Annals of Clinical and Translational Neurology

Papers
(The TQCC of Annals of Clinical and Translational Neurology is 8. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Persistent neurologic symptoms and cognitive dysfunction in non‐hospitalized Covid‐19 “long haulers”467
Blood neurofilament light: a critical review of its application to neurologic disease155
DMTs and Covid‐19 severity in MS: a pooled analysis from Italy and France95
Long COVID‐19: Objectifying most self‐reported neurological symptoms88
Anakinra usage in febrile infection related epilepsy syndrome: an international cohort87
Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study69
Risk factors and abnormal cerebrospinal fluid associate with cognitive symptoms after mild COVID‐1965
Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study61
Brain dysfunction in COVID‐19 and CAR‐T therapy: cytokine storm‐associated encephalopathy57
Diaphragm dysfunction in severe COVID‐19 as determined by neuromuscular ultrasound57
Comparison of SimoaTM and EllaTM to assess serum neurofilament‐light chain in multiple sclerosis55
A rapid α‐synuclein seed assay of Parkinson’s disease CSF panel shows high diagnostic accuracy52
230 days of ultra long‐term subcutaneous EEG: seizure cycle analysis and comparison to patient diary50
QSM is an imaging biomarker for chronic glial activation in multiple sclerosis lesions48
Evolution of neurologic symptoms in non‐hospitalized COVID‐19 “long haulers”47
Experiences of telemedicine in neurological out‐patient clinics during the COVID‐19 pandemic47
Optical coherence tomography in multiple sclerosis: A 3‐year prospective multicenter study44
The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention43
Type I SMA “new natural history”: long‐term data in nusinersen‐treated patients43
Onasemnogene abeparvovec in spinal muscular atrophy: an Australian experience of safety and efficacy42
The gut microbiota in pediatric multiple sclerosis and demyelinating syndromes41
Age‐ and disease‐specific reference values for neurofilament light presented in an online interactive support interface40
Dopamine transporter imaging predicts clinically‐defined α‐synucleinopathy in REM sleep behavior disorder39
Acute disseminated encephalomyelitis in a patient vaccinated against SARS‐CoV‐239
Spinocerebellar ataxia clinical trials: opportunities and challenges38
Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children37
Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment37
Obesity and the risk of Multiple Sclerosis. The role of Leptin37
Intrathecal dexamethasone therapy for febrile infection‐related epilepsy syndrome36
Synaptic density in carriers of C9orf72 mutations: a [11C]UCB‐J PET study35
Choroid plexus volume in multiple sclerosis predicts expansion of chronic lesions and brain atrophy35
Interictal spike networks predict surgical outcome in patients with drug‐resistant focal epilepsy35
Mendelian etiologies identified with whole exome sequencing in cerebral palsy33
Plasma lipid metabolites associate with diabetic polyneuropathy in a cohort with type 2 diabetes32
Isradipine plasma pharmacokinetics and exposure–response in early Parkinson’s disease31
Long‐term efficacy of eculizumab in refractory generalized myasthenia gravis: responder analyses31
Multiple sclerosis, rituximab, and COVID‐1931
Artificial intelligence extension of the OSCAR‐IB criteria31
Nusinersen in pediatric and adult patients with type III spinal muscular atrophy31
Clinical efficacy of plasma exchange in patients with autoimmune encephalitis30
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasia30
Longitudinal evaluation of neurologic‐post acute sequelae SARS‐CoV‐2 infection symptoms30
Nusinersen efficacy data for 24‐month in type 2 and 3 spinal muscular atrophy29
Real‐world experience of ocrelizumab in multiple sclerosis in a Spanish population29
Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD28
Multiple sclerosis and inflammatory bowel disease: A systematic review and meta‐analysis28
Gut microbiome is associated with multiple sclerosis activity in children28
Risdiplam treatment has not led to retinal toxicity in patients with spinal muscular atrophy28
Prevalence and patterns of symptoms of dysautonomia in patients with long‐COVID syndrome: A cross‐sectional study28
KCNQ2‐DEE: developmental or epileptic encephalopathy?27
Recurrent seizure‐related GRIN1 variant: Molecular mechanism and targeted therapy26
Delta power robustly predicts cognitive function in Angelman syndrome26
Multi‐cohort profiling reveals elevated CSF levels of brain‐enriched proteins in Alzheimer’s disease26
Mortality of neuromyelitis optica spectrum disorders in a Chinese population26
Ataluren for drug‐resistant epilepsy in nonsense variant‐mediated Dravet syndrome and CDKL5 deficiency disorder25
Lipid levels and the risk of dementia: A dose–response meta‐analysis of prospective cohort studies25
A Phase 1 study of GDC‐0134, a dual leucine zipper kinase inhibitor, in ALS25
A meta‐analysis comparing first‐line immunosuppressants in neuromyelitis optica25
Effect of diabetes control status on the progression of Parkinson’s disease: A prospective study25
Quantifying regional α ‐synuclein, amyloid β, and tau accumulation in lewy body dementia24
Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study24
CSF parvalbumin levels reflect interneuron loss linked with cortical pathology in multiple sclerosis24
Mechanistic underpinning of an inside–out concept for autoimmunity in multiple sclerosis24
The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease24
Plasma phosphorylated tau181 and neurodegeneration in Alzheimer’s disease24
Subcortical short‐term plasticity elicited by deep brain stimulation23
Development of an age‐adjusted model for blood neurofilament light chain23
Trait impulsivity in Juvenile Myoclonic Epilepsy23
Brain volumetric deficits in MAPT mutation carriers: a multisite study23
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy23
Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy23
Comparison of plasma and CSF biomarkers in predicting cognitive decline22
Central nervous system vascular malformations: A clinical review22
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy22
Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy22
aHSCT is superior to alemtuzumab in maintaining NEDA and improving cognition in multiple sclerosis22
Acute epileptiform abnormalities are the primary predictors of post‐stroke epilepsy: a matched, case–control study22
Baseline characteristics of the North American prodromal Synucleinopathy cohort22
Design of a virtual longitudinal observational study in Parkinson’s disease (AT‐HOME PD)22
Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome21
SARS‐COV‐2 a trigger of myelin oligodendrocyte glycoprotein‐associated disorder20
TDP‐43 as structure‐based biomarker in amyotrophic lateral sclerosis20
Safety and efficacy of dimethyl fumarate in ALS: randomised controlled study20
Manifestations and impact of the COVID‐19 pandemic in neuroinflammatory diseases20
Immune responses to SARS‐CoV‐2 vaccination in multiple sclerosis: a systematic review/meta‐analysis20
Younger age of stroke in low‐middle income countries is related to healthcare access and quality20
Prognostic value of serum/plasma neurofilament light chain for COVID‐19‐associated mortality20
Postoperative changes in cognition and cerebrospinal fluid neurodegenerative disease biomarkers20
Neuronal intermediate filament IgGs in CSF: Autoimmune Axonopathy Biomarkers20
Predictors of cognitive decline in older individuals without dementia: An updated meta‐analysis19
Leveraging electronic health records data to predict multiple sclerosis disease activity19
Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months19
Associations ofsNfLwith clinico‐radiological measures in a largeMSpopulation19
Genetic prediction of impulse control disorders in Parkinson's disease19
Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies19
Neural mechanisms of psychosis vulnerability and perceptual abnormalities in the ALS‐FTD spectrum18
Effects of PB‐TURSO on the transcriptional and metabolic landscape of sporadic ALS fibroblasts18
Sustained immunotolerance in multiple sclerosis after stem cell transplant18
A meta‐analysis of the global impact of the COVID‐19 pandemic on stroke care & the Houston Experience18
Lack of progression of beta dynamics after long‐term subthalamic neurostimulation18
Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset18
Cutaneous amyloid is a biomarker in early ATTRv neuropathy and progresses across disease stages18
Physical activity level and stroke risk in US population: A matched case–control study of 102,578 individuals18
Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes18
Structural brain changes in post‐acute COVID‐19 patients with persistent olfactory dysfunction17
Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy17
Initial findings in traumatic peripheral nerve injury and repair with diffusion tensor imaging17
Cardioselective peripheral noradrenergic deficiency in Lewy body synucleinopathies17
Sirolimus for epileptic seizures associated with focal cortical dysplasia type II17
Safety and efficacy of unilateral and bilateral pallidotomy for primary dystonia17
Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease17
Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study17
Diagnostic capabilities of nanopore long‐read sequencing in muscular dystrophy17
Functional dystonia: A case‐control study and risk prediction algorithm16
CD8+ T cell subpopulations and pro‐inflammatory cytokines in neuromyelitis optica spectrum disorder16
Wearable myoelectric interface enables high‐dose, home‐based training in severely impaired chronic stroke survivors16
No strong HLA association with MOG antibody disease in the UK population16
Plasma calcitonin gene‐related peptide (CGRP) in migraine and endometriosis during the menstrual cycle16
In‐depth peripheral CD4+ T profile correlates with myasthenic crisis16
Decreased serum creatinine levels predict short survival in amyotrophic lateral sclerosis16
Evaluation of SORD mutations as a novel cause of Charcot‐Marie‐Tooth disease16
Impact of T cells on neurodegeneration in anti‐GAD65 limbic encephalitis15
The kynurenine pathway relates to post‐acuteCOVID‐19 objective cognitive impairment andPASC15
Real‐world evaluation of ocrelizumab in multiple sclerosis: A systematic review15
Factors influencing the acute pentylenetetrazole‐induced seizure paradigm and a literature review15
