Results 31 to 40 of about 736,081 (211)

Evolving Evidence in Idiopathic Intracranial Hypertension

open access: yesLife, 2021
Idiopathic intracranial hypertension (IIH) is an enigmatic disorder characterized by raised intracranial pressure (ICP) with no known cause and it affects both children and adults [...]
Susan P. Mollan   +2 more
doaj   +1 more source

Overdiagnosis of idiopathic intracranial hypertension [PDF]

open access: yesNeurology, 2016
To delineate the factors contributing to overdiagnosis of idiopathic intracranial hypertension (IIH) among patients seen in one neuro-ophthalmology service at a tertiary center.We retrospectively reviewed new patients referred with a working diagnosis of IIH over 8 months.
Adeniyi, Fisayo   +3 more
openaire   +4 more sources

Recurrent reflex syncope in idiopathic intracranial hypertension patient resolved after lumbar puncture: pathogenetic implications

open access: yesBMC Neurology, 2023
Background Idiopathic intracranial hypertension is a disease characterized by increased intracranial cerebrospinal fluid volume and pressure without evidence of other intracranial pathology.
Roberto De Simone   +9 more
doaj   +1 more source

Rapid Recovery of Visual Acuity after Lumboperitoneal Shunt Operation in Malignant Idiopathic Intracranial Hypertension

open access: yesCase Reports in Ophthalmological Medicine, 2011
Background. Idiopathic intracranial hypertension can cause rapid deterioration of visual acuity in some severe cases, and these cases are usually thought to have “malignant” form of this disease. Case.
Levent Sinan Bir   +4 more
doaj   +1 more source

When Pediatric Headaches Are Not Benign—Eye Findings

open access: yesChildren, 2023
Headache is the most common neurologic complaint that presents to the pediatrician. While most headaches are benign in nature, patients must be carefully evaluated to rule out life- or vision-threatening causes.
Sam Karimaghaei, Brita S. Rook
doaj   +1 more source

Dural Arteriovenous Fistulas Presenting as Idiopathic Intracranial Hypertension

open access: yes, 2022
Dural arteriovenous fistula (dAVF) and idiopathic intracranial hypertension (IIH) may present similarly.
Roma N. Ahuja; Menachem Weiss; Martha Schatz
core  

Uncommon Presentation of Idiopathic Intracranial Hypertension in a Patient with Polycystic Ovary Syndrome: A Case Report

open access: yesCase Reports in Neurology, 2017
Introduction: Idiopathic intracranial hypertension is a rare condition characterized by increased intracranial pressure without clinical, laboratory, or radiological evidence of intracranial pathology. Early management could prevent irreversible outcomes.
Anas Mohammad Albarrak, Suleiman Kojan
doaj   +1 more source

CSF Cytokine Network Organization Predicts Progression Independent of Relapse and MRI Activity in Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Progression independent of relapse activity is a major determinant of long‐term disability in multiple sclerosis, but its immunopathologic basis remains incompletely understood. We investigated whether relapse‐independent progression in radiologically stable relapsing–remitting multiple sclerosis is associated with distinct ...
Antonio Bruno   +19 more
wiley   +1 more source

Randomised Trial Determining Acute Effects on Intracranial Pressure of Drugs Utilised in Idiopathic Intracranial Hypertension

open access: yes, 2022
Limited data exists to guide treatment of idiopathic intracranial hypertension (IIH). We examined the ability of drugs used in IIH to lower intracranial pressure (ICP)
Alex Sinclair; James Mitchell; Susan Mollan; Andreas Yiangou; Hannah Lyons; George Tsermoulas; Kristian Brock
core  

Pathophysiology of Idiopathic Intracranial Hypertension

open access: yesPediatric Neurology Briefs, 2012
Investigators at Emory University, Atlanta, GA review the epidemiology, pathophysiology and management of idiopathic intracranial hypertension (IIH), sometimes called pseudotumor cerebri or benign intracranial hypertension, terms now considered ...
J Gordon Millichap
doaj   +1 more source

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