-
1
-
-
0000280462
-
Deux cas d'atrophie musculaire progressive avec lesions de la substance grise et des faisceaux antero-lateraux de la moelle epiniere
-
Charcot, J.M. and Joffroy, A. (1869) Deux cas d'atrophie musculaire progressive avec lesions de la substance grise et des faisceaux antero-lateraux de la moelle epiniere. Arch. Physiol. Neurol. Pathol., 2, 744.
-
(1869)
Arch. Physiol. Neurol. Pathol.
, vol.2
, pp. 744
-
-
Charcot, J.M.1
Joffroy, A.2
-
2
-
-
0029433185
-
Epidemiology of ALS
-
Nelson, L.M. (1995) Epidemiology of ALS. Clin. Neurosci., 3, 327-331.
-
(1995)
Clin. Neurosci.
, vol.3
, pp. 327-331
-
-
Nelson, L.M.1
-
3
-
-
0031057003
-
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis
-
Cudkowicz, M.E., McKenna-Yasek, D., Sapp, P.E., Chin, W., Geller, B., Hayden, D.L., Schoenfeld, D.A., Hosler, B.A., Horvitz, H.R. and Brown, R.H. (1997) Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis [see comments]. Ann. Neurol., 41, 210-221.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 210-221
-
-
Cudkowicz, M.E.1
McKenna-Yasek, D.2
Sapp, P.E.3
Chin, W.4
Geller, B.5
Hayden, D.L.6
Schoenfeld, D.A.7
Hosler, B.A.8
Horvitz, H.R.9
Brown, R.H.10
-
4
-
-
0030749160
-
Phenotypic heterogeneity in motor neuron discase patients with CuZn-superoxide dismutase mutations in Scandinavia
-
Andersen, P.M., Nilsson, P., Keranen, M.L., Forsgren, L., Hagglund, J., Karlsborg, M., Ronnevi, L.O., Gredal, O. and Marklund, S.L. (1997) Phenotypic heterogeneity in motor neuron discase patients with CuZn-superoxide dismutase mutations in Scandinavia. Brain, 10, 1723-1737.
-
(1997)
Brain
, vol.10
, pp. 1723-1737
-
-
Andersen, P.M.1
Nilsson, P.2
Keranen, M.L.3
Forsgren, L.4
Hagglund, J.5
Karlsborg, M.6
Ronnevi, L.O.7
Gredal, O.8
Marklund, S.L.9
-
5
-
-
0030780350
-
SOD-1 and sporadic ALS: Analysis of 155 cases and identification of a novel insertion mutation
-
Jackson, M., Al-Chalabi, A., Enayat, Z.E., Chioza, B., Leigh, P.N. and Morrison, K.E. (1997) SOD-1 and sporadic ALS: analysis of 155 cases and identification of a novel insertion mutation. Ann. Neurol., 42, 803-806.
-
(1997)
Ann. Neurol.
, vol.42
, pp. 803-806
-
-
Jackson, M.1
Al-Chalabi, A.2
Enayat, Z.E.3
Chioza, B.4
Leigh, P.N.5
Morrison, K.E.6
-
6
-
-
0028916910
-
Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients
-
Jones, C.T., Swingler, R.J., Simpson, S.A. and Brock, D.J. (1995) Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients. J. Med. Genet., 32, 290-292.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 290-292
-
-
Jones, C.T.1
Swingler, R.J.2
Simpson, S.A.3
Brock, D.J.4
-
7
-
-
0021368680
-
Neurofibrillary axonal swellings and amyotrophic lateral sclerosis
-
Delisle, M.B. and Carpenter, S. (1984) Neurofibrillary axonal swellings and amyotrophic lateral sclerosis. J. Neurol. Sci., 63, 241-250.
-
(1984)
J. Neurol. Sci.
, vol.63
, pp. 241-250
-
-
Delisle, M.B.1
Carpenter, S.2
-
8
-
-
0030037799
-
Intermediate filaments in health and disease
-
Steinert, P.M. (1996) Intermediate filaments in health and disease. Exp. Mol. Med., 28, 55-63.
-
(1996)
Exp. Mol. Med.
, vol.28
, pp. 55-63
-
-
Steinert, P.M.1
-
9
-
-
0023823645
-
Ubiquitin deposits in anterior horn cells in motor neurone disease
-
Leigh, P.N., Anderton, B.H., Dodson, A., Gallo, J.M., Swash, M. and Power, D.M. (1988) Ubiquitin deposits in anterior horn cells in motor neurone disease. Neurosci. Lett., 93, 197-203.
