-
1
-
-
0020064620
-
Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
-
Naito H, Oyanagi S. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology 1982;32:798-807.
-
(1982)
Neurology
, vol.32
, pp. 798-807
-
-
Naito, H.1
Oyanagi, S.2
-
3
-
-
0033598346
-
Familial dementia caused by polymerization of mutant neuroserpin
-
Davis RL, Shrimpton AE, Holohan PD, et al. Familial dementia caused by polymerization of mutant neuroserpin. Nature 1999;401:376-379.
-
(1999)
Nature
, vol.401
, pp. 376-379
-
-
Davis, R.L.1
Shrimpton, A.E.2
Holohan, P.D.3
-
4
-
-
0032881391
-
Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24
-
Plaster NM, Uyama E, Uchino M, et al. Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24. Neurology 1999;53:1180-1183.
-
(1999)
Neurology
, vol.53
, pp. 1180-1183
-
-
Plaster, N.M.1
Uyama, E.2
Uchino, M.3
-
5
-
-
0033365214
-
Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1
-
Mikami M, Yasuda T, Terao A, et al. Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am J Hum Genet 1999;65:745-751.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 745-751
-
-
Mikami, M.1
Yasuda, T.2
Terao, A.3
-
6
-
-
0037177082
-
Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)
-
Labauge P, Amer LO, Simonetta-Moreau M, et al. Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME). Neurology 2002;58: 941-944.
-
(2002)
Neurology
, vol.58
, pp. 941-944
-
-
Labauge, P.1
Amer, L.O.2
Simonetta-Moreau, M.3
-
7
-
-
0035208272
-
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2
-
Guerrini R, Bonanni P, Patrignani A, et al. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2. Brain 2001 124(Pt 12):2459-2475.
-
(2001)
Brain
, vol.124
, Issue.PART 12
, pp. 2459-2475
-
-
Guerrini, R.1
Bonanni, P.2
Patrignani, A.3
-
8
-
-
0037461301
-
Benign adult familial myoclonic epilepsy: Genetic heterogeneity and allelism with ADCME
-
de Falco FA, Striano P, De Falco A, et al. Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. Neurology 2003;60:1381-1385.
-
(2003)
Neurology
, vol.60
, pp. 1381-1385
-
-
de Falco, F.A.1
Striano, P.2
De Falco, A.3
-
9
-
-
0842268282
-
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2
-
Striano P, Chifari R, Striano S, et al. A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. Epilepsia 2004;45: 190-192.
-
(2004)
Epilepsia
, vol.45
, pp. 190-192
-
-
Striano, P.1
Chifari, R.2
Striano, S.3
-
10
-
-
22844444789
-
Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features
-
van Rootselaar AF, van Schaik IN, van den Maagdenberg AM, Koelman JH, Callenbach PM, Tijssen MA. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov Disord 2005;20:665-673.
-
(2005)
Mov Disord
, vol.20
, pp. 665-673
-
-
van Rootselaar, A.F.1
van Schaik, I.N.2
van den Maagdenberg, A.M.3
Koelman, J.H.4
Callenbach, P.M.5
Tijssen, M.A.6
-
11
-
-
34247523427
-
Autosomal dominant PME associated with cortical tremor and cerebellar pathology
-
Abstract
-
Carr JA, van der Walt PE, Thomas S, Brink P, Corfield V. Autosomal dominant PME associated with cortical tremor and cerebellar pathology. Neurology 2000;(suppl 3):A51. Abstract.
-
(2000)
Neurology
, Issue.SUPPL. 3
-
-
Carr, J.A.1
van der Walt, P.E.2
Thomas, S.3
Brink, P.4
Corfield, V.5
-
12
-
-
26844555959
-
-
Mayo Clinic Electromyography and Clinical Neurophysiology Laboratory, Rochester, MN
-
Mayo Clinic Electromyography and Clinical Neurophysiology Laboratory. A manual of techniques in motor and sensory clinical neurophysiology. Rochester, MN: 1994; 1-45.
-
(1994)
A manual of techniques in motor and sensory clinical neurophysiology
, pp. 1-45
-
-
-
13
-
-
0027469189
-
Cortical hyperexcitability in progressive myoclonus epilepsy: A study with transcranial magnetic stimulation
-
Reutens DC, Puce A, Berkovic SF. Cortical hyperexcitability in progressive myoclonus epilepsy: a study with transcranial magnetic stimulation. Neurology 1993;43:186-192.
