-
1
-
-
0032898847
-
The clinical sarcoglycanopathies
-
ANGELINI C, FANIN M, FREDA M, DUGGAN DJ, SICILIANO G, HOFFMAN EP. (1999). The clinical sarcoglycanopathies. Neurology, 52:176-179.
-
(1999)
Neurology
, vol.52
, pp. 176-179
-
-
Angelini, C.1
Fanin, M.2
Freda, M.3
Duggan, D.J.4
Siciliano, G.5
Hoffman, E.P.6
-
2
-
-
0036790909
-
Myoclonus-dystonia syndrome: Epsilon-sarcoglycan mutations and phenotype
-
ASMUS F, ZIMPRICH A, TEZENAS DU MONTCEL S et al. (2002). Myoclonus-dystonia syndrome: Epsilon-sarcoglycan mutations and phenotype. Ann Neurol, 52: 489-492.
-
(2002)
Ann Neurol
, vol.52
, pp. 489-492
-
-
Asmus, F.1
Zimprich, A.2
Tezenas, D.U.3
Montcel, S.4
-
3
-
-
0037183501
-
Clinical and genetic heterogeneity in benign hereditary chorea
-
BREEDVELD GJ, PERCY AK, MACDONALD ME et al. (2002). Clinical and genetic heterogeneity in benign hereditary chorea. Neurology, 59: 579-584.
-
(2002)
Neurology
, vol.59
, pp. 579-584
-
-
Breedveld, G.J.1
Percy, A.K.2
Macdonald, M.E.3
-
4
-
-
0034108373
-
Exploration neurophysiologique des tremblements
-
CASSIM F, DERAMBURE P, DEFEBVRE L, BOURRIEZ JL, DESTÉE A, GUIEU JD. (2000). Exploration neurophysiologique des tremblements. Neurophysiol Clin, 30: 81-96.
-
(2000)
Neurophysiol Clin
, vol.30
, pp. 81-96
-
-
Cassim, F.1
Derambure, P.2
Defebvre, L.3
Bourriez, J.L.4
Destée, A.5
Guieu, J.D.6
-
5
-
-
0022658009
-
Nifedipine and myoclonic dystonia
-
DE MEDINA A, BIASINI O, RIVERA A, SAMPERA A. (1986). Nifedipine and myoclonic dystonia. Ann Intern Med, 104: 125.
-
(1986)
Ann Intern Med
, vol.104
, pp. 125
-
-
De Medina, A.1
Biasini, O.2
Rivera, A.3
Sampera, A.4
-
6
-
-
0033940919
-
Benign hereditary chorea of early onset maps to chromosome 14q
-
DE VRIES BBA, ARTS WFM, BREEDVELD GJ et al. (2000). Benign hereditary chorea of early onset maps to chromosome 14q. Am J Hum Genet, 66: 136-144.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 136-144
-
-
De Vries, B.B.A.1
Arts, W.F.M.2
Breedveld, G.J.3
-
7
-
-
0037841384
-
Neurophysiologie des syndromes parkinsoniens
-
DEFEBVRE L, CASSIM F. (2003). Neurophysiologie des syndromes parkinsoniens. Rev Neurol, 159: 3S62-3S74.
-
(2003)
Rev Neurol
, vol.159
-
-
Defebvre, L.1
Cassim, F.2
-
8
-
-
0037159102
-
Phenotypic features of myoclonus-dystonia in three kindreds
-
DOHENY DO, BRIN MF, MORRISON CE et al. (2002a). Phenotypic features of myoclonus-dystonia in three kindreds. Neurology, 59: 1187-1196.
-
(2002)
Neurology
, vol.59
, pp. 1187-1196
-
-
Doheny, D.O.1
Brin, M.F.2
Morrison, C.E.3
-
9
-
-
0037159182
-
Clinical findings of a myoclonus-dystonia family with two distinct mutations
-
DOHENY D, DANISI F, SMITH C et al. (2002b). Clinical findings of a myoclonus-dystonia family with two distinct mutations. Neurology, 59: 1244-1246.
