Annals of Clinical and Translational Neurology

Papers
(The TQCC of Annals of Clinical and Translational Neurology is 7. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
105
Evaluating brain damage in multiple sclerosis with simultaneous multi‐angular‐relaxometry of tissue101
Quantitative signal properties from standardized MRIs correlate with multiple sclerosis disability71
Cerebral hypoperfusion reduces tau accumulation64
Skull defect – Frontotemporal dementia sagging brain syndrome62
Cognitive impairment in pulmonary arterial hypertension60
Assessment of burden and segregation profiles of CNVs in patients with epilepsy60
Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes55
Phosphorylated alpha‐synuclein in Iba1‐positive macrophages in the skin of patients with Parkinson's disease52
Brain imaging signatures in amyotrophic lateral sclerosis: Correlation with peripheral motor degeneration49
Objective sleep was longitudinally associated with brain amyloid burden in mild cognitive impairment47
High‐dose IgG suppresses local inflammation and facilitates functional recovery after olfactory system injury47
Issue Information46
Epitope Mapping of Anti‐Neurofascin 155 Antibody in a Large Cohort of Autoimmune Nodopathy Patients45
Impaired gating of γ‐ and ε‐AChR respectively causes Escobar syndrome and fast‐channel myasthenia43
Cortical lesions impact cognitive decline in multiple sclerosis via volume loss of nonlesional cortex41
Refractory myasthenia gravis treated with autologous hematopoietic stem cell transplantation41
ALS plasma biomarkers reveal neurofilament and pTau correlate with disease onset and progression39
Issue Information39
Neurological diagnoses in hospitalized COVID‐19 patients during the B.1.1.529 surge36
Optimized microburst VNS elicits fMRI responses beyond thalamic‐specific response from standard VNS35
Infarct‐related structural disconnection and delirium in surgical aortic valve replacement patients35
Hypertension management in elderly with severe intracerebral hemorrhage35
Subcutaneous batoclimab in generalized myasthenia gravis: Results from a Phase 2a trial with an open‐label extension35
Amyloid‐dependent and amyloid‐independent effects of Tau in individuals without dementia33
Issue Information31
Discrepant expressive language lateralization in children and adolescents with epilepsy31
Diagnostic capabilities of nanopore long‐read sequencing in muscular dystrophy30
Reduced Bergmann glial process terminations and lateral appendages in essential tremor30
Auditory neuropathy in mice and humans with Friedreich ataxia30
Muscle magnetic resonance imaging involvement patterns in nemaline myopathies30
Issue Information30
Hypotonia–cystinuria 2p21 deletion syndrome: Intrafamilial variability of clinical expression30
Linking autism spectrum disorders and parkinsonism: clinical and genetic association29
The anterior nucleus of the thalamus plays a role in the epileptic network29
HLA in isolated REM sleep behavior disorder and Lewy body dementia29
Longitudinal evaluation of neurologic‐post acute sequelae SARS‐CoV‐2 infection symptoms29
CYLD variants identified in Alzheimer's disease and frontotemporal dementia patients29
SCAR32: Functional characterization and expansion of the clinical‐genetic spectrum28
Serum neurofilament light chain and cognition decline in US elderly: A cross‐sectional study28
Issue Information28
Baseline systolic blood pressure, hypertension history, and efficacy of remote ischemic conditioning28
Glycated hemoglobin A1c, cerebral small vessel disease burden, and disease severity in Parkinson's disease27
The safety and efficacy of intravenous immunoglobulin in autoimmune encephalitis27
Anakinra treatment for refractory cerebral autoinflammatory responses27
A multi‐omics study to monitor senescence‐associated secretory phenotypes of Alzheimer's disease26
WiTNNess: An international natural history study of infantile‐onset TNNT1 myopathy26
PRNP expression predicts imaging findings in sporadic Creutzfeldt‐Jakob disease26
Autophagy‐related 5 in acute ischemic stroke: Variation and linkage with neurofunction, and survival26
Cobb syndrome effectively treated with trametinib25
