Annals of Clinical and Translational Neurology

Papers
(The median citation count of Annals of Clinical and Translational Neurology is 4. 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 2020-03-01 to 2024-03-01.)
ArticleCitations
Persistent neurologic symptoms and cognitive dysfunction in non‐hospitalized Covid‐19 “long haulers”409
Frequent neurologic manifestations and encephalopathy‐associated morbidity in Covid‐19 patients341
Blood neurofilament light: a critical review of its application to neurologic disease128
DMTs and Covid‐19 severity in MS: a pooled analysis from Italy and France86
Anakinra usage in febrile infection related epilepsy syndrome: an international cohort79
Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy67
Long COVID‐19: Objectifying most self‐reported neurological symptoms65
Longitudinal biomarkers in amyotrophic lateral sclerosis62
De Novo Status Epilepticus in patients with COVID‐1959
Serious safety events in rituximab‐treated multiple sclerosis and related disorders57
Neurological manifestations of coronavirus infections – a systematic review56
Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study55
Gut microbiome variation is associated to Multiple Sclerosis phenotypic subtypes54
Risk factors and abnormal cerebrospinal fluid associate with cognitive symptoms after mild COVID‐1951
Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study51
Seizures and risk of epilepsy in anti‐NMDAR, anti‐LGI1, and anti‐GABABR encephalitis49
Brain dysfunction in COVID‐19 and CAR‐T therapy: cytokine storm‐associated encephalopathy49
Retraining and control therapy for pediatric psychogenic non‐epileptic seizures49
Improved ALS clinical trials through frequent at‐home self‐assessment: a proof of concept study48
230 days of ultra long‐term subcutaneous EEG: seizure cycle analysis and comparison to patient diary46
Insular and occipital changes in visual snow syndrome: a BOLD fMRI and MRS study45
Cortical hyperexcitability evolves with disease progression in ALS44
Comparison of SimoaTM and EllaTM to assess serum neurofilament‐light chain in multiple sclerosis44
Centromedian thalamic responsive neurostimulation for Lennox‐Gastaut epilepsy and autism43
Experiences of telemedicine in neurological out‐patient clinics during the COVID‐19 pandemic43
Diaphragm dysfunction in severe COVID‐19 as determined by neuromuscular ultrasound42
Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients42
Neuropsychiatric symptoms and cognitive abilities over the initial quinquennium of Parkinson disease41
Role of homocysteine in the development and progression of Parkinson’s disease41
The A4 study: β‐amyloid and cognition in 4432 cognitively unimpaired adults39
A rapid α‐synuclein seed assay of Parkinson’s disease CSF panel shows high diagnostic accuracy39
Long‐term peripheral immune cell profiling reveals further targets of oral cladribine in MS39
Neuronal intranuclear inclusion disease is genetically heterogeneous38
Evolution of neurologic symptoms in non‐hospitalized COVID‐19 “long haulers”38
Dopamine transporter imaging predicts clinically‐defined α‐synucleinopathy in REM sleep behavior disorder37
Acute disseminated encephalomyelitis in a patient vaccinated against SARS‐CoV‐236
Developmental regression and mitochondrial function in children with autism36
Re‐defining the clinicopathological spectrum of neuronal intranuclear inclusion disease36
The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention36
Optical coherence tomography in multiple sclerosis: A 3‐year prospective multicenter study35
QSM is an imaging biomarker for chronic glial activation in multiple sclerosis lesions35
Spreading in ALS: The relative impact of upper and lower motor neuron involvement34
Type I SMA “new natural history”: long‐term data in nusinersen‐treated patients34
Validation of differentially expressed brain‐enriched microRNAs in the plasma of PD patients34
Temporal association of sNfL and gad‐enhancing lesions in multiple sclerosis34
Prolonged confusional state as first manifestation of COVID‐1933
Spinocerebellar ataxia clinical trials: opportunities and challenges33
Genetic modifiers of respiratory function in Duchenne muscular dystrophy32
