Results 41 to 50 of about 6,570 (214)

Pseudotumor Cerebri After L-Thyroxine Therapy

open access: yesPediatric Neurology Briefs, 1997
Pseudotumor cerebri in an infant treated with L-thyroxine for transient neonatal hypothyroidism is reported from the Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY.
J Gordon Millichap
doaj   +1 more source

Inflammation in Idiopathic Intracranial Hypertension: An Immunometabolic Mechanistic Framework and Clinical Implications

open access: yesCNS Neuroscience &Therapeutics, Volume 32, Issue 3, March 2026.
Systemic metabolic dysfunction and comorbidities may act as upstream modulators converging on inflammatory activation, which is closely intertwined with excessive CSF production and impaired clearance, potentially contributing to sustained ICP elevation.
Guangyu Han   +5 more
wiley   +1 more source

Pseudotumor Cerebri Complicating Measles

open access: yesPediatric Neurology Briefs, 2006
A novel case of pseudotumor cerebri (PTC) that presented in an 8-year-old girl 3 weeks after measles is reported from Ondokuz Mayis University, Samsun, Turkey.
J Gordon Millichap
doaj   +1 more source

Surgical outcome of benign intracranial hypertension in terms of improvement in vision [PDF]

open access: yes, 2016
To know about surgical outcome of benign intracranial hypertension in terms of improvement of vision.METHODOLOGY ; This Prospective observational study was conducted at of 22 patients operated in neurosurgery unit lady reading hospital Peshawar from Jan ...
hassan, Naseer   +3 more
core   +1 more source

Surgical Interventions in Idiopathic Intracranial Hypertension—A Comprehensive Multi‐Center Study of Outcome and the Role of Treatment Indication

open access: yesEuropean Journal of Neurology, Volume 33, Issue 3, March 2026.
In this multicenter retrospective study of idiopathic intracranial hypertension, only 3.6% of patients required surgery, predominantly for acute visual deterioration. Both cerebrospinal fluid diversion and optic nerve sheath fenestration were effective in improving visual outcomes and resolving papilledema, while headache improvement was limited ...
Gabriel Bsteh   +24 more
wiley   +1 more source

Stiff Neck, Torticollis, and Pseudotumor Cerebri

open access: yesPediatric Neurology Briefs, 2002
Three prepubertal children diagnosed with pseudotumor cerebri and presenting with stiff neck and torticollis are reported from Schneider Children’s Medical Center, Sackler School of Medicine, Tel Aviv, Israel.
J Gordon Millichap
doaj   +1 more source

Idiopathic Intracranial Hypertension—Clinical Characteristics, Neuroimaging and Outcome of Patients from Pretoria, South Africa

open access: yesNeurology and Clinical Neuroscience, Volume 14, Issue 1, Page 46-53, January 2026.
ABSTRACT Background Idiopathic intracranial hypertension is a syndrome characterized by symptoms and signs of raised intracranial pressure without a secondary cause. It primarily affects young obese women who present with headache and papilledema. We report the clinical presentation, brain imaging findings and outcomes of patients with IIH from two ...
Bandlakazi Sukwana‐Ncemane   +2 more
wiley   +1 more source

Symptoms and Etiologies of Pseudotumor Cerebri

open access: yesPediatric Neurology Briefs, 2014
Investigators from Ankara Pediatrics, Turkey, evaluate the clinical symptoms and etiology in records of 53 patients (32 female) diagnosed with pseudotumor cerebri (PTC) in a child neurology department between 2005 and 2012.
J Gordon Millichap, John J Millichap
doaj   +1 more source

Is idiopathic intracranial hypertension without papilledema a risk factor for migraine progression?

open access: yes, 2010
The association of chronic migraine (CM) with an idiopathic intracranial hypertension without papilledema (IIHWOP), although much more prevalent than expected in clinical series of CM sufferers, is not included among the risk factors for migraine ...
Bilo L   +4 more
core   +1 more source

An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]

open access: yes, 2016
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F.   +5 more
core   +2 more sources

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