-
1
-
-
0001372737
-
Progressive motor neuron disease in adults: A clinical study with special reference to the course of the disease
-
Müller R. Progressive motor neuron disease in adults: a clinical study with special reference to the course of the disease. Acta Psychiatr Neurol Scand. 1952;27(1-2):137-156.
-
(1952)
Acta Psychiatr Neurol Scand
, vol.27
, Issue.1-2
, pp. 137-156
-
-
Müller, R.1
-
2
-
-
0027327087
-
Onset, natural history and outcome in idiopathic adult motor neuron disease
-
DOI 10.1016/0022-510X(93)90245-T
-
Norris F, Shepherd R, Denys E, et al. Onset, natural history and outcome in idiopathic adult motor neuron disease. J Neurol Sci. 1993;118(1):48-55. (Pubitemid 23269966)
-
(1993)
Journal of the Neurological Sciences
, vol.118
, Issue.1
, pp. 48-55
-
-
Norris, F.1
Shepherd, R.2
Denys, E.3
-
3
-
-
0027202196
-
The prognosis of adult-onset motor neuron disease: A prospective study based on the Scottish Motor Neuron Disease Register
-
Chancellor AM, Slattery JM, Fraser H, Swingler RJ, Holloway SM, Warlow CP. The prognosis of adult-onset motor neuron disease: a prospective study based on the Scottish Motor Neuron Disease Register. J Neurol. 1993;240(6):339-346. (Pubitemid 23230381)
-
(1993)
Journal of Neurology
, vol.240
, Issue.6
, pp. 339-346
-
-
Chancellor, A.M.1
Slattery, J.M.2
Fraser, H.3
Swingler, R.J.4
Holloway, S.M.5
Warlow, C.P.6
-
4
-
-
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(pt 3):707-719.
-
(1995)
Brain
, vol.118
, Issue.PART 3
, pp. 707-719
-
-
Haverkamp, L.J.1
Appel, V.2
Appel, S.H.3
-
5
-
-
0033905620
-
Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study
-
Traynor BJ, Codd MB, Corr B, Forde C, Frost E, Hardiman O. Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria. Arch Neurol. 2000;57(8):1171-1176. (Pubitemid 30644664)
-
(2000)
Archives of Neurology
, vol.57
, Issue.8
, pp. 1171-1176
-
-
Traynor, B.J.1
Codd, M.B.2
Corr, B.3
Forde, C.4
Frost, E.5
Hardiman, O.M.6
-
6
-
-
0003119862
-
Recherches sur une maladie non encore décrite du système musculaire (atrophie musculaire progressive)
-
Aran FA. Recherches sur une maladie non encore décrite du système musculaire (atrophie musculaire progressive). Arch Gén Méd. 1850;24:5-35.
-
(1850)
Arch Gén Méd
, vol.24
, pp. 5-35
-
-
Aran, F.A.1
-
7
-
-
40349105720
-
The history of progressive muscular atrophy: Syndrome or disease?
-
Visser J, de Jong JM, de Visser M. The history of progressive muscular atrophy: syndrome or disease? Neurology. 2008;70(9):723-727.
-
(2008)
Neurology
, vol.70
, Issue.9
, pp. 723-727
-
-
Visser, J.1
De Jong, J.M.2
De Visser, M.3
-
8
-
-
34247166618
-
Disease course and prognostic factors of progressive muscular atrophy
-
Visser J, Van den Berg-Vos RM, Franssen H, et al. Disease course and prognostic factors of progressive muscular atrophy. Arch Neurol. 2007;64(4):522-528. (Pubitemid 46588340)
-
(2007)
Archives of Neurology
, vol.64
, Issue.4
, pp. 522-528
-
-
Visser, J.1
Van Den Berg-Vos, R.M.2
Franssen, H.3
Van Den Berg, L.H.4
Wokke, J.H.5
De Jong, J.M.V.6
Holman, R.7
De Haan, R.J.8
De Visser, M.9
-
9
-
-
77049139058
-
ALS: Clinico-anatomic study of 53 cases
-
Lawyer T, Netsky MG. ALS: clinico-anatomic study of 53 cases. Arch Neurol Psychiatry. 1953;69(2):171-192.
