNeil, M.3
-
21
-
-
0026100188
-
Familial amyotrophic lateral sclerosis, 1850-1989: A statistical analysis of the world literature
-
Strong MJ, Hudson AJ, Alvord WG. Familial amyotrophic lateral sclerosis, 1850-1989: a statistical analysis of the world literature. Can J Neurol Sci 1991;18:45-58
-
(1991)
Can J Neurol Sci
, vol.18
, pp. 45-58
-
-
Strong, M.J.1
Hudson, A.J.2
Alvord, W.G.3
-
22
-
-
0001061176
-
Epidemiologic investigations of amyotrophic lateral sclerosis
-
Kurland LT, Mulder DW. Epidemiologic investigations of amyotrophic lateral sclerosis. Neurology 1955;5:249-268
-
(1955)
Neurology
, vol.5
, pp. 249-268
-
-
Kurland, L.T.1
Mulder, D.W.2
-
23
-
-
0027597741
-
Dinucleotide repeat polymorphism in the HOX4E locus
-
Rosen DR, Brown RH Jr. Dinucleotide repeat polymorphism in the HOX4E locus. Hum Mol Genet 1993;2:617
-
(1993)
Hum Mol Genet
, vol.2
, pp. 617
-
-
Rosen, D.R.1
Brown Jr., R.H.2
-
24
-
-
33845382806
-
Nonparametric estimation from incomplete observations
-
Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. Am Stat Assoc J 1958:53:457-481
-
(1958)
Am Stat Assoc J
, vol.53
, pp. 457-481
-
-
Kaplan, E.L.1
Meier, P.2
-
26
-
-
0017365573
-
Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. Analysis and examples
-
Peto R, Pike MC, Armitage P, et al. Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. Analysis and examples. Br J Cancer 1977;35:1-39
-
(1977)
Br J Cancer
, vol.35
, pp. 1-39
-
-
Peto, R.1
Pike, M.C.2
Armitage, P.3
-
27
-
-
0000336139
-
Regression models and life-tables
-
Cox DR. Regression models and life-tables. J R Stat Soc B 1972;34:187-202
-
(1972)
J R Stat Soc B
, vol.34
, pp. 187-202
-
-
Cox, D.R.1
-
30
-
-
0028334717
-
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-35
-
Hentati A, Bejaoui K, Pericak-Vance MA, et al. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-35. Nat Genet 1994;7:425-428
-
(1994)
Nat Genet
, vol.7
, pp. 425-428
-
-
Hentati, A.1
Bejaoui, K.2
Pericak-Vance, M.A.3
-
31
-
-
0027407565
-
Apolipoprotein E: High avidity binding to β amyloid and increased frequence of type 4 allele in late-onset familial Alzheimer disease
-
Strittmatter WJ, Saunders AM, Schmechel D, et al. Apolipoprotein E: high avidity binding to β amyloid and increased frequence of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA 1993;90:1977-1981
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1977-1981
-
-
Strittmatter, W.J.1
Saunders, A.M.2
Schmechel, D.3
-
32
-
-
0028991091
-
Apolipoprotein E ε4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis
-
Mui S, Rebeck GW, McKenna-Yasek D, et al. Apolipoprotein E ε4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis. Ann Neurol 1995;38:460-463
-
(1995)
Ann Neurol
, vol.38
, pp. 460-463
-
-
Mui, S.1
Rebeck, G.W.2
McKenna-Yasek, D.3
-
33
-
-
0030025431
-
Early reports: Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease
-
Ammar A, Enayat ZE, Bakker MC, et al. Early reports: association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease. Lancet 1996;347:159-160
-
(1996)
Lancet
, vol.347
, pp. 159-160
-
-
Ammar, A.1
Enayat, Z.E.2
Bakker, M.C.3
-
34
-
-
0027426169
-
Amyotrophic lateral sclerosis and structural defects in Cu,Zn Superoxide dismutase
-
Deng H-X, Hentati A, Tainer JA, et al. Amyotrophic lateral sclerosis and structural defects in Cu,Zn Superoxide dismutase. Science 1993;261:1047-1051
-
(1993)
Science
, vol.261
, pp. 1047-1051
-
-
Deng, H.-X.1
Hentati, A.2
Tainer, J.A.3
-
35
-
-
0037971097
-
Heredity in progressive muscular atrophy as illustrated in Farr family of Vermont
-
Osier W. Heredity in progressive muscular atrophy as illustrated in Farr family of Vermont. Arch Med 1880;4:316-320
-
(1880)
Arch Med
, vol.4
