نتایج جستجو برای: hemiplegic migraine

تعداد نتایج: 14930  

Journal: :Neuroscience letters 2016
Sandra Vilotti Natascha Vana Arn M J M Van den Maagdenberg Andrea Nistri

Migraine is a neurovascular brain disorder suggested to be due to dysfunction of the trigeminovascular system with sensitization of trigeminal ganglion (TG) nociceptors. Since the neuropeptide calcitonin gene-related peptide (CGRP) has been established as a key player in the pathogenesis of migraine, CGRP receptor antagonists have been considered useful compounds to block headache originating f...

Journal: :Cephalalgia : an international journal of headache 2010
F Michael Cutrer Paul Mathew

In this issue of Cephalalgia, Dr Jakob Moller Hansen and his colleagues report a series of very interesting experiments in which they successfully induced migraine-like attacks in patients with migraine with aura via infusion of calcitonin gene related peptide (CGRP). This work echoes similar experiments carried out by the Copenhagen group using the nitric oxide donor, glycerol trinitrate (GTN)...

Journal: :The Proceedings of the Nutrition Society 1983
J A Monro

There is a long history associating food allergy with migraine which has been reviewed recently (Monro, 1982). In all, seventeen studies were reported involving investigations on over 1236 patients. The diagnostic methods used to define allergy were mainly elimination diets and challenge and skin tests. Two specific cases, however, are worth emphasizing. Goltman (1936) reported the case of a wo...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Masashi Suzuki Wim Van Paesschen Ingeborg Stalmans Shoko Horita Hideomi Yamada Bruno A Bergmans Eric Legius Florence Riant Peter De Jonghe Yuehong Li Takashi Sekine Takashi Igarashi Ichiro Fujimoto Katsuhiko Mikoshiba Mitsunobu Shimadzu Masaaki Shiohara Nancy Braverman Lihadh Al-Gazali Toshiro Fujita George Seki

Homozygous mutations in SLC4A4, encoding the electrogenic Na(+)-HCO(3)(-) cotransporter NBCe1, have been known to cause proximal renal tubular acidosis (pRTA) and ocular abnormalities. In this study, we report two sisters with pRTA, ocular abnormalities, and hemiplegic migraine. Genetic analysis ruled out pathological mutations in the known genes for familial hemiplegic migraine, but identified...

Journal: :Arquivos de neuro-psiquiatria 2009
Reinaldo Teixeira Ribeiro Mariana Machado Pereira Pinto Thaís Rodrigues Villa Luana Tesser Gamba Célia Harumi Tengan Deusvenir de Souza-Carvalho

Dr. Deusvenir de Souza-Carvalho – Rua Pedro de Toledo 980 / 33 04039-002 São Paulo SP Brasil. E-mail: [email protected] According to the second edition of the International Classification of Headache Disorders (ICHD-II), migrainous infarction (MI) is a complication of migraine with aura. MI is diagnosed when one or more aura symptoms last longer than 60 minutes, and neuroradiological stud...

Journal: :The Lancet. Neurology 2002
Anne Ducros Elisabeth Tournier-Lasserve Marie-Germaine Bousser

The search for genes involved in the pathophysiology of migraine poses major difficulties. First, there is no objective diagnostic method to assess the status of the individuals studied. Second, migraine is a polygenic multifactorial disorder. Familial hemiplegic migraine (FHM) is the only known autosomal dominant subtype of migraine. In half the families with FHM who have been studied, there a...

Journal: :Pain 2015
Else A Tolner Thijs Houben Gisela M Terwindt Boukje de Vries Michel D Ferrari Arn M J M van den Maagdenberg

Migraine is a common multifactorial episodic brain disorder with strong genetic basis. Monogenic subtypes include rare familial hemiplegic migraine, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, familial advanced sleep-phase syndrome (FASPS), and retinal vasculopathy with cerebral leukodystrophy. Functional studies of disease-causing mutations in ce...

Journal: :Neurology 2005
J P Dreier K Jurkat-Rott G C Petzold O Tomkins R Klingebiel U A Kopp F Lehmann-Horn A Friedman M Dichgans

The authors report a patient with familial hemiplegic migraine type II who developed a long-lasting attack including fever, right-sided hemiplegia, aphasia, and coma. Quantitative analysis of early gadolinium-enhanced MRI revealed a mild but significant left-hemispheric blood-brain barrier (BBB) opening limited to the cortex and preceding cortical edema. The findings suggest that the delayed co...

2016
Dildar Konukoglu Eda Merve Kurtulus

Migraine is a common neurological disorder. It is characterized by recurrent attacks of pulsatile headaches. Data achieved through familial hemiplegic migraine suggest that; mutations in channel proteins can lead dysregulation of calcium and sodium levels and hyperexcitability in nervous system. Even though, genetic tendencies can be responsible for migraine, accumulating data show that many me...

2005
Mari Kaunisto Maija Wessman

 8 ABSTRACT Migraine with aura (MA) is a common headache disorder with a population prevalence of approximately 5%. This subtype of migraine is characterized by neurological, typically visual, symptoms that precede the headache. Twin and family studies have provided strong evidence of genetic factors in MA susceptibility and have shown that the mode ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید