31 results on '"Familial hemiplegic migraine"'
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2. Chronic pregabalin treatment protects against spreading depolarization and alters hippocampal synaptic characteristics in a model of familial hemiplegic migraine-type 1
3. Genetics of migraine: where are we now?
4. Hemiplegic Migraine
5. Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms
6. Large-Scale Mass Spectrometry Imaging Investigation of Consequences of Cortical Spreading Depression in a Transgenic Mouse Model of Migraine
7. Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models
8. Ionenkanalerkrankungen des Gehirns – monogene Migräneformen
9. Headache and Epilepsy
10. Familial and Sporadic Hemiplegic Migraine: Diagnosis and Treatment
11. Perfusion-weighted MR imaging in persistent hemiplegic migraine
12. Identification of molecular genetic factors that influence migraine
13. Génétique de la migraine
14. Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
15. The S218L familial hemiplegic migraine mutation promotes deinhibition of Cav2.1 calcium channels during direct G-protein regulation
16. Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family
17. Migraine as a sex-conditioned inherited disorder: evidences from China and the world
18. Genetische Grundlagen der Migräne
19. Migraine-related vertigo: Diagnosis and treatment
20. Genetik der Migräne
21. The physiopathology of migraine: the contribution of genetics
22. A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
23. Is the CACNA1A gene involved in familial migraine with aura?
24. Calcium channels — basic aspects of their structure, function and gene encoding; anesthetic action on the channels — a review
25. The genetics of migraine
26. Symposia lectures
27. Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice
28. Die Genetik der Migräne
29. Meeting report: 10th international mouse genome conference
30. Mapping of the human Ca2+ channel β4 subunit to 2q22-23 and its expression in developing mouse
31. Mutation watch
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