, pp. 316-320
-
-
Osier, W.1
-
36
-
-
0027952571
-
Cu/Zn Superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis
-
Robberecht W, Sapp P, Viaene MK, et al. Cu/Zn Superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis. J Neurochem 1994;62:384-387
-
(1994)
J Neurochem
, vol.62
, pp. 384-387
-
-
Robberecht, W.1
Sapp, P.2
Viaene, M.K.3
-
37
-
-
0028106044
-
Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn Superoxide dismutase gene
-
Takahashi H, Makifuchi T, Nakano R, et al. Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn Superoxide dismutase gene. Acta Neuropathol (Berl) 1994;88:185-188
-
(1994)
Acta Neuropathol (Berl)
, vol.88
, pp. 185-188
-
-
Takahashi, H.1
Makifuchi, T.2
Nakano, R.3
-
38
-
-
0028132231
-
A new variant Cu/Zn superoxide dismutase (Val 7 to Glu) deduced from lymphocyte mRNA sequences from Japanese patients with familial amyotrophic lateral sclerosis
-
Hirano M, Fujii J, Nagai Y, et al. A new variant Cu/Zn superoxide dismutase (Val 7 to Glu) deduced from lymphocyte mRNA sequences from Japanese patients with familial amyotrophic lateral sclerosis. Biochem Biophys Res Commun 1994;204:572-577
-
(1994)
Biochem Biophys Res Commun
, vol.204
, pp. 572-577
-
-
Hirano, M.1
Fujii, J.2
Nagai, Y.3
-
39
-
-
0028199849
-
SOD1 missense mutation in an Italian family with ALS
-
Rainero I, Pinessi L, Tsuda T, et al. SOD1 missense mutation in an Italian family with ALS. Neurology 1994;44:347-349
-
(1994)
Neurology
, vol.44
, pp. 347-349
-
-
Rainero, I.1
Pinessi, L.2
Tsuda, T.3
-
40
-
-
0028168971
-
Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn Superoxide dismutase gene: A possible new subtype of familial ALS
-
Aoki M, Ogasawara M, Matsubara Y, et al. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn Superoxide dismutase gene: a possible new subtype of familial ALS. J Neurol Sci 1994;126:77-83
-
(1994)
J Neurol Sci
, vol.126
, pp. 77-83
-
-
Aoki, M.1
Ogasawara, M.2
Matsubara, Y.3
-
41
-
-
0029005002
-
Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn Superoxide dismutase mutation
-
Aoki M, Abe K, Houi K, et al. Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn Superoxide dismutase mutation. Ann Neurol 1995;37:676-679
-
(1995)
Ann Neurol
, vol.37
, pp. 676-679
-
-
Aoki, M.1
Abe, K.2
Houi, K.3
-
42
-
-
0028987929
-
Superoxide dismutase (glu100gly) in a family with inherited motor neuron disease: Detection of mutant Superoxide dismutase activity and the presence of heterodimers
-
Calder VL, Domigan NM, George PM, et al. Superoxide dismutase (glu100gly) in a family with inherited motor neuron disease: detection of mutant Superoxide dismutase activity and the presence of heterodimers. Neurosci Lett 1995:189:143-146
-
(1995)
Neurosci Lett
, vol.189
, pp. 143-146
-
-
Calder, V.L.1
Domigan, N.M.2
George, P.M.3
-
43
-
-
0028771134
-
Leu106 to Val (CTC→GTC) mutation of Superoxide dismutase-1 gene in patients with familial amyotrophic lateral sclerosis in Japan
-
Kawamata J, Hasegawa H, Shimorhama S, et al. Leu106 to Val (CTC→GTC) mutation of Superoxide dismutase-1 gene in patients with familial amyotrophic lateral sclerosis in Japan. Lancet 1994;343:1501
-
(1994)
Lancet
, vol.343
, pp. 1501
-
-
Kawamata, J.1
Hasegawa, H.2
Shimorhama, S.3
-
44
-
-
0029080304
-
Familial amyotrophic lateral sclerosis with a point mutation of SOD 1: Intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles
-
Orrell RW, King AW, Hilton DA. Familial amyotrophic lateral sclerosis with a point mutation of SOD 1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles. J Neurol Neurosurg Psychiatry 1995;59:266-270
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.59
, pp. 266-270
-
-
Orrell, R.W.1
King, A.W.2
Hilton, D.A.3
-
45
-
-