Cerebellar cognitive disorder parallels cerebellar motor symptoms in Friedreich ataxia32
The gut microbiota in pediatric multiple sclerosis and demyelinating syndromes32
Automated cot‐side tracking of functional brain age in preterm infants32
Deep learning with diffusion basis spectrum imaging for classification of multiple sclerosis lesions31
Interictal spike networks predict surgical outcome in patients with drug‐resistant focal epilepsy31
Obesity and the risk of Multiple Sclerosis. The role of Leptin31
Onasemnogene abeparvovec in spinal muscular atrophy: an Australian experience of safety and efficacy30
Elevated matrix metalloproteinase‐9 levels in neuronal extracellular vesicles in Alzheimer’s disease30
Early life metal dysregulation in amyotrophic lateral sclerosis29
Walking in multiple sclerosis improves with tDCS: a randomized, double‐blind, sham‐controlled study29
Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children29
Artificial intelligence extension of the OSCAR‐IB criteria29
Intrathecal dexamethasone therapy for febrile infection‐related epilepsy syndrome28
FGF14‐related episodic ataxia: delineating the phenotype of Episodic Ataxia type 928
Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment28
Risdiplam treatment has not led to retinal toxicity in patients with spinal muscular atrophy27
Plasma lipid metabolites associate with diabetic polyneuropathy in a cohort with type 2 diabetes27
11C‐PK11195 PET–based molecular study of microglia activation in SOD1 amyotrophic lateral sclerosis27
Phase I clinical trial of temsirolimus and perifosine for recurrent glioblastoma27
Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience27
Nusinersen in pediatric and adult patients with type III spinal muscular atrophy27
Synaptic density in carriers of C9orf72 mutations: a [11C]UCB‐J PET study27
Parkinson disease clinical subtypes: key features & clinical milestones27
Isradipine plasma pharmacokinetics and exposure–response in early Parkinson’s disease26
Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD26
Multiple sclerosis, rituximab, and COVID‐1926
CSF chitinases before and after symptom onset in amyotrophic lateral sclerosis26
Comparing progression biomarkers in clinical trials of early Alzheimer’s disease26
Adeno‐associated virus serotype 1‐based gene therapy for FTD caused by GRN mutations25
LAMA2‐related muscular dystrophy: Natural history of a large pediatric cohort25
Neuronal RNA‐binding protein dysfunction in multiple sclerosis cortex25
Clinical efficacy of plasma exchange in patients with autoimmune encephalitis24
Vocal music enhances memory and language recovery after stroke: pooled results from two RCTs24
Clinical implication of serum biomarkers and patient age in inflammatory demyelinating diseases24
Ratio and index of Neurofilament light chain indicate its origin in Guillain‐Barré Syndrome24
Remote ischemic conditioning combined with intravenous thrombolysis for acute ischemic stroke24
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasia24
Plasma phosphorylated tau181 and neurodegeneration in Alzheimer’s disease23
Levels of brain‐derived neurotrophic factor in patients with multiple sclerosis23
Idebenone increases chance of stabilization/recovery of visual acuity in OPA1‐dominant optic atrophy23
HLA‐B27 association of autoimmune encephalitis induced by PD‐L1 inhibitor23
Longitudinal Measurements of Glucocerebrosidase activity in Parkinson’s patients23
Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?23
Delta power robustly predicts cognitive function in Angelman syndrome23
Real‐world experience of ocrelizumab in multiple sclerosis in a Spanish population23
Prevalence and patterns of symptoms of dysautonomia in patients with long‐COVID syndrome: A cross‐sectional study23
Choroid plexus volume in multiple sclerosis predicts expansion of chronic lesions and brain atrophy22
Ataluren for drug‐resistant epilepsy in nonsense variant‐mediated Dravet syndrome and CDKL5 deficiency disorder22
Neurological manifestations of Erdheim–Chester Disease22
Mortality of neuromyelitis optica spectrum disorders in a Chinese population22
