Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024
Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023
The Phenotypic Continuum of ATP1A3-Related Disorders
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021
A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Clinical Manifestations of the anti-IgLON5 Disease
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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Transglutaminase 6 Antibodies in the Diagnosis of Gluten Ataxia
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
JNNP 79:672-677, Wagner,J.N.,et al, 2008
JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008
Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
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Late-Onset Friedreich Ataxia
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Gluten Sensitivity as a Neurological Illness
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Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Niemann-Pick Disease Type C: Two Cases and an Update
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
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Clinicopath Conf
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Paraneoplastic Cerebellar Degeneration
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Mitochondrial DNA and Disease
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Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
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Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Paraneoplastic Syndrome Manifesting as Chronic Cerebellar Ataxia in a Child with Hodgkin Disease
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