-
(2002)
Neurology
, vol.59
, pp. 1244-1246
-
-
Doheny, D.1
Danisi, F.2
Smith, C.3
-
10
-
-
0343932572
-
D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus
-
DÜRR A, TASSIN J, VIDAILHET M et al. (2000). D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus. Ann Neurol, 48:127-128.
-
(2000)
Ann Neurol
, vol.48
, pp. 127-128
-
-
Dürr, A.1
Tassin, J.2
Vidailhet, M.3
-
12
-
-
0025740808
-
Hereditary essential myoclonus in a large Norwegian family
-
FAHN S, SJAASTAD O. (1991). Hereditary essential myoclonus in a large Norwegian family. Mov Disord, 6: 237-247.
-
(1991)
Mov Disord
, vol.6
, pp. 237-247
-
-
Fahn, S.1
Sjaastad, O.2
-
13
-
-
10744233866
-
Hereditary myoclonus-dystonia associated with epilepsy
-
FONCKE EMJ, KLEIN C, KOELMAN JHTM et al. (2003). Hereditary myoclonus-dystonia associated with epilepsy. Neurology, 60: 1988-1990.
-
(2003)
Neurology
, vol.60
, pp. 1988-1990
-
-
Foncke, E.M.J.1
Klein, C.2
Koelman, J.H.T.M.3
-
14
-
-
0037159249
-
Inherited myoclonus-dystonia: How many causative genes and clinical phenotypes?
-
FURUKAWA Y, RAJPUT AH. (2002). Inherited myoclonus-dystonia: how many causative genes and clinical phenotypes? Neurology, 59: 1130-1131.
-
(2002)
Neurology
, vol.59
, pp. 1130-1131
-
-
Furukawa, Y.1
Rajput, A.H.2
-
15
-
-
0031604087
-
Inherited myoclonus-dystonia syndrome
-
GASSER T. (1998). Inherited myoclonus-dystonia syndrome. Adv Neurol, 78: 325-334.
-
(1998)
Adv Neurol
, vol.78
, pp. 325-334
-
-
Gasser, T.1
-
16
-
-
0030062198
-
Linkage studies in alcohol-responsive myoclonic dystonia
-
GASSER T, BEREZNAI B, MULLER B, PRUSZAK-SEEL R, DAMRICH R, DEUSCHL G, OERTEL WH. (1996). Linkage studies in alcohol-responsive myoclonic dystonia. Mov Disord, 11: 363-370.
-
(1996)
Mov Disord
, vol.11
, pp. 363-370
-
-
Gasser, T.1
Bereznai, B.2
Muller, B.3
Pruszak-Seel, R.4
Damrich, R.5
Deuschl, G.6
Oertel, W.H.7
-
17
-
-
0037301222
-
The ε-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted
-
GRABOWSKI M, ZIMPRICH A, LORENZ-DEPIEREUX B et al. (2003). The ε-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted. Eur J Hum Genet, 11: 138-144.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 138-144
-
-
Grabowski, M.1
Zimprich, A.2
Lorenz-Depiereux, B.3
-
18
-
-
0035241272
-
Inherited myoclonus-dystDnia: Evidence supporting genetic heterogeneity
-
GRIMES DA, BULMAN D, GEORGE-HYSLOP PS, LANG AE. (2001). Inherited myoclonus-dystDnia: evidence supporting genetic heterogeneity. Mov Disord, 16: 106-110.
-
(2001)
Mov Disord
, vol.16
, pp. 106-110
-
-
Grimes, D.A.1
Bulman, D.2
George-Hyslop, P.S.3
Lang, A.E.4
-
19
-
-
0037159230
-
A novel locus for inherited myoclonus-dystonia on 18p11
-
GRIMES DA, HAN F, LANG AE, ST GEORGE-HYSSOP P, RACACHO L, BULMAN DE. (2002). A novel locus for inherited myoclonus-dystonia on 18p11. Neurology, 59: 1183-1186.
-
(2002)
Neurology
, vol.59
, pp. 1183-1186
-
-
Grimes, D.A.1
Han, F.2
Lang, A.E.3
George-Hyssop, P.S.T.4
Racacho, L.5
Bulman, D.E.6
-
20
-
-
0024474855
-
Myoclonic dystonia: Effective treatment by cervical cord stimulation. A case report
-
GROEN RJ, LAMBOOY N, TAVY DL. (1989). Myoclonic dystonia: effective treatment by cervical cord stimulation. A case report. Surg Neurol, 32: 72-74.
-
(1989)
Surg Neurol
, vol.32
, pp. 72-74
-
-
Groen, R.J.1
Lambooy, N.2
Tavy, D.L.3
-
21
-
-
0001470912
-
Hereditary non-progressive chorea of early onset
-
HAERER AF, CURRIER RD, JACKSON JF. (1966). Hereditary non-progressive chorea of early onset. Neurology, 16: 307.
-
(1966)
Neurology
, vol.16
, pp. 307
-
-
Haerer, A.F.1
Currier, R.D.2
Jackson, J.F.3
-
22
-
-
0021795735
-
Verapamil and myoclonic dystonia
-
HICKS CB, ABRAHAM K. (1985). Verapamil and myoclonic dystonia. Ann Intern Med, 103: 154.
-
(1985)
Ann Intern Med
, vol.103
, pp. 154
-
-
Hicks, C.B.1
Abraham, K.2
-
23
-
-
0037883231
-
A novel mutation in the Epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome
-
HJERMIND LE, WERDELIN LM, EIBERG H, KRAG-OLSEN B, DUPONT E, SORENSEN SA. (2003). A novel mutation in the Epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome. Neurology, 60: 1536-1539.
-
(2003)
Neurology
, vol.60
, pp. 1536-1539
-
-
Hjermind, L.E.1
Werdelin, L.M.2
Eiberg, H.3
Krag-Olsen, B.4
Dupont, E.5
Sorensen, S.A.6
-
24
-
-
0036311809
-
Dystonia: Clinical features, genetics, and treatment
-
KLEIN C, OZELIUS LJ. (2002). Dystonia: clinical features, genetics, and treatment. Curr Opin Neurol, 15: 491-497.
-
(2002)
Curr Opin Neurol
, vol.15
, pp. 491-497
-
-
Klein, C.1
Ozelius, L.J.2
-
25
-
-
4243978485
-
Association of a missense change in the D2 dopamine receptor in myoclonus dystonia
-
KLEIN C, BRIN MF, KRAMER P et al. (1999). Association of a missense change in the D2 dopamine receptor in myoclonus dystonia. Proc Natl Acad Sci USA, 96: 5173-5176.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 5173-5176
-
-
Klein, C.1
Brin, M.F.2
Kramer, P.3
-
26
-
-
0034010735
-
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia
-
KLEIN C, GURVICH N, SENA-ESTEVES M et al. (2000a). Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia. Ann Neurol, 47: 369-373.
-
(2000)
Ann Neurol
, vol.47
, pp. 369-373
-
-
Klein, C.1
Gurvich, N.2
Sena-Esteves, M.3
-
27
-
-
0033754411
-
A major locus for myoclonus-dystonia maps to chromosome 7q in eight families
-
KLEIN C, SCHILLING K, SAUNDERS-PULLMAN RJ et al. (2000b). A major locus for myoclonus-dystonia maps to chromosome 7q in eight families. Am J Hum Genet, 67: 1314-1319.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1314-1319
-
-
Klein, C.1
Schilling, K.2
Saunders-Pullman, R.J.3
-
28
-
-
0036826889
-
Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations
-
KLEIN C, LIU L, DOHENY D, KOCK N et al. (2002). Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations. Ann Neurol, 52: 675-679.