-
(1953)
Arch Neurol Psychiatry
, vol.69
, Issue.2
, pp. 171-192
-
-
Lawyer, T.1
Netsky, M.G.2
-
11
-
-
0037461283
-
Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS
-
Ince PG, Evans J, Knopp M, et al. Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS. Neurology. 2003;60(8):1252-1258. (Pubitemid 36460979)
-
(2003)
Neurology
, vol.60
, Issue.8
, pp. 1252-1258
-
-
Ince, P.G.1
Evans, J.2
Knopp, M.3
Forster, G.4
Hamdalla, H.H.M.5
Wharton, S.B.6
Shaw, P.J.7
-
12
-
-
0242584410
-
Sporadic lower motor neuron disease with adult onset: Classification of subtypes
-
DOI 10.1093/brain/awg117
-
Van den Berg-Vos RM, Visser J, Franssen H, et al. Sporadic lower motor neuron disease with adult onset: classification of subtypes. Brain. 2003;126(pt 5):1036-1047. (Pubitemid 36522947)
-
(2003)
Brain
, vol.126
, Issue.5
, pp. 1036-1047
-
-
Van Den Berg-Vos, R.M.1
Visser, J.2
Franssen, H.3
De Visser, M.4
De Jong, J.M.B.V.5
Kalmijn, S.6
Wokke, J.H.J.7
Van Den Berg, L.H.8
-
13
-
-
50049094756
-
Interpretation of electrodiagnostic findings in sporadic progressive muscular atrophy
-
Visser J, de Visser M, Van den Berg-Vos RM, et al. Interpretation of electrodiagnostic findings in sporadic progressive muscular atrophy. J Neurol. 2008;255(6):903-909.
-
(2008)
J Neurol
, vol.255
, Issue.6
, pp. 903-909
-
-
Visser, J.1
De Visser, M.2
Van Den Berg-Vos, R.M.3
-
14
-
-
0033673058
-
Multifocal motor neuropathy: Diagnostic criteria that predict the response to immunoglobulin treatment
-
Van den Berg-Vos RM, Franssen H, Wokke JHJ, Van Es HW, Van den Berg LH. Multifocal motor neuropathy: diagnostic criteria that predict the response to immunoglobulin treatment. Ann Neurol. 2000;48(6):919-926.
-
(2000)
Ann Neurol
, vol.48
, Issue.6
, pp. 919-926
-
-
Van Den Berg-Vos, R.M.1
Franssen, H.2
Wokke, J.H.J.3
Van Es, H.W.4
Van Den Berg, L.H.5
-
16
-
-
0003499342
-
-
Medical Research Council. London, England: Her Majesty's Stationery Office
-
Medical Research Council. Aid to the Examination of the Peripheral Nervous System. London, England: Her Majesty's Stationery Office; 1976:1-2.
-
(1976)
Aid to the Examination of the Peripheral Nervous System
, pp. 1-2
-
-
-
17
-
-
0024332294
-
Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy
-
Mendell JR, Moxley RT, Griggs RC, et al. Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy. N Engl J Med. 1989;320(24):1592-1597. (Pubitemid 19154573)
-
(1989)
New England Journal of Medicine
, vol.320
, Issue.24
, pp. 1592-1597
-
-
Mendell, J.R.1
Moxley, R.T.2
Griggs, R.C.3
Brooke, M.H.4
Fenichel, G.M.5
Miller, J.P.6
King, W.7
Signore, L.8
Pandya, S.9
Florence, J.10
Schierbecker, J.11
Robison, J.12
Kaiser, K.13
Mandel, S.14
Arfken, C.15
Gilder, B.16
-
18
-
-
0031034093
-
A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): Implications for therapeutic trials
-
FSH-DY Group. A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): implications for therapeutic trials. Neurology. 1997;48(1):38-46. (Pubitemid 27039514)
-
(1997)
Neurology
, vol.48
, Issue.1
, pp. 38-46
-
-
McDermott, M.P.1
-
19
-
-
0023130157
-
Interrater reliability of a modified Ashworth scale of muscle spasticity
-
Bohannon RW, Smith MB. Interrater reliability of a modified Ashworth scale of muscle spasticity. Phys Ther. 1987;67(2):206-207. (Pubitemid 17026064)
-
(1987)
Physical Therapy
, vol.67
, Issue.2
, pp. 206-207
-
-
Bohannon, R.W.1
Smith, M.B.2
-
20
-
-
0027763494
-
NINDS myotatic reflex scale
-
Hallett M. NINDS myotatic reflex scale. Neurology. 1993;43(12):2723. (Pubitemid 24004582)
-
(1993)
Neurology
, vol.43
, Issue.12 I
, pp. 2723
-
-
Hallett, M.1
-
21
-
-
0242469500
-
Prospective quality control of vital capacity as primary endpoint in international multi-center therapeutic trial of SR567746A (Xaliproden) in amyotrophic lateral sclerosis
-
Sanjak M, Salachas F, Frija-Orvoen F, et al. Prospective quality control of vital capacity as primary endpoint in international multi-center therapeutic trial of SR567746A (Xaliproden) in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1(suppl 3):59-60.
