Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy (English)
- New search for: Stogmann, E.
- New search for: Zimprich, A.
- New search for: Zimprich, F.
- New search for: Stogmann, E.
- New search for: Zimprich, A.
- New search for: Zimprich, F.
In:
BRAIN
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136
, 10
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e254-e254
;
2013
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ISSN:
- Article (Journal) / Print
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Title:Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy
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Contributors:
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Published in:BRAIN ; 136, 10 ; e254-e254
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Publisher:
- New search for: Oxford University Press
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Publication date:2013-01-01
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Size:e254-e254
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616.8 -
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© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 136, Issue 10
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 2925
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EditorialCompston, A. et al. | 2013
- 2928
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From The ArchivesCompston, A. et al. | 2013
- 2933
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Defining and treating leucine-rich glioma inactivated 1 antibody associated autoimmunityZandi, M. S. et al. | 2013
- 2935
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Off to never-never land: losing consciousness to gain thoughtCruse, D. et al. | 2013
- 2937
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Beyond taxol: microtubule-based treatment of disease and injury of the nervous systemBaas, P. W. / Ahmad, F. J. et al. | 2013
- 2952
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White matter structural connectivity underlying semantic processing: evidence from brain damaged patientsHan, Z. / Ma, Y. / Gong, G. / He, Y. / Caramazza, A. / Bi, Y. et al. | 2013
- 2966
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Impairment only on the fluency subtest of the Frontal Assessment Battery after prefrontal lesionsChapados, C. / Petrides, M. et al. | 2013
- 2979
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Anterior temporal lobe degeneration produces widespread network-driven dysfunctionGuo, C. C. / Gorno-Tempini, M. L. / Gesierich, B. / Henry, M. / Trujillo, A. / Shany-Ur, T. / Jovicich, J. / Robinson, S. D. / Kramer, J. H. / Rankin, K. P. et al. | 2013
- 2992
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The orbitofrontal cortex is involved in emotional enhancement of memory: evidence from the dementiasKumfor, F. / Irish, M. / Hodges, J. R. / Piguet, O. et al. | 2013
- 3004
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Alterations in a4b2 nicotinic receptors in cognitive decline in Alzheimer's aetiopathologyOkada, H. / Ouchi, Y. / Ogawa, M. / Futatsubashi, M. / Saito, Y. / Yoshikawa, E. / Terada, T. / Oboshi, Y. / Tsukada, H. / Ueki, T. et al. | 2013
- 3018
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DNA methylation map of mouse and human brain identifies target genes in Alzheimer's diseaseSanchez-Mut, J. V. / Aso, E. / Panayotis, N. / Lott, I. / Dierssen, M. / Rabano, A. / Urdinguio, R. G. / Fernandez, A. F. / Astudillo, A. / Martin-Subero, J. I. et al. | 2013
- 3028
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Correlation of dopaminergic terminal dysfunction and microstructural abnormalities of the basal ganglia and the olfactory tract in Parkinson's diseaseScherfler, C. / Esterhammer, R. / Nocker, M. / Mahlknecht, P. / Stockner, H. / Warwitz, B. / Spielberger, S. / Pinter, B. / Donnemiller, E. / Decristoforo, C. et al. | 2013
- 3038
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Ursocholanic acid rescues mitochondrial function in common forms of familial Parkinson's diseaseMortiboys, H. / Aasly, J. / Bandmann, O. et al. | 2013
- 3051
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Purkinje cell axonal anatomy: quantifying morphometric changes in essential tremor versus control brainsBabij, R. / Lee, M. / Cortes, E. / Vonsattel, J. P. / Faust, P. L. / Louis, E. D. et al. | 2013
- 3062