-
(1988)
Neurosci. Lett.
, vol.93
, pp. 197-203
-
-
Leigh, P.N.1
Anderton, B.H.2
Dodson, A.3
Gallo, J.M.4
Swash, M.5
Power, D.M.6
-
10
-
-
0024419525
-
Inclusion bodies in motor cortex and brainstem of patients with motor neurone disease are detected by immunocytochemical localisation of ubiquitin
-
Lowe, J., Aldridge, F. Lennox, G., Doherty, F., Jefferson, D., Landon, M. and Mayer, R.J. (1989) Inclusion bodies in motor cortex and brainstem of patients with motor neurone disease are detected by immunocytochemical localisation of ubiquitin. Neurosci. Lett., 105, 7-13.
-
(1989)
Neurosci. Lett.
, vol.105
, pp. 7-13
-
-
Lowe, J.1
Aldridge, F.2
Lennox, G.3
Doherty, F.4
Jefferson, D.5
Landon, M.6
Mayer, R.J.7
-
11
-
-
0023738162
-
A filamentous inclusion body within anterior horn neurones in motor neurone disease defined by immunocytochemical localisation of ubiquitin
-
Lowe, J., Lennox, G., Jefferson, D., Morrell, K., McQuire, D., Gray, T., Landon, M., Doherty, F.J. and Mayer, R.J. (1988) A filamentous inclusion body within anterior horn neurones in motor neurone disease defined by immunocytochemical localisation of ubiquitin. Neurosci. Lett., 94, 203-210.
-
(1988)
Neurosci. Lett.
, vol.94
, pp. 203-210
-
-
Lowe, J.1
Lennox, G.2
Jefferson, D.3
Morrell, K.4
McQuire, D.5
Gray, T.6
Landon, M.7
Doherty, F.J.8
Mayer, R.J.9
-
12
-
-
0027067890
-
The hypotrophic axonopathy mutant in Japanese quail
-
Mizutani, M., Nunoya, T., Yamasaki, H. and Itakura, C. (1992) The hypotrophic axonopathy mutant in Japanese quail. J. Hered., 83, 234-235.
-
(1992)
J. Hered.
, vol.83
, pp. 234-235
-
-
Mizutani, M.1
Nunoya, T.2
Yamasaki, H.3
Itakura, C.4
-
13
-
-
0027530064
-
Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
-
Ohara, O., Gahara, Y., Miyake, T., Teraoka, H. and Kitamura, T. (1993) Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene. J. Cell Biol., 121, 387-395.
-
(1993)
J. Cell Biol.
, vol.121
, pp. 387-395
-
-
Ohara, O.1
Gahara, Y.2
Miyake, T.3
Teraoka, H.4
Kitamura, T.5
-
14
-
-
0029062287
-
Mice overexpressing the human neurofilament heavy gene as a model of ALS
-
Julien, J.P., Cote, F. and Collard, J.F. (1995) Mice overexpressing the human neurofilament heavy gene as a model of ALS. Neurobiol. Aging, 16, 487-490.
-
(1995)
Neurobiol. Aging
, vol.16
, pp. 487-490
-
-
Julien, J.P.1
Cote, F.2
Collard, J.F.3
-
15
-
-
0030050727
-
Benefit of vitamin E, riluzole and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis
-
Gurney, M.E., Cutting, F.B., Zhai, P., Dohle, A., Taylor, C.P., Andrus, P.K. and Hall, E.D. (1996) Benefit of vitamin E, riluzole and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis. Ann. Neurol., 39, 147-157.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 147-157
-
-
Gurney, M.E.1
Cutting, F.B.2
Zhai, P.3
Dohle, A.4
Taylor, C.P.5
Andrus, P.K.6
Hall, E.D.7
-
16
-
-
0027410516
-
Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease
-
Xu, Z., Cork, L.C., Griffin, J.W. and Cleveland, D.W. (1993) Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease. Cell, 73, 23-33.
