Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management
MB Russell, A Ducros - The Lancet Neurology, 2011 - thelancet.com
Hemiplegic migraine is a rare form of migraine with aura that involves motor aura
(weakness). This type of migraine can occur as a sporadic or a familial disorder. Familial …
(weakness). This type of migraine can occur as a sporadic or a familial disorder. Familial …
Na+, K+-ATPase: Functions in the nervous system and involvement in neurologic disease
EE Benarroch - Neurology, 2011 - AAN Enterprises
The adenosine triphosphatases (ATPases) are integral membrane proteins that actively
exchange ions across cell membranes; the energy required for this process is derived from …
exchange ions across cell membranes; the energy required for this process is derived from …
Studies on the pathophysiology and genetic basis of migraine
CF Gasparini, HG Sutherland, LR Griffiths - Current genomics, 2013 - ingentaconnect.com
Migraine is a neurological disorder that affects the central nervous system causing painful
attacks of headache. A genetic vulnerability and exposure to environmental triggers can …
attacks of headache. A genetic vulnerability and exposure to environmental triggers can …
ATP1A2 mutations in migraine: seeing through the facets of an ion pump onto the neurobiology of disease
T Friedrich, NN Tavraz, C Junghans - Frontiers in physiology, 2016 - frontiersin.org
Mutations in four genes have been identified in familial hemiplegic migraine (FHM), from
which CACNA1A (FHM type 1) and SCN1A (FHM type 3) code for neuronal voltage-gated …
which CACNA1A (FHM type 1) and SCN1A (FHM type 3) code for neuronal voltage-gated …
[HTML][HTML] Epilepsy in patients with familial hemiplegic migraine
BRH Bayır, K Tutkavul, M Eser, B Baykan - Seizure, 2021 - Elsevier
Objective: The coexistence of epilepsy in familial hemiplegic migraine (FHM) has not been
reviewed systematically. We investigated the associations of epilepsy in patients with FHM …
reviewed systematically. We investigated the associations of epilepsy in patients with FHM …
[HTML][HTML] Migraine and epilepsy—shared mechanisms within the family of episodic disorders
MA Rogawski - 2012 - europepmc.org
Migraine and epilepsy are episodic disorders that share many clinical features and
underlying pathophysiological mechanisms. Cortical spreading depression (CSD), a wave …
underlying pathophysiological mechanisms. Cortical spreading depression (CSD), a wave …
Epilepsy in hemiplegic migraine: genetic mutations and clinical implications
P Prontera, P Sarchielli, S Caproni, C Bedetti… - …, 2018 - journals.sagepub.com
Objective We performed a systematic review on the comorbidities of familial/sporadic
hemiplegic migraine (F/SHM) with seizure/epilepsy in patients with CACNA1A, ATP1A2 or …
hemiplegic migraine (F/SHM) with seizure/epilepsy in patients with CACNA1A, ATP1A2 or …
Migraine-and dystonia-related disease-mutations of Na+/K+-ATPases: relevance of behavioral studies in mice to disease symptoms and neurological manifestations …
P Bøttger, C Doğanlı, K Lykke-Hartmann - Neuroscience & Biobehavioral …, 2012 - Elsevier
The two autosomal dominantly inherited neurological diseases: familial hemiplegic migraine
type 2 (FHM2) and familial rapid-onset of dystonia-parkinsonism (Familial RDP) are caused …
type 2 (FHM2) and familial rapid-onset of dystonia-parkinsonism (Familial RDP) are caused …
The borderland of migraine and epilepsy in children
T Rajapakse, J Buchhalter - … : The Journal of Head and Face …, 2016 - Wiley Online Library
Objective To provide a review on the spectrum of migraine‐epilepsy disorders in children.
Background The migraine‐epilepsy continuum covers a fascinating array of disorders that …
Background The migraine‐epilepsy continuum covers a fascinating array of disorders that …
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation
N Pelzer, DE Blom, AH Stam, LS Vijfhuizen… - …, 2017 - journals.sagepub.com
Background Familial hemiplegic migraine (FHM) is a rare monogenic migraine subtype
characterised by attacks associated with transient motor weakness. Clinical information is …
characterised by attacks associated with transient motor weakness. Clinical information is …