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Cerebellar Theta Burst Stimulation Impairs Working Memory
Cerebellar Theta Burst Stimulation Impairs Working Memory
Working memory refers to the process of temporarily storing and manipulating information. The role of the cerebellum in wo...
Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases
Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases
Gillespie syndrome is a rare disorder caused by pathogenic variants in ITPR1 gene and characterized by the typical associa...
Cerebellar Contributions to Traumatic Autobiographical Memory in People with Post-Traumatic Stress Disorder
Cerebellar Contributions to Traumatic Autobiographical Memory in People with Post-Traumatic Stress Disorder
Post-traumatic stress disorder (PTSD) is a debilitating mental health condition characterized by recurrent re-experiencing...
Polyneuropathy in Patients with Spinocerebellar Ataxias Types 2, 3, and 10: A Systematic Review
Polyneuropathy in Patients with Spinocerebellar Ataxias Types 2, 3, and 10: A Systematic Review
Spinocerebellar ataxia (SCA) is an autosomal dominant hereditary disease with a low prevalence, for which more than 50 typ...
Differential Effects of Continuous Theta Burst Stimulation over the Bilateral and Unilateral Cerebellum on Working Memory
Differential Effects of Continuous Theta Burst Stimulation over the Bilateral and Unilateral Cerebellum on Working Memory
Recent functional MRI studies have implicated the cerebellum in working memory (WM) alongside the prefrontal cortex. Some ...
Postmortem Fatty Acid Abnormalities in the Cerebellum of Patients with Essential Tremor
Postmortem Fatty Acid Abnormalities in the Cerebellum of Patients with Essential Tremor
Fatty acids play many critical roles in brain function but have not been investigated in essential tremor (ET), a frequent...
Development of Extubation Success Prediction Model for Mechanically Ventilated Patients with Spontaneous Cerebellar Hemorrhage
Development of Extubation Success Prediction Model for Mechanically Ventilated Patients with Spontaneous Cerebellar Hemorrhage
Spontaneous cerebellar hemorrhage (SCH) patients have a low success rate in extubation, but there are currently no guideli...
Pseudodominance in RFC1-Spectrum Disorder
Pseudodominance in RFC1-Spectrum Disorder
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) and disease spectrum is an autosomal recessive disor...
Purkinje Cell Dendritic Swellings: A Postmortem Study of Essential Tremor and Other Cerebellar Degenerative Disorders
Purkinje Cell Dendritic Swellings: A Postmortem Study of Essential Tremor and Other Cerebellar Degenerative Disorders
Under stress, Purkinje cells (PCs) undergo a variety of reactive morphological changes. These can include swellings of neu...
Neuropsychiatric Symptoms in Rhombencephalosynapsis: A Clinical Report
Neuropsychiatric Symptoms in Rhombencephalosynapsis: A Clinical Report
Rhombencephalosynapsis (RES) is a hindbrain malformation characterized by a missing cerebellar vermis with apposition or f...
Investigating Cerebello-Frontal Circuits Associated with Emotional Prosody: A Double-Blind tDCS and fNIRS study
Investigating Cerebello-Frontal Circuits Associated with Emotional Prosody: A Double-Blind tDCS and fNIRS study
The emotional and cognitive cerebellum has been explored by several studies in the past years. Recent evidence suggested t...
CACNA1G Causes Dominantly Inherited Myoclonus-Ataxia with Intellectual Disability: A Case Report
CACNA1G Causes Dominantly Inherited Myoclonus-Ataxia with Intellectual Disability: A Case Report
Spinocerebellar ataxias (SCAs) are characterized by substantial phenotypic variability. Among them, SCA42 is a rare non-ex...
De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation
De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation
Bi-allelic pathogenic variants in GRID2 have been initially associated to an autosomal recessive form of spinocerebellar a...
Silica Nanoparticles from Melon Seed Husk Abrogated Binary Metal(loid) Mediated Cerebellar Dysfunction by Attenuation of Oxido-inflammatory Response and Upregulation of Neurotrophic Factors in Male Albino Rats
Silica Nanoparticles from Melon Seed Husk Abrogated Binary Metal(loid) Mediated Cerebellar Dysfunction by Attenuation of Oxido-inflammatory Response and Upregulation of Neurotrophic Factors in Male Albino Rats
Silica nanoparticles (SiNPs) have been touted for their role in the management of non-communicable diseases. Their neuropr...
The Latest Developments for the Treatment of Ataxia Telangiectasia: A Narrative Review
The Latest Developments for the Treatment of Ataxia Telangiectasia: A Narrative Review
Ataxia telangiectasia (AT), Louis-Bar syndrome, is a rare neurodegenerative disorder caused by autosomal recessive biallel...