-
(2002)
Ann Neurol
, vol.52
, pp. 675-679
-
-
Klein, C.1
Liu, L.2
Doheny, D.3
Kock, N.4
-
29
-
-
0016137329
-
Familial essential myoclonus
-
KORTEN JJ, NOTERMANS SLH, FRENKEN CWGM, GABREELS FJM, JOOSTEN EMG. (1974). Familial essential myoclonus. Brain, 97: 131-138.
-
(1974)
Brain
, vol.97
, pp. 131-138
-
-
Korten, J.J.1
Notermans, S.L.H.2
Frenken, C.W.G.M.3
Gabreels, F.J.M.4
Joosten, E.M.G.5
-
30
-
-
0031762056
-
Dystonia after striatopallidal and thalamic stroke
-
KRYSTKOWIAK P, MARTINAT P, DEFEBVRE L, PRUVO JP, LEYS D, DESTÉE A. (1998). Dystonia after striatopallidal and thalamic stroke. J Neurol Neurosurg Psychiatry, 65: 703-708.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, pp. 703-708
-
-
Krystkowiak, P.1
Martinat, P.2
Defebvre, L.3
Pruvo, J.P.4
Leys, D.5
Destée, A.6
-
31
-
-
0023674738
-
Myoclonus and dystonia: A family study
-
KURLAN R, BEHR J, MEDVED L, SHOULSON I. (1988). Myoclonus and dystonia: a family study. Adv Neurol, 50: 385-389.
-
(1988)
Adv Neurol
, vol.50
, pp. 385-389
-
-
Kurlan, R.1
Behr, J.2
Medved, L.3
Shoulson, I.4
-
32
-
-
0025084837
-
Alcohol-responsive myoclonic dystonia in a large family: Dominant inheritance and phenotypic variation
-
KYLLERMAN M, FORSGREN L, SANNER G, HOLMGREN G, WAHLSTROM J, DRUGGE U. (1990). Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation. Mov Disord, 5: 270-279.
-
(1990)
Mov Disord
, vol.5
, pp. 270-279
-
-
Kyllerman, M.1
Forsgren, L.2
Sanner, G.3
Holmgren, G.4
Wahlstrom, J.5
Drugge, U.6
-
33
-
-
0029932039
-
Striatopallidal and thalamic dystonia. A magnetic resonance imaging anatomoclinical study
-
LEHÉRICY S, VIDAILHET M, DORMONT D et al. (1996). Striatopallidal and thalamic dystonia. A magnetic resonance imaging anatomoclinical study. Arch Neurol, 53:241-250.
-
(1996)
Arch Neurol
, vol.53
, pp. 241-250
-
-
Lehéricy, S.1
Vidailhet, M.2
Dormont, D.3
-
34
-
-
0035949736
-
Clinical characteristics and topography of lesions in movement disorders due to thalamic lesions
-
LEHERICY S, GRAND S, POLLAK P et al. (2001). Clinical characteristics and topography of lesions in movement disorders due to thalamic lesions. Neurology, 57: 1055-1066.
-
(2001)
Neurology
, vol.57
, pp. 1055-1066
-
-
Lehericy, S.1
Grand, S.2
Pollak, P.3
-
35
-
-
18044403431
-
Novel mutation in the TorlA (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism
-
LEUNG JC, KLEIN C, FRIEDMAN J et al. (2001). Novel mutation in the TorlA (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism. Neurogenetics, 3: 133-143.
-
(2001)
Neurogenetics
, vol.3
, pp. 133-143
-
-
Leung, J.C.1
Klein, C.2
Friedman, J.3
-
36
-
-
0037159199
-
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome
-
LEUZZI V, CARDUCCI C, CARDUCCI C, CARDONA F, ARTIOLA C, ANTONOZZI I. (2002). Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome. Neurology, 59: 1241-1243.
-
(2002)
Neurology
, vol.59
, pp. 1241-1243
-
-
Leuzzi, V.1
Carducci, C.2
Carducci, C.3
Cardona, F.4
Artiola, C.5
Antonozzi, I.6
-
37
-
-
0000209102
-
Familial myoclonus occurring in three successive generations
-
LINDENMULDER FG. (1933). Familial myoclonus occurring in three successive generations. J Nerv Ment Dis, 77: 489-491.