-
(1993)
Neurology
, vol.43
, pp. 186-192
-
-
Reutens, D.C.1
Puce, A.2
Berkovic, S.F.3
-
14
-
-
0029994692
-
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q
-
Virtaneva K, Miao J, Traskelin AL, et al. Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. Am J Hum Genet 1996;58:1247-1253.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1247-1253
-
-
Virtaneva, K.1
Miao, J.2
Traskelin, A.L.3
-
15
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide R, Ikeuchi T, Onodera O, et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet 1994;6:9-13.
-
(1994)
Nat Genet
, vol.6
, pp. 9-13
-
-
Koide, R.1
Ikeuchi, T.2
Onodera, O.3
-
16
-
-
0020561801
-
Baltic myoclonus epilepsy: Hereditary disorder of childhood made worse by phenytoin
-
Eldridge R, Iivanainen M, Stern R, Koerber T, Wilder BJ. "Baltic" myoclonus epilepsy: hereditary disorder of childhood made worse by phenytoin. Lancet 1983;2: 838-842.
-
(1983)
Lancet
, vol.2
, pp. 838-842
-
-
Eldridge, R.1
Iivanainen, M.2
Stern, R.3
Koerber, T.4
Wilder, B.J.5
-
17
-
-
0025043869
-
Cortical tremor: A variant of cortical reflex myoclonus
-
Ikeda A, Kakigi R, Funai N, Neshige R, Kuroda Y, Shibasaki H. Cortical tremor: a variant of cortical reflex myoclonus. Neurology 1990;40:1561-1565.
-
(1990)
Neurology
, vol.40
, pp. 1561-1565
-
-
Ikeda, A.1
Kakigi, R.2
Funai, N.3
Neshige, R.4
Kuroda, Y.5
Shibasaki, H.6
-
18
-
-
0036301962
-
A Dutch family with 'familial cortical tremor with epilepsy'. Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1
-
van Rootselaar F, Callenbach PM, Hottenga JJ, et al. A Dutch family with 'familial cortical tremor with epilepsy'. Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1. J Neurol 2002;249:829-834.
-
(2002)
J Neurol
, vol.249
, pp. 829-834
-
-
van Rootselaar, F.1
Callenbach, P.M.2
Hottenga, J.J.3
-
19
-
-
1542360720
-
Familial cortical tremor with epilepsy and cerebellar pathological findings
-
van Rootselaar AF, Aronica E, Jansen Steur EN, Rozemuller-Kwakkel JM, de Vos RA, Tijssen MA. Familial cortical tremor with epilepsy and cerebellar pathological findings. Mov Disord 2004;19:213-217.
-
(2004)
Mov Disord
, vol.19
, pp. 213-217
-
-
van Rootselaar, A.F.1
Aronica, E.2
Jansen Steur, E.N.3
Rozemuller-Kwakkel, J.M.4
de Vos, R.A.5
Tijssen, M.A.6
-
20
-
-
0021883175
-
Primary generalised epileptic myoclonus: A frequent manifestation of minipolymyoclonus of central origin
-
Wilkins DE, Hallett M, Erba G. Primary generalised epileptic myoclonus: a frequent manifestation of minipolymyoclonus of central origin. J Neurol Neurosurg Psychiatry 1985;48:506-516.
-
(1985)
J Neurol Neurosurg Psychiatry
, vol.48
, pp. 506-516
-
-
Wilkins, D.E.1
Hallett, M.2
Erba, G.3
-
21
-
-
0037866865
-
Exaggerated 16-20 Hz motor cortical oscillation in patients with positive or negative myoclonus
-
Ugawa Y, Hanajima R, Terao Y, Kanazawa I. Exaggerated 16-20 Hz motor cortical oscillation in patients with positive or negative myoclonus. Clin Neurophysiol 2003; 114:1278-1284.
-
(2003)
Clin Neurophysiol
, vol.114
, pp. 1278-1284
-
-
Ugawa, Y.1
Hanajima, R.2
Terao, Y.3
Kanazawa, I.4
|