-
1
-
-
34548388987
-
Amyotrophic lateral sclerosis genetics with Mendelian inheritance
-
(Brown Jr RH, Swash M, Pasinelli P, eds), Informa Healthcare, Lodon
-
Andersen PM. Amyotrophic lateral sclerosis genetics with Mendelian inheritance. In Amyotrophic lateral sclerosis (Brown Jr RH, Swash M, Pasinelli P, eds), 2006, 187-207, Informa Healthcare, Lodon
-
(2006)
Amyotrophic Lateral Sclerosis
, pp. 187-207
-
-
Andersen, P.M.1
-
2
-
-
0016788436
-
Frequency of nerve fiber degeneration of peripheral motor and sensory neurons in amyotrophic lateral sclerosis. Morphometry of deep and superficial peroneal nerves
-
Dyck PJ, Stevens JC, Mulder DW, Espinosa RE. Frequency of nerve fiber degeneration of peripheral motor and sensory neurons in amyotrophic lateral sclerosis. Morphometry of deep and superficial peroneal nerves. Neurology 1975;25:781-785
-
(1975)
Neurology
, vol.25
, pp. 781-785
-
-
Dyck, P.J.1
Stevens, J.C.2
Mulder, D.W.3
Espinosa, R.E.4
-
3
-
-
0034773568
-
Presymptomatic motor neuron loss and reactive astrocytosis in the sod1 mouse model of amyotrophic lateral sclerosis
-
DOI 10.1002/mus.1176
-
Feeney SJ, McKelvie PA, Austin L, Jean-Francois MJ, Kapsa R, Tombs SM, Byrne E. Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis. Muscle Nerve 2001;24:1510-1519 (Pubitemid 32995587)
-
(2001)
Muscle and Nerve
, vol.24
, Issue.11
, pp. 1510-1519
-
-
Feeney, S.J.1
McKelvie, P.A.2
Austin, L.3
Bernadette Jean-Francois, M.J.4
Kapsa, R.5
Tombs, S.M.6
Byrne, E.7
-
4
-
-
0345742771
-
Amyotrophic lateral sclerosis is a distal axonopathy: Evidence in mice and man
-
DOI 10.1016/j.expneurol.2003.10.004
-
Fischer LR, Culver DG, Tennant P, Davis AA, Wang M, Castellano-Sanchez A, Khan J, Polak MA, Glass JD. Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp Neurol 2004;185:232-240 (Pubitemid 38084849)
-
(2004)
Experimental Neurology
, vol.185
, Issue.2
, pp. 232-240
-
-
Fischer, L.R.1
Culver, D.G.2
Tennant, P.3
Davis, A.A.4
Wang, M.5
Castellano-Sanchez, A.6
Khan, J.7
Polak, M.A.8
Glass, J.D.9
-
5
-
-
20244390181
-
The WldS gene modestly prolongs survival in the SOD1G93A fALS mouse
-
Fischer LR, Culver DG, Davis AA, Tennant P, Wang M, Coleman M, Asress S, Adalbert R, Alexander GM, Glass JD. The WldS gene modestly prolongs survival in the SOD1G93A fALS mouse. Neurobiol Dis 2005;19:293-300
-
(2005)
Neurobiol Dis
, vol.19
, pp. 293-300
-
-
Fischer, L.R.1
Culver, D.G.2
Davis, A.A.3
Tennant, P.4
Wang, M.5
Coleman, M.6
Asress, S.7
Adalbert, R.8
Alexander, G.M.9
Glass, J.D.10
-
6
-
-
0028228160
-
LES POTENTIELS EVOQUES SOMESTHESIQUES DANS la SCLEROSE LATERALE AMYOTROPHIQUE et la SCLEROSE LATERALE PRIMAIRE
-
Georgesco M, Salerno A, Carlander B, Leger JJ, Camu W, Billiard M, Cadilhac J. Somatosensory evoked potentials in amyotrophic lateral sclerosis and primary lateral sclerosis. Rev Neurol (Paris) 1994;150:292-298 (Pubitemid 24205320)
-
(1994)
Revue Neurologique
, vol.150
, Issue.4
, pp. 292-298
-
-
Georgesco, M.1
Salerno, A.2
Carlander, B.3
Leger, J.J.4
Camu, W.5
Billiard, M.6
Cadilhac, J.7
-
7
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation
-
Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX et al. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science 1994;264:1772-1775
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.2
Chiu, A.Y.3
Dal Canto, M.C.4
Polchow, C.Y.5
Alexander, D.D.6
Caliendo, J.7
Hentati, A.8
Kwon, Y.W.9
Deng, H.X.10
-
8
-
-
10744223086
-
The crucial role of caspase-9 in the disease progression of a transgenic ALS mouse model
-
Inoue H, Tsukita K, Iwasato T, Suzuki Y, Tomioka M, Tateno M, Nagao M, Kawata A, Saido TC, Miura M et al. The crucial role of caspase-9 in the disease progression of a transgenic ALS mouse model. Embo J 2003;22:6665-6674
-
(2003)
Embo J
, vol.22
, pp. 6665-6674
-
-
Inoue, H.1
Tsukita, K.2
Iwasato, T.3
Suzuki, Y.4
Tomioka, M.5
Tateno, M.6
Nagao, M.7
Kawata, A.8
Saido, T.C.9
Miura, M.10
-
9
-
-
34347212891
-
Amyotrophic lateral sclerosis with sensory neuropathy: Part of a multisystem disorder?
