-
1
-
-
0023924673
-
Somatosensory and acoustic brain stem reflex myoclonus
-
Shibasaki H, Kakigi R, Oda K, Masukawa S. Somatosensory and acoustic brain stem reflex myoclonus. J Neurol Neurosurg Psychiatry 1988;51(4):572-575.
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, Issue.4
, pp. 572-575
-
-
Shibasaki, H.1
Kakigi, R.2
Oda, K.3
Masukawa, S.4
-
2
-
-
65349140039
-
Propriospinal myoclonus revisited: Clinical, neurophysiologic, and neuroradiologic findings
-
Roze E, Bounolleau P, Ducreux D, et al. Propriospinal myoclonus revisited: clinical, neurophysiologic, and neuroradiologic findings. Neurology 2009;72(15):1301-1309.
-
(2009)
Neurology
, vol.72
, Issue.15
, pp. 1301-1309
-
-
Roze, E.1
Bounolleau, P.2
Ducreux, D.3
-
3
-
-
77955918761
-
Axial jerks: A clinical spectrum ranging from propriospinal to psychogenic myoclonus
-
van der Salm SM, Koelman JH, Henneke S, et al. Axial jerks: a clinical spectrum ranging from propriospinal to psychogenic myoclonus. J Neurol 2010;257(8):1349-1355.
-
(2010)
J Neurol
, vol.257
, Issue.8
, pp. 1349-1355
-
-
Van Der Salm, S.M.1
Koelman, J.H.2
Henneke, S.3
-
4
-
-
0042474234
-
Unique form of propriospinal myoclonus as a possible complication of an enteropathogenic toxin
-
DOI 10.1002/mds.10453
-
Espay AJ, Ashby P, Hanajima R, et al. Unique form of propriospinal myoclonus as a possible complication of an enteropathogenic toxin. Mov Disord 2003;18(8):942-948. (Pubitemid 37021172)
-
(2003)
Movement Disorders
, vol.18
, Issue.8
, pp. 942-948
-
-
Espay, A.J.1
Ashby, P.2
Hanajima, R.3
Jog, M.S.4
Lang, A.E.5
-
5
-
-
34249017259
-
Orthostatic myoclonus: A contributor to gait decline in selected elderly
-
DOI 10.1212/01.wnl.0000260225.46732.af
-
Glass GA, Ahlskog JE, Matsumoto JY. Orthostatic myoclonus: a contributor to gait decline in selected elderly. Neurology 2007; 68(21):1826-1830. (Pubitemid 46791396)
-
(2007)
Neurology
, vol.68
, Issue.21
, pp. 1826-1830
-
-
Glass, G.A.1
Ahlskog, J.E.2
Matsumoto, J.Y.3
-
6
-
-
37549039055
-
Myoclonus or tremor in orthostatism: An under-recognized cause of unsteadiness in parkinson's disease
-
Leu-Semenescu S, Roze E, Vidailhet M, et al. Myoclonus or tremor in orthostatism: an under-recognized cause of unsteadiness in Parkinson's disease. Mov Disord 2007;22(14): 2063-2069.
-
(2007)
Mov Disord
, vol.22
, Issue.14
, pp. 2063-2069
-
-
Leu-Semenescu, S.1
Roze, E.2
Vidailhet, M.3
-
8
-
-
67651183916
-
Myoclonus-dystonia: An update
-
Kinugawa K, Vidailhet M, Clot F, et al. Myoclonus-dystonia: an update. Mov Disord 2009;24(4):479-489.
-
(2009)
Mov Disord
, vol.24
, Issue.4
, pp. 479-489
-
-
Kinugawa, K.1
Vidailhet, M.2
Clot, F.3
-
9
-
-
80052294248
-
Psychiatric disorders myoclonus dystonia and the epsilon-sarcoglycan gene: A systematic review
-
Peall KJ, Waite AJ, Blake DJ, et al. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Mov Disord 2011;26(10):1939-1942.