-
(1933)
J Nerv Ment Dis
, vol.77
, pp. 489-491
-
-
Lindenmulder, F.G.1
-
38
-
-
0036523784
-
Involvement of the medial pallidum in focal myoclonic dystonia: A clinical and neurophysiological case study
-
LIU X, GRIFFIN IC, PARKIN SG et al. (2002). Involvement of the medial pallidum in focal myoclonic dystonia: A clinical and neurophysiological case study. Mov Disord, 17: 346-353.
-
(2002)
Mov Disord
, vol.17
, pp. 346-353
-
-
Liu, X.1
Griffin, I.C.2
Parkin, S.G.3
-
39
-
-
0038746977
-
Focal myoclonus-dystonia of the leg secondary to a lesion of the posterolateral putamen: Clinical and neurophysiological features
-
MAHANT N, CORDATO DJ, FUNG VS. (2003). Focal myoclonus-dystonia of the leg secondary to a lesion of the posterolateral putamen: Clinical and neurophysiological features. Mov Disord, 18: 452-455.
-
(2003)
Mov Disord
, vol.18
, pp. 452-455
-
-
Mahant, N.1
Cordato, D.J.2
Fung, V.S.3
-
40
-
-
0014127906
-
Hereditary essential myoclonus
-
MAHLOUDJI M, PIKIELNY RT. (1967). Hereditary essential myoclonus. Brain, 90: 669-674.
-
(1967)
Brain
, vol.90
, pp. 669-674
-
-
Mahloudji, M.1
Pikielny, R.T.2
-
41
-
-
10744230382
-
Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation
-
MARECHAL L, RAUX G, DUMANCHIN C et al. (2003). Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation. Am J Med Genet, 119B: 114-117.
-
(2003)
Am J Med Genet
, vol.119 B
, pp. 114-117
-
-
Marechal, L.1
Raux, G.2
Dumanchin, C.3
-
42
-
-
0036916437
-
Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia
-
MULLER B, HEDRICH K, KOCK N et al. (2002). Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia. Am J Hum Genet, 71: 1303-1311.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1303-1311
-
-
Muller, B.1
Hedrich, K.2
Kock, N.3
-
43
-
-
0036212214
-
The genetics of primary dystonias and related disorders
-
NEMETH AH. (2002). The genetics of primary dystonias and related disorders. Brain, 125: 695-721.
-
(2002)
Brain
, vol.125
, pp. 695-721
-
-
Nemeth, A.H.1
-
44
-
-
0032705097
-
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31
-
NYGAARD TG, RAYMOND D, CHEN C et al. (1999). Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Ann Neurol, 46:794-798.
-
(1999)
Ann Neurol
, vol.46
, pp. 794-798
-
-
Nygaard, T.G.1
Raymond, D.2
Chen, C.3
-
45
-
-
0020519139
-
Myoclonic dystonia
-
OBESO JA, ROTHWELL JC, LANG AE, MARSDEN CD. (1983). Myoclonic dystonia. Neurology, 33: 825-830.
-
(1983)
Neurology
, vol.33
, pp. 825-830
-
-
Obeso, J.A.1
Rothwell, J.C.2
Lang, A.E.3
Marsden, C.D.4
-
46
-
-
0034102396
-
Gamma-hydroxybutyric acid for alcohol-sensitive myoclonus with dystonia
-
PRIORI A, BERTOLASI L, PESENTI A, CAPPELLARI A, BARBIERI S. (2000). Gamma-hydroxybutyric acid for alcohol-sensitive myoclonus with dystonia. Neurology, 54: 1706.
-
(2000)
Neurology
, vol.54
, pp. 1706
-
-
Priori, A.1
Bertolasi, L.2
Pesenti, A.3
Cappellari, A.4
Barbieri, S.5
-
47
-
-
0029882099
-
Essential myoclonus and myoclonic dystonia
-
QUINN NP. (1996). Essential myoclonus and myoclonic dystonia. Mov Disord, 11: 119-124.