-
Isaacs JD, Dean AF, Shaw CE, Al-Chalabi A, Mills KR, Leigh PN. Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder? J Neurol Neurosurg Psychiatry 2007;78:750-753
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 750-753
-
-
Isaacs, J.D.1
Dean, A.F.2
Shaw, C.E.3
Al-Chalabi, A.4
Mills, K.R.5
Leigh, P.N.6
-
10
-
-
0034520591
-
Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1
-
DOI 10.1006/nbdi.2000.0299
-
Jaarsma D, Haasdijk ED, Grashorn JA, Hawkins R, van Duijn W, Verspaget HW, London J, Holstege JC. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1. Neurobiol Dis 2000;7:623-643 (Pubitemid 32044287)
-
(2000)
Neurobiology of Disease
, vol.7
, Issue.6
, pp. 623-643
-
-
Jaarsma, D.1
Haasdijk, E.D.2
Grashorn, J.A.C.3
Hawkins, R.4
Van Duijn, W.5
Verspaget, H.W.6
London, J.7
Holstege, J.C.8
-
11
-
-
0031458389
-
Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene
-
DOI 10.1016/S0022-510X(97)00176-7, PII S0022510X97001767
-
Kawata A, Kato S, Hayashi H, Hirai S. Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene. J Neurol Sci 1997;153:82-85 (Pubitemid 28010071)
-
(1997)
Journal of the Neurological Sciences
, vol.153
, Issue.1
, pp. 82-85
-
-
Kawata, A.1
Kato, S.2
Hayashi, H.3
Hirai, S.4
-
12
-
-
34548287969
-
Activation of the Nrf2-ARE pathway in muscle and spinal cord during ALS-like pathology in mice expressing mutant SOD1
-
DOI 10.1016/j.expneurol.2007.05.026, PII S001448860700235X
-
Kraft AD, Resch JM, Johnson DA, Johnson JA. Activation of the Nrf2-ARE pathway in muscle and spinal cord during ALS-like pathology in mice expressing mutant SOD1. Exp Neurol 2007;207:107-117 (Pubitemid 47332487)
-
(2007)
Experimental Neurology
, vol.207
, Issue.1
, pp. 107-117
-
-
Kraft, A.D.1
Resch, J.M.2
Johnson, D.A.3
Johnson, J.A.4
-
13
-
-
0034647003
-
Functional role of caspase-1 and caspase-3 in an ALS transgenic mouse model
-
Li M, Ona VO, Guegan C, Chen M, Jackson-Lewis V, Andrews LJ, Olszewski AJ, Stieg PE, Lee JP, Przedborski S et al. Functional role of caspase-1 and caspase-3 in an ALS transgenic mouse model. Science 2000;288:335-339
-
(2000)
Science
, vol.288
, pp. 335-339
-
-
Li, M.1
Ona, V.O.2
Guegan, C.3
Chen, M.4
Jackson-Lewis, V.5
Andrews, L.J.6
Olszewski, A.J.7
Stieg, P.E.8
Lee, J.P.9
Przedborski, S.10
-
14
-
-
34248571777
-
The distribution of primary nitric oxide synthase- and parvalbumin- immunoreactive afferents in the dorsal funiculus of the lumbosacral spinal cord in a dog
-
DOI 10.1007/s10571-007-9140-6
-
Marsala J, Lukacova N, Kolesar D, Sulla I, Galik J, Marsala M. The distribution of primary nitric oxide synthase- and parvalbumin-immunoreactive afferents in the dorsal funiculus of the lumbosacral spinal cord in a dog. Cell Mol Neurobiol 2007;27:475-504 (Pubitemid 46763892)
-
(2007)
Cellular and Molecular Neurobiology
, vol.27
, Issue.4
, pp. 475-504
-
-
Marsala, J.1
Lukacova, N.2
Kolesar, D.3
Sulla, I.4
Galik, J.5
Marsala, M.6
-
15
-
-
0032956096
-
The spinal somatosensory evoked potentials in amyotrophic lateral sclerosis in relation to the spinal cord conduction velocities
-
Matsumoto A, Kawashima A, Doi S, Moriwaka F, Tashiro K. The spinal somatosensory evoked potentials in amyotrophic lateral sclerosis in relation to the spinal cord conduction velocities. No To Shinkei 1999;51:41-47 (Pubitemid 29093342)
-
(1999)
Brain and Nerve
, vol.51
, Issue.1
, pp. 41-47
-
-
Matsumoto, A.1
Kawashima, A.2
Doi, S.3
Moriwaka, F.4
Tashiro, K.5
-
16
-
-
34347247316
-
Generalised sensory system abnormalities in amyotrophic lateral sclerosis: A European multicentre study