T1−/T2‐weighted ratio reveals no alterations to gray matter myelination in temporal lobe epilepsy25
Impact of cerebral collateral flow on stroke outcomes after carotid stenting25
B cell and aquaporin‐4 antibody relationships with neuromyelitis optica spectrum disorder activity24
Issue Information23
Increased systemic HSP70B levels in spinal muscular atrophy infants23
Postoperative changes in cognition and cerebrospinal fluid neurodegenerative disease biomarkers23
Sensitivity and specificity of the Salzburg EEG criteria for nonconvulsive status epilepticus23
Juvenile‐onset Huntington's disease – Spectrum and evolution of presenting movement disorders23
Order from chaos: Using CSF proteomics to predict ALS progression23
Early‐onset leukoencephalomyelopathy due to a biallelic NDUFV1 variant in a mid‐forties patient23
Characterizing mortality in patients with AQP4‐Ab+ neuromyelitis optica spectrum disorder23
Micro‐diffusely abnormal white matter: An early multiple sclerosis lesion phase with intensified myelin blistering22
Immune responses to SARS‐CoV‐2 vaccination in multiple sclerosis: a systematic review/meta‐analysis22
Repeated iv anti‐CD20 treatment in multiple sclerosis: Long‐term effects on peripheral immune cell subsets22
Lactate dehydrogenase predicting mortality in patients with aneurysmal subarachnoid hemorrhage22
Consistency of electrical source imaging in presurgical evaluation of epilepsy across different vigilance states22
COVID‐19 clinical outcomes and DMT of MS patients and population‐based controls22
Novel pathogenic mtDNA variants in Chinese children with neurological mitochondrial disorders22
Reliability and validity of digital health metrics for assessing arm and hand impairments in an ataxic disorder21
In vivo detection of poststroke cerebral cell proliferation in rodents and humans21
Associations of Cerebrospinal Fluid Orexin‐A, Alzheimer Disease Biomarkers, and Cognitive Performance20
Incremental clinical value of intraplaque neovascularization in predicting recurrent ischemic stroke20
Neuromuscular transmission deficits in patients with CMT and ClC‐1 inhibition in CMT animal models20
Issue Information20
Cocaine use is associated with cerebral white matter hyperintensities in HIV disease20
Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 120
Artificial intelligence extension of the OSCAR‐IB criteria19
Well‐being on supportive techniques in amyotrophic lateral sclerosis: from neurologists' perspective19
Blended phenotype of TECPR2‐associated hereditary sensory‐autonomic neuropathy and Temple syndrome19
Psychotropic medication use and Parkinson's disease risk amongst older women19
Natural history and survival rate of familial amyloidosis with polyneuropathy: A nationwide databank19
Late‐onset Krabbe disease presenting as spastic paraplegia – implications of GCase and CTSB/D19
Retinal hypoplasia and degeneration result in vision loss in Friedreich ataxia19
Clinicoradiologic data of familial cerebral cavernous malformation with age‐related disease burden18
Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders18
Structural and functional connectivity alteration patterns of the cingulate gyrus in Type 2 diabetes18
Plasma calcitonin gene‐related peptide (CGRP) in migraine and endometriosis during the menstrual cycle18
Comparison of two corticosteroid regimens on brain volumetrics in patients with Duchenne muscular dystrophy18
Circannual seizure provocation as the day lengthens in the northern and southern hemispheres18
Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome18
Mexiletine in spinal and bulbar muscular atrophy: a randomized controlled trial17
A contemporary review of therapeutic and regenerative management of intracerebral hemorrhage17
Automated assessment of EEG background for neurodevelopmental prediction in neonatal encephalopathy17
Safety and efficacy of intravenous thrombolytic therapy in the extended window up to 24 hours: A systematic review and meta‐analysis17
Rethinking antisense oligonucleotide therapeutics for amyotrophic lateral sclerosis17
FDGPET patterns associate with survival in patients with prion disease17
