Results 41 to 50 of about 3,232,639 (308)
Neurology of endocrine disease [PDF]
Clinical Medicine, 2010 #### Key Points Endocrine disorders are common and have a wide range of neurological presentations and potential complications Diabetes is a common cause of painful third and sixth nerve palsies, with good recovery over 3–6 months Diabetic lumbosacral radiculoplexus neuropathy ...
John Winer, Mike Douglas
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Genetically engineered pig models of neurological diseases
, 2022 Genetically modified animal models are commonly used for in vivo studies of human diseases. Mice are the most common animal models used in biomedical research, which have provided important insights into disease pathogenesis and are widely used to find ...
Li, Jun +4 more
core
肌萎缩侧索硬化医疗质量控制指标 Medical Quality Control Indicators for Amyotrophic Lateral Sclerosis
Zhongguo cuzhong zazhi国家神经系统疾病医疗质量控制中心于2022年设立了运动神经元病（motor neuron disease，MND）质控专病组，启动了肌萎缩侧索硬化（amyotrophic lateral sclerosis，ALS）/MND医疗质量控制体系建设。通过系统调研循证医学证据和国内外指南，MND质控专病组利用德尔菲法制定了ALS医疗质量控制指标体系，从统一诊断标准，建立患者全面管理概念，规范治疗方案等方面系统完善ALS的住院诊疗质量控制过程。该ALS医疗质量控制指标体系共15个指标 ...
The Motor Neuron Disease Working Group of National Center for Healthcare Quality Management in Neurological Diseases
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Deep-learning tool for early identification of non-traumatic intracranial hemorrhage etiology and application in clinical diagnostics based on computed tomography (CT) scans [PDF]
PeerJBackground To develop an artificial intelligence system that can accurately identify acute non-traumatic intracranial hemorrhage (ICH) etiology (aneurysms, hypertensive hemorrhage, arteriovenous malformation (AVM), Moyamoya disease (MMD), cavernous ...
Meng Zhao +16 more
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Autoantibody-mediated neurological diseases [PDF]
, 2020 Autoimmune neurological diseases are an expanding group of phenotypically characteristic, potentially treatable syndromes. A number of these conditions are mediated by autoantibodies.
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Genome-edited rabbit, a prospective alternative model for neurological diseases
, 2022 Animal models have great importance in the research of human neurodegenerative diseases due to their value in symptom mimicking, mechanism investigation, and preclinical tests.
Song, Yuning +3 more
core
Frontiers in Neurology, 2021 Mutations in the ATP1A3 gene encoding the α3 subunit of Na+/K+-ATPase are associated with different neurological manifestations that may be elicited by febrile episodes.
Raffaella Pisapia +4 more
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Neurologic Wilson's disease [PDF]
Annals of the New York Academy of Sciences, 2010 Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains a commonly misdiagnosed import disease. Mutations in ATP7B result in abnormal copper metabolism and subsequent toxic accumulation of copper.
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Pediatric Blood &Cancer, EarlyView.ABSTRACT Rates of cancer among adolescents and young adults (AYA), age 15–39 years, are increasing. Consequently, radiation oncologists are treating more AYAs who have diagnoses spanning both pediatric and adult practices. Compared to pediatric and older adult patients, AYAs face a unique set of challenges.
Hesham Elhalawani +7 more
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Multicystic Cerebral Hydatid Cyst: Uncommon Presentation of A Rare Disease
Nepal Journal of Neuroscience, 2016 Hydatid cyst is a common zoonosis, affecting the liver and lungs in the endemic areas. Occasionally it involves the brain. We present a rare case of multicystic cerebral Hydatid cyst present over a long time in an adult patient with some odd radiological
Sil Kaushik +3 more
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