Showing 271-280 of 1354 results for "".
Decreasing Door-to-Reperfusion Time
https://practicalneurology.com/diseases-diagnoses/stroke/decreasing-door-to-reperfusion-time/30392/Steps taken at Foothills Medical Centre to improve stroke care.Dementia Insights:
Short- and Long-Term Cognitive Consequences of Acute Non-Neurological Hospitalizationhttps://practicalneurology.com/diseases-diagnoses/alzheimer-disease-dementias/dementia-insights-brshort--and-long-term-cognitive-consequences-of-acute-non-neurological-hospitalization/30786/Most neurologists are not surprised to hear that a patient has cognitively or physically deteriorated after hospitalization, but what is the evidence and mechanism for this?Genetic Testing & Neuromuscular Disorders
https://practicalneurology.com/diseases-diagnoses/neuromuscular/genetic-testing-neuromuscular-disorders/31920/The cost of genetic testing has decreased significantly, and the results are priceless.Etiology and Treatment of Urogenital Dysfunction in Individuals with Parkinson Disease
https://practicalneurology.com/diseases-diagnoses/movement-disorders/etiology-and-treatment-of-urogenital-dysfunction-in-individuals-with-parkinson-disease/37653/Urogenital dysfunction is a common nonmotor symptom observed in people with Parkinson disease which can negatively impact quality of life, necessitating careful investigation and prompt treatment.Quantitative Structural MRI for Neurocognitive Disorders
https://practicalneurology.com/diseases-diagnoses/alzheimer-disease-dementias/quantitative-structural-mri-for-neurocognitive-disorders/31730/Alzheimer disease dementia, frontotemporal dementia, and traumatic brain injury can be differentiated with quantitative MRI.Inherited Neuropathies: Giant Axonal Neuropathy, Charcot-Marie-Tooth Disease, and Hereditary Transthyretin Amyloidosis
https://practicalneurology.com/diseases-diagnoses/neuromuscular/inherited-neuropathies-giant-axonal-neuropathy-charcot-marie-tooth-disease-and-hereditary-transthyretin-amyloidosis/32026/A review of 3 of the most common causes of inherited neuropathies, with a focus on pathogenesis, presentation, diagnosis, and management for each disease.Stroke Snapshot: Platelet Function Testing in Ischemic Stroke and Transient Ischemic Attack
https://practicalneurology.com/diseases-diagnoses/stroke/stroke-snapshot-platelet-function-testing-in-ischemic-stroke-and-transient-ischemic-attack/32146/Platelet function testing allows antiplatelet regimens to be tailored more effectively for individuals with ischemic stroke or TIA, and an understanding of antiplatelet pharmacokinetics is essential to its implementation.Management of Poststroke Epilepsy: An Update
https://practicalneurology.com/diseases-diagnoses/epilepsy-seizures/management-of-poststroke-epilepsy-an-update/32188/Poststroke seizure management is a clinical and research priority to improve prognosis.Neuromuscular Amyloidosis
https://practicalneurology.com/diseases-diagnoses/neuromuscular/neuromuscular-amyloidosis/31815/The most common amyloidosis are both treatable; accurate diagnosis is paramount.Therapeutic Approaches to Neuromuscular Repeat Disorders: Facioscapulohumeral Muscular Dystrophy and Myotonic Dystrophy Type 1
https://practicalneurology.com/diseases-diagnoses/neuromuscular/therapeutic-approaches-to-neuromuscular-repeat-disorders-facioscapulohumeral-muscular-dystrophy-and-myotonic-dystrophy-type-1/32027/A promising pipeline of therapeutics target toxic RNA.