Plasma exchange with albumin replacement for Alzheimer's disease treatment induced changes in serum and cerebrospinal fluid inflammatory mediator levels17
A meta‐analysis comparing first‐line immunosuppressants in neuromyelitis optica16
Study on clinical features and factors related to long‐term outcomes of antibody‐negative autoimmune encephalitis16
Exhaustive clinical examination of etiology and initial response to first‐line treatment in 577 children with infantile epileptic spasm syndrome children: A 5‐year retrospective observational study16
Endovascular thrombectomy versus medical management on outcomes with infarct volumes more than 70 mL15
Alemtuzumab treatment for multiple sclerosis in Austria: An observational long‐term outcome study15
Focal lesions following intracerebral gene therapy for mucopolysaccharidosis IIIA15
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Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature15
Abnormal dynamic functional connectivity in young nondisabling intracerebral hemorrhage patients15
Epilepsy in Duchenne and Becker muscular dystrophies15
ALS Identified: two‐year findings from a sponsored ALS genetic testing program15
Vinpocetine improved neuropsychiatric and epileptic outcomes in a patient with a GABRA1 loss‐of‐function variant15
Issue Information15
Impact of the National Amyotrophic Lateral Sclerosis Registry: Analysis of Registry‐funded Research14
The predictive value of normal EEGs in dementia due to Alzheimer’s disease14
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Clinical trial of raltegravir, an integrase inhibitor, in HAM/TSP14
Intranasal neuropeptide Y1 receptor antagonism improves motor deficits in symptomatic SOD1 ALS mice14
Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia14
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS‐associated mtDNA mutations14
Aseptic meningitis and Fabry disease14
Efficacy of immunotherapy and prognosis in anti‐LGI1 encephalitis patients: A meta‐analysis14
Using electronic health data to explore effectiveness of ICU EEG and anti‐seizure treatment13
Infantile‐onset parkinsonism, dyskinesia, and developmental delay: do not forget polyglutamine defects!13
In‐hospital recurrent stroke in ipsilateral carotid web patients undergoing thrombectomy13
Heart meets brain: A 25‐year‐old with a constellation of neurologic symptoms and heart failure13
Spatiotemporal spinal cord stimulation with real‐time triggering exoskeleton restores walking capability: a case report13
MicroRNAsignatures in genetic frontotemporal dementia and amyotrophic lateral sclerosis13
Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh13
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Issue Information13
Proteomic networks of gray and white matter reveal tissue‐specific changes in human tauopathy13
Cardiac troponin T as a serum biomarker of respiratory impairment in amyotrophic lateral sclerosis13
Scrambler therapy for treatment of poststroke pain13
Expanding molecular and clinical spectrum of CPT1C‐associated hereditary spastic paraplegia (SPG73)—a case series13
Alterations in metabolic biomarkers and their potential role in amyotrophic lateral sclerosis13
Epigenetic control of ataxin‐1 in multiple sclerosis12
Testing awareness in focal seizures: Clinical practice and interpretation of current guidelines12
Corrigendum12
COVID‐19‐associated immune‐mediated encephalitis mimicking acute‐onset Creutzfeldt‐Jakob disease12
The case of a 49‐year‐old man with involuntary toe movements12
Dynamic effects of prognostic factors and individual survival prediction for amyotrophic lateral sclerosis disease12
Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan12
Subclinical imaging activity in multiple sclerosis patients during war‐related psychological stress12
Association of serum Spp1 levels with disease progression in ALS and SBMA12
Evolution of disability in spinocerebellar ataxias type 1, 2, 3, and 612
Recurrent seizure‐related GRIN1 variant: Molecular mechanism and targeted therapy12
Peripheral nervous system manifestations of MOG antibody associated disease12
Comparison of SimoaTM and EllaTM to assess serum neurofilament‐light chain in multiple sclerosis12
Corrigendum12