-
(2011)
Mov Disord
, vol.26
, Issue.10
, pp. 1939-1942
-
-
Peall, K.J.1
Waite, A.J.2
Blake, D.J.3
-
10
-
-
84866087908
-
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency
-
Stamelou M, Mencacci NE, Cordivari C, et al. Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency. Neurology 2012;79(5):435-441.
-
(2012)
Neurology
, vol.79
, Issue.5
, pp. 435-441
-
-
Stamelou, M.1
Mencacci, N.E.2
Cordivari, C.3
-
11
-
-
54049098434
-
Myoclonus-dystonia due to maternal uniparental disomy
-
Guettard E, Portnoi MF, Lohmann-Hedrich K, et al. Myoclonus-dystonia due to maternal uniparental disomy. Arch Neurol 2008;65(10):1380-1385.
-
(2008)
Arch Neurol
, vol.65
, Issue.10
, pp. 1380-1385
-
-
Guettard, E.1
Portnoi, M.F.2
Lohmann-Hedrich, K.3
-
12
-
-
79960773144
-
Difficulties with neurological prognostication in a young woman with delayed-onset generalised status myoclonus after cardiac arrest due to acute severe asthma
-
Rajamani A, Seppelt I, Bourne J. Difficulties with neurological prognostication in a young woman with delayed-onset generalised status myoclonus after cardiac arrest due to acute severe asthma. Indian J Crit Care Med 2011;15(2):137-139.
-
(2011)
Indian J Crit Care Med
, vol.15
, Issue.2
, pp. 137-139
-
-
Rajamani, A.1
Seppelt, I.2
Bourne, J.3
-
14
-
-
0024333221
-
Severe acute asthma in a pediatric intensive care unit: Six years' experience
-
Stein R, Canny GJ, Bohn DJ, et al. Severe acute asthma in a pediatric intensive care unit: six years' experience. Pediatrics 1989; 83(6):1023-1028. (Pubitemid 19154680)
-
(1989)
Pediatrics
, vol.83
, Issue.6
, pp. 1023-1028
-
-
Stein, R.1
Canny, G.J.2
Bohn, D.J.3
Reisman, J.J.4
Levison, H.5
-
15
-
-
33847408907
-
Myoclonus and extrapyramidal diseases
-
Defebvre L. Myoclonus and extrapyramidal diseases. Neurophysiol Clin 2006;36(5-6): 319-325.
-
(2006)
Neurophysiol Clin
, vol.36
, Issue.5-6
, pp. 319-325
-
-
Defebvre, L.1
-
16
-
-
0036371759
-
Myoclonus in parkinsonian disorders
-
Shafiq M, Lang AE. Myoclonus in parkinsonian disorders. Adv Neurol 2002;89:77-83.
-
(2002)
Adv Neurol
, vol.89
, pp. 77-83
-
-
Shafiq, M.1
Lang, A.E.2
-
17
-
-
0034100242
-
Negative myoclonus in Creutzfeldt-Jakob disease
-
DOI 10.1016/S1388-2457(99)00277-1, PII S1388245799002771
-
Matsunaga K, Uozumi T, Akamatsu N, et al. Negative myoclonus in Creutzfeldt-Jakob disease. Clin Neurophysiol 2000;111(3): 471-476. (Pubitemid 30123117)
-
(2000)
Clinical Neurophysiology
, vol.111
, Issue.3
, pp. 471-476
-
-
Matsunaga, K.1
Uozumi, T.2
Akamatsu, N.3
Nagashio, Y.4
Qingrui, L.5
Hashimoto, T.6
Tsuji, S.7
-
18
-
-
78649349873
-
Drug-induced cranial myoclonus
-
Gupta A, Lang AE. Drug-induced cranial myoclonus. Mov Disord 2010;25(13): 2264-2265.
