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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 1 |
2008 | 1 |
2012 | 1 |
2019 | 1 |
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Familial hemiplegic migraine type 1 shows no hypersensitivity to nitric oxide.
Cephalalgia. 2008 May;28(5):496-505. doi: 10.1111/j.1468-2982.2008.01559.x. Epub 2008 Mar 31.
Cephalalgia. 2008.
PMID: 18384418
Clinical Trial.
Familial hemiplegic migraine type 1 (FHM-1) is a dominantly inherited subtype of migraine with aura and transient hemiplegia associated with mutations in the CACNA1A gene. ...
Familial hemiplegic migraine type 1 (FHM-1) is a dominantly inherited subtype of migraine with aura and t …
Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children.
Asghar SJ, Milesi-Hallé A, Kaushik C, Glasier C, Sharp GB.
Asghar SJ, et al.
Pediatr Neurol. 2012 Sep;47(3):201-4. doi: 10.1016/j.pediatrneurol.2012.05.006.
Pediatr Neurol. 2012.
PMID: 22883286
Genetic testing demonstrated variable results: one child manifested a CACNA1A mutation compatible with familial hemiplegic migraine type 1, whereas another demonstrated an ATP1A2 sequence alteration. No known mutations were evident in the third …
Genetic testing demonstrated variable results: one child manifested a CACNA1A mutation compatible with familial hemiplegic …
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Basal astrocyte and microglia activation in the central nervous system of Familial Hemiplegic Migraine Type I mice.
Magni G, Boccazzi M, Bodini A, Abbracchio MP, van den Maagdenberg AM, Ceruti S.
Magni G, et al.
Cephalalgia. 2019 Dec;39(14):1809-1817. doi: 10.1177/0333102419861710. Epub 2019 Jul 1.
Cephalalgia. 2019.
PMID: 31260335
Free article.
BACKGROUND: Gain-of-function missense mutations in the alpha(1A) subunit of neuronal Ca(V)2.1 channels, which define Familial Hemiplegic Migraine Type 1 (FHM1), result in enhanced cortical glutamatergic transmission and a higher susceptibility t …
BACKGROUND: Gain-of-function missense mutations in the alpha(1A) subunit of neuronal Ca(V)2.1 channels, which define Familial Hemi …
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Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report.
Luan H, Zhang L, Zhang S, Zhang M.
Luan H, et al.
Medicine (Baltimore). 2021 Dec 23;100(51):e28141. doi: 10.1097/MD.0000000000028141.
Medicine (Baltimore). 2021.
PMID: 34941060
Free PMC article.
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Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C.
Cricchi F, et al.
J Neurol Sci. 2007 Mar 15;254(1-2):69-71. doi: 10.1016/j.jns.2007.01.008. Epub 2007 Feb 12.
J Neurol Sci. 2007.
PMID: 17292920
Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca( …
Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2 …
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