Results 61 to 70 of about 54,391 (157)
ICTAL AND INTERICTAL EEG ABNORMALITIES IN 100 MIGRAINEURS WITH AND WITHOUT AURA [PDF]
Acta Medica Iranica, 2007 There are several conflicting reports about the EEG of the migraineurs. In this study we report the ictal and interictal EEGs of 100 migraineurs, in comparison with control group.
H. Pourmahmoodian +4 more
doaj +1 more source
‘What's in a Name?’ Naming Genetically Determined Movement Disorders: Gap and Controversy
Movement Disorders, Volume 41, Issue 2, Page 342-350, February 2026.Abstract In 2016, the International Parkinson and Movement Disorder Society (MDS) Task Force for Genetic Nomenclature in Movement Disorders laid out a new proposal for naming genetically determined movement disorders. This proposal sought to address the difficulties arising from the practical usage of numbered loci (eg, DYT1, DYT2, DYT3, etc.) as names
Connie Marras +19 more
wiley +1 more source
Exploring the Hereditary Nature of Migraine
Neuropsychiatric Disease and Treatment, 2021 Charlene Bron, Heidi G Sutherland, Lyn R Griffiths Queensland University of Technology (QUT), Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland,
Bron C, Sutherland HG, Griffiths LR
doaj
Pediatric Neurology Briefs, 2004 A family with a stereotyped unilateral or bilateral transient visual loss, that recurred many times daily and was associated with childhood epilepsy and familial hemiplegic migraine, is reported from University Hospitals, Geneva, Switzerland.
J Gordon Millichap
doaj +1 more source
Familial Hemiplegic Migraine and Spreading Depression [PDF]
, 2014 How to Cite This Article: Kazemi H, Speckmann EJ, Gorji A. Familial Hemiplegic Migraine and Spreading Depression. Iran J Child Neurol. 2014 Summer;8(3): 6-11.
SPECKMANN, Erwin Josef +2 more
core +1 more source
Moyamoya Disease Masquerading as Hemiplegic Migraine in a Child: A Case Report from India
The Journal of Pediatric AcademyMoyamoya disease (MMD) is a chronic progressive steno-occlusive disease of the intracranial arterial vessels and their branches characterized by puff smoke appearance on angiography.
Kunal Kumar, Deepak Kumar, S. B. Mathur
doaj +1 more source
Advances in genetics of migraine
The Journal of Headache and Pain, 2019 Background Migraine is a complex neurovascular disorder with a strong genetic component. There are rare monogenic forms of migraine, as well as more common polygenic forms; research into the genes involved in both types has provided insights into the ...
Heidi G. Sutherland +2 more
doaj +1 more source
Migraine and patent foramen ovale: correlation, coexistence, dependence. A narrative review
Headache: The Journal of Head and Face Pain, Volume 66, Issue 1, Page 307-321, January 2026.Plain Language Summary This review looked at what scientists know about the connection between migraine and a small heart opening called a patent foramen ovale (PFO). It showed that people with migraine, especially with aura, often have PFO, but it is not certain whether closing this heart opening helps prevent strokes in these patients.
Olga Grodzka +5 more
wiley +1 more source
Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations
Pediatric Neurology Briefs, 2009 Two novel SCN1A mutations are identified in two unrelated families with familial hemiplegic migraine and a unique phenotype of elicited repetitive daily blindness, in a report from Hopital Lariboisiere, and other centers in Paris, France, and Geneva ...
J Gordon Millichap
doaj +1 more source
Journal of Paediatrics and Child Health, Volume 62, Issue 6, Page 1060-1065, June 2026.
Briana Davis +3 more
wiley +1 more source