-
1
-
-
84872246996
-
A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia
-
Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, et al. A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. PLoS One 2013; 8: e53826.
-
(2013)
PLoS One
, vol.8
-
-
Ben Ammar, A.1
Soltanzadeh, P.2
Bauché, S.3
Richard, P.4
Goillot, E.5
Herbst, R.6
-
2
-
-
0027361165
-
Motor unit number estimation, isometric strength, and electromyographic measures in amyotrophic lateral sclerosis
-
Bromberg MB, Forshew DA, Nau KL, Bromberg J, Simmons Z, Fries TJ. Motor unit number estimation, isometric strength, and electromyographic measures in amyotrophic lateral sclerosis. Muscle Nerve 1993; 16: 1213-9.
-
(1993)
Muscle Nerve
, vol.16
, pp. 1213-1219
-
-
Bromberg, M.B.1
Forshew, D.A.2
Nau, K.L.3
Bromberg, J.4
Simmons, Z.5
Fries, T.J.6
-
3
-
-
0014530017
-
Some comments on the histochemical characterization of muscle adenosine triphosphatase
-
Brooke MH, Kaiser KK. Some comments on the histochemical characterization of muscle adenosine triphosphatase. J Histochem Cytochem 1969; 17: 431-2.
-
(1969)
J Histochem Cytochem
, vol.17
, pp. 431-432
-
-
Brooke, M.H.1
Kaiser, K.K.2
-
5
-
-
0000280462
-
Deux cas d'atrophie musculaire progressive avec lésions de la substance grise et des faisceaux antéro-latéraux de la moelle épinière
-
Charcot JM, Joffroy A. Deux cas d'atrophie musculaire progressive avec lésions de la substance grise et des faisceaux antéro- latéraux de la moelle épinière. Arch Physiol Neurol Pathol 1869; 2: 744-60.
-
(1869)
Arch Physiol Neurol Pathol
, vol.2
, pp. 744-760
-
-
Charcot, J.M.1
Joffroy, A.2
-
6
-
-
84887403257
-
Morphologie de la jonction neuromusculaire
-
Cöers C. Morphologie de la jonction neuromusculaire. Arch Biol (Liège) 1964; 75: 905-41.
-
(1964)
Arch Biol (Liège)
, vol.75
, pp. 905-941
-
-
Cöers, C.1
-
7
-
-
58249119457
-
The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity
-
Cohen TJ, Barrientos T, Hartman ZC, Garvey SM, Cox GA, Yao TP. The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity. FASEB J 2009; 23: 99-106.
-
(2009)
FASEB J
, vol.23
, pp. 99-106
-
-
Cohen, T.J.1
Barrientos, T.2
Hartman, Z.C.3
Garvey, S.M.4
Cox, G.A.5
Yao, T.P.6
-
8
-
-
36348988617
-
The histone deacetylase HDAC4 connects neural activity to muscle transcriptional reprogramming
-
Cohen TJ, Waddell DS, Barrientos T, Lu Z, Feng G, Cox GA, et al. The histone deacetylase HDAC4 connects neural activity to muscle transcriptional reprogramming. J Biol Chem 2007; 282: 33752-9.
-
(2007)
J Biol Chem
, vol.282
, pp. 33752-33759
-
-
Cohen, T.J.1
Waddell, D.S.2
Barrientos, T.3
Lu, Z.4
Feng, G.5
Cox, G.A.6
-
9
-
-
0024213603
-
On the role of the 200-kDa neurofilament protein at the developing neuromuscular junction
-
Donahue SP, Wood JG, English AW. On the role of the 200-kDa neurofilament protein at the developing neuromuscular junction. Dev Biol 1988; 130: 154-66.
-
(1988)
Dev Biol
, vol.130
, pp. 154-166
-
-
Donahue, S.P.1
Wood, J.G.2
English, A.W.3
-
10
-
-
0034175513
-
Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases
-
Frey D, Schneider C, Xu L, Borg J, Spooren W, Caroni P. Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases. J Neurosci 2000; 20: 2534-42.
-
(2000)
J Neurosci
, vol.20
, pp. 2534-2542
-
-
Frey, D.1
Schneider, C.2
Xu, L.3
Borg, J.4
Spooren, W.5
Caroni, P.6
-
11
-
-
0036260266
-
Expression of foetal type acetylcholine receptor is restricted to type 1 muscle fibres in human neuromuscular disorders
-
Gattenlohner S, Schneider C, Thamer C, Klein R, Roggendorf W, Gohlke F, et al. Expression of foetal type acetylcholine receptor is restricted to type 1 muscle fibres in human neuromuscular disorders. Brain 2002; 125: 1309-19.
-
(2002)
Brain
, vol.125
, pp. 1309-1319
-
-
Gattenlohner, S.1
Schneider, C.2
Thamer, C.3
Klein, R.4
Roggendorf, W.5
Gohlke, F.6
-
12
-
-
0017844051
-
A quantitative electrophysiological study of motor neurone disease
-
Hansen S, Ballantyne JP. A quantitative electrophysiological study of motor neurone disease. J Neurol Neurosurg Psychiatry 1978; 41: 773-83.
-
(1978)
J Neurol Neurosurg Psychiatry
, vol.41
, pp. 773-783
-
-
Hansen, S.1
Ballantyne, J.P.2
-
13
-
-
68349151039
-
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function
-
Huzé C, Bauche S, Richard P, Chevessier F, Goillot E, Gaudon K, et al. Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. Am J Hum Genet 2009; 85: 155-67.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 155-167
-
-
Huzé, C.1
Bauche, S.2
Richard, P.3
Chevessier, F.4
Goillot, E.5
Gaudon, K.6
-
14
-
-
0015547811
-
Data on the distribution of fibre types in thirty-six human muscles. An autopsy study
-
Johnson MA, Polgar J, Weightman D, Appleton D. Data on the distribution of fibre types in thirty-six human muscles. An autopsy study. J Neurol Sci 1973; 18: 111-29.
-
(1973)
J Neurol Sci
, vol.18
, pp. 111-129
-
-
Johnson, M.A.1
Polgar, J.2
Weightman, D.3
Appleton, D.4
-
15
-
-
78651012385
-
A histochemical method for localizing cholinesterase activity
-
Koelle GB, Friedenwald JA. A histochemical method for localizing cholinesterase activity. Proc Soc Exp Biol Med 1949; 70: 617-22.
-
(1949)
Proc Soc Exp Biol Med
, vol.70
, pp. 617-622
-
-
Koelle, G.B.1
Friedenwald, J.A.2
-
16
-
-
0029977337
-
Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II
-
Lacomblez L, Bensimon G, Leigh PN, Guillet P, Meininger V. Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II. Lancet 1996; 347: 1425-31.
-
(1996)
Lancet
, vol.347
, pp. 1425-1431
-
-
Lacomblez, L.1
Bensimon, G.2
Leigh, P.N.3
Guillet, P.4
Meininger, V.5
-
17
-
-
0023113842
-
Differences between motor unit firing rate, twitch characteristics and fibre type composition in an agonistic muscle group in man
-
Le Bozec S, Maton B. Differences between motor unit firing rate, twitch characteristics and fibre type composition in an agonistic muscle group in man. Eur J Appl Physiol Occup Physiol 1987; 56: 350-5.
-
(1987)
Eur J Appl Physiol Occup Physiol
, vol.56
, pp. 350-355
-
-
Le Bozec, S.1
Maton, B.2
-
18
-
-
0025888399
-
Anconeus muscle: A human muscle preparation suitable for in-vitro microelectrode studies
-
Maselli RA, Mass DP, Distad BJ, Richman DP. Anconeus muscle: a human muscle preparation suitable for in-vitro microelectrode studies. Muscle Nerve 1991; 14: 1189-92.
-
(1991)
Muscle Nerve
, vol.14
, pp. 1189-1192
-
-
Maselli, R.A.1
Mass, D.P.2
Distad, B.J.3
Richman, D.P.4
-
19
-
-
0027484081
-
Neuromuscular transmission in amyotrophic lateral sclerosis
-
Maselli RA, Wollman RL, Leung C, Distad B, Palombi S, Richman DP, et al. Neuromuscular transmission in amyotrophic lateral sclerosis. Muscle Nerve 1993; 16: 1193-203.
-
(1993)
Muscle Nerve
, vol.16
, pp. 1193-1203
-
-
Maselli, R.A.1
Wollman, R.L.2
Leung, C.3
Distad, B.4
Palombi, S.5
Richman, D.P.6
-
20
-
-
77958121094
-
Patients who survive 5 years or more with ALS in Olmsted County, 1925-2004
-
Mateen FJ, Carone M, Sorenson EJ. Patients who survive 5 years or more with ALS in Olmsted County, 1925-2004. J Neurol Neurosurg Psychiatry 2010; 81: 1144-6.
-
(2010)
J Neurol Neurosurg Psychiatry
, vol.81
, pp. 1144-1146
-
-
Mateen, F.J.1
Carone, M.2
Sorenson, E.J.3
-
21
-
-
0027522111
-
Motor unit populations in healthy and diseased muscles
-
McComas AJ, Galea V, de Bruin H. Motor unit populations in healthy and diseased muscles. Phys Ther 1993; 73: 868-77.
-
(1993)
Phys Ther
, vol.73
, pp. 868-877
-
-
McComas, A.J.1
Galea, V.2
De Bruin, H.3
-
22
-
-
0029433185
-
Epidemiology of ALS
-
Nelson LM. Epidemiology of ALS. Clin Neurosci 1995; 3: 327-31.