Adult‐onset leukoencephalopathy caused by CSF1R mutations: Is all that glitters gold?11
Disease progression and brain atrophy in NMDAR encephalitis: Associated factor & clinical implication11
Visual atrophy rating scales and amyloid PET status in an Alzheimer's disease clinical cohort11
Corneal nerve loss predicts dementia in patients with mild cognitive impairment11
High diagnostic performance of plasma and cerebrospinal fluid beta‐synuclein for sporadic Creutzfeldt–Jakob disease11
Longitudinal Trajectories of Digital Cognitive Biomarkers for Multiple Sclerosis11
No evidence that herpes zoster is associated with increased risk of dementia diagnosis11
Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data11
Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early‐onset psychosis11
A potential biomarker of cognitive impairment: The olfactory dysfunction and its genes expression11
Cerebellar impulsivity–compulsivity assessment scale11
Home infusions of natalizumab for people with multiple sclerosis: a pilot randomised crossover trial11
Comparison of stress hyperglycemia ratio and glycemic gap on acute ICH in‐hospital outcomes11
Adaptive behavior assessed by Vineland‐3 as comprehensive outcome measure in vanishing white matter11
Association between brain health outcomes and metabolic risk factors in persons with diabetes11
Factors influencing the acute pentylenetetrazole‐induced seizure paradigm and a literature review11
Lipid levels and the risk of dementia: A dose–response meta‐analysis of prospective cohort studies11
Systemic inflammatory markers and EEG features of children with FIRES receiving anakinra11
Molecularly targeted treatment of recurrent anaplastic astrocytoma – a case report11
Correlation between spinal cord stimulation analgesia and cortical dynamics in pain management11
Asymptomatic spinal lesions in patients with AQP4‐IgG‐positive NMOSD: A real‐world cohort study11
Multiple sclerosis and inflammatory bowel disease: A systematic review and meta‐analysis11
Responsive neurostimulation for focal motor status epilepticus11
Novel Phenotypes and Deep Intronic Variant Expand TH‐Associated Dopa‐Responsive Dystonia Spectrum11
Seizure reduction in TSC2‐mutant mouse model by an mTOR catalytic inhibitor11
Effects of tirofiban on large vessel occlusion stroke are modified by etiology and renal function11
Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset11
Childhood‐onset progressive dystonia associated with pathogenic truncating variants in CHD810
Issue Information10
Diagnostic Challenge in Frontal Variant Alzheimer's Disease With Low Amyloid‐β PET Retention10
Multiple sclerosis clinical decision support system based on projection to reference datasets10
Identification of fibrinogen as a plasma protein binding partner for lecanemab biosimilar IgG10
Does long‐term phenytoin have a place in Dravet syndrome?10
Visual Snow Syndrome is unstable: A longitudinal investigation of VSS symptoms in a Naïve population10
White matter microstructures in Parkinson's disease with and without impulse control behaviors10
Longitudinal change in TSPO PET imaging in progressive multiple sclerosis10
The case of a 60‐year‐old man with decline in job performance and changes in personality and judgment10
Women's reproductive traits and ischemic stroke: a two‐sample Mendelian randomization study10
RNA mis‐splicing in children with congenital myotonic dystrophy is associated with physical function10
aHSCT is superior to alemtuzumab in maintaining NEDA and improving cognition in multiple sclerosis10
Correlation of slow‐wave sleep with motor and nonmotor progression in Parkinson's disease10
Issue Information10
Provisional practice recommendation for the management of myopathy in VCP‐associated multisystem proteinopathy10
Mobile digital gait analysis objectively measures progression in hereditary spastic paraplegia10
Reply to: “Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic”10
Annual stability of the plasma Aß40/42 ratio and associated factors10
LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials10
A sequential guide to identify neonates with low bacterial meningitis risk: a multicenter study10
