-
1
-
-
0036263895
-
Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: Synonyms for the same disorder?
-
Jonghe PD, Auer-Grumbach M, Irobi J, et al.: Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? Brain 2002, 125:1320-1325.
-
(2002)
Brain
, vol.125
, pp. 1320-1325
-
-
Jonghe, P.D.1
Auer-Grumbach, M.2
Irobi, J.3
-
2
-
-
0034792793
-
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
-
Forestier NL, Maisonobe T, Piquard A, et al.: Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature. Brain 2001, 124:1989-1999.
-
(2001)
Brain
, vol.124
, pp. 1989-1999
-
-
Forestier, N.L.1
Maisonobe, T.2
Piquard, A.3
-
3
-
-
15844401527
-
Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: Discrete entities or spectrum?
-
Strong M, Gordon PH: Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum? Amyotroph Lateral Scler Other Motor Neuron Disord 2005, 6:8-16.
-
(2005)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.6
, pp. 8-16
-
-
Strong, M.1
Gordon, P.H.2
-
4
-
-
3142628291
-
Word retrieval in amyotrophic lateral sclerosis: A functional magnetic resonance imaging study
-
Abrahams S, Goldstein LH, Simmons A, et al.: Word retrieval in amyotrophic lateral sclerosis: a functional magnetic resonance imaging study. Brain 2004, 127:1507-1517.
-
(2004)
Brain
, vol.127
, pp. 1507-1517
-
-
Abrahams, S.1
Goldstein, L.H.2
Simmons, A.3
-
5
-
-
8144227320
-
Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: Broadening the clinical picture to include progressive supranuclear palsy
-
Paviour DC, Lees AJ, Josephs KA, et al.: Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy. Brain 2004, 127:2441-2451.
-
(2004)
Brain
, vol.127
, pp. 2441-2451
-
-
Paviour, D.C.1
Lees, A.J.2
Josephs, K.A.3
-
6
-
-
0030026082
-
Avoiding false positive diagnoses of motor neuron disease: Lessons from the Scottish Motor Neuron Disease Register
-
Davenport RJ, Swingler RJ, Chancellor AM, Warlow CP: Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register. J Neurol Neurosurg Psychiatry 1996, 60:147-151.
-
(1996)
J Neurol Neurosurg Psychiatry
, vol.60
, pp. 147-151
-
-
Davenport, R.J.1
Swingler, R.J.2
Chancellor, A.M.3
Warlow, C.P.4
-
7
-
-
23144445291
-
Incidence of amyotrophic lateral sclerosis in southern Italy: A population based study
-
Logroscino G, Beghi E, Zoccolella S, et al.: Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study. J Neurol Neurosurg Psychiatry 2005, 76:1094-1098.
-
(2005)
J Neurol Neurosurg Psychiatry
, vol.76
, pp. 1094-1098
-
-
Logroscino, G.1
Beghi, E.2
Zoccolella, S.3
-
8
-
-
15044342282
-
Severely increased risk of amyotrophic lateral sclerosis among Italian professional football players
-
Chiò A, Benzi G, Dossena M, et al.: Severely increased risk of amyotrophic lateral sclerosis among Italian professional football players. Brain 2005, 128:472-476.
-
(2005)
Brain
, vol.128
, pp. 472-476
-
-
Chiò, A.1
Benzi, G.2
Dossena, M.3
-
9
-
-
0030749160
-
Phenotypic heterogeneity in MND-patients with CuZn-superoxide dismutase mutations in Scandinavia
-
Andersen PM, Nilsson P, Keränen ML, et al.: Phenotypic heterogeneity in MND-patients with CuZn-superoxide dismutase mutations in Scandinavia. Brain 1997, 10:1723-1737.
