Subclinical cerebellar impairment in the common types of migraine: A three-dimensional analysis of reaching movements

Annals of Neurology

Volumn 49, Issue 5, 2001, Pages 668-672

  Sándor, Peter S ^a   Mascia, Addolorata ^b   Seidel, Laurence ^c   De Pasqua, Victor ^c   Schoenen, Jean ^c,d  

^a UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c UNIVERSITY OF LIÈGE   (Belgium)

^d CHR   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

ADULT; ARM MOVEMENT; ARTICLE; CEREBELLUM DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE MUTATION; HUMAN; MALE; MIGRAINE; PRIORITY JOURNAL;

ADULT; ARM; CEREBELLAR DISEASES; FEMALE; HUMANS; MALE; MIGRAINE DISORDERS; MOVEMENT;

EID: 0342936409     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1019     Document Type: Article

References (20)

1. 2+ channel gene CACNL1A4. Cell 1996; 87:543-552.
2. Terwindt GM, Ophoff RA, Haan J, et al. Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19. Cephalalgia 1996;16:153-155.
3. Craig PJ, McAinsh AD, McCormack AL, et al. Distribution of the voltage-dependent calcium channel alpha(1A) subunit throughout the mature rat brain and its relationship to neuro-transmitter pathways. J Comp Neurol 1998;397:251-267.
4. Ambrosini A, Maertens de Noordhout AM, Alagona G, et al. Impairment of neuromuscular transmission in a subgroup of migraine patients. Neurosci Lett 1999;276:201-203.
5. Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, et al. Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha (1A) Ca (2+) channel mutation. Brain 2000;123:463-471.
6. May A, Ophoff RA, Terwindt GM, et al. Familial hemiplégie migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Hum Genet 1995;96:604-608.
7. Nyholt DR, Lea RA, Goadsby PJ, et al. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology 1998;50:1428-1432.
8. Schoenen J. Sympathetic hyperarousal in migraine? Evaluation by contingent negative variation and psychomotor testing. Effects of beta-blockers. In: Clifford Rose F, ed. Advances in headache research. London: John Libbey, 1987. p 155-160.
9. International Headache Society. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988;8(Suppl 7):1-96.
10. Holmes G. The symptoms of acute cerebellar injuries due to gunshot injuries. Brain 1917;40:461-535.
11. Day BL, Thompson PD, Harding AE, Marsden CD. Influence of vision on upper limb reaching movements in patients with cerebellar ataxia. Brain 1998;121:357-372.
12. Manto M, Godaux E, Jacquy J. Detection of silent cerebellar lesions by increasing the inertial load of the moving hand. Ann Neurol 1995;37:344-350.
13. Ghez C. The control of movements. In: Kandel ER, Schwartz JH, Jessel TM, eds. Principles of neural science. London: Prentice Hall International; 1991. p 533-547.
14. Flament D, Hore J. Movement and electromyographic disorders associated with cerebellar dysmetria. J Neurophysiol 1986; 55:1221-1233.
15. Wray SH, Mijovic-Prelec D, Kosslyn SM. Visual processing in migraineurs. Brain 1995;118:25-35.
16. Silberstein SD, Lipton RB, Breslau N. Migraine: association with personality characteristics and psychopathology. Cephalalgia 1995;15:358-369.
17. Mulder EJCM, Linssen WHJP, Passchier J, et al. Interictal and postictal cognitive changes in migraine. Cephalalgia 1999;19: 557-565.
18. Baloh RW. Neurootology of migraine. Headache 1997;37:615-621.
19. Gervil M, Ulrich V, Kaprio J, et al. The relative role of genetic and environmental factors in migraine without aura. Neurology 1999;53:995-999.
20. Ulrich V, Gervil M, Kyvik KO, et al. Evidence of a genetic factor in migraine with aura: a population-based Danish twin study. Ann Neural 1999;45:242-246.