-
1
-
-
30544454938
-
The global burden of migraine: Measuring disability in headache disorders with WHO's Classification of Functioning, Disability and Health (ICF)
-
Leonardi M, Steiner TJ, Scher AT, Lipton RB. The global burden of migraine: Measuring disability in headache disorders with WHO's Classification of Functioning, Disability and Health (ICF). J Headache Pain. 2005 6 : 429 440.
-
(2005)
J Headache Pain.
, vol.6
, pp. 429-440
-
-
Leonardi, M.1
Steiner, T.J.2
Scher, A.T.3
Lipton, R.B.4
-
2
-
-
0142106002
-
Migraine: Diagnosis and management
-
Goadsby PJ. Migraine: Diagnosis and management. Intern Med J. 2003 33 : 436 442.
-
(2003)
Intern Med J.
, vol.33
, pp. 436-442
-
-
Goadsby, P.J.1
-
3
-
-
1442265540
-
The International Classification of Headache Disorders
-
Headache Classification Subcommittee of the International Headache Society.
-
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders. Cephalalgia. 2004 24 (suppl 1).
-
(2004)
Cephalalgia.
, vol.24
, Issue.1
-
-
-
5
-
-
0037302967
-
The neuronal versus vascular hypothesis of migraine and cortical spreading depression
-
Parsons AA, Strijbos PJ. The neuronal versus vascular hypothesis of migraine and cortical spreading depression. Curr Opin Pharmacol. 2003 3 : 73 77.
-
(2003)
Curr Opin Pharmacol.
, vol.3
, pp. 73-77
-
-
Parsons, A.A.1
Strijbos, P.J.2
-
6
-
-
0019435433
-
Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine
-
Olesen J, Larsen B, Lauritzen M. Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine. Ann Neurol. 1981 9 : 344 352.
-
(1981)
Ann Neurol.
, vol.9
, pp. 344-352
-
-
Olesen, J.1
Larsen, B.2
Lauritzen, M.3
-
7
-
-
17244367125
-
Brain hyperexcitability: The basis for antiepileptic drugs in migraine prevention
-
Welch KM. Brain hyperexcitability: The basis for antiepileptic drugs in migraine prevention. Headache. 2005 45 (suppl 1 S25 S32.
-
(2005)
Headache.
, vol.45
, Issue.1
-
-
Welch, K.M.1
-
8
-
-
21044434650
-
Migraine genetics: An update
-
Haan J, Kors EE, Vanmolkot KR, van den Maagdenberg AM, Frants RR, Ferrari MD. Migraine genetics: An update. Curr Pain Headache Rep. 2005 9 : 213 220.
-
(2005)
Curr Pain Headache Rep.
, vol.9
, pp. 213-220
-
-
Haan, J.1
Kors, E.E.2
Vanmolkot, K.R.3
Van Den Maagdenberg, A.M.4
Frants, R.R.5
Ferrari, M.D.6
-
9
-
-
1242343820
-
Consecutive transcranial magnetic stimulation: Phosphene thresholds in migraineurs and controls
-
Young WB, Oshinsky ML, Shechter AL, Gebeline-Myers C, Bradley KC, Wassermann EM. Consecutive transcranial magnetic stimulation: Phosphene thresholds in migraineurs and controls. Headache. 2004 44 : 131 135.
-
(2004)
Headache.
, vol.44
, pp. 131-135
-
-
Young, W.B.1
Oshinsky, M.L.2
Shechter, A.L.3
Gebeline-Myers, C.4
Bradley, K.C.5
Wassermann, E.M.6
-
10
-
-
0014931112
-
Electrophysiological concomitants of spreading depression in caudate and thalamic nuclei of the cat
-
Trachtenberg MC, Hull CD, Buchwald NA. Electrophysiological concomitants of spreading depression in caudate and thalamic nuclei of the cat. Brain Res. 1970 20 : 219 231.
-
(1970)
Brain Res.
, vol.20
, pp. 219-231
-
-
Trachtenberg, M.C.1
Hull, C.D.2
Buchwald, N.A.3
-
11
-
-
0025601914
-
Re-entry waves of Leao's spreading depression between neocortex and caudate nucleus
-
Vinogradova LV, Koroleva VI, Bures J. Re-entry waves of Leao's spreading depression between neocortex and caudate nucleus. Brain Res. 1991 538 : 161 164.
-
(1991)
Brain Res.
, vol.538
, pp. 161-164
-
-
Vinogradova, L.V.1
Koroleva, V.I.2
Bures, J.3
-
12
-
-
34250634965
-
Nota acerca da depressão alastrante no cerebelo, tubérculo quadrigêmino anterior e bulbo olfativo
-
Leão AAP, Martins-Ferreira H. Nota acerca da depressão alastrante no cerebelo, tubérculo quadrigêmino anterior e bulbo olfativo. An Acad Bras Cienc. 1961 22 : 34 40.
-
(1961)
An Acad Bras Cienc.
, vol.22
, pp. 34-40
-
-
Leão, A.A.P.1
Martins-Ferreira, H.2
-
14
-
-
0018858938
-
Spreading depression in elasmobranch cerebellum
-
Young W. Spreading depression in elasmobranch cerebellum. Brain Res. 1980 199 : 113 126.
-
(1980)
Brain Res.
, vol.199
, pp. 113-126
-
-
Young, W.1
-
15
-
-
0021696849
-
Comparative neurophysiology of spreading depression in the cerebellum
-
Nicholson C. Comparative neurophysiology of spreading depression in the cerebellum. An Acad Bras Cienc. 1984 56 : 481 494.
-
(1984)
An Acad Bras Cienc.
, vol.56
, pp. 481-494
-
-
Nicholson, C.1
-
17
-
-
0015161422
-
Spreading depression in isolated chick retina
-
Martins-Ferreira H, de Oliveira Castro G. Spreading depression in isolated chick retina. Vision Res. 1971 11 (suppl 3 71 84.
-
(1971)
Vision Res.
, vol.11
, Issue.3
, pp. 71-84
-
-
Martins-Ferreira, H.1
De Oliveira Castro, G.2
-
19
-
-
0000669998
-
Spreading depression in the chicken retina
-
In: Ookawa, T., ed. Tokyo: Japan Scientific Societies Press
-
Martins-Ferreira H. Spreading depression in the chicken retina. In : Ookawa T, ed. The Brain and Behavior of the Fowl. 1st ed. Tokyo : Japan Scientific Societies Press 1983 : 317 333.
-
(1983)
The Brain and Behavior of the Fowl. 1st Ed.
, pp. 317-333
-
-
Martins-Ferreira, H.1
-
20
-
-
0031441331
-
Sumatriptan blocks spreading depression in isolated chick retina
-
Maranhão-Filho PA, Martins-Ferreira H, Vincent MB, Ribeiro LJ, Novis SA. Sumatriptan blocks spreading depression in isolated chick retina. Cephalalgia. 1997 17 : 822 825.
-
(1997)
Cephalalgia.
, vol.17
, pp. 822-825
-
-
Maranhão-Filho, P.A.1
Martins-Ferreira, H.2
Vincent, M.B.3
Ribeiro, L.J.4
Novis, S.A.5
-
21
-
-
0013367905
-
Propagation of spreading depression in isolated chick retina
-
In: Lehmenkühler, A., Grotemaier, K.H., Tegtmeier, F., eds. Wien, Baltimore: Urban and Schwarzenberg
-
Martins-Ferreira H. Propagation of spreading depression in isolated chick retina. In : Lehmenkühler A, Grotemaier KH, Tegtmeier F, eds. Migraine: Basic Mechanisms and Treatment. Monchen. Wien, Baltimore : Urban and Schwarzenberg 1993 : 533 546.
