neuritis/headache

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Cluster headache-like headache, Hageman trait deficiency, retrobulbar neuritis, and giant aneurysm. Autonomic function studies.

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A 56-year-old, previously reported woman with cluster headache-like headache with bouts of unilateral (the side of predominance changing through the years) severe headache had a familial history (three generations) of partial Hageman factor deficiency and bleeding episodes. A giant aneurysm was

Prodromal headache in MOG-antibody positive optic neuritis.

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Myelin oligodendrocyte glycoprotein antibody (MOG-Ab) disease is an inflammatory autoimmune condition of the central nervous system, defined by antibodies (Abs) against MOG. Of the various clinical phenotypes optic neuritis (ON) is the commonest. We have observed that some patients

[Role of the vascular component in the pathogenesis of headaches in neurotic patients].

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The authors studied the volume velocity of extracranial blood flow by an original method of venous occlusional cranial pletysmography in 40 individuals with headaches of stress and in 30 examinees without headaches in conditions of calmness and in stress influences (cold test, terminal

Prolotherapy for headache. Pain in the head and neck, and neuritis.

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[Neurotic character of outpatients with headache at the pain clinic. A study by Cornell Medical Index].

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Radiology case of the month. Unilateral vision loss with ipsilateral eye and head pain. Optic neuritis.

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[Cerebral nerves and headache-on the evaluation of trigeminal and facial neuralgia, neuritis etc].

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[Diagnostic clues for giant cell arteritis: beyond headache and ischemic optic neuritis].

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A new headache syndrome? Headache resembling cluster headache (Horton's headache), with recurring bouts of homolateral retrobulbar neuritis, partial factor XII deficiency, bleeding tendency and a heterolateral convulsive episode.

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[Headache as neurotic somatization].

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[Headache caused by supraorbital neuritis].

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Treating neurotic headache by point-injection with Novocain.

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Cause and mechanism of headache, pain and neuritis.

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[Orbital inflammatory pseudotumor with optic neuritis in Behçet's disease].

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OBJECTIVE To report an atypical case of orbital inflammatory pseudotumor associated with optic neuritis revealing Behçet's disease. METHODS A 37-year-old man was worked up for headache and progressive decreased bilateral visual acuity most profound in the left eye. Initial ophthalmologic exam was

[Isolated neuritis of the oculomotor nerve in infectious mononucleosis].

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A 19-year-old immune-competent patient developed right-sided headache and, subsequently, subacute diplopia. On clinical examination he had incomplete right oculomotor palsy. Cranial MRI showed pathologic contrast enhancement of the right oculomotor nerve at its exit point from the mesencephalon, and

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