-
(1997)
Brain
, vol.10
, pp. 1723-1737
-
-
Andersen, P.M.1
Nilsson, P.2
Keränen, M.L.3
-
11
-
-
0028916910
-
Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients
-
Jones CT, Swingler RJ, Simpson SA, Brock DJ: Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients. J Med Genet 1995, 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
-
12
-
-
22244438889
-
Age dependent penetrance of three different superoxide dismutase 1 (SOD1) mutations
-
Aggarwal A, Nicholson G: Age dependent penetrance of three different superoxide dismutase 1 (SOD1) mutations. Int J Neurosci 2005, 115:1119-1130.
-
(2005)
Int J Neurosci
, vol.115
, pp. 1119-1130
-
-
Aggarwal, A.1
Nicholson, G.2
-
14
-
-
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
-
15
-
-
31544461165
-
Toxicity from copper chaperone and dismutase activity-independent accumulation of familial ALS-causing SOD1 mutants with spinal cord mitochondria
-
Liu J, Concepcion L, Jonsson PA, et al.: Toxicity from copper chaperone and dismutase activity-independent accumulation of familial ALS-causing SOD1 mutants with spinal cord mitochondria. Neuron 2004, 43:5-17.
-
(2004)
Neuron
, vol.43
, pp. 5-17
-
-
Liu, J.1
Concepcion, L.2
Jonsson, P.A.3
-
16
-
-
3242703300
-
ALS-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria
-
Pasinelli P, Belford ME, Lennon N, et al.: ALS-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria. Neuron 2004, 43:19-30.
-
(2004)
Neuron
, vol.43
, pp. 19-30
-
-
Pasinelli, P.1
Belford, M.E.2
Lennon, N.3
-
17
-
-
0347358915
-
Motor neuron disease in ALS patient and transgenic mice carrying Gly127insTGGG mutant Human CuZn-Superoxide Dismutase
-
Jonsson A, Ernhill K, Andersen PM, et al.: Motor neuron disease in ALS patient and transgenic mice carrying Gly127insTGGG mutant Human CuZn-Superoxide Dismutase. Brain 2004, 127:73-88.
-
(2004)
Brain
, vol.127
, pp. 73-88
-
-
Jonsson, A.1
Ernhill, K.2
Andersen, P.M.3
-
19
-
-
21344457470
-
Hoarseness due to bilateral vocal cord paralysis as an initial manifestation of familial ALS
-
Fukae J, Kubo SI, Hattori N, et al.: Hoarseness due to bilateral vocal cord paralysis as an initial manifestation of familial ALS. Amyotroph Lateral Scler Other Motor Neuron Disord 2005, 6:122-124.
-
(2005)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.6
, pp. 122-124
-
-
Fukae, J.1
Kubo, S.I.2
Hattori, N.3
-
20
-
-
0031854283
-
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis
-
Boukaftane Y, Khoris J, Moulard B, et al.: Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis. Can J Neurol Sci 1998, 25:192-196.
-
(1998)
Can J Neurol Sci
, vol.25
, pp. 192-196
-
-
Boukaftane, Y.1
Khoris, J.2
Moulard, B.3
-
21
-
-
22144446302
-
SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study
-
Battistini S, Giannini F, Greco G, et al.: SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study. J Neurol 2005, 252:782-788.
-
(2005)
J Neurol
, vol.252
, pp. 782-788
-
-
Battistini, S.1
Giannini, F.2
Greco, G.3
-
22
-
-
0030780350
-
Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: Analysis of 155 cases and identification of a novel insertion mutation
-
Jackson M, Al-Chalabi A, Enayat ZE, et al.: Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation. Ann Neurol 1997, 42:803-807.
-
(1997)
Ann Neurol
, vol.42
, pp. 803-807
-
-
Jackson, M.1
Al-Chalabi, A.2
Enayat, Z.E.3
-
23
-
-
0036338710
-
Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis
-
Garcia-Redondo A, Bustos F, Juan Y, et al.: Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis. Muscle Nerve 2002, 26:274-278.
-
(2002)
Muscle Nerve
, vol.26
, pp. 274-278
-
-
Garcia-Redondo, A.1
Bustos, F.2
Juan, Y.3
-
25
-
-
0029854883
-
D90A heterozygosity in the SOD1 gene is associated with familial and apprently sporadic ALS
-
Robberecht W, Aguirre T, Bosch LV, et al.: D90A heterozygosity in the SOD1 gene is associated with familial and apprently sporadic ALS. Neurology 1996, 47:1336-1339.