Phospho‐specific plasma p‐tau181 assay detects clinical as well as asymptomatic Alzheimer's disease15
Plasma lipidomics of monozygotic twins discordant for multiple sclerosis15
JKAP relates to disease risk, severity, and Th1 and Th17 differentiation in Parkinson's disease14
Dopamine D1 + D3 receptor density may correlate with parkinson disease clinical features14
Characteristics and outcome of facial nerve palsy from Lyme neuroborreliosis in the United States14
TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function14
Scientific rationale for a higher dose of nusinersen14
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult‐onset disorder14
Home‐based biofeedback speech treatment improves dysarthria in repeat‐expansion SCAs14
Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy14
PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy14
Stiff person spectrum disorder diagnosis, misdiagnosis, and suggested diagnostic criteria14
Dynamics of pseudo‐atrophy in RRMS reveals predominant gray matter compartmentalization14
Congenital myasthenic syndrome in China: genetic and myopathological characterization14
Nusinersen in type 0 spinal muscular atrophy: should we treat?13
A population‐based meta‐analysis of circulating GFAP for cognition and dementia risk13
Disease progression in Parkinson‘s disease patients with subjective cognitive complaint13
Plasma GFAP associates with secondary Alzheimer's pathology in Lewy body disease13
Systematic review of CMTX1 patients with episodic neurological dysfunction13
Nanopore 16S sequencing enhances the detection of bacterial meningitis after neurosurgery13
Altered executive control network connectivity in anti‐NMDA receptor encephalitis13
Correlation of plasma and neuroimaging biomarkers in Alzheimer's disease13
Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 513
Central and peripheral α‐synuclein in Parkinson disease detected by seed amplification assay13
Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy13
Ante‐ and postmortem tau in autosomal dominant and late‐onset Alzheimer’s disease13
Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort13
National and subnational burden of stroke in Iran from 1990 to 201913
Deep brain stimulation effects on verbal fluency dissociated by target and active contact location13
Long‐term adherence and response to botulinum toxin in different indications13
Proteomics and mathematical modeling of longitudinal CSF differentiates fast versus slow ALS progression12
Air pollution is associated with faster cognitive decline in Alzheimer's disease12
Peripheral synucleinopathy in Parkinson disease with LRRK2 G2385R variants12
Characteristics of systemic inflammation and brain iron deposition in Parkinson's disease patients12
The altered expression of neurofilament in mouse models and patients with spinal muscular atrophy12
No evidence that herpes zoster is associated with increased risk of dementia diagnosis12
“Brain age” predicts disability accumulation in multiple sclerosis12
New approaches for the quantification and targeting of noradrenergic dysfunction in Alzheimer's disease12
Neutrophil to lymphocyte ratio predicts early growth of traumatic intracerebral haemorrhage12
Digital endpoints for self‐administered home‐based functional assessment in pediatric Friedreich’s ataxia12
Diminished muscle oxygen uptake and fatigue in spinal muscular atrophy12
The safety and efficacy of intravenous immunoglobulin in autoimmune encephalitis12
Evaluation of the EFNS/PNS diagnostic criteria in a cohort of CIDP patients12
Unilateral pallidothalamic tractotomy at Forel's field H1 for cervical dystonia12
Swallowing‐related neural oscillation: an intracranial EEG study12
Multisystem proteinopathies (MSPs) and MSP‐like disorders: Clinical‐pathological‐molecular spectrum12
The potassium channel Kv1.3 as a therapeutic target for immunocytoprotection after reperfusion12
Anakinra treatment for refractory cerebral autoinflammatory responses12
A new clustering method identifies multiple sclerosis‐specific T‐cell receptors11
Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia11
Remyelination in humans due to a retinoid‐X receptor agonist is age‐dependent11
Identifying miRNAs in multiple sclerosis gray matter lesions that correlate with atrophy measures11
Independent study demonstrates amyloid probability score accurately indicates amyloid pathology11
Amyloid‐β, cortical thickness, and subsequent cognitive decline in cognitively normal oldest‐old11
Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations11
KCNA1 gain‐of‐function epileptic encephalopathy treated with 4‐aminopyridine11
Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosis11
Newborn screening for Duchenne muscular dystrophy: A two‐year pilot study11
Continuous and interval training attenuate encephalomyelitis by separate immunomodulatory mechanisms11
Humoral response to neurofilaments and dipeptide repeats in ALS progression11
Human Leukocyte Antigen Class II associations in late‐onset Myasthenia Gravis11
Increased atrial fibrillation risk in Parkinson’s disease: A nationwide population‐based study11
Sciatic nerve microvascular permeability in type 2 diabetes decreased in patients with neuropathy11