Restorative treatments of dystrophin expression in Duchenne muscular dystrophy: A systematic review22
Mendelian etiologies identified with whole exome sequencing in cerebral palsy22
Long‐term efficacy of eculizumab in refractory generalized myasthenia gravis: responder analyses22
Quantifying regional α ‐synuclein, amyloid β, and tau accumulation in lewy body dementia21
Prognosis and risk factors for reocclusion after mechanical thrombectomy21
Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies21
Nusinersen efficacy data for 24‐month in type 2 and 3 spinal muscular atrophy21
Gut microbiome is associated with multiple sclerosis activity in children21
Trait impulsivity in Juvenile Myoclonic Epilepsy21
Brain volumetric deficits in MAPT mutation carriers: a multisite study21
Transmission of CJD from nasal brushings but not spinal fluid or RT‐QuIC product21
Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study21
Rituximab versus natalizumab, fingolimod, and dimethyl fumarate in multiple sclerosis treatment21
Longitudinal evaluation of neurologic‐post acute sequelae SARS‐CoV‐2 infection symptoms21
Neurotoxicity after hematopoietic stem cell transplant in multiple sclerosis20
Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect20
Genetic factors for susceptibility to and manifestations of neuromyelitis optica20
Magnetization transfer ratio quantifies polyneuropathy in hereditary transthyretin amyloidosis20
Mechanistic underpinning of an inside–out concept for autoimmunity in multiple sclerosis20
A Phase 1 study of GDC‐0134, a dual leucine zipper kinase inhibitor, in ALS20
Multiple sclerosis and inflammatory bowel disease: A systematic review and meta‐analysis20
Age‐ and disease‐specific reference values for neurofilament light presented in an online interactive support interface19
Subcortical short‐term plasticity elicited by deep brain stimulation19
White matter and neurite morphology differ in psychogenic nonepileptic seizures19
Inflammatory pathway analytes predicting rapid cognitive decline in MCI stage of Alzheimer’s disease19
Association of rare variants in neurodegenerative genes with familial Alzheimer’s disease19
Manifestations and impact of the COVID‐19 pandemic in neuroinflammatory diseases19
KCNQ2‐DEE: developmental or epileptic encephalopathy?19
Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy19
Multi‐cohort profiling reveals elevated CSF levels of brain‐enriched proteins in Alzheimer’s disease19
A meta‐analysis comparing first‐line immunosuppressants in neuromyelitis optica19
Plasma NfL and GFAP as biomarkers of spinal cord degeneration in adrenoleukodystrophy19
Impaired cerebral autoregulation is associated with poststroke cognitive impairment19
CSF parvalbumin levels reflect interneuron loss linked with cortical pathology in multiple sclerosis19
Development of an age‐adjusted model for blood neurofilament light chain19
Comparison of plasma and CSF biomarkers in predicting cognitive decline18
Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R918
Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies18
The influence of white matter hyperintensity on cognitive impairment in Parkinson's disease18
Vorinostat in the acute neuroinflammatory form of X‐linked adrenoleukodystrophy18
Design of a virtual longitudinal observational study in Parkinson’s disease (AT‐HOME PD)18
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders18
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy18
Effect of diabetes control status on the progression of Parkinson’s disease: A prospective study18
Impaired phonemic discrimination in logopenic variant primary progressive aphasia18
Selenoprotein N‐related myopathy: a retrospective natural history study to guide clinical trials17
Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy17
Habitual sleep disturbances and migraine: a Mendelian randomization study17
Cognitive reserve and midlife vascular risk: Cognitive and clinical outcomes17
Demographic characteristics and neuropsychological assessments of subjective cognitive decline (SCD) (plus)17
Serum neurofilament light chain in FTLD: association with C9orf72, clinical phenotype, and prognosis17
Prognostic value of serum/plasma neurofilament light chain for COVID‐19‐associated mortality17