-
(1996)
Neurology
, vol.47
, pp. 1336-1339
-
-
Robberecht, W.1
Aguirre, T.2
Bosch, L.V.3
-
26
-
-
0141726584
-
A rare Cu/Zn superoxide dismutase mutation causing familial ALS with variable age of onset, incomplete penetrance and a sensory neuropathy
-
Rezania K, Yan J, Dellefave L, et al.: A rare Cu/Zn superoxide dismutase mutation causing familial ALS with variable age of onset, incomplete penetrance and a sensory neuropathy. Amyotroph Lateral Scler Other Motor Neuron Disord 2003, 4:162-166.
-
(2003)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.4
, pp. 162-166
-
-
Rezania, K.1
Yan, J.2
Dellefave, L.3
-
28
-
-
9544236295
-
Autosomal recessive adult-onset ALS associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients
-
Andersen PM, Forsgren L, Binzer M, et al.: Autosomal recessive adult-onset ALS associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients. Brain 1996, 119:1153-1172.
-
(1996)
Brain
, vol.119
, pp. 1153-1172
-
-
Andersen, P.M.1
Forsgren, L.2
Binzer, M.3
-
29
-
-
0036828798
-
"True" sporadic ALS associated with novel SOD-1 mutation
-
Alexander MD, Traynor BJ, Miller N, et al.: "True" sporadic ALS associated with novel SOD-1 mutation. Ann Neurol 2002, 52:680-683.
-
(2002)
Ann Neurol
, vol.52
, pp. 680-683
-
-
Alexander, M.D.1
Traynor, B.J.2
Miller, N.3
-
30
-
-
0033947274
-
Preserved slow conducting corticomotoneuronal projections in ALS patients with autosomal recessive D90A CuZn-SOD mutation
-
Weber M, Eisen A, Stewart HG, Andersen PM: Preserved slow conducting corticomotoneuronal projections in ALS patients with autosomal recessive D90A CuZn-SOD mutation. Brain 2000, 123:1505-1515.
-
(2000)
Brain
, vol.123
, pp. 1505-1515
-
-
Weber, M.1
Eisen, A.2
Stewart, H.G.3
Andersen, P.M.4
-
31
-
-
0031057003
-
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis
-
Cudkowicz ME, McKenna-Yasek D, Sapp PE, et al.: Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis. Ann Neurol 1997, 41:210-221.
-
(1997)
Ann Neurol
, vol.41
, pp. 210-221
-
-
Cudkowicz, M.E.1
McKenna-Yasek, D.2
Sapp, P.E.3
-
32
-
-
3442899724
-
Familial ALS in Germany: Origin of the R115G SOD1 mutation by a founder effect
-
Niemann S, Joos H, Meyer T, et al.: Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect. J Neurol Neurosurg Psychiatry 2004, 75:1186-1188.
-
(2004)
J Neurol Neurosurg Psychiatry
, vol.75
, pp. 1186-1188
-
-
Niemann, S.1
Joos, H.2
Meyer, T.3
-
33
-
-
20444470252
-
Distinct cerebral lesions in sporadic and 'D90A' SOD1 ALS: Studies with [11C]-flumazenil PET
-
Turner MR, Hammers A, Al-Chalabi A, et al.: Distinct cerebral lesions in sporadic and 'D90A' SOD1 ALS: Studies with [11C]-flumazenil PET. Brain 2005, 128:1323-1329.
-
(2005)
Brain
, vol.128
, pp. 1323-1329
-
-
Turner, M.R.1
Hammers, A.2
Al-Chalabi, A.3
-
34
-
-
0031960868
-
Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis
-
Hayward C, Brock DJ, Minns RA, Swingler RJ: Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis. J Med Genet 1998, 35:174.