-
(2000)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.1
, Issue.SUPPL. 3
, pp. 59-60
-
-
Sanjak, M.1
Salachas, F.2
Frija-Orvoen, F.3
-
22
-
-
0001163277
-
The amyotrophic lateral sclerosis functional rating scale: Assessment of activities of daily living in patients with amyotrophic lateral sclerosis
-
ALS CNTF Treatment Study Phase I-II Study Group. The Amyotrophic Lateral Sclerosis Functional Rating Scale: assessment of activities of daily living in patients with amyotrophic lateral sclerosis. Arch Neurol. 1996;53(2):141-147. (Pubitemid 26056465)
-
(1996)
Archives of Neurology
, vol.53
, Issue.2
, pp. 141-147
-
-
Cedarbaum, J.M.1
-
23
-
-
0001596952
-
Non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease)
-
Vinken PJ, Bruyn GW, Klawans HL, de Jong JMBV, eds. Amsterdam, the Netherlands: Elsevier Science Publishers
-
Hirayama K. Non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease). In: Vinken PJ, Bruyn GW, Klawans HL, de Jong JMBV, eds. Handbook of Clinical Neurology. Amsterdam, the Netherlands: Elsevier Science Publishers; 1991:107-118.
-
(1991)
Handbook of Clinical Neurology
, pp. 107-118
-
-
Hirayama, K.1
-
24
-
-
0034169549
-
Juvenile muscular atrophy of distal upper extremity (Hirayama disease)
-
Hirayama K. Juvenile muscular atrophy of distal upper extremity (Hirayama disease). Intern Med. 2000;39(4):283-290.
-
(2000)
Intern Med
, vol.39
, Issue.4
, pp. 283-290
-
-
Hirayama, K.1
-
25
-
-
0033595565
-
Brachial amyotrophic diplegia: A slowly progressive motor neuron disorder
-
Katz JS, Wolfe GI, Andersson PB, et al. Brachial amyotrophic diplegia: a slowly progressive motor neuron disorder. Neurology. 1999;53(5):1071-1076. (Pubitemid 29442125)
-
(1999)
Neurology
, vol.53
, Issue.5
, pp. 1071-1076
-
-
Katz, J.S.1
Wolfe, G.I.2
Andersson, P.B.3
Saperstein, D.S.4
Elliott, J.L.5
Nations, S.P.6
Bryan, W.W.7
Barohn, R.J.8
-
26
-
-
33645113923
-
Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan
-
Tashiro K, Kikuchi S, Itoyama Y, et al. Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan. Amyotroph Lateral Scler. 2006;7(1):38-45.
-
(2006)
Amyotroph Lateral Scler
, vol.7
, Issue.1
, pp. 38-45
-
-
Tashiro, K.1
Kikuchi, S.2
Itoyama, Y.3
-
27
-
-
0032252416
-
Flail arm syndrome: A distinctive variant of amyotrophic lateral sclerosis
-
Hu MT, Ellis CM, al Chalabi A, Leigh PN, Shaw CE. Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 1998;65(6):950-951.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, Issue.6
, pp. 950-951
-
-
Hu, M.T.1
Ellis, C.M.2
Al Chalabi, A.3
Leigh, P.N.4
Shaw, C.E.5
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