… of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine -
M Hans, S Luvisetto, ME Williams, M Spagnolo, A … - J Neurosci, 1999 - Soc Neuroscience
... Pagnutti, S. Luvisetto, J. Striessnig, C. Fletcher, and D. Pietrobon Familial
hemiplegic migraine mutations increase ... Chem., March 1, 2002; 277(9): 6960 - 6966. ...
Familial Hemiplegic Migraine Mutations Change a1A Ca2+ Channel Kinetics -
RL Kraus, MJ Sinnegger, H Glossmann, S Hering, J … - Journal of Biological Chemistry, 1998 - ASBMB
... J Biol Chem, Vol. 273, Issue 10, 5586-5590, March 6, 1998. Familial Hemiplegic
Migraine Mutations Change 1A Ca 2+ Channel Kinetics *. ...
Prevalence of Migraine and Cluster Headache in Swedish Men of 18 -
K Ekbom, B Ahlborg, R Schele - Headache: The Journal of Head and Face Pain, 1978 - Blackwell Synergy
... number of neurological diseases was recorded in a random sample of 6960 residents ...
which have caused loss of time from work or school?" A "migraine-like syndrome ...
Familial hemiplegic migraine mutations increase Ca2+ influx through single human CaV2. 1 channels … -
A Tottene, T Fellin, S Pagnutti, S Luvisetto, J … - Proceedings of the National Academy of Sciences, 2002 - National Acad Sciences
... Physiology Familial hemiplegic migraine mutations increase Ca 2+ influx through
single human Ca V 2.1 channels and decrease maximal Ca V 2.1 current density in ...
The molecular genetics of migraine -
M Wessman, M Kaunisto, M Kallela, A Palotie - Annals of Medicine, 2004 - ingentaconnect.com
Page 1. The molecular genetics of migraine Maija Wessman 1 ... The best been
described in these common forms of migraine. The best genetic ...
… Channels Produced by Mutation S218L Causing Familial Hemiplegic Migraine and Delayed Cerebral Edema … -
A Tottene, F Pivotto, T Fellin, T Cesetti, AMJM … - Journal of Biological Chemistry, 2005 - ASBMB
... Specific Kinetic Alterations of Human Ca V 2.1 Calcium Channels Produced by Mutation
S218L Causing Familial Hemiplegic Migraine and Delayed Cerebral Edema and ...
Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Cav2. 1 Ca2+ Channel … -
C Mullner, LAM Broos, AMJM van den Maagdenberg, J … - Journal of Biological Chemistry, 2004 - ASBMB
... protein receptor; EA2, episodic ataxia type 2; FHM1, familial hemiplegic migraine
type 1 ... 277, 6960?6966 [Abstract/Free Full Text]; Jen, J., Wan, J., Graves, M ...
Maternal severe migraine and risk of congenital limb deficiencies
F Banhidy, N Acs, E Horv?th-Puh?, AE Czeizel - Birth Defects Research (Part A): Clinical and Molecular …, 2006 - doi.wiley.com
... and Malformed Control Groups with or without Migraine and Other Headaches at Anytime
during ... 17,3 41 47.0 25?2 9 194 34.3 6960 31.2 264 37.0 12,6 21 33.7 6 ...
Neurological diseases: Neurobiology of migraine
R Rizzuto, T Pozzan - Nature Genetics, 2003 - nature.com
... nervous system are associated with a few rare human diseases: X-linked congenital
stationary night blindness, familial hemiplegic migraine (FHM), episodic ...
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Triptans in migraine. A review of side effects, improvement and recurrence -
A Pino, A Vaccaro, GS Mela - The Pain Clinic, 2004 - Springer
... Review Triptans in migraine. A review of side effects, ... summary Key words: Triptans;
5-HT1B/1D receptors agonists; headache treatment; migraine. ...
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