-
(1998)
J Med Genet
, vol.35
, pp. 174
-
-
Hayward, C.1
Brock, D.J.2
Minns, R.A.3
Swingler, R.J.4
-
35
-
-
0035955486
-
Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial ALS with the homozygous mutation
-
Kato M, Aoki M, Ohta M, et al.: Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial ALS with the homozygous mutation. Neurosci Lett 2001, 312:165-168.
-
(2001)
Neurosci Lett
, vol.312
, pp. 165-168
-
-
Kato1
Aoki, M.2
Ohta, M.3
-
36
-
-
0242643434
-
Relevance of oxidative injury in the pathogenesis of motor neuron disease
-
Agar J, Durham H: Relevance of oxidative injury in the pathogenesis of motor neuron disease. Amyotroph Lateral Scler Other Motor Neuron Disord 2003, 4:232-242.
-
(2003)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.4
, pp. 232-242
-
-
Agar, J.1
Durham, H.2
-
37
-
-
0141642203
-
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice
-
Clement AM, Nguyen MD, Roberts EA, et al.: Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice. Science 2003, 302:113-117.
-
(2003)
Science
, vol.302
, pp. 113-117
-
-
Clement, A.M.1
Nguyen, M.D.2
Roberts, E.A.3
-
38
-
-
0036209082
-
Minocycline prevents neurotoxicity induced by cerebrospinal fluid from patients with motor neuron disease
-
Tikka TM, Vartiainen NE, Goldsteins G, et al.: Minocycline prevents neurotoxicity induced by cerebrospinal fluid from patients with motor neuron disease. Brain 2002, 125:722-731.
-
(2002)
Brain
, vol.125
, pp. 722-731
-
-
Tikka, T.M.1
Vartiainen, N.E.2
Goldsteins, G.3
-
40
-
-
0034812835
-
Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers
-
Aggarwal A, Nicholson G: Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers. J Neurol Neurosurg Psychiatry 2001, 71:478-481.
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.71
, pp. 478-481
-
-
Aggarwal, A.1
Nicholson, G.2
-
41
-
-
23444445882
-
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies
-
Krasnianski A, Deschauer M, Neudecker S, et al.: Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies. Brain 2005, 128:1870-1876.
-
(2005)
Brain
, vol.128
, pp. 1870-1876
-
-
Krasnianski, A.1
Deschauer, M.2
Neudecker, S.3
-
42
-
-
22244489417
-
Systematically perturbed folding patterns of ALS-associated SOD1 mutants
-
Lindberg MJ, Byström R, Bokanäs N, et al.: Systematically perturbed folding patterns of ALS-associated SOD1 mutants. Proc Natl Acad Sci U S A 2005, 102:9754-9759.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 9754-9759
-
-
Lindberg, M.J.1
Byström, R.2
Bokanäs, N.3
-
43
-
-
2442624720
-
Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial ALS
-
Rakhit R, Crow JP, Lepock JR, et al.: Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial ALS. J Biol Chem 2004, 279:15499-15504.
-
(2004)
J Biol Chem
, vol.279
, pp. 15499-15504
-
-
Rakhit, R.1
Crow, J.P.2
Lepock, J.R.3
-
44
-
-
2442436685
-
Long term proteasome inhibition does not preferentially afflict motor neurons in organo-typical spinal cord cultures
-
Vlug AS, Jaarsma D: Long term proteasome inhibition does not preferentially afflict motor neurons in organo-typical spinal cord cultures. Amyotroph Lateral Scler Other Motor Neuron Disord 2004, 5:16-21.
-
(2004)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.5
, pp. 16-21
-
-
Vlug, A.S.1
Jaarsma, D.2
-
45
-
-
0036310142
-
Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis
-
Menzies FM, Cookson MR, Taylor RW, et al.: Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis. Brain 2002, 125:1522-1533.
-
(2002)
Brain
, vol.125
, pp. 1522-1533
-
-
Menzies, F.M.1
Cookson, M.R.2
Taylor, R.W.3
-
46
-
-
12844269876
-
Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA
-
Ge WW, Wen W, Strong W, et al.: Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA. J Biol Chem 2005, 280:118-124.