Reversing 21 years of chronic paralysis via non‐invasive spinal cord neuromodulation: a case study17
Recurrent seizure‐related GRIN1 variant: Molecular mechanism and targeted therapy17
Relation of plasma β‐amyloid, clusterin, and tau with cerebral microbleeds: Framingham Heart Study17
Tau pathology associates with in vivo cortical thinning in Lewy body disorders17
Leveraging electronic health records data to predict multiple sclerosis disease activity17
Safety and efficacy of dimethyl fumarate in ALS: randomised controlled study17
Postoperative changes in cognition and cerebrospinal fluid neurodegenerative disease biomarkers17
TDP‐43 as structure‐based biomarker in amyotrophic lateral sclerosis17
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy17
Acute epileptiform abnormalities are the primary predictors of post‐stroke epilepsy: a matched, case–control study16
MRI and flortaucipir relationships in Alzheimer's phenotypes are heterogeneous16
A meta‐analysis of the global impact of the COVID‐19 pandemic on stroke care & the Houston Experience16
Sustained immunotolerance in multiple sclerosis after stem cell transplant16
Cardioselective peripheral noradrenergic deficiency in Lewy body synucleinopathies16
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay16
Accuracy of FGF‐21 and GDF‐15 for the diagnosis of mitochondrial disorders: A meta‐analysis16
SARS‐COV‐2 a trigger of myelin oligodendrocyte glycoprotein‐associated disorder16
GYS1 or PPP1R3C deficiency rescues murine adult polyglucosan body disease16
Hematoma enlargement characteristics in deep versus lobar intracerebral hemorrhage16
aHSCT is superior to alemtuzumab in maintaining NEDA and improving cognition in multiple sclerosis16
Lipid levels and the risk of dementia: A dose–response meta‐analysis of prospective cohort studies16
Immune responses to SARS‐CoV‐2 vaccination in multiple sclerosis: a systematic review/meta‐analysis15
Genetic prediction of impulse control disorders in Parkinson's disease15
Efficacy of Ciprofloxacin/Celecoxib combination in zebrafish models of amyotrophic lateral sclerosis15
Safety and efficacy of unilateral and bilateral pallidotomy for primary dystonia15
Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome15
Evolution of white matter damage in amyotrophic lateral sclerosis15
Neuroprotective effects of FK866 against traumatic brain injury: Involvement of p38/ERK pathway15
Consistent improvement with eculizumab across muscle groups in myasthenia gravis15
UCHL1 from serum and CSF is a candidate biomarker for amyotrophic lateral sclerosis15
Amyloid‐β PET and CSF in an autopsy‐confirmed cohort15
Altered coupling between resting‐state glucose metabolism and functional activity in epilepsy15
Hippocampal sclerosis, TDP‐43, and the duration of the symptoms of dementia of AD patients15
Effect of plasma exchange in neuromyelitis optica spectrum disorder: A systematic review and meta‐analysis15
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 5215
Machine learning prediction of the adverse outcome for nontraumatic subarachnoid hemorrhage patients14
Central nervous system vascular malformations: A clinical review14
Dynamics of pseudo‐atrophy in RRMS reveals predominant gray matter compartmentalization14
Neurodegeneration trajectory in pediatric and adult/late DM1: A follow‐up MRI study across a decade14
Association between amphetamine‐related disorders and dementia‐a nationwide cohort study in Taiwan14
Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy14
Younger age of stroke in low‐middle income countries is related to healthcare access and quality14
In‐depth peripheral CD4+ T profile correlates with myasthenic crisis14
Baseline characteristics of the North American prodromal Synucleinopathy cohort14
Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study14
Lack of progression of beta dynamics after long‐term subthalamic neurostimulation14
Neuronal intermediate filament IgGs in CSF: Autoimmune Axonopathy Biomarkers13
Evaluation of SORD mutations as a novel cause of Charcot‐Marie‐Tooth disease13
Cognitive impairment in patients with Neuro‐Sjögren13
