-
1
-
-
79954880590
-
Sporadic and familial hemiplegic migraine: Pathophysiological mechanisms, clinical characteristics, diagnosis, and management
-
Russell MB, Ducros A. Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management. Lancet Neurol 2011; 10:457-470.
-
(2011)
Lancet Neurol
, vol.10
, pp. 457-470
-
-
Russell, M.B.1
Ducros, A.2
-
2
-
-
82255186531
-
Exome sequencing identifies truncating mutations in prrt2 that cause paroxysmal kinesigenic dyskinesia
-
Chen WJ, Lin Y, Xiong ZQ, et al. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nat Genet 2011;43:1252-1255.
-
(2011)
Nat Genet
, vol.43
, pp. 1252-1255
-
-
Chen, W.J.1
Lin, Y.2
Xiong, Z.Q.3
-
3
-
-
84855827661
-
Prrt2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
-
Heron SE, Grinton BE, Kivity S, et al. PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome. Am J Hum Genet 2012;90:152-160.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 152-160
-
-
Heron, S.E.1
Grinton, B.E.2
Kivity, S.3
-
4
-
-
84862912899
-
Mutations in prrt2 result in paroxysmal dyskinesias with marked variability in clinical expression
-
Liu Q, Qi Z, Wan XH, et al. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression. J Med Genet 2012;49:79-82.
-
(2012)
J Med Genet
, vol.49
, pp. 79-82
-
-
Liu, Q.1
Qi, Z.2
Wan, X.H.3
-
5
-
-
1442265540
-
The international classification of headache disorders 2nd edition
-
The International Classification of Headache Disorders: 2nd edition. Cephalalgia 2004;24(suppl 1):9-160.
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 9-160
-
-
-
6
-
-
77957280532
-
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
-
Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. Neurology 2010;75:967-972.
-
(2010)
Neurology
, vol.75
, pp. 967-972
-
-
Riant, F.1
Ducros, A.2
Ploton, C.3
Barbance, C.4
Depienne, C.5
Tournier-Lasserve, E.6
-
7
-
-
39749203582
-
Epilepsy as part of the phenotype associated with atp1a2 mutations
-
Deprez L, Weckhuysen S, Peeters K, et al. Epilepsy as part of the phenotype associated with ATP1A2 mutations. Epilepsia 2008;49:500-508.
-
(2008)
Epilepsia
, vol.49
, pp. 500-508
-
-
Deprez, L.1
Weckhuysen, S.2
Peeters, K.3
-
8
-
-
84856144700
-
Mutations in the gene prrt2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions
-
Lee HY, Huang Y, Bruneau N, et al. Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. Cell Rep 2012;1:2-12.
-
(2012)
Cell Rep
, vol.1
, pp. 2-12
-
-
Lee, H.Y.1
Huang, Y.2
Bruneau, N.3
-
9
-
-
25144498379
-
A human proteinprotein interaction network: A resource for annotating the proteome
-
Stelzl U, Worm U, Lalowski M, et al. A human proteinprotein interaction network: a resource for annotating the proteome. Cell 2005;122:957-968.
-
(2005)
Cell
, vol.122
, pp. 957-968
-
-
Stelzl, U.1
Worm, U.2
Lalowski, M.3
-
10
-
-
77956466889
-
Cav2.1 (p/q channel) interaction with synaptic proteins is essential for depolarization-evoked release
-
Cohen-Kutner M, Nachmanni D, Atlas D. CaV2.1 (P/Q channel) interaction with synaptic proteins is essential for depolarization-evoked release. Channels 2010;4:266-277.
-
(2010)
Channels
, vol.4
, pp. 266-277
-
-
Cohen-Kutner, M.1
Nachmanni, D.2
Atlas, D.3
-
11
-
-
16244412642
-
Masters or slaves? Vesicle release machinery and the regulation of presynaptic calcium channels
-
Jarvis SE, Zamponi GW. Masters or slaves? Vesicle release machinery and the regulation of presynaptic calcium channels. Cell Calcium 2005;37:483-488.
-
(2005)
Cell Calcium
, vol.37
, pp. 483-488
-
-
Jarvis, S.E.1
Zamponi, G.W.2
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