0028598738
-
"Sporadic" motorneuron disease due to familial SOD1 mutation with low penetrance
-
Suthers G, Laing N, Wilton S, et al. "Sporadic" motorneuron disease due to familial SOD1 mutation with low penetrance. Lancet 1994;344:1773
-
(1994)
Lancet
, vol.344
, pp. 1773
-
-
Suthers, G.1
Laing, N.2
Wilton, S.3
-
46
-
-
0028956222
-
A novel point mutation in the Cu/Zn Superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis
-
Ikeda M, Abe K, Ogasawara M, et al. A novel point mutation in the Cu/Zn Superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis. Hum Mol Genet 1995;4:491-492
-
(1995)
Hum Mol Genet
, vol.4
, pp. 491-492
-
-
Ikeda, M.1
Abe, K.2
Ogasawara, M.3
-
47
-
-
0030050727
-
Benefit of vitamin E, riluzole and gabapentin in a transgenic model of familial ALS
-
Gurney ME, Cutting FB, Zhai P, et al. Benefit of vitamin E, riluzole and gabapentin in a transgenic model of familial ALS. Ann Neurol 1996;39:147-157
-
(1996)
Ann Neurol
, vol.39
, pp. 147-157
-
-
Gurney, M.E.1
Cutting, F.B.2
Zhai, P.3
-
48
-
-
0028097839
-
A controlled trial of riluzole in amyotrophic lateral sclerosis
-
Bensimon G, Lacomblez L, Meininger V, et al. A controlled trial of riluzole in amyotrophic lateral sclerosis. N Engl J Med 1994;330:585-591
-
(1994)
N Engl J Med
, vol.330
, pp. 585-591
-
-
Bensimon, G.1
Lacomblez, L.2
Meininger, V.3
-
49
-
-
0029584941
-
Superoxide dismutase in familial amyotrophic lateral sclerosis: Models for gain of function
-
Brown RH. Superoxide dismutase in familial amyotrophic lateral sclerosis: models for gain of function. Curr Opin Neurobiol 1995;5:841-846
-
(1995)
Curr Opin Neurobiol
, vol.5
, pp. 841-846
-
-
Brown, R.H.1
-
50
-
-
0027359334
-
Superoxide dismutase activity, oxidative damage and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis
-
Bowling AC, Schulz JB, Brown RH Jr, Beal MF. Superoxide dismutase activity, oxidative damage and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis. J Neurochem 1993;61:2322-2325
-
(1993)
J Neurochem
, vol.61
, pp. 2322-2325
-
-
Bowling, A.C.1
Schulz, J.B.2
Brown Jr., R.H.3
Beal, M.F.4
-
51
-
-
12044249765
-
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity
-
Siddique TS, Figlewicz DA, Pericak-Vance MA, et al. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. N Engl J Med 1991;324:1381-1384
-
(1991)
N Engl J Med
, vol.324
, pp. 1381-1384
-
-
Siddique, T.S.1
Figlewicz, D.A.2
Pericak-Vance, M.A.3
-
53
-
-
0027965073
-
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
-
Borchelt DR, Lee MK, Slunt HS, et al. Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity. Proc Natl Acad Sci USA 1994;91:8292-8296
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8292-8296
-
-
Borchelt, D.R.1
Lee, M.K.2
Slunt, H.S.3
-
54
-
-
0023221049
-
Phenotypic and genotypic heterogeneity of dominantly inherited amyotrophic lateral sclerosis
-
Chio A, Brignolio F, Meinere D, Schiffer D. Phenotypic and genotypic heterogeneity of dominantly inherited amyotrophic lateral sclerosis. Acta Neurol Scand 1986;75:277-282
-
(1986)
Acta Neurol Scand
, vol.75
, pp. 277-282
-
-
Chio, A.1
Brignolio, F.2
Meinere, D.3
Schiffer, D.4
-
55
-
-
0028816033
-
Parental influence on inheritance of familial amyotrophic lateral sclerosis
-
Orrell RW, King AW, deBelleroche JS. Parental influence on inheritance of familial amyotrophic lateral sclerosis. Lancet 1995;345:391-392
-
(1995)
Lancet
, vol.345
, pp. 391-392
-
-
Orrell, R.W.1
King, A.W.2
DeBelleroche, J.S.3
-
56
-
-
0025815333
-
Parental sex effect in familial amyotrophic lateral sclerosis
-
Leone M. Parental sex effect in familial amyotrophic lateral sclerosis. Neurology 1991;41:1292-1294
-
(1991)
Neurology
, vol.41
, pp. 1292-1294
-
-
Leone, M.1
|