Heritability of alpha and sensorimotor network changes in temporal lobe epilepsy13
Congenital myasthenic syndrome in China: genetic and myopathological characterization13
Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset13
Optic, trigeminal, and facial neuropathy related to anti‐neurofascin 155 antibody13
Effects of PB‐TURSO on the transcriptional and metabolic landscape of sporadic ALS fibroblasts13
Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy13
Ocular ultrasonography to detect intracranial pressure in aneurysmal subarachnoid hemorrhage13
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult‐onset disorder13
Sirolimus for epileptic seizures associated with focal cortical dysplasia type II13
Functional and pharmacological evaluation of a novel SCN2A variant linked to early‐onset epilepsy12
Dopamine D1 + D3 receptor density may correlate with parkinson disease clinical features12
No strong HLA association with MOG antibody disease in the UK population12
Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 512
Expansion of the genetic landscape of ERLIN2‐related disorders12
Factors influencing the acute pentylenetetrazole‐induced seizure paradigm and a literature review12
Plasma calcitonin gene‐related peptide (CGRP) in migraine and endometriosis during the menstrual cycle12
Association of serum Apolipoprotein B with cerebrospinal fluid biomarkers of Alzheimer’s pathology12
Systematic review of CMTX1 patients with episodic neurological dysfunction12
Abolishing spontaneous epileptiform activity in human brain tissue through AMPA receptor inhibition12
Home‐based biofeedback speech treatment improves dysarthria in repeat‐expansion SCAs12
CD8+ T cell subpopulations and pro‐inflammatory cytokines in neuromyelitis optica spectrum disorder12
Anakinra treatment for refractory cerebral autoinflammatory responses12
Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes12
Predictors of cognitive decline in older individuals without dementia: An updated meta‐analysis12
Functional dystonia: A case‐control study and risk prediction algorithm12
Electrophysiological properties and seizure networks in hypothalamic hamartoma12
Predictors of worsening neuropathy and neuropathic pain after 12 years in people with HIV12
Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 512
Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome12
Test–retest reliability of the Friedreich’s ataxia rating scale12
Initial findings in traumatic peripheral nerve injury and repair with diffusion tensor imaging11
The safety and efficacy of intravenous immunoglobulin in autoimmune encephalitis11
Excitatory and inhibitory neuron defects in a mouse model of Scn1b‐linked EIEE5211
Genetic variation contributes to gene expression response in ischemic stroke: an eQTL study11
Phospho‐specific plasma p‐tau181 assay detects clinical as well as asymptomatic Alzheimer's disease11
Long‐term continuation of anti‐seizure medications after acute stroke11
Swallowing‐related neural oscillation: an intracranial EEG study11
Using urine to diagnose large‐scale mtDNA deletions in adult patients11
Physical activity level and stroke risk in US population: A matched case–control study of 102,578 individuals11
Evaluation of peripherin in biofluids of patients with motor neuron diseases11
Vitamin D concentration and focal brain atrophy in older adults: a voxel‐based morphometric study11
Correlation of plasma and neuroimaging biomarkers in Alzheimer's disease11
Peripheral synucleinopathy in Parkinson disease with LRRK2 G2385R variants11
Reliability and accuracy of EEG interpretation for estimating age in preterm infants11
Cardiac arrhythmias in Dravet syndrome: an observational multicenter study11
Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy11
Expanding the clinical and genetic heterogeneity of SPAX511
Characteristics and outcome of facial nerve palsy from Lyme neuroborreliosis in the United States11
Decreased serum creatinine levels predict short survival in amyotrophic lateral sclerosis11
Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease11
The CSF Levels of Neutrophil‐Related Chemokines in Patients with Neuromyelitis Optica11
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