Results 111 to 120 of about 182,556 (397)

Congenital heart disease does not entail an increased risk for severe COVID‐19

open access: yesActa Paediatrica, Volume 112, Issue 2, Page 286-289, February 2023., 2023
Abstract Aim To analyse the risk of developing serious disease or death due to COVID‐19 among patients who underwent heart surgery during childhood. Methods A retrospective combined register and patient file study. We identified all individuals who had undergone surgery for congenital heart disease in childhood between 1994 and 2019 in our Local ...
Britt‐Marie Ekman‐Joelsson   +1 more
wiley   +1 more source

Design of a sustainable pre-polarizing magnetic resonance imaging system for infant hydrocephalus [PDF]

open access: yesarXiv, 2018
The need for affordable and appropriate medical technologies for developing countries continue to rise as challenges such as inadequate energy supply, limited technical expertise and poor infrastructure persists. Low-field MRI is a technology that can be tailored to meet specific imaging needs within such countries.
arxiv  

MR diffusion changes in the perimeter of the lateral ventricles demonstrate periventricular injury in post-hemorrhagic hydrocephalus of prematurity [PDF]

open access: yes, 2019
OBJECTIVES: Injury to the preterm lateral ventricular perimeter (LVP), which contains the neural stem cells responsible for brain development, may contribute to the neurological sequelae of intraventricular hemorrhage (IVH) and post-hemorrhagic ...
Alexopoulos, Dimitrios   +10 more
core   +1 more source

Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment [PDF]

open access: yes, 2004
BACKGROUND: Thirty-nine patients have been described with deletions involving chromosome 6p25. However, relatively few of these deletions have had molecular characterization.
A Plaja   +45 more
core   +3 more sources

Decreased homovanillic acid and 5‐hydroxyindoleacetic acid levels in the cerebrospinal fluid of patients with Dravet syndrome with parkinsonism

open access: yesEpilepsia Open, EarlyView.
Abstract Dravet syndrome (DS) is an early onset, developmental, and epileptic encephalopathy characterized by drug‐resistant seizures and multiple comorbidities. It has been reported that in adulthood, it may be accompanied by parkinsonism, but the pathogenesis of this condition remains unclear.
Ryo Sugiyama   +5 more
wiley   +1 more source

Automated Segmentation of CT Scans for Normal Pressure Hydrocephalus [PDF]

open access: yesarXiv, 2019
Normal Pressure Hydrocephalus (NPH) is one of the few reversible forms of dementia, Due to their low cost and versatility, Computed Tomography (CT) scans have long been used as an aid to help diagnose intracerebral anomalies such as NPH. However, no well-defined and effective protocol currently exists for the analysis of CT scan-based ventricular ...
arxiv  

Cryptococcal infection of the ventriculoperitoneal shunt in an immunocompetent patient [PDF]

open access: yes, 2016
Patient: Male, 52 Final Diagnosis: Cryptococcal ventriculoperitoneal shunt infection Symptoms: Confusion • fever • Lethargy Medication: Amphotericin B • Flucytosine Clinical Procedure: Ventriculoperitoneal shunt removal Specialty: Infectious disease ...
Foong, Kap Sum   +2 more
core   +2 more sources

Treated hydrocephalus in individuals with myelomeningocele in the National Spina Bifida Patient Registry.

open access: yesJournal of Neurosurgery: Pediatrics, 2018
OBJECTIVEAlthough the majority of patients with myelomeningocele have hydrocephalus, reported rates of hydrocephalus treatment vary widely. The purpose of this study was to determine the rate of surgical treatment for hydrocephalus in patients with ...
Irene Kim   +12 more
semanticscholar   +1 more source

The Genetic Basis of Hydrocephalus.

open access: yesAnnual Review of Neuroscience, 2016
Studies of syndromic hydrocephalus have led to the identification of >100 causative genes. Even though this work has illuminated numerous pathways associated with hydrocephalus, it has also highlighted the fact that the genetics underlying this phenotype
M. Kousi, N. Katsanis
semanticscholar   +1 more source

SUMMARY [PDF]

open access: yes
Objectives: Severe post-hemorrhaghic internal hydrocephalus with almost complete atrophy of the cerebral parenchyma, as in the following case, is rare.
Internal Hydrocephalus
core  

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