Results 51 to 60 of about 4,697 (184)

Cognitive Impairment in Patients with Pseudotumor Cerebri Syndrome

open access: yesBehavioural Neurology, 2011
Introduction: Patients with Pseudotumor Cerebri Syndrome (PTCS) may complain of difficulty in thinking or concentrating; however there has been little formal cognitive evaluation in this population.
Siddharth Kharkar   +6 more
doaj   +1 more source

Elucidating the Molecular Landscape of Cystic Kidney Disease: Old Friends, New Friends and Some Surprises

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 6, June 2025.
ABSTRACT Cystic kidney diseases (CyKD) are a diverse group of disorders affecting more than 1 in 1000 individuals. Over 120 genes are implicated, primarily encoding components of the primary cilium, transcription factors, and morphogens. Prognosis varies greatly by molecular diagnosis. Causal variants are not identified in 10%–60% of individuals due to
Deborah Watson   +10 more
wiley   +1 more source

Pseudotumor Cerebri and Sickle Cell Disease

open access: yesPediatric Neurology Briefs, 2004
Three children, all girls, ages 9, 8, and 16 years, with sickle cell disease (SCD) presented with headache and were diagnosed with pseudotumor cerebri (PC) at the Children’s National Medical Center, Washington, DC.
J Gordon Millichap
doaj   +1 more source

Idiopathic Intracranial Hypertension in Pregnancy. A Systematic Review on Clinical Course, Treatments, Delivery and Maternal‐Fetal Outcome

open access: yesEuropean Journal of Neurology, Volume 32, Issue 5, May 2025.
ABSTRACT Background Idiopathic intracranial hypertension (IIH) during pregnancy presents significant challenges due to the physiological gestational changes, which can exacerbate its symptoms. Methods We conducted a systematic review on studies reporting maternal‐fetal outcomes of IIH during pregnancy, selecting 49 papers reporting on clinical course ...
Matteo Palermo   +3 more
wiley   +1 more source

Miller Fisher Syndrome Presenting as Pseudotumor

open access: yesPediatric Neurology Briefs, 2002
Two female children, ages 9 and 2 years, who presented with pseudotumor cerebri and within 2 to 3 days, were diagnosed with Miller Fisher syndrome are reported from the Hopital Universitaire des Enfants Reine Fabiola, Brussels, Belgium.
J Gordon Millichap
doaj   +1 more source

The association of early passive mobilization with intracranial pressure in the adult intensive care unit: A prospective, cohort study

open access: yesNursing in Critical Care, Volume 30, Issue 3, May 2025.
Abstract Background Early mobilization are key components of the ABCDEF Care Bundle and critical treatments to reduce acquired muscle weakness, delirium and prolonged intensive care unit (ICU) stay. Aim This study aimed to determine whether routine early mobilization related to intracranial pressure in intensive care patients on mechanical ventilation,
Ahmet Oğuzhan Küçük   +4 more
wiley   +1 more source

Efficacy of Tirzepatide Dual GIP/GLP‐1 Receptor Agonist in Patients With Idiopathic Intracranial Hypertension. A Real‐World Propensity Score‐Matched Study

open access: yesEndocrinology, Diabetes &Metabolism, Volume 8, Issue 2, March 2025.
Tirzepatide in Idiopathic Intracranial Hypertension (IIH) Management. ABSTRACT Introduction Idiopathic intracranial hypertension (IIH) is a neurological disorder characterised by elevated intracranial pressure (ICP), predominantly affecting obese women of reproductive age.
Ahmed Y. Azzam   +16 more
wiley   +1 more source

Incidence Rates of Pediatric Pseudotumor Cerebri

open access: yesPediatric Neurology Briefs, 1997
Twenty nine cases of pseudotumor cerebri were identified in a retrospective study of records of 205,765 children aged 2-15 years presenting between 1979 and 1994 at the IWK Grace Health Centre, Dalhousie University, Halifax, Canada.
J Gordon Millichap
doaj   +1 more source

Unusual Presentation of Classical Galactosemia: A Case Report of Iranian Experience

open access: yesClinical Case Reports, Volume 13, Issue 2, February 2025.
ABSTRACT Galactosemia is a rare autosomal recessive metabolic disorder with four main types, and classic galactosemia is the most prevalent. These patients have galactose‐1‐phosphate‐uridyltransferase deficiency. We report on a case of an infant who was admitted with poor feeding, lethargy, and poor weight gain.
Mohammadreza Alaee   +4 more
wiley   +1 more source

A Presentation of Lyme Disease: Pseudotumor Cerebri

open access: yesThe Turkish Journal of Pediatrics, 2015
Lyme disease is caused by a tick-transmitted spirochete, B. burgdorferi. It can present with both central and peripheral nervous system manifestations, including aseptic meningitis, meningoencephalitis, Bell's palsy and other cranial neuropathies,
Burcu Şahin   +4 more
doaj  

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