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A case of a heterozygous ABCC6 mutation showing recurrent ischemic strokes and intracranial hemorrhages
A case of a heterozygous ABCC6 mutation showing recurrent ischemic strokes and intracranial hemorrhages
Abstract Mutations in the ATP-binding cassette subfamily C member 6 (ABCC6) gene are responsible for pseudoxanthoma elasti...
Case of cortical superficial siderosis presenting with corticobasal syndrome
Case of cortical superficial siderosis presenting with corticobasal syndrome
Abstract A 70-year-old man presented with slow gait and a clumsy hand on the right side. Neurological examination revealed...
A Case of Cortical Superficial Siderosis Presenting with Corticobasal Syndrome
A Case of Cortical Superficial Siderosis Presenting with Corticobasal Syndrome
Abstract A 70-year-old man presented with slow gait and a clumsy hand on the right side. Neurological examination revealed...
Critical illness neuropathy: a clinicopathological case
Critical illness neuropathy: a clinicopathological case
Abstract We report a case of an older woman who, after a long-lasting systemic inflammation in a non-ICU hospital ward, de...
Long‐term changes of the neural network in case of improved post‐hypoxic myoclonus and gait
Long‐term changes of the neural network in case of improved post‐hypoxic myoclonus and gait
Abstract Chronic post-hypoxic myoclonus (PHM) is a rare complication after successful cardiopulmonary resuscitation that c...
Endovascular revascularization for internal carotid artery dissection during stroke‐like episode in MELAS: A case report
Endovascular revascularization for internal carotid artery dissection during stroke‐like episode in MELAS: A case report
Abstract A 45-year-old woman was admitted to our hospital because of speech difficulties. Initial magnetic resonance imagi...
Isolated sensory impairment of the ear auricle in a patient with cerebral infarction localized to the postcentral gyrus
Isolated sensory impairment of the ear auricle in a patient with cerebral infarction localized to the postcentral gyrus
Abstract Pure sensory stroke, a well-defined clinical entity characterized by sensory symptoms, sometimes causes atypical ...
Unusual brain morphological changes in amyotrophic lateral sclerosis after long‐term tracheostomy invasive ventilation
Unusual brain morphological changes in amyotrophic lateral sclerosis after long‐term tracheostomy invasive ventilation
Abstract We report the cases of two patients who developed unusual brain morphological changes reminiscent of disproportio...
Brain diseases and aspiration pneumonia in older person
Brain diseases and aspiration pneumonia in older person
Abstract Objective Age-related brain symptoms (gait, speech and swallowing difficulties, and dementia) increase the risk o...
Autoimmune myositis – mechanism and therapy development
Autoimmune myositis – mechanism and therapy development
Abstract Over the recent decades, notable progress has been made in the understanding of the pathomechanism of autoimmune ...
Morphological and Functional Changes of Striatal Neurons with L‐dopa‐induced Dyskinesia
Morphological and Functional Changes of Striatal Neurons with L‐dopa‐induced Dyskinesia
Abstract Priming and expression of L-dopa-induced dyskinesia (LID) is associated with maladaptive plasticity of striatal s...
Challenges of persons with Multiple Sclerosis on ocrelizumab treatment during COVID‐19 pandemic
Challenges of persons with Multiple Sclerosis on ocrelizumab treatment during COVID‐19 pandemic
Abstract Background Coronavirus disease of the 2019 pandemic caused much fear among people with chronic diseases and those...
Three Cases of GFAP Astrocytopathy, One with Bilateral Ovarian Teratoma
Three Cases of GFAP Astrocytopathy, One with Bilateral Ovarian Teratoma
Abstract Glial fibrillary acidic protein (GFAP) astrocytopathy is a novel autoimmune meningoencephalomyelitis. Case 1 is a...
Spontaneous Conus Medullary Infarction in the absence of Cardiovascular Risk Factors
Spontaneous Conus Medullary Infarction in the absence of Cardiovascular Risk Factors
Abstract Spinal cord infarction (SCI) is a rare but devastating disease that occurs in association with trauma or predispo...
Aseptic meningitis and myelitis as presenting features of SLE
Aseptic meningitis and myelitis as presenting features of SLE
Abstract Systemic lupus erythematosus (SLE) is an autoimmune disorder affecting multiple organs of body. We present a case...
Autonomic manifestations in autoimmune encephalitis
Autonomic manifestations in autoimmune encephalitis
Abstract Autoimmune encephalitis represented by anti-NMDA receptor antibody positive encephalitis is a type of non-herpeti...
Evaluation of headaches in primary brain calcification in Japan
Evaluation of headaches in primary brain calcification in Japan
Abstract Background Primary brain calcification (PBC) is a rare neurodegenerative disorder characterized by bilateral calc...
Internal carotid artery dissection due to Eagle syndrome: Case report and review of literatures
Internal carotid artery dissection due to Eagle syndrome: Case report and review of literatures
Abstract Eagle syndrome is a rare condition induced by an elongated styloid process. A 51-year-old man became aware of wea...
The Processes Underlying Chronic Migraine Pathophysiology and its Treatment with Botulinum Toxin Type A
The Processes Underlying Chronic Migraine Pathophysiology and its Treatment with Botulinum Toxin Type A
Abstract Objective To comprehensively review both the models of migraine pathophysiology and transformation to chronic mig...
Validation of hyperacute stroke protocol modification aiming for time saving
Validation of hyperacute stroke protocol modification aiming for time saving
Abstract Background and Purpose Since efforts to save time in hyperacute cerebral infarction largely depend on each facili...
Autophagic vacuolar myopathy: Danon disease and related myopathies
Autophagic vacuolar myopathy: Danon disease and related myopathies
Abstract Autophagic vacuolar myopathy is a subgroup of muscle diseases defined as a condition in which autophagic vacuoles...
A nationwide survey of episodic ataxia in Japan
A nationwide survey of episodic ataxia in Japan
Abstract Background Episodic ataxia (EA) is a rare inherited disorder characterized by recurrent cerebellar ataxic attacks...
A case of cutis verticis gyrata‐mental retardation syndrome accompanied by various neurological abnormalities
A case of cutis verticis gyrata‐mental retardation syndrome accompanied by various neurological abnormalities
Abstract We report a 44-year-old male with cutis verticis gyrate (CVG)-mental retardation syndrome. His backhead skin form...