-
(1993)
Migraine: Basic Mechanisms and Treatment. Monchen.
, pp. 533-546
-
-
Martins-Ferreira, H.1
-
22
-
-
0021731235
-
Spreading depression of Leao probed with ion-selective microelectrodes in isolated chick retina
-
do Carmo RJ, Martins-Ferreira H. Spreading depression of Leao probed with ion-selective microelectrodes in isolated chick retina. An Acad Bras Cienc. 1984 56 : 401 421.
-
(1984)
An Acad Bras Cienc.
, vol.56
, pp. 401-421
-
-
Do Carmo, R.J.1
Martins-Ferreira, H.2
-
24
-
-
0002247105
-
Propagation of spreading cortical depression
-
Leão AAP, Morison RS. Propagation of spreading cortical depression. J Neurophysiol. 1945 8 : 33 45.
-
(1945)
J Neurophysiol.
, vol.8
, pp. 33-45
-
-
Leão, A.A.P.1
Morison, R.S.2
-
25
-
-
0001152951
-
Pial circulation and spreading depression of activity in the cerebral cortex
-
Leão AAP. Pial circulation and spreading depression of activity in the cerebral cortex. J Neurophysiol. 1944 7 : 391 396.
-
(1944)
J Neurophysiol.
, vol.7
, pp. 391-396
-
-
Leão, A.A.P.1
-
27
-
-
0035836628
-
Mechanisms of migraine aura revealed by functional MRI in human visual cortex
-
Hadjikhani N, Sanchez Del Rio M, Wu O, et al Mechanisms of migraine aura revealed by functional MRI in human visual cortex. Proc Natl Acad Sci U S A. 2001 98 : 4687 4692.
-
(2001)
Proc Natl Acad Sci U S A.
, vol.98
, pp. 4687-4692
-
-
Hadjikhani, N.1
Sanchez Del Rio, M.2
Wu, O.3
Al, E.4
-
28
-
-
0027478975
-
Neocortical spreading depression provokes the expression of c-fos protein-like immunoreactivity within trigeminal nucleus caudalis via trigeminovascular mechanisms
-
Moskowitz MA, Nozaki K, Kraig RP. Neocortical spreading depression provokes the expression of c-fos protein-like immunoreactivity within trigeminal nucleus caudalis via trigeminovascular mechanisms. J Neurosci. 1993 13 : 1167 1177.
-
(1993)
J Neurosci.
, vol.13
, pp. 1167-1177
-
-
Moskowitz, M.A.1
Nozaki, K.2
Kraig, R.P.3
-
29
-
-
0021183491
-
The neurobiology of vascular head pain
-
Moskowitz MA. The neurobiology of vascular head pain. Ann Neurol. 1984 16 : 157 168.
-
(1984)
Ann Neurol.
, vol.16
, pp. 157-168
-
-
Moskowitz, M.A.1
-
30
-
-
0025103363
-
The antimigraine drug, sumatriptan (GR43175), selectively blocks neurogenic plasma extravasation from blood vessels in dura mater
-
Buzzi MG, Moskowitz MA. The antimigraine drug, sumatriptan (GR43175), selectively blocks neurogenic plasma extravasation from blood vessels in dura mater. Br J Pharmacol. 1990 99 : 202 209.
-
(1990)
Br J Pharmacol.
, vol.99
, pp. 202-209
-
-
Buzzi, M.G.1
Moskowitz, M.A.2
-
31
-
-
0025940826
-
Evidence for 5-HT1B/1D receptors mediating the antimigraine effect of sumatriptan and dihydroergotamine
-
Buzzi MG, Moskowitz MA. Evidence for 5-HT1B/1D receptors mediating the antimigraine effect of sumatriptan and dihydroergotamine. Cephalalgia. 1991 11 : 165 168.
-
(1991)
Cephalalgia.
, vol.11
, pp. 165-168
-
-
Buzzi, M.G.1
Moskowitz, M.A.2
-
32
-
-
0026697460
-
Sumatriptan is a potent vasoconstrictor of human dural arteries via a 5-HT1-like receptor
-
Jansen I, Edvinsson L, Mortensen A, Olesen J. Sumatriptan is a potent vasoconstrictor of human dural arteries via a 5-HT1-like receptor. Cephalalgia. 1992 12 : 202 205.
-
(1992)
Cephalalgia.
, vol.12
, pp. 202-205
-
-
Jansen, I.1
Edvinsson, L.2
Mortensen, A.3
Olesen, J.4
-
34
-
-
4544259147
-
Disorders of the cerebellum: Ataxia, dysmetria of thought, and the cerebellar cognitive affective syndrome
-
Schmahmann JD. Disorders of the cerebellum: Ataxia, dysmetria of thought, and the cerebellar cognitive affective syndrome. J Neuropsychiatry Clin Neurosci. 2004 16 : 367 378.
-
(2004)
J Neuropsychiatry Clin Neurosci.
, vol.16
, pp. 367-378
-
-
Schmahmann, J.D.1
-
35
-
-
0031928291
-
The cells and molecules that make a cerebellum
-
Goldowitz D, Hamre K. The cells and molecules that make a cerebellum. Trends Neurosci. 1998 21 : 375 382.
-
(1998)
Trends Neurosci.
, vol.21
, pp. 375-382
-
-
Goldowitz, D.1
Hamre, K.2
-
36
-
-
0036164187
-
Static stabilometry in patients with migraine and tension-type headache during a headache-free period
-
Ishizaki K, Mori N, Takeshima T, et al Static stabilometry in patients with migraine and tension-type headache during a headache-free period. Psychiatry Clin Neurosci. 2002 56 : 85 90.
-
(2002)
Psychiatry Clin Neurosci.
, vol.56
, pp. 85-90
-
-
Ishizaki, K.1
Mori, N.2
Takeshima, T.3
Al, E.4
-
37
-
-
0028937262
-
Visually triggered migraine headaches affect spatial orientation and balance in a helicopter pilot
-
Cho AA, Clark JB, Rupert AH. Visually triggered migraine headaches affect spatial orientation and balance in a helicopter pilot. Aviat Space Environ Med. 1995 66 : 353 358.
-
(1995)
Aviat Space Environ Med.
, vol.66
, pp. 353-358
-
-
Cho, A.A.1
Clark, J.B.2
Rupert, A.H.3
-
38
-
-
9144254640
-
Subclinical vestibulocerebellar dysfunction in migraine with and without aura
-
Harno H, Hirvonen T, Kaunisto MA, et al Subclinical vestibulocerebellar dysfunction in migraine with and without aura. Neurology. 2003 61 : 1748 1752.
-
(2003)
Neurology.
, vol.61
, pp. 1748-1752
-
-
Harno, H.1
Hirvonen, T.2
Kaunisto, M.A.3
Al, E.4
-
39
-
-
0342936409
-
Subclinical cerebellar impairment in the common types of migraine: A three-dimensional analysis of reaching movements
-
Sandor PS, Mascia A, Seidel L, de Pasqua V, Schoenen J. Subclinical cerebellar impairment in the common types of migraine: A three-dimensional analysis of reaching movements. Ann Neurol. 2001 49 : 668 672.