-
(2005)
J Biol Chem
, vol.280
, pp. 118-124
-
-
Ge, W.W.1
Wen, W.2
Strong, W.3
-
47
-
-
21344472483
-
A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice
-
Kieran D, Hafezparast M, Bohnert S, et al.: A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice. J Cell Biol 2005, 169:561-567.
-
(2005)
J Cell Biol
, vol.169
, pp. 561-567
-
-
Kieran, D.1
Hafezparast, M.2
Bohnert, S.3
-
48
-
-
17844399774
-
Mutant superoxide dismutase disrupts cytoplasmic dynein in motor neurons
-
Ligon LA, LaMonte BL, Wallace KE, et al.: Mutant superoxide dismutase disrupts cytoplasmic dynein in motor neurons. Neuroreport 2005, 16:533-536.
-
(2005)
Neuroreport
, vol.16
, pp. 533-536
-
-
Ligon, L.A.1
LaMonte, B.L.2
Wallace, K.E.3
-
49
-
-
22844436451
-
Dynein mutations impair autophagic clerance of aggregate-prone proteins
-
Ravikumar B, Acevedo-Arozena A, Imarisio S, et al.: Dynein mutations impair autophagic clerance of aggregate-prone proteins. Nat Genet 2005, 37:771-776.
-
(2005)
Nat Genet
, vol.37
, pp. 771-776
-
-
Ravikumar, B.1
Acevedo-Arozena, A.2
Imarisio, S.3
-
50
-
-
0141614845
-
No association with genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial ALS
-
Fischer EM, Ahmad-Annuar A, Shah P, et al.: No association with genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial ALS. Amyotroph Lateral Scler Other Motor Neuron Disord 2003, 4:150-157.
-
(2003)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.4
, pp. 150-157
-
-
Fischer, E.M.1
Ahmad-Annuar, A.2
Shah, P.3
-
51
-
-
20944448536
-
Distal spinal and bulbar muscular atrophy caused by dynactin mutation
-
Puls I, Oh SJ, Sumner CJ, et al.: Distal spinal and bulbar muscular atrophy caused by dynactin mutation. Ann Neurol 2005, 57:687-694.
-
(2005)
Ann Neurol
, vol.57
, pp. 687-694
-
-
Puls, I.1
Oh, S.J.2
Sumner, C.J.3
-
52
-
-
4143084861
-
Point mutation of the p150 subunit of dynactin (DCTN1) gene in ALS
-
Münch C, Sedlmeier R, Meyer T, et al.: Point mutation of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology 2004, 63:724-726.
-
(2004)
Neurology
, vol.63
, pp. 724-726
-
-
Münch, C.1
Sedlmeier, R.2
Meyer, T.3
-
53
-
-
27644558934
-
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD
-
Münch C, Rosenbohm A, Sperfeld AD, et al.: Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD. Ann Neurol 2005, 58:777-780.
-
(2005)
Ann Neurol
, vol.58
, pp. 777-780
-
-
Münch, C.1
Rosenbohm, A.2
Sperfeld, A.D.3
-
54
-
-
0031936175
-
Mutations in all five exons of SOD-1 may cause ALS
-
Shaw CE, Enayat ZE, Chioza BA, et al.: Mutations in all five exons of SOD-1 may cause ALS. Ann Neurol 1998, 43:390-394.
-
(1998)
Ann Neurol
, vol.43
, pp. 390-394
-
-
Shaw, C.E.1
Enayat, Z.E.2
Chioza, B.A.3
-
55
-
-
0030945491
-
Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis
-
Orrell RW, Habgood JJ, Gardiner I, et al.: Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis. Neurology 1997, 48:746-751.
-
(1997)
Neurology
, vol.48
, pp. 746-751
-
-
Orrell, R.W.1
Habgood, J.J.2
Gardiner, I.3
|