Adjunct Professor, Neurology, Baylor College of Medicine
Neurology
Dr. Tetsuo Ashizawa, MD
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Tetsuo Ashizawa, MD is an expert in the field of Neurology. He attended Baylor College of Medicine. He over the years received 2 awards: "America's Top Doctors" and "CMS Meaningful Use Stage 1 Certification". Tetsuo Ashizawa is also published. He has 99 publications published. The lastest publication: "Getting a grip on the myotonic dystrophies.' Dr. Tetsuo Ashizawa accepts Medicare payments and is listed with Medicare.gov.
Publications
- Genome Modification Leads to Phenotype Reversal in Human Myotonic Dystrophy type 1 iPS-cell Derived Neural Stem Cells.
- Dynamic changes of nuclear RNA foci in proliferating DM1 cells.
- Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.
- Bolivian kindred with combined spinocerebellar Ataxia types 2 and 10.
- The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar Ataxia type 3 pathogenesis.
- Clinical Evaluation of Eye Movements in Spinocerebellar Ataxias: A Prospective Multicenter Study.
- Modulation of the age at onset in spinocerebellar Ataxia by CAG tracts in various genes.
- Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar Ataxias.
- Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other Muscular dystrophies.
- Spinocerebellar Ataxia type 10: from amerindians to latin americans.
- Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian Disorders.
- Analysis of the visual system in Friedreich Ataxia.
- Comprehensive Phenotype of the p.Arg420his Allelic Form of Spinocerebellar Ataxia Type 13.
- Diagnostic odyssey of patients with myotonic Dystrophy.
- Purkinje cell loss is the major brain pathology of spinocerebellar Ataxia type 10.
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's Disease motor onset.
- Generation of Neural Cells from DM1 Induced Pluripotent Stem Cells As Cellular Model for the Study of Central Nervous System Neuropathogenesis.
- Paradoxical effects of repeat interruptions on spinocerebellar Ataxia type 10 expansions and repeat instability.
- Acute onset of cerebellar Ataxia in a spinocerebellar Ataxia type 10 patient after use of steroids.
- Generation of Human-Induced Pluripotent Stem Cells to Model Spinocerebellar Ataxia Type 2 In vitro.
- Affective communication deficits associated with cerebellar degeneration.
- Oculomotor and visual axis systems sparing in spinocerebellar Ataxia type 13.
- Muscleblind-like 2-Mediated Alternative Splicing in the Developing Brain and Dysregulation in Myotonic Dystrophy.
- GGCCTG repeats put a hex on Purkinje cells and motor neurons in SCA36.
- Two Novel SNPs in ATXN3 3' UTR May Decrease Age at Onset of SCA3/MJD in Chinese Patients.
- Vascular risk factors and clinical progression in spinocerebellar Ataxias.
- Mutation in the kv3.3 voltage-gated potassium channel causing spinocerebellar Ataxia 13 disrupts sound-localization mechanisms.
- Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry.
- Endogenous inhibitor of ligand binding to the muscarinic acetylcholine receptor.
- The role of plasmapheresis therapy for perioperative management in ABO-incompatible adult living donor liver transplantation.
- Ethnic distribution of myotonic Dystrophy gene.
- Anticellular and antitumor activity of duocarmycins, novel antitumor antibiotics.
- Pi35(t), a new gene conferring partial resistance to leaf blast in the rice cultivar Hokkai 188.
- Ligation and catheterization of the hepatic artery for palliative treatment of malignant hepatic tumors.
- The hot bath test.
- Antigenic determinants of hen egg-white lysozyme in delayed hypersensitivity. II. Antigenicity and immunogenicity of the N- and C-terminal peptide.
- Proton magnetic resonance spectroscopy: an in vivo window to study neurodegenerative Disorders.
- Spastic pure motor monoparesis.
- Progressive multifocal leukoencephalopathy and magnetic resonance imaging.
- Interaction of myasthenic immunoglobulins and cholinergic agonists on acetylcholine receptors of rat myotubes.