-
(2001)
Ann Neurol.
, vol.49
, pp. 668-672
-
-
Sandor, P.S.1
Mascia, A.2
Seidel, L.3
De Pasqua, V.4
Schoenen, J.5
-
40
-
-
0031436665
-
Neurotology of migraine
-
Baloh RW. Neurotology of migraine. Headache. 1997 37 : 615 621.
-
(1997)
Headache.
, vol.37
, pp. 615-621
-
-
Baloh, R.W.1
-
41
-
-
0026747814
-
Migraine-associated dizziness
-
Cutrer FM, Baloh RW. Migraine-associated dizziness. Headache. 1992 32 : 300 304.
-
(1992)
Headache.
, vol.32
, pp. 300-304
-
-
Cutrer, F.M.1
Baloh, R.W.2
-
42
-
-
0019413588
-
Common migraine and vestibular function. Electronystagmographic study and pathogenesis
-
3pt1
-
Toglia JU, Thomas D, Kuritzky A. Common migraine and vestibular function. Electronystagmographic study and pathogenesis. Ann Otol Rhinol Laryngol. 1981 90 (3pt1 267 271.
-
(1981)
Ann Otol Rhinol Laryngol.
, vol.90
, pp. 267-271
-
-
Toglia, J.U.1
Thomas, D.2
Kuritzky, A.3
-
43
-
-
0021740986
-
Neuro-otological manifestations of migraine
-
pt4
-
Kayan A, Hood JD. Neuro-otological manifestations of migraine. Brain. 1984 107 (pt4 1123 1142.
-
(1984)
Brain.
, vol.107
, pp. 1123-1142
-
-
Kayan, A.1
Hood, J.D.2
-
44
-
-
0034897531
-
Visual vertigo: Symptom assessment, spatial orientation and postural control
-
pt8
-
Guerraz M, Yardley L, Bertholon P, et al Visual vertigo: Symptom assessment, spatial orientation and postural control. Brain. 2001 124 (pt8 1646 1656.
-
(2001)
Brain.
, vol.124
, pp. 1646-1656
-
-
Guerraz, M.1
Yardley, L.2
Bertholon, P.3
Al, E.4
-
46
-
-
2442585558
-
Motion processing deficits in migraine
-
McKendrick AM, Badcock DR. Motion processing deficits in migraine. Cephalalgia. 2004 24 : 363 372.
-
(2004)
Cephalalgia.
, vol.24
, pp. 363-372
-
-
McKendrick, A.M.1
Badcock, D.R.2
-
47
-
-
34250689803
-
Assessment of spatial-contrast function and short-wavelength sensitivity deficits in patients with migraine
-
Yenice O, Onal S, Incili B, Temel A, Afsar N, Tanrida Gcaron T. Assessment of spatial-contrast function and short-wavelength sensitivity deficits in patients with migraine. Eye. 2006.
-
(2006)
Eye.
-
-
Yenice, O.1
Onal, S.2
Incili, B.3
Temel, A.4
Afsar, N.5
Tanrida Gcaron, T.6
-
48
-
-
84939686814
-
Kleinhirnmigräne bei basilarer impression
-
Polak O, Grof P. Kleinhirnmigräne bei basilarer impression. Psychiatr Neurol (Basel). 1966 152 : 246 257.
-
(1966)
Psychiatr Neurol (Basel).
, vol.152
, pp. 246-257
-
-
Polak, O.1
Grof, P.2
-
51
-
-
0002772672
-
Basilar artery migraine
-
Bickerstaff ER. Basilar artery migraine. Lancet. 1961 277 : 15 17.
-
(1961)
Lancet.
, vol.277
, pp. 15-17
-
-
Bickerstaff, E.R.1
-
52
-
-
0016747320
-
Basilar artery migraine in young children
-
Golden GS, French JH. Basilar artery migraine in young children. Pediatrics. 1975 56 : 722 726.
-
(1975)
Pediatrics.
, vol.56
, pp. 722-726
-
-
Golden, G.S.1
French, J.H.2
-
53
-
-
33645806292
-
Basilar-type migraine. Clinical, epidemiologic and genetic features
-
Kirchmann M, Thomsen LL, Olesen J. Basilar-type migraine. Clinical, epidemiologic and genetic features. Neurology. 2006 66 : 880 886.
-
(2006)
Neurology.
, vol.66
, pp. 880-886
-
-
Kirchmann, M.1
Thomsen, L.L.2
Olesen, J.3
-
55
-
-
0025392111
-
Cerebellar and thalamic infarctions in basilar artery migraine
-
Sabharwal RK, Mehndiratta MM, Gupta M, Anjaneyulu A, Malhotra LK, Khwaja G. Cerebellar and thalamic infarctions in basilar artery migraine. J Assoc Physicians India. 1990 38 : 237 238.
-
(1990)
J Assoc Physicians India.
, vol.38
, pp. 237-238
-
-
Sabharwal, R.K.1
Mehndiratta, M.M.2
Gupta, M.3
Anjaneyulu, A.4
Malhotra, L.K.5
Khwaja, G.6
-
56
-
-
0026665894
-
Bilateral occipital lobe infarction in acute migraine: Clinical, neurophysiological, and neuroradiological study
-
Ganji S, Williams W, Furlow J. Bilateral occipital lobe infarction in acute migraine: Clinical, neurophysiological, and neuroradiological study. Headache. 1992 32 : 360 365.
-
(1992)
Headache.
, vol.32
, pp. 360-365
-
-
Ganji, S.1
Williams, W.2
Furlow, J.3
-
57
-
-
0028211685
-
Basilar artery migraine. Reversible ischemia demonstrated by Tc-99m HMPAO brain SPECT
-
Seto H, Shimizu M, Futatsuya R, et al Basilar artery migraine. Reversible ischemia demonstrated by Tc-99m HMPAO brain SPECT. Clin Nucl Med. 1994 19 : 215 218.
-
(1994)
Clin Nucl Med.
, vol.19
, pp. 215-218
-
-
Seto, H.1
Shimizu, M.2
Futatsuya, R.3
Al, E.4
-
58
-
-
0028247003
-
Prolonged impaired consciousness in basilar artery migraine
-
Muellbacher W, Mamoli B. Prolonged impaired consciousness in basilar artery migraine. Headache. 1994 34 : 282 285.
-
(1994)
Headache.
, vol.34
, pp. 282-285
-
-
Muellbacher, W.1
Mamoli, B.2
-
59
-
-
33645062190
-
Familial basilar migraine associated with a new mutation in the ATP1A 2 gene
-
Ambrosini A, D'Onofrio M, Grieco GS, et al Familial basilar migraine associated with a new mutation in the ATP1A 2 gene. Neurology. 2005 65 : 1826 1828.
-
(2005)
Neurology.
, vol.65
, pp. 1826-1828
-
-
Ambrosini, A.1
D'Onofrio, M.2
Grieco, G.S.3
Al, E.4
-
60
-
-
0038076033
-
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: A description of 5 families with familial hemiplegic migraine
-
Kors EE, Haan J, Giffin NJ, et al Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: A description of 5 families with familial hemiplegic migraine. Arch Neurol. 2003 60 : 684 688.
-
(2003)
Arch Neurol.
, vol.60
, pp. 684-688
-
-
Kors, E.E.1
Haan, J.2
Giffin, N.J.3
Al, E.4
-
61
-
-
16044370232
-
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
-
Ophoff RA, Terwindt GM, Vergouwe MN, et al Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell. 1996 87 : 543 552.
