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Page 1 from 1077 results
A juvenile case of cerebellar arteriovenous malformation (AVM) with gradual onset of headache and ataxia.
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An 11-year-old male was admitted because of frequent vomiting and truncal ataxia which had lasted for over one week. He had clear consciousness but slowly-progressive mild headache and ataxic gait. Cranial CT revealed a 4 cm hematoma in the right cerebellar hemisphere. Angiography showed a 2 x 2 cm
A novel CACNA1A mutation results in episodic ataxia with migrainous features without headache.
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BACKGROUND
The mechanisms subtending migrainous features, like sensoriphobia, remain poorly understood even though recent works have shed new light on their mechanisms.
METHODS
A 24-year-old woman consulted the headache clinic because of frequent paroxysmal attacks of strong sensoriphobia, digestive
Ataxia and Headache in a Child: A Case of Acute Cerebellar Infarction.
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A 4-year-old female patient presents to the pediatric emergency department with acute onset of ataxia and occipital headache. Initial investigation, including computed tomography imaging, failed to demonstrate any focal neurologic lesion. Subsequent studies, however, reveal an acute thrombosis of
Ataxia and migraine-like headache in a girl with a cerebellar developmental venous anomaly.
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Cerebral developmental venous anomalies (DVAs) are generally considered as anatomical variants of the venous system without clinical importance. We report the case of a 15-year-old girl with recurrent episodes of migraine-like headache who presented with subacute vertigo and ataxia associated with
Flunarizine in prevention of headache, ataxia, and memory deficits during decompression to 4559 m.
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Our purpose was to study the preventive effect of the calcium channel blocker flunarizine on headache, postural ataxia, and memory deficits occurring during decompression to high altitude in a randomized, placebo-controlled, double-blind study. After 7-day pretreatment with the study drugs, 20
A novel amyloidogenic transthyretin variant, Gly53Ala, associated with intermittent headaches and ataxia.
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We report a novel transthyretin variant, Gly53Ala, in a 44-year-old British woman who presented with severe episodic headaches, often with focal neurological deficit, before developing progressive ataxia, depression, dementia and eventually peripheral neuropathy. Transthyretin amyloidosis was
A 3-year-old girl with headaches and ataxia.
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A case of intermittent ataxia associated with migraine headaches.
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Severe headache, dysarthria and ataxia in a 62-year-old man.
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Clinical cases in neurology from Johns Hopkins--case 3: 44-year-old man with fever, headache, confusion, and ataxia.
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Case of the month: August 1998 - 45 year old man with headache and ataxia.
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Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 38-1996. An 18-year-old man with severe headache, pleocytosis, and ataxia.
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Primary Angiitis of the Central Nervous System Presenting With Headache and Ataxia.
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Clinical Reasoning: An adolescent female presenting with worsening vertigo, headache, and ataxia
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A 52-year-old woman with headache, ataxia and loss of consciousness.
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