-
(2010)
Mov Disord
, vol.25
, Issue.13
, pp. 2264-2265
-
-
Gupta, A.1
Lang, A.E.2
-
19
-
-
0033960019
-
Postural and action myoclonus in patients with parkinsonian type multiple system atrophy
-
DOI 10.1002/1531-8257(200001)15:1<77::AID-MDS1013>3.0.CO;2-N
-
Salazar G, Valls-Sole J, Marti MJ, et al. Postural and action myoclonus in patients with parkinsonian type multiple system atrophy. Mov Disord 2000;15(1):77-83. (Pubitemid 30037991)
-
(2000)
Movement Disorders
, vol.15
, Issue.1
, pp. 77-83
-
-
Salazar, G.1
Valls-Sole, J.2
Marti, M.J.3
Chang, H.4
Tolosa, E.S.5
-
20
-
-
0028289351
-
Facial action myoclonus in patients with olivopontocerebellar atrophy
-
Lou JS, Valls-Sole J, Toro C, Hallett M. Facial action myoclonus in patients with olivopontocerebellar atrophy. Mov Disord 1994;9(2):223-226. (Pubitemid 24092343)
-
(1994)
Movement Disorders
, vol.9
, Issue.2
, pp. 223-226
-
-
Lou, J.-S.1
Valls-Sole, J.2
Toro, C.3
Hallett, M.4
-
21
-
-
69549085108
-
Alzheimer's disease and corticobasal degeneration presenting as corticobasal syndrome
-
Hu WT, Rippon GW, Boeve BF, et al. Alzheimer's disease and corticobasal degeneration presenting as corticobasal syndrome. Mov Disord 2009;24(9): 1375-1379.
-
(2009)
Mov Disord
, vol.24
, Issue.9
, pp. 1375-1379
-
-
Hu, W.T.1
Rippon, G.W.2
Boeve, B.F.3
-
22
-
-
84873639356
-
Criteria for the diagnosis of corticobasal degeneration
-
Armstrong MJ, Litvan I, Lang AE, et al. Criteria for the diagnosis of corticobasal degeneration. Neurology 2013;80(5):496-503.
-
(2013)
Neurology
, vol.80
, Issue.5
, pp. 496-503
-
-
Armstrong, M.J.1
Litvan, I.2
Lang, A.E.3
-
23
-
-
23244448102
-
Surface-binding autoantibodies to cerebellar neurons in opsoclonus syndrome
-
DOI 10.1002/ana.20539
-
Blaes F, Fuhlhuber V, Korfei M, et al. Surface-binding autoantibodies to cerebellar neurons in opsoclonus syndrome. Ann Neurol 2005;58(2):313-317. (Pubitemid 41098889)
-
(2005)
Annals of Neurology
, vol.58
, Issue.2
, pp. 313-317
-
-
Blaes, F.1
Fuhlhuber, V.2
Korfei, M.3
Tschernatsch, M.4
Behnisch, W.5
Rostasy, K.6
Hero, B.7
Kaps, M.8
Preissner, K.T.9
-
24
-
-
70449364101
-
Scarb2 mutations in progressive myoclonus epilepsy (pme) without renal failure
-
Dibbens LM, Michelucci R, Gambardella A, et al. SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure. Ann Neurol 2009;66(4):532-536.
-
(2009)
Ann Neurol
, vol.66
, Issue.4
, pp. 532-536
-
-
Dibbens, L.M.1
Michelucci, R.2
Gambardella, A.3
-
25
-
-
0025167681
-
Progressive myoclonic ataxia (The Ramsay Hunt syndrome)
-
Marsden CD, Harding AE, Obeso JA, Lu CS, et al. Progressive myoclonic ataxia (the Ramsay Hunt syndrome). Arch Neurol 1990;47(10):1121-1125. (Pubitemid 20326671)
-
(1990)
Archives of Neurology
, vol.47
, Issue.10
, pp. 1121-1125
-
-
Marsden, C.D.1
Harding, A.E.2
Obeso, J.A.3
Lu, C.-S.4
-
26
-
-
0028864352
-
Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum
-
Bhatia KP, Brown P, Gregory R, et al. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain 1995;118(pt 5):1087-1093.
-
(1995)
Brain
, vol.118
, Issue.PART 5
, pp. 1087-1093
-
-
Bhatia, K.P.1
Brown, P.2
Gregory, R.3
-
27
-
-
65549107903
-
The autosomal recessively inherited progressive myoclonus epilepsies and their genes
-
Ramachandran N, Girard JM, Turnbull J, Minassian BA. The autosomal recessively inherited progressive myoclonus epilepsies and their genes. Epilepsia 2009;50(suppl 5): 29-36.