-
(1993)
Cell
, vol.73
, pp. 23-33
-
-
Xu, Z.1
Cork, L.C.2
Griffin, J.W.3
Cleveland, D.W.4
-
17
-
-
0030910404
-
Oxidative stress, mutant SOD1 and neurofilament pathology in transgenic mouse models of human motor neuron disease
-
Tu, P.H., Gurney, M.E., Julien, J.P., Lee, V.M. and Trojanowski, J.Q. (1997) Oxidative stress, mutant SOD1 and neurofilament pathology in transgenic mouse models of human motor neuron disease [review]. Lab. Invest., 76, 441-456.
-
(1997)
Lab. Invest.
, vol.76
, pp. 441-456
-
-
Tu, P.H.1
Gurney, M.E.2
Julien, J.P.3
Lee, V.M.4
Trojanowski, J.Q.5
-
18
-
-
0031456315
-
Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation
-
Shaw, C.E., Enayat, Z.E., Powell, J.F., Anderson, V.E., Radunovic, A., al-Sarraj, S. and Leigh, P.N. (1997) Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation. Neurology, 49, 1612-1616.
-
(1997)
Neurology
, vol.49
, pp. 1612-1616
-
-
Shaw, C.E.1
Enayat, Z.E.2
Powell, J.F.3
Anderson, V.E.4
Radunovic, A.5
Al-Sarraj, S.6
Leigh, P.N.7
-
19
-
-
0030034545
-
SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis
-
Rouleau, G.A., Clark, A.W., Rooke, K., Pramatarova, A., Krizus, A., Suchowersky, O., Julien, J.P. and Figlewicz, D. (1996) SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis. Ann. Neurol., 39, 128-131.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 128-131
-
-
Rouleau, G.A.1
Clark, A.W.2
Rooke, K.3
Pramatarova, A.4
Krizus, A.5
Suchowersky, O.6
Julien, J.P.7
Figlewicz, D.8
-
20
-
-
0027424206
-
Polymorphism in the multi-phosphorylation domain of the human neurofilament heavy-subunit-encoding gene
-
Figlewicz, D.A., Rouleau, G.A., Krizus, A. and Julien, J.P. (1993) Polymorphism in the multi-phosphorylation domain of the human neurofilament heavy-subunit-encoding gene. Gene, 132, 297-300.
-
(1993)
Gene
, vol.132
, pp. 297-300
-
-
Figlewicz, D.A.1
Rouleau, G.A.2
Krizus, A.3
Julien, J.P.4
-
21
-
-
0028001606
-
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
-
Figlewicz, D.A., Krizus, A., Martinoli, M.G., Meininger, V., Dib, M., Rouleau, G.A. and Julien, J.P. (1994) Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis. Hum. Mol. Genet., 3, 1757-1761.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1757-1761
-
-
Figlewicz, D.A.1
Krizus, A.2
Martinoli, M.G.3
Meininger, V.4
Dib, M.5
Rouleau, G.A.6
Julien, J.P.7
-
22
-
-
0024042469
-
The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it
-
Lees, J.F., Shneidman, P.S., Skuntz, S.F., Carden, M.J. and Lazzarini, R.A. (1988) The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it. EMBO J., 7, 1947-1955.
-
(1988)
EMBO J.
, vol.7
, pp. 1947-1955
-
-
Lees, J.F.1
Shneidman, P.S.2
Skuntz, S.F.3
Carden, M.J.4
Lazzarini, R.A.5
-
23
-
-
0030000608
-
Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis
-
Rooke, K., Figlewicz, D.A., Han, F.Y. and Rouleau, G.A. (1996) Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis. Neurology, 46, 789-790.
-
(1996)
Neurology
, vol.46
, pp. 789-790
-
-
Rooke, K.1
Figlewicz, D.A.2
Han, F.Y.3
Rouleau, G.A.4
-
24
-
-
0029970685
-
Sequence variants in human neurofilament proteins: Absence of linkage to familial amyotrophic lateral sclerosis
-
Vechio, J.D., Bruijn, L.I., Xu, Z., Brown, R.H. Jr and Cleveland, D.W. (1996) Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis. Ann. Neurol., 40, 603-610.
-
(1996)
Ann. Neurol.