SARS‐COV‐2 a trigger of myelin oligodendrocyte glycoprotein‐associated disorder10
Capturing what matters: Patient‐reported LGI1‐ANTibody encephalitis outcome RatiNg scale (LANTERN)9
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations9
Transcriptomic signature of painful human neurofibromatosis type 2 schwannomas9
Longitudinal study of immunity toSARS‐CoV2in ocrelizumab‐treatedMSpatients up to 2 years afterCOVID‐19 vaccination9
Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant9
First‐ever acute ischemic strokes in HIV‐infected persons: A case–control study from stroke units9
The Impact of In‐Hospital Disease Modifying Treatments on Mental and Physical Burden in Caregiver of Patients With MS9
Genotype‐function‐phenotype correlations for SCN1A variants identified by clinical genetic testing9
Radiomics in glioma: emerging trends and challenges9
Issue Information9
Socioeconomic status moderates associations between hippocampal development and cognition in preterms9
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Pituitary neuroendocrine tumor: A neuropsychological comparison with intra‐axial tumor9
Change of guard at ACTN9
Dynamic FDG‐PET demonstration of functional brain abnormalities9
Comparison of offspring outcomes in women with and without epilepsy9
High‐Fat and Low‐Carbohydrate Dietary Environments Are Linked to Reduced Idiopathic Epilepsy Incidence and Prevalence9
An ordinal clinical score predicts seizure freedom after minimally invasive epilepsy surgery9
Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics9
Where neurostimulation meets neurodegeneration in Parkinson's disease related to GBA variants9
Epidemiology of autoimmune encephalitis and comparison to infectious causes—Experience from a tertiary center9
Percentage brain volume change in multiple sclerosis mainly reflects white matter and cortical volume9
Interaction between sex and neurofilament light chain on brain structure and clinical severity in Huntington’s disease8
Issue Information8
B‐cell depletion limits HTLV‐1‐infected T‐cell expansion and ameliorate HTLV‐1‐associated myelopathy8
Effects of intravenous pulse methylprednisolone in neuromyelitis optica during the acute phase8
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Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants8
Clinical utility of cerebrospinal fluid biomarkers measured by LUMIPULSE® system8
Fulminant leptomeningeal disease diagnosed as comutant H3F3A and FGFR diffuse midline glioma8
Novel mutations in HTRA1‐related cerebral small vessel disease and comparison with CADASIL8
Proteomic profiling of sporadic late‐onset nemaline myopathy8
Dystonia, spastic tetraplegia, and ataxia due to a novel mutation in the dynamin domain of OPA18
Comparison between mono‐tacrolimus and mono‐glucocorticoid in the treatment of myasthenia gravis8
Sustained immunotolerance in multiple sclerosis after stem cell transplant8
Issue Information8
No pain, no strain: Targin® mitigates pain and constipation following spinal cord injury8
Accuracy of artificial intelligence software for CT angiography in stroke8
The case of a 75‐year‐old male with confusion and acute blindness8
Issue Information8
New phenotype of RTN2‐related spectrum: Complicated form of spastic paraplegia‐128
Reply to: The need for evidence‐based treatment decisions in spinal muscular atrophy type 08
Clinical characteristics of double negative atypical inflammatory demyelinating disease: A prospective study8
Clinical importance of changes in magnetic resonance biomarkers for Duchenne muscular dystrophy8
Temporopolar blurring signifies abnormalities of white matter in mesial temporal lobe epilepsy8
Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutation8
Shifting patterns of multiple sclerosis treatment in a highly prevalent United States population8
Issue Information8
Issue Information8
The potassium channel Kv1.3 as a therapeutic target for immunocytoprotection after reperfusion7
Pituitary cyclase‐activating polypeptide targeted treatments for the treatment of primary headache disorders7
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone7
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