Differences in the Impact of Intensive Rehabilitation on Hereditary Ataxias and the Cerebellar Subtype of Multiple System Atrophy
Differences in the Impact of Intensive Rehabilitation on Hereditary Ataxias and the Cerebellar Subtype of Multiple System Atrophy
Multiple system atrophy-cerebellar type (MSA-C) exhibits faster disease progression than does hereditary spinocerebellar d...
Differential Effects of Cerebellar Transcranial Direct Current Stimulation with Gait Training on Functional Mobility, Balance, and Ataxia Symptoms
Differential Effects of Cerebellar Transcranial Direct Current Stimulation with Gait Training on Functional Mobility, Balance, and Ataxia Symptoms
Cerebellar transcranial direct current stimulation (ctDCS) has emerged as a promising, non-invasive, and safe neuromodulat...
A Case of Coexistent Spinocerebellar Ataxia Type 2 and Primary Progressive Multiple Sclerosis—Coincidental or Associated?
A Case of Coexistent Spinocerebellar Ataxia Type 2 and Primary Progressive Multiple Sclerosis—Coincidental or Associated?
Spinocerebellar ataxia type 2 (SCA2) is a dominantly inherited ataxia primarily characterised by progressive cerebellar sy...
CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1
CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1
Spinocerebellar ataxia type 1 (SCA1) is the third most common type of spinocerebellar ataxias in China. CAT interruptions ...
Serum Neurofilament Light-Chain Concentrations in Essential Tremor: a Case–Control Study
Serum Neurofilament Light-Chain Concentrations in Essential Tremor: a Case–Control Study
Essential tremor (ET) is a common neurological disorder, with clinical and pathophysiological links to the cerebellum. Inq...
The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does Not Alter Cerebellar Neuron Populations in a Rat Model
The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does Not Alter Cerebellar Neuron Populations in a Rat Model
Spinocerebellar ataxia 34 (SCA34) is an autosomal dominant disease that arises from point mutations in the fatty acid elon...
Psychometric Validation of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) in Patients With Spinocerebellar Ataxia
Psychometric Validation of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) in Patients With Spinocerebellar Ataxia
This study aimed to generate evidence to support psychometric validity of the modified functional Scale for the Assessment...
Spatiotemporal Gait Analysis of Patients with Spinocerebellar Ataxia Types 3 and 10 Using Inertial Measurement Units: A Comparative Study
Spatiotemporal Gait Analysis of Patients with Spinocerebellar Ataxia Types 3 and 10 Using Inertial Measurement Units: A Comparative Study
Given the high morbidity related to the progression of gait deficits in spinocerebellar ataxias (SCA), there is a growing ...
Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene
Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene
The CACNA1A gene encodes the alpha-1A subunit of P/Q type voltage-gated calcium channel Cav2.1, which is associated with a...
Plasmapheresis and IVIG for Treatment of Non-Tumor Anti-Tr/DNER Antibody-Associated Ataxia: A Case Report
Plasmapheresis and IVIG for Treatment of Non-Tumor Anti-Tr/DNER Antibody-Associated Ataxia: A Case Report
Autoimmune cerebellar ataxia (ACA) is a condition characterized by progressive ataxia resulting from an immune-mediated at...
Scale for Ocular Motor Disorders in Ataxia (SODA) in Patients with Multiple System Atrophy
Scale for Ocular Motor Disorders in Ataxia (SODA) in Patients with Multiple System Atrophy
A clinical scale fully dedicated to evaluating ocular motor abnormalities is required for now. We investigated the utility...
Toward a Better Understanding of Walking Speed in Ataxia of Charlevoix-Saguenay: a Factor Exploratory Study
Toward a Better Understanding of Walking Speed in Ataxia of Charlevoix-Saguenay: a Factor Exploratory Study
Mobility limitations, including a decrease in walking speed, are major issues for people with autosomal recessive spastic ...
Cerebellar Direct Current Stimulation Reveals the Causal Role of the Cerebellum in Temporal Prediction
Cerebellar Direct Current Stimulation Reveals the Causal Role of the Cerebellum in Temporal Prediction
Temporal prediction (TP) influences our perception and cognition. The cerebellum could mediate this multi-level ability in...
Cerebellar Asymmetry of Motivational Direction: Anger-Dependent Effects of Cerebellar Transcranial Direct Current Stimulation on Aggression in Healthy Volunteers
Cerebellar Asymmetry of Motivational Direction: Anger-Dependent Effects of Cerebellar Transcranial Direct Current Stimulation on Aggression in Healthy Volunteers
It has recently been theorized that the frontal asymmetry of approach- and avoidance-related motivation is mirrored in the...
The Phenotypic Spectrum of Spinocerebellar Ataxia Type 19 in a Series of Latin American Patients
The Phenotypic Spectrum of Spinocerebellar Ataxia Type 19 in a Series of Latin American Patients
Spinocerebellar ataxia 19 (SCA19) represents a rare autosomal dominant genetic disorder resulting in progressive ataxia an...
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