Results 81 to 90 of about 234,110 (135)

Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report. [PDF]

Medicine (Baltimore), 2021
Luan H, Zhang L, Zhang S, Zhang M.
europepmc   +1 more source

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2. [PDF]

J Headache Pain, 2021
Antonaci F, Ravaglia S, Grieco GS, Gagliardi S, Cereda C, Costa A.   +5 more
europepmc   +1 more source

Involvement of kainate glutamate receptors in the modulation of neuronal transmission in brain areas involved in migraine pathophysiology [PDF]

, 2009
Migraine pathophysiology is thought to involve activation of the trigeminal fibres which innervate dural structures. The nociceptive inflow from the meninges is relayed to the trigeminocervical complex (TCC), before ascending to higher brain areas ...
Andreou, A.
core  

Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.

, 2010
Familial hemiplegic migraine (FHM) is a clinically and genetically heterogeneous disease most commonly linked to CACNA1A gene mutation. Epilepsy rarely occurs in FHM and is seen predominantly with specific CACNA1A gene mutations.
Sperling, Michael R, Asadi-Pooya, Ali A, Ashkenazi, Avi, Zangaladze, Andro   +3 more
core   +1 more source

Ca_V2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury. [PDF]

Elife, 2022
Terpolilli NA, Dolp R, Waehner K, Schwarzmaier SM, Rumbler E, Todorov B, Ferrari MD, van den Maagdenberg AMJM, Plesnila N.   +8 more
europepmc   +1 more source

Responsivity to light in familial hemiplegic migraine type 1 mutant mice reveals frequency-dependent enhancement of visual network excitability. [PDF]

Eur J Neurosci, 2021
Perenboom MJL, Schenke M, Ferrari MD, Terwindt GM, van den Maagdenberg AMJM, Tolner EA.   +5 more
europepmc   +1 more source

Deciphering in silico the Role of Mutated Na _V 1.1 Sodium Channels in Enhancing Trigeminal Nociception in Familial Hemiplegic Migraine Type 3. [PDF]

Front Cell Neurosci, 2021
Suleimanova A, Talanov M, van den Maagdenberg AMJM, Giniatullin R.   +3 more
europepmc   +1 more source

Familial Syndrome of Hemiplegic Migraine and Nystagmus: Chromosomal Defect Localization and Ocular Motility Characteristics

, 1994
Familial hemiplegic migraine (FHM) is an autosomal dominant disorder characterized by transient hemiplegia during the aura phase of a migraine attack. This disease has recently been mapped to chromosome 19 in two families. Prominent gaze-evoked nystagmus
Michael A. Elliott, MD; S.J. Peroutka, MD, PhD; S. Welsh, MD, PhD; E. May, MD
core  

Genetics of Familial Hemiplegic Migraine: state of the art

, 2000
At present, very few is known on the genetics of common Migraines, most likely to be considered a multifactorial disease. Recently, the CACNA1A gene encoding the brain-specific P/Q type calcium channel alpha 1 subunit, has been cloned and mutations in ...
CARRERA, P., BATTISTINI, S.
core   +1 more source

Familial hemiplegic migraine, epilepsy, and a suspicion of intracranial hypertension in a patient with a positive family history. [PDF]

Arch Med Sci
Grodzka O, Chądzyński P, Makulec A, Domitrz I.   +3 more
europepmc   +1 more source