-
(1996)
Cell.
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouwe, M.N.3
Al, E.4
-
62
-
-
0031470730
-
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
-
Ducros A, Joutel A, Vahedi K, et al Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ann Neurol. 1997 42 : 885 890.
-
(1997)
Ann Neurol.
, vol.42
, pp. 885-890
-
-
Ducros, A.1
Joutel, A.2
Vahedi, K.3
Al, E.4
-
63
-
-
0041835844
-
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
-
Vanmolkot KR, Kors EE, Hottenga JJ, et al Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol. 2003 54 : 360 366.
-
(2003)
Ann Neurol.
, vol.54
, pp. 360-366
-
-
Vanmolkot, K.R.1
Kors, E.E.2
Hottenga, J.J.3
Al, E.4
-
64
-
-
23044459961
-
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
-
Dichgans M, Freilinger T, Eckstein G, et al Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet. 2005 366 : 371 377.
-
(2005)
Lancet.
, vol.366
, pp. 371-377
-
-
Dichgans, M.1
Freilinger, T.2
Eckstein, G.3
Al, E.4
-
65
-
-
5444222541
-
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs
-
Spadaro M, Ursu S, Lehmann-Horn F, et al A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. Neurogenetics. 2004 5 : 177 185.
-
(2004)
Neurogenetics.
, vol.5
, pp. 177-185
-
-
Spadaro, M.1
Ursu, S.2
Lehmann-Horn, F.3
Al, E.4
-
66
-
-
0026595617
-
P-type calcium channels blocked by the spider toxin omega-Aga-IVA
-
Mintz IM, Venema VJ, Swiderek KM, Lee TD, Bean BP, Adams ME. P-type calcium channels blocked by the spider toxin omega-Aga-IVA. Nature. 1992 355 : 827 829.
-
(1992)
Nature.
, vol.355
, pp. 827-829
-
-
Mintz, I.M.1
Venema, V.J.2
Swiderek, K.M.3
Lee, T.D.4
Bean, B.P.5
Adams, M.E.6
-
67
-
-
0025775195
-
Primary structure and functional expression from complementary DNA of a brain calcium channel
-
Mori Y, Friedrich T, Kim MS, et al Primary structure and functional expression from complementary DNA of a brain calcium channel. Nature. 1991 350 : 398 402.
-
(1991)
Nature.
, vol.350
, pp. 398-402
-
-
Mori, Y.1
Friedrich, T.2
Kim, M.S.3
Al, E.4
-
68
-
-
0028985125
-
Exocytotic Ca2+ channels in mammalian central neurons
-
Dunlap K, Luebke JI, Turner TJ. Exocytotic Ca2+ channels in mammalian central neurons. Trends Neurosci. 1995 18 : 89 98.
-
(1995)
Trends Neurosci.
, vol.18
, pp. 89-98
-
-
Dunlap, K.1
Luebke, J.I.2
Turner, T.J.3
-
69
-
-
0031841241
-
Specificity in the interaction of HVA Ca2+ channel types with Ca2+-dependent AHPs and firing behavior in neocortical pyramidal neurons
-
Pineda JC, Waters RS, Foehring RC. Specificity in the interaction of HVA Ca2+ channel types with Ca2+-dependent AHPs and firing behavior in neocortical pyramidal neurons. J Neurophysiol. 1998 79 : 2522 2534.
-
(1998)
J Neurophysiol.
, vol.79
, pp. 2522-2534
-
-
Pineda, J.C.1
Waters, R.S.2
Foehring, R.C.3
-
70
-
-
0033103648
-
Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine
-
Hans M, Luvisetto S, Williams ME, et al Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine. J Neurosci. 1999 19 : 1610 1619.
-
(1999)
J Neurosci.
, vol.19
, pp. 1610-1619
-
-
Hans, M.1
Luvisetto, S.2
Williams, M.E.3
Al, E.4
-
71
-
-
12144286750
-
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression
-
van den Maagdenberg AM, Pietrobon D, Pizzorusso T, et al A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression. Neuron. 2004 41 : 701 710.
-
(2004)
Neuron.
, vol.41
, pp. 701-710
-
-
Van Den Maagdenberg, A.M.1
Pietrobon, D.2
Pizzorusso, T.3
Al, E.4
-
72
-
-
0033364409
-
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
-
Ducros A, Denier C, Joutel A, et al Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia. Am J Hum Genet. 1999 64 : 89 98.
-
(1999)
Am J Hum Genet.
, vol.64
, pp. 89-98
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
Al, E.4
-
73
-
-
0034633752
-
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
-
Vahedi K, Denier C, Ducros A, et al CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy. Neurology. 2000 55 : 1040 1042.
-
(2000)
Neurology.
, vol.55
, pp. 1040-1042
-
-
Vahedi, K.1
Denier, C.2
Ducros, A.3
Al, E.4
-
74
-
-
0033551452
-
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia
-
Battistini S, Stenirri S, Piatti M, et al A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia. Neurology. 1999 53 : 38 43.
-
(1999)
Neurology.
, vol.53
, pp. 38-43
-
-
Battistini, S.1
Stenirri, S.2
Piatti, M.3
Al, E.4
-
75
-
-
0036725082
-
The spinocerebellar ataxias: Order emerges from chaos
-
Margolis RL. The spinocerebellar ataxias: Order emerges from chaos. Curr Neurol Neurosci Rep. 2002 2 : 447 456.
-
(2002)
Curr Neurol Neurosci Rep.
, vol.2
, pp. 447-456
-
-
Margolis, R.L.1
-
76
-
-
0026591574
-
Familial paroxysmal ataxia: Report of a family
-
Hawkes CH. Familial paroxysmal ataxia: Report of a family. J Neurol Neurosurg Psychiatry. 1992 55 : 212 213.
-
(1992)
J Neurol Neurosurg Psychiatry.
, vol.55
, pp. 212-213
-
-
Hawkes, C.H.1
-
77
-
-
0032497574
-
Downbeat nystagmus in two siblings with spinocerebellar ataxia type 6 (SCA 6)
-
Harada H, Tamaoka A, Watanabe M, Ishikawa K, Shoji S. Downbeat nystagmus in two siblings with spinocerebellar ataxia type 6 (SCA 6). J Neurol Sci. 1998 160 : 161 163.
-
(1998)
J Neurol Sci.
, vol.160
, pp. 161-163
-
-
Harada, H.1
Tamaoka, A.2
Watanabe, M.3
Ishikawa, K.4
Shoji, S.5
-
78
-
-
0032872916
-
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
-
Friend KL, Crimmins D, Phan TG, et al Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM. Hum Genet. 1999 105 : 261 265.
-
(1999)
Hum Genet.
, vol.105
, pp. 261-265
-
-
Friend, K.L.1
Crimmins, D.2
Phan, T.G.3
Al, E.4
-
79
-
-
0347722572
-
Clinical spectrum of episodic ataxia type 2
-
Jen J, Kim GW, Baloh RW. Clinical spectrum of episodic ataxia type 2. Neurology. 2004 62 : 17 22.
-
(2004)
Neurology.
, vol.62
, pp. 17-22
-
-
Jen, J.1
Kim, G.W.2
Baloh, R.W.3
-
80
-
-
0035115339
-
Missense CACNA1A mutation causing episodic ataxia type 2
-
Denier C, Ducros A, Durr A, Eymard B, Chassande B, Tournier-Lasserve E. Missense CACNA1A mutation causing episodic ataxia type 2. Arch Neurol. 2001 58 : 292 295.