Clinical profile of autoimmune nodopathy with anti‐neurofascin 186 antibody11
Vascular endothelial‐cadherin as a marker of endothelial injury in preclinical Alzheimer disease11
LRRK2 and Parkinson's disease: from genetics to targeted therapy11
Hold that pose: capturing cervical dystonia's head deviation severity from video11
Evaluation of peripherin in biofluids of patients with motor neuron diseases11
Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy11
Long‐term continuation of anti‐seizure medications after acute stroke11
Hybrid and vaccine‐induced immunity against SAR‐CoV‐2 in MS patients on different disease‐modifying therapies11
Mitochondrial morphology and MAVS‐IFN1 signaling pathway in muscles of anti‐MDA5 dermatomyositis10
COVID‐19 clinical outcomes and DMT of MS patients and population‐based controls10
Epilepsy inMTATP6‐ related mils/NARP: correlation of elettroclinical features with heteroplasmy10
Clinical trial of raltegravir, an integrase inhibitor, in HAM/TSP10
Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases10
Cognitive reserve protects ALS‐typical cognitive domains: A longitudinal study.10
Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis10
The α2δ‐1/NMDA receptor complex is involved in brain injury after intracerebral hemorrhage in mice10
The systemic inflammation markers as possible indices for predicting respiratory failure and outcome in patients with myasthenia gravis10
COVID‐19 and the risk of Alzheimer's disease, amyotrophic lateral sclerosis, and multiple sclerosis10
Exosomal circ‐AHCY promotes glioblastoma cell growth via Wnt/β‐catenin signaling pathway10
Transcriptome analysis of collagen VI‐related muscular dystrophy muscle biopsies10
Clinical and diagnostic features of anti‐neurofascin‐155 antibody‐positive neuropathy in Han Chinese10
MAPT R406W increases tau T217 phosphorylation in absence of amyloid pathology10
Improving quality, affordability, and equity of multiple sclerosis care10
Responsive neurostimulation for focal motor status epilepticus10
Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP10
Using electronic health data to explore effectiveness of ICU EEG and anti‐seizure treatment10
Clinical and transcriptional recovery profiles in pediatric and adult multiple sclerosis patients10
Guanabenz ameliorates disease in vanishing white matter mice in contrast to sephin110
Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease10
Cyclical underreporting of seizures in patient‐based seizure documentation10
Accelerated long‐term forgetting over three months in asymptomatic APOE ɛ4 carriers10
A double‐blind, randomized, placebo‐controlled phase 2 trial evaluating the selective dihydroorotate dehydrogenase inhibitor vidofludimus calcium in relapsing‐remitting multiple sclerosis10
Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings10
Plasma phosphorylated tau181 predicts cognitive and functional decline10
Vestibular syncope: clinical characteristics and mechanism10
Effects of simvastatin on white matter integrity in healthy middle‐aged adults10
Evidence‐based consensus guidelines for ALS genetic testing and counseling10
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS‐associated mtDNA mutations10
Serum neurofilament levels and patient‐reported outcomes in multiple sclerosis10
Exploring diazoxide and continuous glucose monitoring as treatment for Glut1 deficiency syndrome10
A blood biomarker test for brain amyloid impacts the clinical evaluation of cognitive impairment10
Genetic defects are common in myopathies with tubular aggregates10
Response to ibudilast treatment according to progressive multiple sclerosis disease phenotype10
Improving risk‐stratification of natalizumab‐associated PML10
Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency10
Efficacy of melatonin in term neonatal models of perinatal hypoxia‐ischaemia10
PINK1 antagonize intracerebral hemorrhage by promoting mitochondrial autophagy10
Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A119
Clinical features, investigations, and outcomes of pediatric limbic encephalitis: A multicenter study9
Adult‐onset rapidly worsening progressive myoclonic epilepsy caused by a novel variant in DHDDS9
Visceral and emotional responses to direct electrical stimulations of the cortex9
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness9
MRI and fluid biomarkers reveal determinants of myelin and axonal loss with aging9
Results of a randomized double‐blind study evaluating luvadaxistat in adults with Friedreich ataxia9
Sleep disturbance and memory dysfunction in early multiple sclerosis9
Longitudinal change in TSPO PET imaging in progressive multiple sclerosis9
Phosphorylated alpha‐synuclein in Iba1‐positive macrophages in the skin of patients with Parkinson's disease9
Triacetyluridine treats epileptic encephalopathy from CAD mutations: a case report and review9
Associative cued asynchronous BCI induces cortical plasticity in stroke patients9
Hyperventilation‐induced focal seizures in adults: think autoimmune encephalitis9
HCMV infection and IFITM3 rs12252 are associated with Rasmussen's encephalitis disease progression9
Quantitative signal properties from standardized MRIs correlate with multiple sclerosis disability9
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