, vol.40
, pp. 603-610
-
-
Vechio, J.D.1
Bruijn, L.I.2
Xu, Z.3
Brown R.H., Jr.4
Cleveland, D.W.5
-
25
-
-
17544370807
-
Phosphorylation of the high molecular weight neurofilament protein (NF-H) by Cdk5 and p35
-
Sun, D., Leung, C.L. and Liem, R.K.H. (1996) Phosphorylation of the high molecular weight neurofilament protein (NF-H) by Cdk5 and p35. J. Biol. Chem., 271, 14245-14251.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 14245-14251
-
-
Sun, D.1
Leung, C.L.2
Liem, R.K.H.3
-
26
-
-
0029999175
-
A cdc2-like kinase distinct from cdk5 is associated with neurofilaments
-
Starr, R., Hall, F.L. and Monteiro, M.J. (1996) A cdc2-like kinase distinct from cdk5 is associated with neurofilaments. J. Cell Sci., 109, 1565-1573.
-
(1996)
J. Cell Sci.
, vol.109
, pp. 1565-1573
-
-
Starr, R.1
Hall, F.L.2
Monteiro, M.J.3
-
27
-
-
0344625369
-
Characterization of the phosphorylation sites of human high molecular weight neurofilament protein by electrospray ionization tandem mass spectrometry and database searching
-
Jaffe, H., Veeranna, Shetty, K.T. and Pant, H.C. (1998) Characterization of the phosphorylation sites of human high molecular weight neurofilament protein by electrospray ionization tandem mass spectrometry and database searching. Biochemistry, 37, 3931-3940.
-
(1998)
Biochemistry
, vol.37
, pp. 3931-3940
-
-
Jaffe, H.1
Veeranna2
Shetty, K.T.3
Pant, H.C.4
-
28
-
-
0026787142
-
Evidence for unequal crossing over in the evolution of the neurofilament polypeptide H
-
Soppet, D.R., Beasley, L.L. and Willard, M.B. (1992) Evidence for unequal crossing over in the evolution of the neurofilament polypeptide H. J. Biol. Chem., 267, 17354-17361.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 17354-17361
-
-
Soppet, D.R.1
Beasley, L.L.2
Willard, M.B.3
-
29
-
-
0024601998
-
Cloning of a cDNA encoding the rat high molecular weight neurofilament peptide (NF-H): Developmental and tissue expression in the rat and mapping of its human homologue to chromosomes 1 and 22
-
Lieberburg, I., Spinner, N., Snyder, S., Anderson, J., Goldgaber, D., Smulowitz, M., Carroli, Z., Emanuel, B., Breitner, J. and Rubin, L. (1989) Cloning of a cDNA encoding the rat high molecular weight neurofilament peptide (NF-H): developmental and tissue expression in the rat and mapping of its human homologue to chromosomes 1 and 22. Proc. Natl Acad. Sci. USA, 86, 2463-2467.
-
(1989)
Proc. Natl Acad. Sci. USA
, vol.86
, pp. 2463-2467
-
-
Lieberburg, I.1
Spinner, N.2
Snyder, S.3
Anderson, J.4
Goldgaber, D.5
Smulowitz, M.6
Carroli, Z.7
Emanuel, B.8
Breitner, J.9
Rubin, L.10
-
30
-
-
0022896464
-
Isolation of a cDNA for the rat heavy neurofilament polypeptide (NF-H)
-
Robinson, P.A., Wion, D. and Anderton, B.H. (1986) Isolation of a cDNA for the rat heavy neurofilament polypeptide (NF-H). FEBS Lett., 209, 203-205.
-
(1986)
FEBS Lett.
, vol.209
, pp. 203-205
-
-
Robinson, P.A.1
Wion, D.2
Anderton, B.H.3
-
31
-
-
0029918466
-
Neurogenetic diseases: Molecular diagnosis and therapeutic approaches
-
Muller, U. and Graeber, M.B. (1996) Neurogenetic diseases: molecular diagnosis and therapeutic approaches. J. Mol. Med., 74, 71-84.
-
(1996)
J. Mol. Med.
, vol.74
, pp. 71-84
-
-
Muller, U.1
Graeber, M.B.2
-
32
-
-
0030479536
-
The origin of interspersed repeats in the human genome
-
Smit, A.F. (1996) The origin of interspersed repeats in the human genome (review). Curr. Opin. Genet. Dev., 6, 743-748.
-
(1996)
Curr. Opin. Genet. Dev.
, vol.6
, pp. 743-748
-
-
Smit, A.F.1
-
33
-
-
0029367097
-
Neurofilament phosphorylation
-
Pant, H.C. and Veeranna (1995) Neurofilament phosphorylation [review]. Biochem. Cell Biol., 73, 575-592.
-
(1995)
Biochem. Cell Biol.
