Results 11 to 20 of about 234,110 (135)

Sporadic Hemiplegic Migraine: A Separate Entity

Pediatric Neurology Briefs, 2003
The clinical characteristics of 105 patients with sporadic hemiplegic migraine (SHM) were compared with those of patients with migraine with typical aura (MA) and patients with familial hemiplegic migraine (FHM) in a study at the Danish Headache Center ...
J Gordon Millichap
doaj   +2 more sources

The genetic relationship between epilepsy and hemiplegic migraine

Neuropsychiatric Disease and Treatment, 2017
Yiqing Huang,1 Hai Xiao,1 Xingyue Qin,1 Yuan Nong,1 Donghua Zou,2 Yuan Wu3 1Department of Neurology, Guigang City People’s Hospital and the Eighth Affiliated Hospital of Guangxi Medical University, Guigang, People’s Republic of China ...
Huang Y, Xiao H, Qin X, Nong Y, Zou D, Wu Y   +5 more
doaj   +1 more source

Sporadic Hemiplegic Migraine with Seizures and Transient MRI Abnormalities

Case Reports in Neurological Medicine, 2011
Hemiplegic migraines are characterised by attacks of migraine with aura accompanied by transient motor weakness. There are both familial and sporadic subtypes, which are now recognised as separate entities by the International Classification of Headache ...
Harsha Bhatia, Fawzi Babtain
doaj   +2 more sources

Anàlisi genètica i funcional de la migranya hemiplègica i la migranya comuna [PDF]

, 2011
[cat] Aquesta tesi es centra en la genètica de la migranya. La migranya comuna és un trastorn neurològic caracteritzat per episodis recurrents de mal de cap.
Carreño, Oriel
core   +6 more sources

Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy [PDF]

Brain Sciences, 2020
Floriana D'Onofrio, Luigi Vetri, Francesca Operto   +2 more
exaly   +2 more sources

Mouse Models of Familial Hemiplegic Migraine for Studying Migraine Pathophysiology [PDF]

Current Neuropharmacology, 2019
Anisa Dehghani, Hulya Karatas
exaly   +2 more sources

Clinical characterization of a novel ATP1A2 p.Gly615Glu mutation in nine family members with familial hemiplegic migraine. [PDF]

Brain Commun
Familial hemiplegic migraine type 2 results from pathogenic variants in the ATP1A2 gene, which encodes for a catalytic subunit of sodium/potassium ATPase.
Romozzi M, Spartano S, L'Erario FF, Iannone LF, Trigila V, Gentile A, Sanginario P, Calabresi P, Tiziano FD, Vollono C.   +9 more
europepmc   +2 more sources

Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis [PDF]

, 1999
Familial hemiplegic migraine is a rare autosomal dominant disorder associated with stereotypic neurologic au ra phenomena including hemiparesis, So far two chromosomal loci have been identified. Families linked to the chromosome 19 locus display missense
Spranger, S., Benninger, C., Schwab, S., Spranger, Matthias, Dichgans, Martin   +4 more
core   +1 more source

P/Q-type calcium-channel blockade in the periaqueductal gray facilitates trigeminal nociception: a functional genetic link for migraine? [PDF]

, 2002
The discovery of mis-sense mutations in the alpha1A subunit of the P/Q-type calcium channel in patients with familial hemiplegic migraine indicates the potential involvement of dysfunctional ion channels in migraine.
Goadsby, PJ, Yolande E. Knight, Knight, Yolande E., Knight, YE, Goadsby, Peter J., Bartsch, Thorsten, Peter J. Goadsby, Kaube, Holger, Holger Kaube, Kaube, H, Thorsten Bartsch, Bartsch, T   +11 more
core   +1 more source

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine

Frontiers in Molecular Neuroscience, 2022
Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes, CACNA1A, SCN1A, and ATP1A2, have been implicated. However, more than 80% of referred diagnostic cases of hemiplegic migraine (HM) are negative for exonic ...
Neven Maksemous, Claire D. Blayney, Heidi G. Sutherland, Robert A. Smith, Rod A. Lea, Kim Ngan Tran, Omar Ibrahim, Jeffrey R. McArthur, Larisa M. Haupt, M. Zameel Cader, Rocio K. Finol-Urdaneta, David J. Adams, Lyn R. Griffiths   +12 more
doaj   +1 more source