Tetsuo Ashizawa


Ontology type: schema:Person     


Person Info

NAME

Tetsuo

SURNAME

Ashizawa

Publications in SciGraph latest 50 shown

  • 2019-02 Intravenously Administered Novel Liposomes, DCL64, Deliver Oligonucleotides to Cerebellar Purkinje Cells in THE CEREBELLUM
  • 2019-02 Olfactory Function in SCA10 in THE CEREBELLUM
  • 2018-12 Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies in CURRENT STEM CELL REPORTS
  • 2018-11-08 Author Correction: Spinocerebellar ataxias: prospects and challenges for therapy development in NATURE REVIEWS NEUROLOGY
  • 2018-10 Spinocerebellar ataxias: prospects and challenges for therapy development in NATURE REVIEWS NEUROLOGY
  • 2017-12 Correction to: SPG7 and Impaired Emotional Communication in THE CEREBELLUM
  • 2017-12 Nonmotor Symptoms in Patients with Spinocerebellar Ataxia Type 10 in THE CEREBELLUM
  • 2017-08 A Comparative Optical Coherence Tomography Study of Spinocerebellar Ataxia Types 3 and 10 in THE CEREBELLUM
  • 2017-06 The Initial Symptom and Motor Progression in Spinocerebellar Ataxias in THE CEREBELLUM
  • 2017-04 SPG7 and Impaired Emotional Communication in THE CEREBELLUM
  • 2017-03 Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6 in BRAIN STRUCTURE AND FUNCTION
  • 2016-04 Rare neurological channelopathies — networks to study patients, pathogenesis and treatment in NATURE REVIEWS NEUROLOGY
  • 2015-12 High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression in THE CEREBELLUM
  • 2015-06 Dynamic changes of nuclear RNA foci in proliferating DM1 cells in HISTOCHEMISTRY AND CELL BIOLOGY
  • 2014-09 Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease in JOURNAL OF NEUROLOGY
  • 2014-04 Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias in THE CEREBELLUM
  • 2014-03 Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures in NEUROGENETICS
  • 2013-12 Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study in ORPHANET JOURNAL OF RARE DISEASES
  • 2013-12 Comprehensive Phenotype of the p.Arg420his Allelic Form of Spinocerebellar Ataxia Type 13 in THE CEREBELLUM
  • 2013-11 Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset in NEUROGENETICS
  • 2013-11 Spinocerebellar Ataxia Type 10: From Amerindians to Latin Americans in CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS
  • 2013-11 Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-10 Generation of Human-Induced Pluripotent Stem Cells to Model Spinocerebellar Ataxia Type 2 In vitro in JOURNAL OF MOLECULAR NEUROSCIENCE
  • 2013-10 Diagnostic odyssey of patients with myotonic dystrophy in JOURNAL OF NEUROLOGY
  • 2013-09 Analysis of the visual system in Friedreich ataxia in JOURNAL OF NEUROLOGY
  • 2008-02 Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2006-12 Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study in BMC MEDICAL GENETICS
  • 2006 Recent Progress in Spinocerebellar Ataxia Type 10 in HUMAN NUCLEOTIDE EXPANSION DISORDERS
  • 2005-03 Recent progress in spinocerebellar ataxia type-10 (SCA10) in THE CEREBELLUM
  • 2004-10 Abstracts from ASENT 2004 Annual Meeting March 11–13, 2004 in NEUROTHERAPEUTICS
  • 2003-08 Haplotype analysis of the ETM2 locus in familial essential tremor in NEUROGENETICS
  • 2002-04 The Hereditary Ataxias in THE CEREBELLUM
  • 2002 Spinocerebellar Ataxia Type 10: A Disease Caused by a Large ATTCT Repeat Expansion in TRIPLE REPEAT DISEASES OF THE NERVOUS SYSTEMS
  • 2000-10 Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 in NATURE GENETICS
  • 2000-05 Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells? in MOLECULAR PSYCHIATRY
  • 1999-11 DNA microarray-based profiling of global gene-expression changes in myotonic dystrophy in NATURE GENETICS
  • 1997-01 Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel in NATURE GENETICS
  • 1996-10 Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An entity distinct from proximal myotonic myopathy (PROMM)? in JOURNAL OF NEUROLOGY
  • 1994-11 Analysis of exposed regions on the main extracellular domain of mouse acetylcholine receptor α subunit in live muscle cells by binding profiles of antipeptide antibodies in THE PROTEIN JOURNAL
  • 1994 Mapping of the Polypeptide Chain Organization of the Main Extracellular Domain of the α-Subunit in Membrane-Bound Acetylcholine Receptor by Anti-Peptide Antibodies Spanning the Entire Domain in IMMUNOBIOLOGY OF PROTEINS AND PEPTIDES VII
  • 1991 Autoimmune Recognition Profile of the Alpha Chain of Human Acetylcholine Receptor in Myasthenia Gravis in IMMUNOBIOLOGY OF PROTEINS AND PEPTIDES VI
  • 1985-08 Immunopathologic events at the endplate in myasthenia gravis in SEMINARS IN IMMUNOPATHOLOGY
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