, vol.73
, pp. 575-592
-
-
Pant, H.C.1
Veeranna2
-
34
-
-
0023766743
-
MAP2 is a component of crossbridges between microtubules and neurofilaments in the neuronal cytoskeleton: Quick-freeze, deep-etch immunoelectron microscopy and reconstitution studies
-
Hirokawa, N., Hisanaga, S.I. and Shiomura, Y. (1988) MAP2 is a component of crossbridges between microtubules and neurofilaments in the neuronal cytoskeleton: quick-freeze, deep-etch immunoelectron microscopy and reconstitution studies. J. Neurosci., 8, 2769-2779.
-
(1988)
J. Neurosci.
, vol.8
, pp. 2769-2779
-
-
Hirokawa, N.1
Hisanaga, S.I.2
Shiomura, Y.3
-
35
-
-
0026784910
-
Macromolecular structure of reassembled neurofilaments as revealed by the quick-freeze deep-etch mica method: Difference between NF-M and NF-H subunits in their ability to form cross-bridges
-
Gotow, T., Takeda, M., Tanaka, T. and Hashimoto, P.H. (1992) Macromolecular structure of reassembled neurofilaments as revealed by the quick-freeze deep-etch mica method: difference between NF-M and NF-H subunits in their ability to form cross-bridges. Eur. J. Cell Biol., 58, 331-345.
-
(1992)
Eur. J. Cell Biol.
, vol.58
, pp. 331-345
-
-
Gotow, T.1
Takeda, M.2
Tanaka, T.3
Hashimoto, P.H.4
-
36
-
-
0024565972
-
Cytoskeletal abnormalities in motor neuron disease. An immunocytochemical study
-
Leigh, P.N., Dodson, A., Swash, M., Brion, J.P. and Anderton, B.H. (1989) Cytoskeletal abnormalities in motor neuron disease. An immunocytochemical study. Brain, 112, 521-535.
-
(1989)
Brain
, vol.112
, pp. 521-535
-
-
Leigh, P.N.1
Dodson, A.2
Swash, M.3
Brion, J.P.4
Anderton, B.H.5
-
37
-
-
0025943790
-
Neurofilament phosphorylation: A new look at regulation and function
-
Nixon, R.A. and Sihag, R.K. (1991) Neurofilament phosphorylation: a new look at regulation and function. Trends Neurosci., 14, 501-506.
-
(1991)
Trends Neurosci.
, vol.14
, pp. 501-506
-
-
Nixon, R.A.1
Sihag, R.K.2
-
38
-
-
0027531842
-
The regulation of neurofilament protein dynamics by phosphorylation: Clues to neurofibrillary pathobiology
-
Nixon, R.A. (1993) The regulation of neurofilament protein dynamics by phosphorylation: clues to neurofibrillary pathobiology. Brain Pathol., 3, 29-38.
-
(1993)
Brain Pathol.
, vol.3
, pp. 29-38
-
-
Nixon, R.A.1
-
40
-
-
0025988453
-
Transport complexes associated with slow axonal flow
-
Bray, J.J. and Mills, R.G. (1991) Transport complexes associated with slow axonal flow. Neurochem. Res., 16, 645-649.
-
(1991)
Neurochem. Res.
, vol.16
, pp. 645-649
-
-
Bray, J.J.1
Mills, R.G.2
-
41
-
-
0028142392
-
El Escorial world federation of neurology criteria for the diagnosis of amyotrophic lateral sclerosis
-
Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial 'Clinical limits of amyotrophic lateral sclerosis' workshop contributors
-
Brooks, B.R. (1994) El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial 'Clinical limits of amyotrophic lateral sclerosis' workshop contributors. J. Neurol. Sci., 124 (suppl.), 96-107.
-
(1994)
J. Neurol. Sci.
, vol.124
, Issue.SUPPL.
, pp. 96-107
-
-
Brooks, B.R.1
-
42
-
-
0030094146
-
CENSOR - A program for identification and elimination of repetitive elements from DNA sequences
-
Jurka, J., Klonowski, P., Dagman, V. and Pelton, P. (1996) CENSOR - a program for identification and elimination of repetitive elements from DNA sequences. Comput. Chem., 20, 119-121.
-
(1996)
Comput. Chem.
, vol.20
, pp. 119-121
-
-
Jurka, J.1
Klonowski, P.2
Dagman, V.3
Pelton, P.4
|