-
(2001)
Arch Neurol.
, vol.58
, pp. 292-295
-
-
Denier, C.1
Ducros, A.2
Durr, A.3
Eymard, B.4
Chassande, B.5
Tournier-Lasserve, E.6
-
81
-
-
0035089729
-
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2
-
Guida S, Trettel F, Pagnutti S, et al Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2. Am J Hum Genet. 2001 68 : 759 764.
-
(2001)
Am J Hum Genet.
, vol.68
, pp. 759-764
-
-
Guida, S.1
Trettel, F.2
Pagnutti, S.3
Al, E.4
-
82
-
-
0021800846
-
Autosomal recessive non-progressive ataxia with an early childhood debut
-
Kvistad PH, Dahl A, Skre H. Autosomal recessive non-progressive ataxia with an early childhood debut. Acta Neurol Scand. 1985 71 : 295 302.
-
(1985)
Acta Neurol Scand.
, vol.71
, pp. 295-302
-
-
Kvistad, P.H.1
Dahl, A.2
Skre, H.3
-
83
-
-
0042566063
-
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13
-
Tranebjaerg L, Teslovich TM, Jones M, et al Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13. Hum Genet. 2003 113 : 293 295.
-
(2003)
Hum Genet.
, vol.113
, pp. 293-295
-
-
Tranebjaerg, L.1
Teslovich, T.M.2
Jones, M.3
Al, E.4
-
84
-
-
0035940624
-
An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus
-
Steckley JL, Ebers GC, Cader MZ, McLachlan RS. An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Neurology. 2001 57 : 1499 1502.
-
(2001)
Neurology.
, vol.57
, pp. 1499-1502
-
-
Steckley, J.L.1
Ebers, G.C.2
Cader, M.Z.3
McLachlan, R.S.4
-
85
-
-
0344962372
-
Spinocerebellar ataxia type 6 and episodic ataxia type 2: Differences and similarities between two allelic disorders
-
Mantuano E, Veneziano L, Jodice C, Frontali M. Spinocerebellar ataxia type 6 and episodic ataxia type 2: Differences and similarities between two allelic disorders. Cytogenet Genome Res. 2003 100 : 147 153.
-
(2003)
Cytogenet Genome Res.
, vol.100
, pp. 147-153
-
-
Mantuano, E.1
Veneziano, L.2
Jodice, C.3
Frontali, M.4
-
86
-
-
0035503901
-
Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?
-
Frontali M. Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder? Brain Res Bull. 2001 56 : 227 231.
-
(2001)
Brain Res Bull.
, vol.56
, pp. 227-231
-
-
Frontali, M.1
-
87
-
-
0002079429
-
Familial episodic ataxias and related ion channel disorders
-
Jen J. Familial episodic ataxias and related ion channel disorders. Curr Treat Options Neurol. 2000 2 : 429 431.
-
(2000)
Curr Treat Options Neurol.
, vol.2
, pp. 429-431
-
-
Jen, J.1
-
88
-
-
9844263366
-
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
-
Jodice C, Mantuano E, Veneziano L, et al Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. Hum Mol Genet. 1997 6 : 1973 1978.
-
(1997)
Hum Mol Genet.
, vol.6
, pp. 1973-1978
-
-
Jodice, C.1
Mantuano, E.2
Veneziano, L.3
Al, E.4
-
89
-
-
23844500344
-
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures
-
Jen JC, Wan J, Palos TP, Howard BD, Baloh RW. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures. Neurology. 2005 65 : 529 534.
-
(2005)
Neurology.
, vol.65
, pp. 529-534
-
-
Jen, J.C.1
Wan, J.2
Palos, T.P.3
Howard, B.D.4
Baloh, R.W.5
-
90
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko O, Bailey J, Bonnen P, et al Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet. 1997 15 : 62 69.
-
(1997)
Nat Genet.
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
Al, E.4
-
91
-
-
0344406276
-
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family
-
Alonso I, Barros J, Tuna A, et al Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. Arch Neurol. 2003 60 : 610 614.
-
(2003)
Arch Neurol.
, vol.60
, pp. 610-614
-
-
Alonso, I.1
Barros, J.2
Tuna, A.3
Al, E.4
-
92
-
-
1642555626
-
A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine
-
Alonso I, Barros J, Tuna A, et al A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine. Clin Genet. 2004 65 : 70 72.
-
(2004)
Clin Genet.
, vol.65
, pp. 70-72
-
-
Alonso, I.1
Barros, J.2
Tuna, A.3
Al, E.4
-
93
-
-
24944531664
-
Degree of cerebellar ataxia correlates with three-dimensional MRI-based cerebellar volume in pure cerebellar degeneration
-
Richter S, Dimitrova A, Maschke M, et al Degree of cerebellar ataxia correlates with three-dimensional MRI-based cerebellar volume in pure cerebellar degeneration. Eur Neurol. 2005 54 : 23 27.
-
(2005)
Eur Neurol.
, vol.54
, pp. 23-27
-
-
Richter, S.1
Dimitrova, A.2
Maschke, M.3
Al, E.4
-
94
-
-
0035811775
-
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
-
Ducros A, Denier C, Joutel A, et al The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med. 2001 345 : 17 24.
-
(2001)
N Engl J Med.
, vol.345
, pp. 17-24
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
Al, E.4
-
95
-
-
0030052699
-
Familial hemiplegic migraine, nystagmus, and cerebellar atrophy
-
Elliott MA, Peroutka SJ, Welch S, May EF. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy. Ann Neurol. 1996 39 : 100 106.
-
(1996)
Ann Neurol.
, vol.39
, pp. 100-106
-
-
Elliott, M.A.1
Peroutka, S.J.2
Welch, S.3
May, E.F.4
-
96
-
-
4644282550
-
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation
-
Kors EE, Melberg A, Vanmolkot KR, et al Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation. Neurology. 2004 63 : 1136 1137.
-
(2004)
Neurology.
, vol.63
, pp. 1136-1137
-
-
Kors, E.E.1
Melberg, A.2
Vanmolkot, K.R.3
Al, E.4
-
97
-
-
0033551468
-
A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia
-
Jen J, Yue Q, Nelson SF, et al A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia. Neurology. 1999 53 : 34 37.
-
(1999)
Neurology.
, vol.53
, pp. 34-37
-
-
Jen, J.1
Yue, Q.2
Nelson, S.F.3
Al, E.4
-
98
-
-
0030949087
-
Analysis of spontaneous electrical activity in cerebellar Purkinje cells acutely isolated from postnatal rats
-
Nam SC, Hockberger PE. Analysis of spontaneous electrical activity in cerebellar Purkinje cells acutely isolated from postnatal rats. J Neurobiol. 1997 33 : 18 32.
-
(1997)
J Neurobiol.
, vol.33
, pp. 18-32
-
-
Nam, S.C.1
Hockberger, P.E.2
-
99
-
-
33344454896
-
Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia
-
Walter JT, Alvina K, Womack MD, Chevez C, Khodakhah K. Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia. Nat Neurosci. 2006 9 : 389 397.
-
(2006)
Nat Neurosci.
, vol.9
, pp. 389-397
-
-
Walter, J.T.1
Alvina, K.2
Womack, M.D.3
Chevez, C.4
Khodakhah, K.5
-
100
-
-
0034988145
-
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
-
Kors EE, Terwindt GM, Vermeulen FL, et al Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol. 2001 49 : 753 760.
