Home › Research › Topics › hydrocephalus
hydrocephalus
73 studies tagged hydrocephalus, dated 1968-06-01 to 2026-09-01. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Five Decades of Infusion Testing in Idiopathic Normal Pressure Hydrocephalus: A Biomarker in Search of a Gold Standard 2026-09-01
- Reduced Dementia Incidence Following Neck Dissection: A Population-based Matched Cohort Study 2026-08-31
- Effectiveness of Modern Diagnostic and Therapeutic Interventions for Major Neurological Disorders: A Systematic Literature Review 2026-08-12
Studies
73 studies carry this tag.
Date range
1968 to 2026
Top journals
- Neurology 7
- Brain : a journal of neurology 5
- Journal of neurosurgery 5
- Archives of Neurology 3
- Research Square 3
45 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
-
The accuracy of the clinical diagnosis of corticobasal degeneration (CBD) is unknown.
-
Many cases of central nervous system (CNS) Whipple's disease are not diagnosed until postmortem.
-
The cause of progressive supranuclear palsy (PSP) is not known and has been little studied.
-
To review the evidence for risk factors of Creutzfeldt-Jakob disease (CJD), we pooled and reanalyzed the raw data of three case-control studies.
-
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human transmissible spongiform encephalopathies (prion diseases) are proposed for the following disease entities: CJD--sporadic, iatrogenic (recognised risk) or familial (same disease in 1st degree relative): spongiform encephalopathy in cerebral and/or cerebellar cortex and/or subcortical grey matter; or encephalopathy with prion protein (PrP) immunoreactivity (plaque and/or diffuse synaptic and/or patchy/perivacuolar types).
-
There have been 87 cases of superficial siderosis of the CNS reported in the world literature and 63 cases had developed the clinical syndrome with sufficient details to be reviewed.
-
Gait was improved in 25 (72%) of the 35 patients, whereas the Bartel index remained unchanged.
-
The dominantly inherited ataxias comprise a series of clinical phenotypes that include ataxia, dysarthria, dysmetria, and intention tremor resulting from the involvement of the cerebellum and its afferent and efferent pathways.
-
We present the preliminary neuropathologic criteria for progressive supranuclear palsy (PSP) as proposed at a workshop held at the National Institutes of Health, Bethesda, MD, April 24 and 25, 1993.
-
Hereditary dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurologic disorder characterized by variable combinations of myoclonus, epilepsy, cerebellar ataxia, choreoathetosis and dementia.
-
There appears to be a new syndrome in this family that is characterized by recurrent subcortical strokelike episodes, leukoencephalopathy, immunologic anomalies, muscular lipidosis, and an autosomal dominant pattern of transmission.
-
The authors blindly reviewed the charts of 20 patients with normal-pressure hydrocephalus (a disease of unknown cause characterized radiologically as chronic communicating hydrocephalus and clinically by gait apraxia, dementia, and incontinence) who had undergone creation of a ventriculoperitoneal shunt.
-
Quinolinic acid is an "excitotoxic" metabolite and an agonist of N-methyl-D-aspartate receptors.
-
The coexistence of cerebrovascular disease leading to deep white matter infarction and normal-pressure hydrocephalus has been noted previously in clinical studies, as both diseases can present with the triad of gait disturbance, dementia, and incontinence.
-
Section I: Pathophysiology of Stroke. Epidemiology of Stroke.
-
In order to define the histopathological substrate of the dementia that frequently complicates the acquired immune deficiency syndrome (AIDS), we analyzed the neuropathological findings in 70 autopsied adult AIDS patients, 46 of whom had suffered clinically overt dementia.
-
We conducted virus-isolation studies on 56 specimens from the nervous system of 45 patients in order to determine whether human T-cell lymphotropic virus Type III (HTLV-III) is directly involved in the pathogenesis of the neurologic disorders frequently encountered in the acquired immunodeficiency syndrome (AIDS) and the AIDS-related complex.
-
Twenty-three elderly patients were found to have a consistent pattern of leukoencephalopathy by computed tomography and nuclear magnetic resonance imaging.
-
In most cell types intermediate or 10-mm filaments (IF) are a major cytoskeletal organization and, thus, directly or indirectly influence the structural appearance of the cytoplasm.
-
Conductance to outflow of CSF was measured in a prospective study of 80 patients with normal pressure hydrocephalus.
-
The cases of six patients are presented to delineate the clinical profile of delayed radiation necrosis of the brain.
-
✓ Thirty-eight cases of colloid cyst of the third ventricle are reviewed.
-
36/100
CONSIDERABLE interest has been focused on the entity of progressive external ophthalmoplegia (PEO) since the report of Kiloh and Nevin in 1951.1These authors were primarily concerned with the pathogenesis of the ocular muscle weakness, concluding that it was virtually always the result of a myopathic process.
From across this tag
10 of the 73 studies in this tag, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 10. The same 10 appear here every time.
- Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype
- Global, regional, and national burden of neurological disorders, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016
- Steroid-responsive encephalopathy with a peculiar CSF biomarker profile in an 89-year-old man
- Five Decades of Infusion Testing in Idiopathic Normal Pressure Hydrocephalus: A Biomarker in Search of a Gold Standard
- Rhabdomyolysis Secondary to Reactivated Herpes Simplex Virus Type 1 Coinfected with Klebsiella pneumoniae in an Elderly Patient: A Case Report
- Susac syndrome: challenges in the diagnosis and treatment
- Guidelines for management of idiopathic normal pressure hydrocephalus: second edition
- Juvenile neuronal ceroid lipofuscinosis (Batten disease): current insights
- A new enzyme-linked immunosorbent assay for neurofilament light in cerebrospinal fluid: analytical validation and clinical evaluation
- Does corticobasal degeneration exist? A clinicopathological re-evaluation