Results 131 to 140 of about 34,604,755 (154)

Contractures of the Hands As a Prenatal Phenotype of CACNA1A-Related Disorder. [PDF]

Prenat Diagn
Menzies L, Gibbs A, Ashraf T, Beesley C, Roberts R, Chandler NJ.   +5 more
europepmc   +1 more source

Migraine triggers, phases, and classification using machine learning models. [PDF]

Front Neurol
Reddy A, Reddy A.
europepmc   +1 more source

Genotype and Age at Onset Drive Vermis Atrophy in CACNA1A- and GAA-FGF14-related Ataxias. [PDF]

Cerebellum
Indelicato E, Nachbauer W, Amprosi M, Pellerin D, Mangesius S, Gizewski ER, Kiechl S, Brais B, Boesch S, Krismer F, Alzheimer’s Disease Neuroimaging Initiative.   +10 more
europepmc   +1 more source

Familial Hemiplegic Migraine (FHM) with Transient Psychotic Symptoms: A Case Report and Literature Review. [PDF]

Turk Psikiyatri Derg
Öz T, Gürel ŞC.
europepmc   +1 more source

Trigger factors for familial hemiplegic migraine

Cephalalgia, 2011
The aim was to identify and describe migraine trigger factors in patients with familial hemiplegic migraine (FHM) from a population-based ...
Jes Olesen, Jakob Møller Hansen, Messoud Ashina   +2 more
exaly   +2 more sources

Transcranial Doppler Sonography in Familial Hemiplegic Migraine

Cephalalgia, 1991
A patient affected by familial hemiplegic migraine underwent Transcranial Doppler Sonography twice: the first during a spontaneous attack with right hemiparesis and aphasia, the second during a headache-free period.
Flavia Pauri, Letizia Maria Cupini, Francesco Pierelli   +2 more
exaly   +2 more sources

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

Lancet, The, 2005
BACKGROUND: Familial hemiplegic migraine is an autosomal dominant severe subtype of migraine with aura characterised by some degree of hemiparesis during the attacks.
Michel D Ferrari, Martin Dichgans, Michael Pusch   +2 more
exaly   +2 more sources

Familial Hemiplegic Migraine Type 1 Shows no Hypersensitivity to Nitric Oxide

Cephalalgia, 2008
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.
Jes Olesen, Jakob Møller Hansen, Messoud Ashina   +2 more
exaly   +2 more sources

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Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy

Brain and Development, 2020
Rika Kosaki, Kenjiro Kosaki, Sato Suzuki-Muromoto   +2 more
exaly  

Is Familial Hemiplegic Migraine a Hereditary form of Basilar Migraine?

Cephalalgia, 1995
Michel D Ferrari, Gisela Terwindt, R R Frants   +2 more
exaly