-
(2009)
Epilepsia
, vol.50
, Issue.SUPPL. 5
, pp. 29-36
-
-
Ramachandran, N.1
Girard, J.M.2
Turnbull, J.3
Minassian, B.A.4
-
28
-
-
84864080212
-
Novel mutations consolidate kctd7 as a progressive myoclonus epilepsy gene
-
Kousi M, Anttila V, Schulz A, et al. Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. J Med Genet 2012;49(6):391-399.
-
(2012)
J Med Genet
, vol.49
, Issue.6
, pp. 391-399
-
-
Kousi, M.1
Anttila, V.2
Schulz, A.3
-
29
-
-
0026598675
-
Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (may and white syndrome)
-
Vaamonde J, Muruzabal J, Tunon T, et al. Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome). J Neurol Neurosurg Psychiatry 1992;55(2):128-132.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, Issue.2
, pp. 128-132
-
-
Vaamonde, J.1
Muruzabal, J.2
Tunon, T.3
-
30
-
-
76549106531
-
Galloway-mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature
-
Pezzella M, Yeghiazaryan NS, Veggiotti P, et al. Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature. Seizure 2010;19(2):132-135.
-
(2010)
Seizure
, vol.19
, Issue.2
, pp. 132-135
-
-
Pezzella, M.1
Yeghiazaryan, N.S.2
Veggiotti, P.3
-
31
-
-
82955232423
-
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by scarb2 mutations
-
Rubboli G, Franceschetti S, Berkovic SF, et al. Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. Epilepsia 2011;52(12):2356-2363.
-
(2011)
Epilepsia
, vol.52
, Issue.12
, pp. 2356-2363
-
-
Rubboli, G.1
Franceschetti, S.2
Berkovic, S.F.3
-
32
-
-
0025900901
-
The hyperekplexias and their relationship to the normal startle reflex
-
Brown P, Rothwell JC, Thompson PD, et al. The hyperekplexias and their relationship to the normal startle reflex. Brain 1991; 114(pt 4):1903-1928.
-
(1991)
Brain
, vol.114
, Issue.PART 4
, pp. 1903-1928
-
-
Brown, P.1
Rothwell, J.C.2
Thompson, P.D.3
-
33
-
-
0036652637
-
Major and minor form of hereditary hyperekplexia
-
DOI 10.1002/mds.10168
-
Tijssen MA, Vergouwe MN, van Dijk JG, et al. Major and minor form of hereditary hyperekplexia. Mov Disord 2002;17(4): 826-830. (Pubitemid 41295034)
-
(2002)
Movement Disorders
, vol.17
, Issue.4
, pp. 826-830
-
-
Tijssen, M.A.J.1
Vergouwe, M.N.2
Van Dijk, J.G.3
Rees, M.4
Frants, R.R.5
Brown, P.6
-
34
-
-
84873526942
-
Novel missense mutations in the glycine receptor beta subunit gene (glrb) in startle disease
-
James VM, Bode A, Chung SK, et al. Novel missense mutations in the glycine receptor beta subunit gene (GLRB) in startle disease. Neurobiol Dis 2013;52:137-149.
-
(2013)
Neurobiol Dis
, vol.52
, pp. 137-149
-
-
James, V.M.1
Bode, A.2
Chung, S.K.3
-
35
-
-
84865234977
-
Mutations in the glyt2 gene (slc6a5) are a second major cause of startle disease
-
Carta E, Chung SK, James VM, et al. Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease. J Biol Chem 2012;287(34):28975- 28985.
