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Abstract:

Keywords:	A3243G mutation ABPM acrodermatitis chronica atrophicans acute ischemic neurological event adhesion molecules ageing aging Alzheimer's disease amino acids amyotrophic lateral sclerosis angiogenesis antibodies anti‐ganglioside antibody anti‐GM1 antibodies antihypertensive therapy arterial hypertension arterio‐jugular venous difference of oxygen artery‐to‐artery embolism astheno‐emotional disorder astrocyte atrial fibrillation atrial natriuretic peptide atrio‐ventricular block auditory brainstem response autonomic function blood pressure Borrelia Boston questionnaire brain dysplasia brain natriuretic peptide brain tumor branched‐chain amino acid therapy calcium carbon disulfide cardiac arrhythmias caregivers carpal tunnel syndrome cataract central nervous system involvement cerebral circulation cerebral embolism cerebral infarction cerebrospinal fluid cerebrovascular reactivity cholesterol chronic chronic acquired hepatocerebral degeneration clinical characteristics clinical severity scale cognition cold pressor test Commission Report compound muscle action potentials computerized tomography scan congenital muscular dystrophy coping corpus callosum cranial nerves CSF dementia dentatorubral‐pallidoluysian atrophy (DRPLA) diabetes mellitus diagnosis of epilepsy diffusion‐weighted MRI dopamine agonist Doppler dosing double discharges dystonia early diagnosis eclampsia EEG reporting electrodiagnosis electroencephalography ELISA embolism enoxaparin epidemiology epilepsy epilepsy surgery epileptic seizures essential tremor estrogen receptor 1 European Guidelines excitatory and inhibitory amino acids fasciculation potentials flow cytometry fukutin gene Fukuyama disease gene glycemic control GM1 ganglioside GT1a Guillain–Barré syndrome head tremor head‐up tilt health‐related quality of life hepatocyte growth factor hereditary spastic paraplegia high‐sensitive C‐reactive protein human human herpes virus 6 Huntington's disease hypercoagulability hyperexcitability hypothermia IgG immunosupressive therapy inflammation interferon‐β 1a interleukin‐12 ischaemic stroke jugular venous oxygen saturation lactic acidosis and stroke‐like episodes Leber's hereditary optic neuropathy (LHON) lipoproteins long‐term follow‐up low‐dose low‐molecular‐weight heparin Lyme disease lymphocyte subsets lysophosphatidylcholine magnetic resonance imaging magnetoencephalography MELAS memory methodology middle cerebral artery middle‐latency response mild cognitive impairment mitochondrial DNA mitochondrial encephalomyopathy mitoxantrone motoneuron motor nerve conduction velocity multifocal motor neuropathy multimodality MRI multiple multiple sclerosis muscle force myasthenia gravis with hyperthyroidism neuroborreliosis neurofibroma neurofibromatosis neurofibromin neurological symptoms neuropathy neuropsychological effects neuropsychology normal pressure hydrocephalus olanzapine oligodendroglioma outcome organic psychiatric disorders outcome painful neuropathy parkinsonism Parkinson's disease partial‐onset patient satisfaction PCDD peripheral nerve pharyngeal cervical‐brachial variant phosphatidylcholine plasma polychlorinated dioxins polymerase chain reaction polymorphism prevalence progressive supranuclear palsy resource utilization Riluzole ropinirole secondary hyperparathyroidism seizure serum severe subarachnoid hemorrhage shunt surgery siblings simultanagnosia single photon emission computed tomography skeletal muscle slow cortical potential small sodium valproate somatosensory‐evoked potential sPECAM‐1 spinocerebellar ataxia type 6 spinocerebellar degeneration sPLA2 stenosis stroke subarachnoid hemorrhage sudden unexpected death associated with epilepsy surgery surgical decompression synaptosome syndrome TCDD TGF‐β1 therapeutics thromboprophylaxis thyroid gland tick‐borne encephalitis topiramate transcranial transcranial Doppler transforming growth factor‐β1 treatment treatment outcome tumour supressor gene ultrasonography visual recovery white matter damage

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