-
(1996)
Mov Disord
, vol.11
, pp. 119-124
-
-
Quinn, N.P.1
-
48
-
-
0001071534
-
Dominantly inherited myoclonic dystonia with dramatic response to alcohol
-
QUINN NP, MARSDEN CD. (1984). Dominantly inherited myoclonic dystonia with dramatic response to alcohol [abstract]. Neurology, 34:236.
-
(1984)
Neurology
, vol.34
, pp. 236
-
-
Quinn, N.P.1
Marsden, C.D.2
-
49
-
-
0023763764
-
Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: An area of confusion
-
QUINN NP, ROTHWELL JC, THOMPSON PD, MARSDEN CD. (1988). Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion. Adv Neurol, 50: 391-401.
-
(1988)
Adv Neurol
, vol.50
, pp. 391-401
-
-
Quinn, N.P.1
Rothwell, J.C.2
Thompson, P.D.3
Marsden, C.D.4
-
51
-
-
0037154246
-
Myoclonus dystonia: Possible association with obsessive-compulsive disorder and alcohol dependence
-
SAUNDERS-PULLMAN R, SHRIBERG J et al. (2002b). Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence. Neurology, 58: 242-245.
-
(2002)
Neurology
, vol.58
, pp. 242-245
-
-
Saunders-Pullman, R.1
Shriberg, J.2
-
52
-
-
0034073531
-
Benign hereditary chorea - Entity or syndrome?
-
SCHRAG A, QUINN NP, BHATIA KP, MARSDEN CD. (2000). Benign hereditary chorea - entity or syndrome? Mov Disord, 15: 280-288.
-
(2000)
Mov Disord
, vol.15
, pp. 280-288
-
-
Schrag, A.1
Quinn, N.P.2
Bhatia, K.P.3
Marsden, C.D.4
-
53
-
-
0028153437
-
The myoclonus in corticobasal degeneration. Evidence for two forms of cortical reflex myoclonus
-
THOMPSON PD, DAY BL, ROTHWELL JC, BROWN P, BRITTON TC, MARSOLEN CD. (1994). The myoclonus in corticobasal degeneration. Evidence for two forms of cortical reflex myoclonus Brain, 117: 1197-1207.
-
(1994)
Brain
, vol.117
, pp. 1197-1207
-
-
Thompson, P.D.1
Day, B.L.2
Rothwell, J.C.3
Brown, P.4
Britton, T.C.5
Marsolen, C.D.6
-
54
-
-
0035412886
-
Neurostimulation of the ventral intermediate thalamic nucleus in inherited myoclonus-dystonia syndrome
-
TROTTENBERG T, MEISSNER W, KABUS C et al. (2001). Neurostimulation of the ventral intermediate thalamic nucleus in inherited myoclonus-dystonia syndrome. Mov Disord, 16: 769-771.
-
(2001)
Mov Disord
, vol.16
, pp. 769-771
-
-
Trottenberg, T.1
Meissner, W.2
Kabus, C.3
-
55
-
-
0035297141
-
Dystonia in corticobasal degeneration
-
VANEK Z, JANKOVIC J. (2001). Dystonia in corticobasal degeneration. Mov Disord, 16: 252-257.
-
(2001)
Mov Disord
, vol.16
, pp. 252-257
-
-
Vanek, Z.1
Jankovic, J.2
-
56
-
-
0035826884
-
A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q
-
VIDAILHET M, TASSIN J, DURIF F et al. (2001). A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q. Neurology, 56: 1213-1216.
-
(2001)
Neurology
, vol.56
, pp. 1213-1216
-
-
Vidailhet, M.1
Tassin, J.2
Durif, F.3
-
57
-
-
17944378309
-
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome
-
ZIMPRICH A, GRABOWSKI M, ASMUS F et al. (2001). Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet, 29: 66-69.
-
(2001)
Nat Genet
, vol.29
, pp. 66-69
-
-
Zimprich, A.1
Grabowski, M.2
Asmus, F.3
|