-
(1995)
Clin Neurosci
, vol.3
, pp. 327-331
-
-
Nelson, L.M.1
-
23
-
-
80055053362
-
Muscle gene expression is a marker of amyotrophic lateral sclerosis severity
-
Pradat PF, Dubourg O, de Tapia M, di Scala F, Dupuis L, Lenglet T, et al. Muscle gene expression is a marker of amyotrophic lateral sclerosis severity. Neurodegener Dis 2012; 9: 38-52.
-
(2012)
Neurodegener Dis
, vol.9
, pp. 38-52
-
-
Pradat, P.F.1
Dubourg, O.2
De Tapia, M.3
Di Scala, F.4
Dupuis, L.5
Lenglet, T.6
-
24
-
-
33344462702
-
Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF
-
Pun S, Santos AF, Saxena S, Xu L, Caroni P. Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF. Nat Neurosci 2006; 9: 408-19.
-
(2006)
Nat Neurosci
, vol.9
, pp. 408-419
-
-
Pun, S.1
Santos, A.F.2
Saxena, S.3
Xu, L.4
Caroni, P.5
-
25
-
-
0002887220
-
Skeletal muscle adaptability: Significance for metabolism and performance
-
In: Peachey LD, Adrian RH, Geiger SR, editors. Bethesda: American Physiological Society
-
Saltin B, Gollnick PD. Skeletal muscle adaptability: significance for metabolism and performance. In: Peachey LD, Adrian RH, Geiger SR, editors. Handbook of physiology. Bethesda: American Physiological Society; 1983. p. 555-631.
-
(1983)
Handbook of Physiology
, pp. 555-631
-
-
Saltin, B.1
Gollnick, P.D.2
-
26
-
-
23744445580
-
A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis
-
Schaefer AM, Sanes JR, Lichtman JW. A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis. J Comp Neurol 2005; 490: 209-19.
-
(2005)
J Comp Neurol
, vol.490
, pp. 209-219
-
-
Schaefer, A.M.1
Sanes, J.R.2
Lichtman, J.W.3
-
27
-
-
0038480212
-
Prolonged survival in motor neuron disease: A descriptive study of the King's database 1990-2002
-
Turner MR, Parton MJ, Shaw CE, Leigh PN, Al Chalabi A. Prolonged survival in motor neuron disease: a descriptive study of the King's database 1990-2002. J Neurol Neurosurg Psychiatry 2003; 74: 995-7.
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, pp. 995-997
-
-
Turner, M.R.1
Parton, M.J.2
Shaw, C.E.3
Leigh, P.N.4
Al Chalabi, A.5
-
28
-
-
34848838292
-
MicroRNAs: Powerful new regulators of heart disease and provocative therapeutic targets
-
van Rooij E, Olson EN. MicroRNAs: powerful new regulators of heart disease and provocative therapeutic targets. J Clin Invest 2007; 117: 2369-76.
-
(2007)
J Clin Invest
, vol.117
, pp. 2369-2376
-
-
Van Rooij, E.1
Olson, E.N.2
-
29
-
-
84857064039
-
ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survival
-
Weber M, Neuwirth C, Thierbach J, Schweikert K, Czaplinski A, Petersen J, et al. ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survival. J Neurol Neurosurg Psychiatry 2012; 83: 351-3.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 351-353
-
-
Weber, M.1
Neuwirth, C.2
Thierbach, J.3
Schweikert, K.4
Czaplinski, A.5
Petersen, J.6
-
30
-
-
72149131804
-
MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice
-
Williams AH, Valdez G, Moresi V, Qi X, McAnally J, Elliott JL, et al. MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice. Science 2009; 326: 1549-54.
-
(2009)
Science
, vol.326
, pp. 1549-1554
-
-
Williams, A.H.1
Valdez, G.2
Moresi, V.3
Qi, X.4
McAnally, J.5
Elliott, J.L.6
-
31
-
-
79961028733
-
Treatment with trichostatin A initiated after disease onset delays disease progression and increases survival in a mouse model of amyotrophic lateral sclerosis
-
Yoo YE, Ko CP. Treatment with trichostatin A initiated after disease onset delays disease progression and increases survival in a mouse model of amyotrophic lateral sclerosis. Exp Neurol 2011; 231: 147-59.
-
(2011)
Exp Neurol
, vol.231
, pp. 147-159
-
-
Yoo, Y.E.1
Ko, C.P.2
-
32
-
-
40849083833
-
Predictors of long survival in amyotrophic lateral sclerosis: A population-based study
-
Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Samarelli V, et al. Predictors of long survival in amyotrophic lateral sclerosis: a population-based study. J Neurol Sci 2008; 268: 28-32.
-
(2008)
J Neurol Sci
, vol.268
, pp. 28-32
-
-
Zoccolella, S.1
Beghi, E.2
Palagano, G.3
Fraddosio, A.4
Guerra, V.5
Samarelli, V.6
|