Results 71 to 80 of about 34,604,755 (154)

Clinical Prediction of Posttreatment Migraine Recurrence Using Biofeedback Data: A Machine Learning Framework for Enhanced Patient Stratification and Treatment Monitoring

BioMed Research International, Volume 2026, Issue 1, 2026.
Migraine is a complex neurological disorder with significant implications for individual well‐being and public health. Predicting migraine occurrences after treatment is crucial for evaluating therapeutic efficacy and enabling personalized care, yet remains largely underexplored.
Shibbir Ahmed Arif, Ferdib-Al-Islam, Mehidy Hasan Sium, Baisakhi Banerjee   +3 more
wiley   +1 more source

Huntington's Disease‐like Syndrome as a Rare Presentation of CACNA1A‐Related Disorder

Movement Disorders Clinical Practice, Volume 13, Issue 5, Page 1322-1325, May 2026.
Petros Boumis, Constantin Potagas, Christos Koros, Vasilios Constantinides, Nikolaos Ragazos, Chrysoula Koniari, Stavroula Aristeidou, Chrisoula Kartanou, Emmanouela Linardaki, Nektarios Tavernarakis, Evangelos Anagnostou, Leonidas Stefanis, Socratis Papageorgiou, Georgia Karadima, Georgios Koutsis   +14 more
wiley   +1 more source

Functional Characterization and Pathogenicity Classification of PRRT2 Splice Variants in PRRT2‐Related Disorders

Annals of Clinical and Translational Neurology, Volume 12, Issue 12, Page 2558-2568, December 2025.
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu, Yu‐Lan Chen, Wan‐Bing Sun, Hong‐Fu Li, Zhi‐Ying Wu, Dian‐Fu Chen   +5 more
wiley   +1 more source

Self-reported muscle pain in adolescents with migraine and tension-type headache [PDF]

, 2012
Aim: To identify possible associations between muscular pain and headache in adolescents in a large population-based sample. Methods: Grammar school students were invited to fill in a questionnaire on headache and associated lifestyle factors.
Straube, Andreas, Schankin, Christoph, Kries, Rüdiger von, Heinen, Florian, Jahn, Klaus, Reiter, Karl, Blaschek, Astrid, Langhagen, Thyra, Milde-Busch, Astrid, Schröder, Sebastian Andreas   +9 more
core   +1 more source

Familial hemiplegic migraine: a ion channel disorder

, 2001
At present, little information is available 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 ...
FERRARI, M., CARRERA, P., STENIRRI, S., BATTISTINI, S.   +3 more
core   +1 more source

Biochemical characterization of sporadic/familial hemiplegic migraine mutations [PDF]

, 2014
Contains fulltext : 133904.pdf (Publisher’s version ) (Open Access)Sporadic hemiplegic migraine type 2 (SHM2) and familial hemiplegic migraine type 2 (FHM2) are rare forms of hemiplegic migraine caused by mutations in the Na(+),K ...
Koenderink, J.B., Koenderink, Jan B., Weigand, K.M., Weigand, Karl M., Russel, F.G., Russel, Frans G.M., Swarts, Herman G.P., Swarts, H.G.P.   +7 more
core   +2 more sources

Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis:A Case Report

, 2015
Familial hemiplegic migraine (FHM) is a rare autosomal dominant form of migraine with motor aura. We present a case report of a father and son with very similar attacks of hemiplegic migraine and recurrent episodes of accompanying psychoses.
Baandrup, Lone, Bendtsen, Lars, van den Maagdenberg, Arn M J M, Bendtsen, L., LaBianca, S., Maagdenberg, A.M.J.M. van den, Baandrup, L., Jensen, Rigmor, LaBianca, Sonja, Jensen, R.   +9 more
core   +1 more source

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

Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L

, 2017
Background Familial hemiplegic migraine type 3 is a monogenic subtype of migraine caused by missense mutations in the neuronal voltage-gated sodium channel gene SCN1A, with 10 different mutations reported so far.
Eva Auffenberg, Victoria Schubert, Tobias Freilinger, Saskia Biskup, Karin Jurkat-Rott   +4 more
core   +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