-
DOI 10.1136/jnnp.2006.098533
-
Pugdahl K, Fuglsang-Frederiksen A, de Carvalho M, Johnsen B, Fawcett PR, Labarre-Vila A, Liguori R, Nix WA, Schofield IS. Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study. J Neurol Neurosurg Psychiatry 2007;78:746-749 (Pubitemid 46998851)
-
(2007)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.78
, Issue.7
, pp. 746-749
-
-
Pugdahl, K.1
Fuglsang-Frederiksen, A.2
De Carvalho, M.3
Johnsen, B.4
Fawcett, P.R.W.5
Labarre-Vila, A.6
Liguori, R.7
Nix, W.A.8
Schofield, I.S.9
-
17
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX 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
Figlewicz, D.A.4
Sapp, P.5
Hentati, A.6
Donaldson, D.7
Goto, J.8
O'Regan, J.P.9
Deng, H.X.10
-
18
-
-
0028915976
-
Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: Studies in yeast and neural cells
-
Rabizadeh S, Gralla EB, Borchelt DR, Gwinn R, Valentine JS, Sisodia S, Wong P, Lee M, Hahn H, Bredesen DE. Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells. Proc Natl Acad Sci USA 1995;92:3024-3028
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3024-3028
-
-
Rabizadeh, S.1
Gralla, E.B.2
Borchelt, D.R.3
Gwinn, R.4
Valentine, J.S.5
Sisodia, S.6
Wong, P.7
Lee, M.8
Hahn, H.9
Bredesen, D.E.10
-
19
-
-
36348993804
-
Mitochondrial alterations in dorsal root ganglion cells in sporadic amyotrophic lateral sclerosis
-
DOI 10.1007/s00401-007-0299-1
-
Sasaki S, Horie Y, Iwata M. Mitochondrial alterations in dorsal root ganglion cells in sporadic amyotrophic lateral sclerosis. Acta Neuropathol 2007;114:633-639 (Pubitemid 350142751)
-
(2007)
Acta Neuropathologica
, vol.114
, Issue.6
, pp. 633-639
-
-
Sasaki, S.1
Horie, Y.2
Iwata, M.3
-
20
-
-
0036703771
-
Overexpression of HGF retards disease progression and prolongs life span in a transgenic mouse model of ALS
-
Sun W, Funakoshi H, Nakamura T. Overexpression of HGF retards disease progression and prolongs life span in a transgenic mouse model of ALS. J Neurosci 2002;22:6537-6548 (Pubitemid 35386410)
-
(2002)
Journal of Neuroscience
, vol.22
, Issue.15
, pp. 6537-6548
-
-
Sun, W.1
Funakoshi, H.2
Nakamura, T.3
-
21
-
-
0029966363
-
Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions
-
DOI 10.1073/pnas.93.7.3155
-
Tu PH, Raju P, Robinson KA, Gurney ME, Trojanowski JQ, Lee VM. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proc Natl Acad Sci USA 1996;93:3155-3160 (Pubitemid 26114380)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.7
, pp. 3155-3160
-
-
Tu, P.-H.1
Raju, P.2
Robinson, K.A.3
Gurney, M.E.4
Trojanowski, J.Q.5
Lee, V.M.-Y.6
-
22
-
-
0037206646
-
G93A G1H transgenic mouse model of familial amyotrophic lateral sclerosis
-
DOI 10.1016/S0304-3940(02)00944-8, PII S0304394002009448
-
Zang DW, Cheema SS. Degeneration of corticospinal and bulbospinal systems in the superoxide dismutase 1(G93A G1H) transgenic mouse model of familial amyotrophic lateral sclerosis. Neurosci Lett 2002;332:99-102 (Pubitemid 35217850)
-
(2002)
Neuroscience Letters
, vol.332
, Issue.2
, pp. 99-102
-
-
Zang, D.W.1
Cheema, S.S.2
-
23
-
-
0030817291
-
Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation
-
DOI 10.1083/jcb.139.5.1307
-
Zhang B, Tu P, Abtahian F, Trojanowski JQ, Lee VM. Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation. J Cell Biol 1997;139:1307-1315 (Pubitemid 27523216)
-
(1997)
Journal of Cell Biology
, vol.139
, Issue.5
, pp. 1307-1315
-
-
Zhang, B.1
Tu, P.-H.2
Abtahian, F.3
Trojanowski, J.Q.4
Lee, V.M.-Y.5
|