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Using an expanded algorithm to estimate prevalence of amyotrophic lateral sclerosis in U.S. and UK
Using an expanded algorithm to estimate prevalence of amyotrophic lateral sclerosis in U.S. and UK
There is an increasing need to better understand the burden of amyotrophic lateral sclerosis (ALS) using real-world data (...
A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS
A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a maternally inherited multis...
Marchiafava-Bignami disease: why not Marchiafava-Bignami-Carducci disease?
Marchiafava-Bignami disease: why not Marchiafava-Bignami-Carducci disease?
The Marchiafava-Bignami disease has a curious backstory, namely, the publication in 1898 of the Contribution to the Study ...
Effects of different modalities of transcranial magnetic stimulation on post-stroke cognitive impairment: a network meta-analysis
Effects of different modalities of transcranial magnetic stimulation on post-stroke cognitive impairment: a network meta-analysis
The study aimed to evaluate, using a network meta-analysis, the effects of different transcranial magnetic stimulation (TM...
Cognitive assessment during the phases of a spontaneous migraine: a prospective cohort study
Cognitive assessment during the phases of a spontaneous migraine: a prospective cohort study
Cognitive symptoms are reported commonly throughout all phases of a migraine; however, there is a paucity of objective cog...
Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
SPG18 is caused by mutations in the endoplasmic reticulum lipid raft associated 2 (ERLIN2) gene. Autosomal recessive (AR) ...
Optimized trans-cranial direct current stimulation for prolonged consciousness disorder in a patient with titanium mesh cranioplasty
Optimized trans-cranial direct current stimulation for prolonged consciousness disorder in a patient with titanium mesh cranioplasty
Transcranial direct current stimulation (tDCS) has been used for the restoration of awareness in patients with a minimal c...
Utilization of EEG microstates as a prospective biomarker for assessing the impact of ketogenic diet in GLUT1-DS
Utilization of EEG microstates as a prospective biomarker for assessing the impact of ketogenic diet in GLUT1-DS
The aim of the study is to analyze microstate patterns in GLUT1-DS, both before and after the ketogenic diet (KD). We cond...
Nusinersen in adults with type 3 spinal muscular atrophy: long-term outcomes on motor and respiratory function
Nusinersen in adults with type 3 spinal muscular atrophy: long-term outcomes on motor and respiratory function
Nusinersen was approved for 5q spinal muscular atrophy (SMA), irrespective of age, SMA type or functional status. Nonethel...
Genetic aspects of ataxias in a cohort of Turkish patients
Genetic aspects of ataxias in a cohort of Turkish patients
Ataxia is one of the clinical findings of the movement disorder disease group. Although there are many underlying etiologi...
Exploring variability in cognitive functioning in patients with spinal muscular atrophy: a scoping review
Exploring variability in cognitive functioning in patients with spinal muscular atrophy: a scoping review
The cognitive functioning of individuals with spinal muscular atrophy (SMA) is not well understood, prompting a call for m...
Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
Literature reporting the onset of Creutzfeldt-Jakob disease (CJD) immediately after COVID-19 infection has strengthened a ...
Sex hormones and neuromyelitis optica spectrum disorder: a bidirectional Mendelian randomization study
Sex hormones and neuromyelitis optica spectrum disorder: a bidirectional Mendelian randomization study
Females are considered to have an increased susceptibility to neuromyelitis optica spectrum disorder (NMOSD) than males, e...
Blurred lines: bilateral optic perineuritis mimicking idiopathic intracranial hypertension
Blurred lines: bilateral optic perineuritis mimicking idiopathic intracranial hypertension
Saitakis G, Chwalisz BK (2022) Optic perineuritis. Curr Opin Ophthalmol 33:519–524Article  PubMed  ...
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia
ATP13A2 is a monogenic causative gene of Parkinson’s disease, whose biallelic mutations can result in Kufor-Rakeb sy...
An unusual stroke chameleon: acute isolated sialorrhea
An unusual stroke chameleon: acute isolated sialorrhea
Candelaresi P, Di Monaco C, Pisano E (2023) Stroke chameleons: diagnostic challenges. Eur J Radiol Open 11:100533Article  ...
An emerging etiology of spinal cord injury resembling neuromyelitis optica spectrum disorder
An emerging etiology of spinal cord injury resembling neuromyelitis optica spectrum disorder
Cite this articleGiramé-Rizzo, L., de Gordoa, E.S., Vilaseca, A. et al. An emerging etiology of spinal cord injury resembl...
A case of female-restricted Wieacker-Wolff syndrome with heart and endocrinological involvement
A case of female-restricted Wieacker-Wolff syndrome with heart and endocrinological involvement
Frints SGM, Hennig F, Colombo R, Jacquemont S, Terhal P, Zimmerman HH, Hunt D, Mendelsohn BA, Kordaß U, Webster R, Sinnema...
Association between renal insufficiency and lesion characteristics of posterior reversible encephalopathy syndrome
Association between renal insufficiency and lesion characteristics of posterior reversible encephalopathy syndrome
Posterior reversible encephalopathy syndrome (PRES) is characterized by cerebral blood flow dysregulation and the blood...
Essential tremor is associated with reduced serum ceruloplasmin levels
Essential tremor is associated with reduced serum ceruloplasmin levels
Essential tremor (ET), a prevalent movement disorder, has an elusive pathogenesis. A reduction in ceruloplasmin (Cp) level...
Emotional atypical arousal ratings for unpleasant stimuli in patients with Parkinson’s disease
Emotional atypical arousal ratings for unpleasant stimuli in patients with Parkinson’s disease
Parkinson’s disease (PD) is a neurodegenerative disorder characterized by motor and non-motor symptoms, including al...