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Phase dependent modulation of tremor amplitude in essential tremor through thalamic stimulationCagnan, H. / Brittain, J. S. / Little, S. / Foltynie, T. / Limousin, P. / Zrinzo, L. / Hariz, M. / Joint, C. / Fitzgerald, J. / Green, A. L. et al. | 2013
- 3076
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Can we still dream when the mind is blank? Sleep and dream mentations in auto-activation deficitLeu-Semenescu, S. / Uguccioni, G. / Golmard, J. L. / Czernecki, V. / Yelnik, J. / Dubois, B. / Forgeot d'Arc, B. / Grabli, D. / Levy, R. / Arnulf, I. et al. | 2013
- 3085
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Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delayThomas, R. H. / Chung, S. K. / Wood, S. E. / Cushion, T. D. / Drew, C. J. / Hammond, C. L. / Vanbellinghen, J. F. / Mullins, J. G. / Rees, M. I. et al. | 2013
- 3096
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ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesWebb, E. A. / AlMutair, A. / Kelberman, D. / Bacchelli, C. / Chanudet, E. / Lescai, F. / Andoniadou, C. L. / Banyan, A. / Alsawaid, A. / Alrifai, M. T. et al. | 2013
- 3106
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Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a modelNemeth, A. H. / Kwasniewska, A. C. / Lise, S. / Parolin Schnekenberg, R. / Becker, E. B. / Bera, K. D. / Shanks, M. E. / Gregory, L. / Buck, D. / Zameel Cader, M. et al. | 2013
- 3119
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Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Vantaggiato, C. / Crimella, C. / Airoldi, G. / Polishchuk, R. / Bonato, S. / Brighina, E. / Scarlato, M. / Musumeci, O. / Toscano, A. / Martinuzzi, A. et al. | 2013
- 3140
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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1AKasperaviciute, D. / Catarino, C. B. / Matarin, M. / Leu, C. / Novy, J. / Tostevin, A. / Leal, B. / Hessel, E. V. / Hallmann, K. / Hildebrand, M. S. et al. | 2013
- 3151
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Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotypeIrani, S. R. / Stagg, C. J. / Schott, J. M. / Rosenthal, C. R. / Schneider, S. A. / Pettingill, P. / Pettingill, R. / Waters, P. / Thomas, A. / Voets, N. L. et al. | 2013
- 3163
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Asymmetry of planum temporale constrains interhemispheric language plasticity in children with focal epilepsyPahs, G. / Rankin, P. / Helen Cross, J. / Croft, L. / Northam, G. B. / Liegeois, F. / Greenway, S. / Harrison, S. / Vargha-Khadem, F. / Baldeweg, T. et al. | 2013
- 3176
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The value of magnetoencephalography for seizure-onset zone localization in magnetic resonance imaging-negative partial epilepsyJung, J. / Bouet, R. / Delpuech, C. / Ryvlin, P. / Isnard, J. / Guenot, M. / Bertrand, O. / Hammers, A. / Mauguiere, F. et al. | 2013
- 3187
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The lifelong course of chronic epilepsy: the Chalfont experienceNovy, J. / Belluzzo, M. / Caboclo, L. O. / Catarino, C. B. / Yogarajah, M. / Martinian, L. / Peacock, J. L. / Bell, G. S. / Koepp, M. J. / Thom, M. et al. | 2013
- 3200
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The reel of consciousnessCornwell, J. et al. | 2013
- e250
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Ocular paradoxical movement and severity of Parkinson's diseaseMatsumoto, H. / Terao, Y. / Ugawa, Y. et al. | 2013
- e251
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The cuneiform nucleus may be involved in the regulation of skeletal muscle tone by motor pathway: a virally mediated trans-synaptic tracing study in surgically sympathectomized miceXiang, H. B. / Zhu, W. Z. / Guan, X. H. / Ye, D. W. et al. | 2013
- e252
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Reply: The cuneiform nucleus may be involved in the regulation of skeletal muscle tone by motor pathway: a virally mediated trans-synaptic tracing study in surgically sympathectomized miceAlam, M. / Schwabe, K. / Krauss, J. K. et al. | 2013
- e253
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Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsyStriano, P. / Zara, F. / Striano, S. / Minetti, C. et al. | 2013
- e254
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Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsyStogmann, E. / Zimprich, A. / Zimprich, F. et al. | 2013
- e255
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Erratum| 2013