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photophobia/illamående

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An item response theory based integrated model of headache, nausea, photophobia, and phonophobia in migraine patients.

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This study developed an integrated model of severity scores of migraine headache and the incidence of nausea, photophobia, and phonophobia to predict the natural time course of migraine symptoms, which are likely to occur by a common disease progression mechanism. Data were acquired from two phase 3

Tryptophan depletion increases nausea, headache and photophobia in migraine sufferers.

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Sensitivity to light was investigated 5 and 8 h after consumption of an amino acid drink which contained L-tryptophan (balanced amino acid condition: 19 controls and 22 migraine sufferers) or which produced a short-term reduction in brain serotonin synthesis by omitting L-tryptophan (tryptophan

Case 28-2014: A man with a rash, headache, fever, nausea, and photophobia.

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Case 28-2014: A man with a rash, headache, fever, nausea, and photophobia.

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Case 28-2014: A man with a rash, headache, fever, nausea, and photophobia.

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Transdermal sumatriptan for acute treatment of migraineurs with baseline nausea.

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OBJECTIVE To evaluate the efficacy and safety of transdermal sumatriptan in migraine patients who have baseline nausea. BACKGROUND Migraine-associated nausea and vomiting can limit the effectiveness of acute treatment with oral agents by causing delays, avoidance, or incomplete absorption of
The aim of this study was to determine whether scalp tenderness and photophobia, two well-recognized symptoms of migraine, develop during the motion sickness induced by optokinetic stimulation. To investigate whether motion sickness has a general influence on pain perception, pain was also assessed
OBJECTIVE To determine whether baseline nausea or prior triptan treatment for migraine impact the effectiveness of diclofenac potassium for oral solution in treating acute migraine. BACKGROUND A great deal of variability exists in patients' response to migraine medications. Migraine-associated

Clinical Predictors for Migraine in Patients Presenting With Nausea and/or Vomiting.

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OBJECTIVE Many migraine patients develop nausea and/or vomiting (N/V) and are referred to gastroenterologists. This can lead to an inappropriate treatment and a delay of the correct diagnosis. We therefore aimed to identify predictors for migraine in patients presenting with N/V as well as
Migraine attacks are typically described as unilateral, throbbing pain that is usually accompanied by nausea, vomiting, and exaggerated sensitivities to light, noise and smell. The headache phase of a migraine attack is mediated by activation of the trigeminovascular pathway; a nociceptive pathway

The use of questions to determine the presence of photophobia and phonophobia during migraine.

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OBJECTIVE To investigate whether the use of more detailed close-ended questions as part of the routine headache history is helpful when patients initially deny that they are sensitive to light and noise during migraine headaches. BACKGROUND According to the International Headache Society 2004
A migraine is a disabling neurovascular disorder characterized by a unilateral throbbing headache that lasts from 4 to 72 h. The headache is often accompanied by nausea, vomiting, phonophobia and photophobia, and may be worsened by physical exercise. The trigeminovascular system (TVS) is speculated

Analysis of dopamine beta hydroxylase gene polymorphisms in migraine.

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BACKGROUND Migraine is a complex neurological disorder characterized by severe recurrent headache, nausea, vomiting, photophobia, and phonophobia. The frequency and duration of these symptoms varies among individuals. Dopaminergic systems are believed to be involved in migraine pathophysiology. We

Randomized, controlled trial of telcagepant over four migraine attacks.

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METHODS This study evaluated the calcitonin gene-related peptide (CGRP) receptor antagonist telcagepant (tablet formulation) for treatment of a migraine attack and across four attacks. Adults with migraine were randomized, double-blind, to telcagepant 140 mg, telcagepant 280 mg, or control treatment
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