-
(2012)
J Biol Chem
, vol.287
, Issue.34
, pp. 28975-28985
-
-
Carta, E.1
Chung, S.K.2
James, V.M.3
-
36
-
-
0035353729
-
Latah in Jakarta, Indonesia
-
DOI 10.1002/mds.1088
-
Tanner CM, Chamberland J. Latah in Jakarta, Indonesia. Mov Disord 2001;16(3): 526-529. (Pubitemid 36041160)
-
(2001)
Movement Disorders
, vol.16
, Issue.3
, pp. 526-529
-
-
Tanner, C.M.1
Chamberland, J.2
-
38
-
-
0035353756
-
The ''ragin' cajuns'' of louisiana
-
McFarling DA. The ''Ragin' Cajuns'' of Louisiana. Mov Disord 2001;16(3):531-532.
-
(2001)
Mov Disord
, vol.16
, Issue.3
, pp. 531-532
-
-
McFarling, D.A.1
-
39
-
-
0029919293
-
Abnormalities of the balance between inhibition and excitation in the motor cortex of patients with cortical myoclonus
-
DOI 10.1093/brain/119.1.309
-
Brown P, Ridding MC, Werhahn KJ, et al. Abnormalities of the balance between inhibition and excitation in the motor cortex of patients with cortical myoclonus. Brain 1996;119(pt 1):309-317. (Pubitemid 26077574)
-
(1996)
Brain
, vol.119
, Issue.1
, pp. 309-317
-
-
Brown, P.1
Ridding, M.C.2
Werhahn, K.J.3
Rothwell, J.C.4
Marsden, C.D.5
-
40
-
-
80052963170
-
Motor cortical plasticity is impaired in unverricht-lundborg disease
-
Danner N, Saisanen L, Maatta S, et al. Motor cortical plasticity is impaired in Unverricht-Lundborg disease. Mov Disord 2011;26(11):2095-2100.
-
(2011)
Mov Disord
, vol.26
, Issue.11
, pp. 2095-2100
-
-
Danner, N.1
Saisanen, L.2
Maatta, S.3
-
41
-
-
0027093628
-
Stimulus-sensitive myoclonus in akinetic-rigid syndromes
-
Chen R, Ashby P, Lang AE. Stimulus-sensitive myoclonus in akinetic-rigid syndromes. Brain 1992;115(pt 6):1875-1888. (Pubitemid 23054869)
-
(1992)
Brain
, vol.115
, Issue.6
, pp. 1875-1888
-
-
Chen, R.1
Ashby, P.2
Lang, A.E.3
-
42
-
-
84869239674
-
The bereitschaftspotential in jerky movement disorders
-
van der Salm SM, Tijssen MA, Koelman JH, van Rootselaar AF. The bereitschaftspotential in jerky movement disorders. J Neurol Neurosurg Psychiatry 2012;83(12):1162-1167.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, Issue.12
, pp. 1162-1167
-
-
Van Der Salm, S.M.1
Tijssen, M.A.2
Koelman, J.H.3
Van Rootselaar, A.F.4
-
43
-
-
68449102380
-
Psychogenic movement disorders
-
Gupta A, Lang AE. Psychogenic movement disorders. Curr Opin Neurol 2009;22(4):430-436.
-
(2009)
Curr Opin Neurol
, vol.22
, Issue.4
, pp. 430-436
-
-
Gupta, A.1
Lang, A.E.2
-
44
-
-
33645738757
-
A single-blind open-label trial of sodium oxybate for myoclonus and essential tremor
-
Frucht SJ, Houghton WC, Bordelon Y, et al. A single-blind, open-label trial of sodium oxybate for myoclonus and essential tremor. Neurology 2005;65(12):1967-1969.
-
(2005)
Neurology
, vol.65
, Issue.12
, pp. 1967-1969
-
-
Frucht, S.J.1
Houghton, W.C.2
Bordelon, Y.3
-
45
-
-
65549094570
-
A patient with intractable posthypoxic myoclonus (lance-adams syndrome) treated with sodium oxybate
-
Arpesella R, Dallocchio C, Arbasino C, et al. A patient with intractable posthypoxic myoclonus (Lance-Adams syndrome) treated with sodium oxybate. Anaesth Intensive Care 2009;37(2):314-318.
-
(2009)
Anaesth Intensive Care
, vol.37
, Issue.2
, pp. 314-318
-
-
Arpesella, R.1
Dallocchio, C.2
Arbasino, C.3
-
46
-
-
0033377858
-
Treatment of childhood myoclonus with botulinum toxin type A
-
Awaad Y, Tayem H, Elgamal A, Coyne MF. Treatment of childhood myoclonus with botulinum toxin type A. J Child Neurol 1999;14(12):781-786. (Pubitemid 30035502)
-
(1999)
Journal of Child Neurology
, vol.14
, Issue.12
, pp. 781-786
-
-
Awaad, Y.1
Tayem, H.2
Elgamal, A.3
Coyne, M.F.4
-
47
-
-
0034102396
-
Gamma-hydroxybutyric acid for alcohol-sensitive myoclonus with dystonia
-
Priori A, Bertolasi L, Pesenti A, et al. gamma-hydroxybutyric acid for alcohol-sensitive myoclonus with dystonia. Neurology 2000;54(8):1706.
-
(2000)
Neurology
, vol.54
, Issue.8
, pp. 1706
-
-
Priori, A.1
Bertolasi, L.2
Pesenti, A.3
-
48
-
-
78651312999
-
Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to (-sarcoglycan mutations: A pilot study
-
Azoulay-Zyss J, Roze E, Welter ML, et al. Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to (-sarcoglycan mutations: a pilot study. Arch Neurol 2011;68(1):94-98.
-
(2011)
Arch Neurol
, vol.68
, Issue.1
, pp. 94-98
-
-
Azoulay-Zyss, J.1
Roze, E.2
Welter, M.L.3
-
49
-
-
33644957867
-
Levetiracetam in patients with cortical myoclonus: A clinical and electrophysiological study
-
Striano P, Manganelli F, Boccella P, et al. Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study. Mov Disord 2005;20(12):1610-1614.
-
(2005)
Mov Disord
, vol.20
, Issue.12
, pp. 1610-1614
-
-
Striano, P.1
Manganelli, F.2
Boccella, P.3
-
50
-
-
84885618264
-
-
In: Pagon RA, Bird TD, Dolan CR, et al, eds. GeneReviews Seattle, WA: University of Washington. Posted June 3, Updated August 18, 2009
-
DiMauro S, Hirano M. MERRF. In: Pagon RA, Bird TD, Dolan CR, et al, eds. GeneReviews Seattle, WA: University of Washington. Posted June 3, 2003. Updated August 18, 2009.
-
(2003)
MERRF
-
-
DiMauro, S.1
Hirano, M.2
-
51
-
-
84555187327
-
Intrathecal baclofen for the treatment of spinal myoclonus: A case series
-
Chiodo AE, Saval A. Intrathecal baclofen for the treatment of spinal myoclonus: a case series. J Spinal Cord Med. 2012;35(1): 64-67.
-
(2012)
J Spinal Cord Med
, vol.35
, Issue.1
, pp. 64-67
-
-
Chiodo, A.E.1
Saval, A.2
-
52
-
-
79960458362
-
The use of intrathecal baclofen therapy for myoclonus in a patient with lance adams syndrome
-
Birthi P, Walters C, Ortiz Vargas O, Karandikar N. The use of intrathecal baclofen therapy for myoclonus in a patient with Lance Adams syndrome. PM R. 2011;3(7):671-673.
-
(2011)
PM R
, vol.3
, Issue.7
, pp. 671-673
-
-
Birthi, P.1
Walters, C.2
Ortiz Vargas, O.3
Karandikar, N.4
-
53
-
-
0029903551
-
Treatment of four siblings with progressive myoclonus epilepsy of the Unverricht-Lundborg type with N-acetylcysteine
-
Hurd RW, Wilder BJ, Helveston WR, Uthman BM. Treatment of four siblings with progressive myoclonus epilepsy of the Unverricht-Lundborg type with N-acetylcysteine. Neurol. 1996;47(5): 1264-1268. (Pubitemid 26374898)
-
(1996)
Neurology
, vol.47
, Issue.5
, pp. 1264-1268
-
-
Hurd, R.W.1
Wilder, B.J.2
Helveston, W.R.3
Uthman, B.M.4
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