-
(2001)
Ann Neurol.
, vol.49
, pp. 753-760
-
-
Kors, E.E.1
Terwindt, G.M.2
Vermeulen, F.L.3
Al, E.4
-
101
-
-
0021799194
-
Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia.
-
pt3
-
Fitzsimons RB, Wolfenden WH. Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia. Brain. 1985 108 (pt3 555 577.
-
(1985)
Brain.
, vol.108
, pp. 555-577
-
-
Fitzsimons, R.B.1
Wolfenden, W.H.2
-
102
-
-
0025017477
-
Familial migraine coma: A case study
-
Munte TF, Muller-Vahl H. Familial migraine coma: A case study. J Neurol. 1990 237 : 59 61.
-
(1990)
J Neurol.
, vol.237
, pp. 59-61
-
-
Munte, T.F.1
Muller-Vahl, H.2
-
103
-
-
0036157992
-
Wide clinical variability in a family with a CACNA1A T666m mutation: Hemiplegic migraine, coma, and progressive ataxia
-
Wada T, Kobayashi N, Takahashi Y, Aoki T, Watanabe T, Saitoh S. Wide clinical variability in a family with a CACNA1A T666m mutation: Hemiplegic migraine, coma, and progressive ataxia. Pediatr Neurol. 2002 26 : 47 50.
-
(2002)
Pediatr Neurol.
, vol.26
, pp. 47-50
-
-
Wada, T.1
Kobayashi, N.2
Takahashi, Y.3
Aoki, T.4
Watanabe, T.5
Saitoh, S.6
-
104
-
-
0025520869
-
Migraine versus glaucoma-A diagnostic dilemma
-
Tan BB. Migraine versus glaucoma-A diagnostic dilemma. Ann Acad Med Singapore. 1990 19 : 856 858.
-
(1990)
Ann Acad Med Singapore.
, vol.19
, pp. 856-858
-
-
Tan, B.B.1
-
106
-
-
0032869936
-
Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1
-
Echenne B, Ducros A, Rivier F, et al Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1. Neuropediatrics. 1999 30 : 214 217.
-
(1999)
Neuropediatrics.
, vol.30
, pp. 214-217
-
-
Echenne, B.1
Ducros, A.2
Rivier, F.3
Al, E.4
-
107
-
-
0034302362
-
Interesting case of migraine presenting with recurrent episodes of migraine coma
-
Sareen D. Interesting case of migraine presenting with recurrent episodes of migraine coma. J Assoc Physicians India. 2000 48 : 1031.
-
(2000)
J Assoc Physicians India.
, vol.48
, pp. 1031
-
-
Sareen, D.1
-
108
-
-
20444388528
-
Specific kinetic alterations of human CaV2. 1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma
-
Tottene A, Pivotto F, Fellin T, Cesetti T, van den Maagdenberg AM, Pietrobon D. Specific kinetic alterations of human CaV2. 1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma. J Biol Chem. 2005 280 : 17678 17686.
-
(2005)
J Biol Chem.
, vol.280
, pp. 17678-17686
-
-
Tottene, A.1
Pivotto, F.2
Fellin, T.3
Cesetti, T.4
Van Den Maagdenberg, A.M.5
Pietrobon, D.6
-
109
-
-
20444428550
-
Migraine: New molecular mechanisms
-
Pietrobon D. Migraine: New molecular mechanisms. Neuroscientist. 2005 11 : 373 386.
-
(2005)
Neuroscientist.
, vol.11
, pp. 373-386
-
-
Pietrobon, D.1
-
110
-
-
2942615488
-
Cortical spreading depression activates and upregulates MMP-9
-
Gursoy-Ozdemir Y, Qiu J, Matsvaka N, et al Cortical spreading depression activates and upregulates MMP-9. J Clin Invest. 2004 113 : 1447 1455.
-
(2004)
J Clin Invest.
, vol.113
, pp. 1447-1455
-
-
Gursoy-Ozdemir, Y.1
Qiu, J.2
Matsvaka, N.3
Al, E.4
-
111
-
-
0022622198
-
Leao's spreading depression in the hippocampus explains transient global amnesia: A hypothesis
-
Olesen J, Jorgensen MB. Leao's spreading depression in the hippocampus explains transient global amnesia: A hypothesis. Acta Neurol Scand. 1986 73 : 219 220.
-
(1986)
Acta Neurol Scand.
, vol.73
, pp. 219-220
-
-
Olesen, J.1
Jorgensen, M.B.2
-
112
-
-
0022618220
-
Transient global amnesia triggered by mild head trauma
-
pt2
-
Haas DC, Ross GS. Transient global amnesia triggered by mild head trauma. Brain. 1986 109 (pt2 251 257.
-
(1986)
Brain.
, vol.109
, pp. 251-257
-
-
Haas, D.C.1
Ross, G.S.2
-
113
-
-
0026597221
-
Familial periodic cerebellar ataxia: A problem of cerebellar intracellular pH homeostasis
-
Bain PG, O'Brien MD, Keevil SF, Porter DA. Familial periodic cerebellar ataxia: A problem of cerebellar intracellular pH homeostasis. Ann Neurol. 1992 31 : 147 154.
-
(1992)
Ann Neurol.
, vol.31
, pp. 147-154
-
-
Bain, P.G.1
O'Brien, M.D.2
Keevil, S.F.3
Porter, D.A.4
-
114
-
-
0018122266
-
Hereditary paroxysmal ataxia: Response to acetazolamide
-
3rd
-
Griggs RC, Moxley RT, 3rd, Lafrance RA, McQuillen J. Hereditary paroxysmal ataxia: Response to acetazolamide. Neurology. 1978 28 : 1259 1264.
-
(1978)
Neurology
, vol.28
, pp. 1259-1264
-
-
Griggs, R.C.1
Moxley, R.T.2
Lafrance, R.A.3
McQuillen, J.4
-
115
-
-
0031726082
-
Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia
-
Jen JC, Yue Q, Karrim J, Nelson SF, Baloh RW. Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia. J Neurol Neurosurg Psychiatry. 1998 65 : 565 568.
-
(1998)
J Neurol Neurosurg Psychiatry.
, vol.65
, pp. 565-568
-
-
Jen, J.C.1
Yue, Q.2
Karrim, J.3
Nelson, S.F.4
Baloh, R.W.5
-
116
-
-
0029807841
-
Acetazolamide responsiveness in familial hemiplegic migraine
-
Athwal BS, Lennox GG. Acetazolamide responsiveness in familial hemiplegic migraine. Ann Neurol. 1996 40 : 820 821.
-
(1996)
Ann Neurol.
, vol.40
, pp. 820-821
-
-
Athwal, B.S.1
Lennox, G.G.2
-
117
-
-
17244373694
-
Acetazolamide efficacy and tolerability in migraine with aura: A pilot study
-
de Simone R, Marano E, Di Stasio E, Bonuso S, Fiorillo C, Bonavita V. Acetazolamide efficacy and tolerability in migraine with aura: A pilot study. Headache. 2005 45 : 385 386.
-
(2005)
Headache.
, vol.45
, pp. 385-386
-
-
De Simone, R.1
Marano, E.2
Di Stasio, E.3
Bonuso, S.4
Fiorillo, C.5
Bonavita, V.6
-
118
-
-
0036167182
-
Efficacy and tolerability of acetazolamide in migraine prophylaxis: A randomised placebo-controlled trial
-
Vahedi K, Taupin P, Djomby R, et al Efficacy and tolerability of acetazolamide in migraine prophylaxis: A randomised placebo-controlled trial. J Neurol. 2002 249 : 206 211.
-
(2002)
J Neurol.
, vol.249
, pp. 206-211
-
-
Vahedi, K.1
Taupin, P.2
Djomby, R.3
Al, E.4
-
120
-
-
17044407601
-
Plasma and whole blood pharmacokinetics of topiramate: The role of carbonic anhydrase
-
Shank RP, Doose DR, Streeter AJ, Bialer M. Plasma and whole blood pharmacokinetics of topiramate: The role of carbonic anhydrase. Epilepsy Res. 2005 63 : 103 112.
-
(2005)
Epilepsy Res.
, vol.63
, pp. 103-112
-
-
Shank, R.P.1
Doose, D.R.2
Streeter, A.J.3
Bialer, M.4
-
121
-
-
33645789260
-
Suppression of cortical spreading depression in migraine prophylaxis
-
Ayata C, Jin H, Kudo C, Dalkara T, Moskowitz MA. Suppression of cortical spreading depression in migraine prophylaxis. Ann Neurol. 2006 59 : 652 661.
-
(2006)
Ann Neurol.
, vol.59
, pp. 652-661
-
-
Ayata, C.1
Jin, H.2
Kudo, C.3
Dalkara, T.4
Moskowitz, M.A.5
-
122
-
-
3843077388
-
Functional implications of a novel EA2 mutation in the P/Q-type calcium channel
-
Spacey SD, Hildebrand ME, Materek LA, Bird TD, Snutch TP. Functional implications of a novel EA2 mutation in the P/Q-type calcium channel. Ann Neurol. 2004 56 : 213 220.
-
(2004)
Ann Neurol.
, vol.56
, pp. 213-220
-
-
Spacey, S.D.1
Hildebrand, M.E.2
Materek, L.A.3
Bird, T.D.4
Snutch, T.P.5
-
123
-
-
0028893022
-
Fatal cerebellar infarction in a migraine sufferer whilst receiving sumatriptan
-
Jayamaha JE, Street MK. Fatal cerebellar infarction in a migraine sufferer whilst receiving sumatriptan. Intensive Care Med. 1995 21 : 82 83.
-
(1995)
Intensive Care Med.
, vol.21
, pp. 82-83
-
-
Jayamaha, J.E.1
Street, M.K.2
-
124
-
-
0030682445
-
Familial hemiplegic migraine with crossed cerebellar diaschisis and unilateral meningeal enhancement
-
Crawford JS, Konkol RJ. Familial hemiplegic migraine with crossed cerebellar diaschisis and unilateral meningeal enhancement. Headache. 1997 37 : 590 593.
-
(1997)
Headache.
, vol.37
, pp. 590-593
-
-
Crawford, J.S.1
Konkol, R.J.2
-
125
-
-
0029805085
-
Reversible cerebellar perfusion in familial hemiplegic migraine
-
Lee TG, Solomon GD, Kunkel RS, Raja S. Reversible cerebellar perfusion in familial hemiplegic migraine. Lancet. 1996 348 : 1383.
-
(1996)
Lancet.
, vol.348
, pp. 1383
-
-
Lee, T.G.1
Solomon, G.D.2
Kunkel, R.S.3
Raja, S.4
-
126
-
-
0020055886
-
Pediatric cerebellar infarction: Case report and review of the literature
-
Harbaugh RE, Saunders RL, Reeves AG. Pediatric cerebellar infarction: Case report and review of the literature. Neurosurgery. 1982 10 : 593 596.
-
(1982)
Neurosurgery.
, vol.10
, pp. 593-596
-
-
Harbaugh, R.E.1
Saunders, R.L.2
Reeves, A.G.3
-
127
-
-
1542365240
-
Migraine as a risk factor for subclinical brain lesions
-
Kruit MC, van Buchem MA, Hofman PA, Bakkers JT, Terwindt GM, Ferrari MD, et al. Migraine as a risk factor for subclinical brain lesions. JAMA. 2004 291 : 427 434.
-
(2004)
JAMA.
, vol.291
, pp. 427-434
-
-
Kruit, M.C.1
Van Buchem, M.A.2
Hofman, P.A.3
Bakkers, J.T.4
Terwindt, G.M.5
Ferrari, M.D.6
-
128
-
-
24344486827
-
Infarcts in the posterior circulation territory in migraine. the population-based MRI CAMERA study
-
Kruit MC, Launer LJ, Ferrari MD, van Buchem MA. Infarcts in the posterior circulation territory in migraine. The population-based MRI CAMERA study. Brain. 2005 128 : 2068 2077.
-
(2005)
Brain.
, vol.128
, pp. 2068-2077
-
-
Kruit, M.C.1
Launer, L.J.2
Ferrari, M.D.3
Van Buchem, M.A.4
-
129
-
-
0021041669
-
The vascularization of the human cerebellar cortex
-
Duvernoy H, Delon S, Vannson JL. The vascularization of the human cerebellar cortex. Brain Res Bull. 1983 11 : 419 480.
-
(1983)
Brain Res Bull.
, vol.11
, pp. 419-480
-
-
Duvernoy, H.1
Delon, S.2
Vannson, J.L.3
-
131
-
-
0032981764
-
Novel form of spreading acidification and depression in the cerebellar cortex demonstrated by neutral red optical imaging
-
Chen G, Hanson CL, Dunbar RL, Ebner TJ. Novel form of spreading acidification and depression in the cerebellar cortex demonstrated by neutral red optical imaging. J Neurophysiol. 1999 81 : 1992 1998.
-
(1999)
J Neurophysiol.
, vol.81
, pp. 1992-1998
-
-
Chen, G.1
Hanson, C.L.2
Dunbar, R.L.3
Ebner, T.J.4
-
132
-
-
0037310734
-
Spreading acidification and depression in the cerebellar cortex
-
Ebner TJ, Chen G. Spreading acidification and depression in the cerebellar cortex. Neuroscientist. 2003 9 : 37 45.
-
(2003)
Neuroscientist.
, vol.9
, pp. 37-45
-
-
Ebner, T.J.1
Chen, G.2
-
133
-
-
0029958199
-
Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1
-
Comu S, Giuliani M, Narayanan V. Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1. Ann Neurol. 1996 40 : 684 687.
-
(1996)
Ann Neurol.
, vol.40
, pp. 684-687
-
-
Comu, S.1
Giuliani, M.2
Narayanan, V.3
-
134
-
-
0025138986
-
Glutamate induces calcium waves in cultured astrocytes: Long-range glial signaling
-
Cornell-Bell AH, Finkbeiner SM, Cooper MS, Smith SJ. Glutamate induces calcium waves in cultured astrocytes: Long-range glial signaling. Science. 1990 247 : 470 473.
-
(1990)
Science.
, vol.247
, pp. 470-473
-
-
Cornell-Bell, A.H.1
Finkbeiner, S.M.2
Cooper, M.S.3
Smith, S.J.4
-
135
-
-
0032171655
-
Intercellular calcium waves in glia
-
Charles A. Intercellular calcium waves in glia. Glia. 1998 24 : 39 49.
-
(1998)
Glia.
, vol.24
, pp. 39-49
-
-
Charles, A.1
-
136
-
-
0141988699
-
Signaling at the gliovascular interface
-
Simard M, Arcuino G, Takano T, Liu QS, Nedergaard M. Signaling at the gliovascular interface. J Neurosci. 2003 23 : 9254 9262.
-
(2003)
J Neurosci.
, vol.23
, pp. 9254-9262
-
-
Simard, M.1
Arcuino, G.2
Takano, T.3
Liu, Q.S.4
Nedergaard, M.5
-
137
-
-
0028212163
-
Direct signaling from astrocytes to neurons in cultures of mammalian brain cells
-
Nedergaard M. Direct signaling from astrocytes to neurons in cultures of mammalian brain cells. Science. 1994 263 : 1768 1771.
-
(1994)
Science.
, vol.263
, pp. 1768-1771
-
-
Nedergaard, M.1
-
138
-
-
0026503603
-
Neuronal activity triggers calcium waves in hippocampal astrocyte networks
-
Dani JW, Chernjavsky A, Smith SJ. Neuronal activity triggers calcium waves in hippocampal astrocyte networks. Neuron. 1992 8 : 429 440.
-
(1992)
Neuron.
, vol.8
, pp. 429-440
-
-
Dani, J.W.1
Chernjavsky, A.2
Smith, S.J.3
-
139
-
-
0031017768
-
Calcium waves in retinal glial cells
-
Newman EA, Zahs KR. Calcium waves in retinal glial cells. Science. 1997 275 : 844 847.
-
(1997)
Science.
, vol.275
, pp. 844-847
-
-
Newman, E.A.1
Zahs, K.R.2
-
140
-
-
0033555444
-
ATP released from astrocytes mediates glial calcium waves
-
Guthrie PB, Knappenberger J, Segal M, Bennett MV, Charles AC, Kater SB. ATP released from astrocytes mediates glial calcium waves. J Neurosci. 1999 19 : 520 528.
-
(1999)
J Neurosci.
, vol.19
, pp. 520-528
-
-
Guthrie, P.B.1
Knappenberger, J.2
Segal, M.3
Bennett, M.V.4
Charles, A.C.5
Kater, S.B.6
-
141
-
-
0032080232
-
Calcium waves precede electrophysiological changes of spreading depression in hippocampal organ cultures
-
Kunkler PE, Kraig RP. Calcium waves precede electrophysiological changes of spreading depression in hippocampal organ cultures. J Neurosci. 1998 18 : 3416 3425.
-
(1998)
J Neurosci.
, vol.18
, pp. 3416-3425
-
-
Kunkler, P.E.1
Kraig, R.P.2
-
142
-
-
0032530759
-
Imaging spreading depression and associated intracellular calcium waves in brain slices
-
Basarsky TA, Duffy SN, Andrew RD, MacVicar BA. Imaging spreading depression and associated intracellular calcium waves in brain slices. J Neurosci. 1998 18 : 7189 7199.
-
(1998)
J Neurosci.
, vol.18
, pp. 7189-7199
-
-
Basarsky, T.A.1
Duffy, S.N.2
Andrew, R.D.3
MacVicar, B.A.4
-
143
-
-
0036175714
-
Calcium channels and channelopathies of the central nervous system
-
Pietrobon D. Calcium channels and channelopathies of the central nervous system. Mol Neurobiol. 2002 25 : 31 50.
-
(2002)
Mol Neurobiol.
, vol.25
, pp. 31-50
-
-
Pietrobon, D.1
-
144
-
-
0034192486
-
Advances in the vascular pathophysiology of ischemic stroke
-
del Zoppo GJ, Hallenbeck JM. Advances in the vascular pathophysiology of ischemic stroke. Thromb Res. 2000 98 : 73 81.
-
(2000)
Thromb Res.
, vol.98
, pp. 73-81
-
-
Del Zoppo, G.J.1
Hallenbeck, J.M.2
-
145
-
-
0032870674
-
Phosphorus and proton magnetic resonance spectroscopy in episodic ataxia type 2
-
Sappey-Marinier D, Vighetto A, Peyron R, Broussolle E, Bonmartin A. Phosphorus and proton magnetic resonance spectroscopy in episodic ataxia type 2. Ann Neurol. 1999 46 : 256 259.
-
(1999)
Ann Neurol.
, vol.46
, pp. 256-259
-
-
Sappey-Marinier, D.1
Vighetto, A.2
Peyron, R.3
Broussolle, E.4
Bonmartin, A.5
-
146
-
-
0031883338
-
Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6)
-
Sasaki H, Kojima H, Yabe I, et al Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6). Acta Neuropathol (Berl). 1998 95 : 199 204.
-
(1998)
Acta Neuropathol (Berl).
, vol.95
, pp. 199-204
-
-
Sasaki, H.1
Kojima, H.2
Yabe, I.3
Al, E.4
-
147
-
-
27244449618
-
Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation
-
Takahashi T, Arai N, Shimamura M, et al Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation. Neuropathology. 2005 25 : 228 234.
-
(2005)
Neuropathology.
, vol.25
, pp. 228-234
-
-
Takahashi, T.1
Arai, N.2
Shimamura, M.3
Al, E.4
-
148
-
-
0023476056
-
Trigeminal nerve pathways to the cerebral arteries in monkeys
-
Ruskell GL, Simons T. Trigeminal nerve pathways to the cerebral arteries in monkeys. J Anat. 1987 155 : 23 37.
-
(1987)
J Anat.
, vol.155
, pp. 23-37
-
-
Ruskell, G.L.1
Simons, T.2
-
149
-
-
0024580720
-
Contributions from the upper cervical dorsal roots and trigeminal ganglia to the feline circle of Willis
-
Saito K, Moskowitz MA. Contributions from the upper cervical dorsal roots and trigeminal ganglia to the feline circle of Willis. Stroke. 1989 20 : 524 526.
-
(1989)
Stroke.
, vol.20
, pp. 524-526
-
-
Saito, K.1
Moskowitz, M.A.2
-
150
-
-
0031015937
-
Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p
-
Baloh RW, Yue Q, Furman JM, Nelson SF. Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p. Ann Neurol. 1997 41 : 8 16.
-
(1997)
Ann Neurol.
, vol.41
, pp. 8-16
-
-
Baloh, R.W.1
Yue, Q.2
Furman, J.M.3
Nelson, S.F.4
-
151
-
-
0001271610
-
Familial occurrence of migraine with a hemiplegic syndrome and cerebellar manifestations
-
8pt1
-
Ohta M, Araki S, Kuroiwa Y. Familial occurrence of migraine with a hemiplegic syndrome and cerebellar manifestations. Neurology. 1967 17 (8pt1 813 817.
-
(1967)
Neurology.
, vol.17
, pp. 813-817
-
-
Ohta, M.1
Araki, S.2
Kuroiwa, Y.3
-
152
-
-
0014848932
-
Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus
-
Young GF, Leon-Barth CA, Green J. Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus. Arch Neurol. 1970 23 : 201 209.
-
(1970)
Arch Neurol.
, vol.23
, pp. 201-209
-
-
Young, G.F.1
Leon-Barth, C.A.2
Green, J.3
-
154
-
-
0018948435
-
An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor
-
Zifkin B, Andermann E, Andermann F, Kirkham T. An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor. Ann Neurol. 1980 8 : 329 332.
-
(1980)
Ann Neurol.
, vol.8
, pp. 329-332
-
-
Zifkin, B.1
Andermann, E.2
Andermann, F.3
Kirkham, T.4
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