- Complement-dependent lysis of cultured rat myotubes by myasthenic immunoglobulins.
- Clinical features of Todd''s post-epileptic paralysis.
- Meige's syndrome.
- Immunohistochemical and molecular analysis of giant cell carcinoma of the pancreas: a report of three cases.
- Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells?
- Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniques.
- Myotonic Dystrophy as a brain disorder.
- A dominantly inherited syndrome with continuous motor neuron discharges.
- Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic Dystrophy locus on chromosome 19.
- Analysis of exposed regions on the main extracellular domain of mouse acetylcholine receptor alpha subunit in live muscle cells by binding profiles of antipeptide anti...
- NcoI and TaqI RFLPs for human M creatine kinase (CKM)
- cDNA surveying of specific tissue expression of human chromosome 19 sequences.
- Cerebral vasculitis in relapsing polychondritis.
- Paroxysmal kinesigenic dyskinesia and infantile Convulsions. Clinical and linkage studies. 2000.
- Repeats may not be everything in anticipation.
- What is Kearns-Sayre syndrome after all?
- Molecular basis of neuromuscular Diseases.
- Getting a grip on the myotonic dystrophies.
- Delayed diagnosis of Friedreich's Ataxia due to coexisting recessive deaf/blind syndrome.
- Instability of the (CTG)n repeat in congenital myotonic Dystrophy.
- Diagnostic value of ophthalmologic findings in myotonic Dystrophy: comparison with risks calculated by haplotype analysis of closely linked restriction fragment length...
- [Instability of myotonic Dystrophy CTG trinucleotide repeat].
- RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1.
- Profile of the regions on the alpha-chain of human acetylcholine receptor recognized by autoantibodies in Myasthenia gravis.
- Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic Dystrophy.
- An unstable triplet repeat in a gene related to myotonic Muscular dystrophy.
- Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
- Antigen mimicry in autoimmune Disease. Can immune responses to microbial antigens that mimic acetylcholine receptor act as initial triggers of Myasthenia gravis?
- Myotonic Dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?
- Symptom onset of spinocerebellar Ataxia type 10 in pregnancy and puerperium.
- Autoimmune T cell recognition of human acetylcholine receptor: the sites of T cell recognition in Myasthenia gravis on the extracellular part of the alpha subunit.
- Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar Ataxia type 10.
- Alcohol dehydrogenase polymorphism and Parkinson''s Disease.
- Phenotypic expression of the myotonic Dystrophy gene in monozygotic twins.
- Anticipation in myotonic Dystrophy. I. Statistical verification based on clinical and haplotype findings.
- Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington Disease.
- Cardiac involvement in a large kindred with myotonic Dystrophy. Quantitative assessment and relation to size of CTG repeat expansion.
- Anticipation in myotonic Dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.
- Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.
- Paroxysmal kinesigenic dyskinesia and infantile Convulsions: clinical and linkage studies.
- Somatic instability of CTG repeat in myotonic Dystrophy.
- Mapping of the polypeptide chain organization of the main extracellular domain of the alpha-subunit in membrane-bound acetylcholine receptor by antipeptide antibodies ...
- Epitope-specific suppression of antibody response in experimental autoimmune Myasthenia gravis by a monomethoxypolyethylene glycol conjugate of a myasthenogenic synthe...
- Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic Dystrophy.
- Emotional and functional impact of DNA testing on patients with symptoms of Huntington''s Disease.
- Objective home-based gait assessment in spinocerebellar Ataxia.
- Autoimmune recognition profile of the alpha chain of human acetylcholine receptor in Myasthenia gravis.
- Measuring Friedreich Ataxia: complementary features of examination and performance measures.
- Measuring Friedreich Ataxia: Interrater reliability of a neurologic rating scale.
- Clinical and genetic analysis of four Mexican families with spinocerebellar Ataxia type 10.
- Effect of myotonic Dystrophy trinucleotide repeat expansion on DMPK transcription and processing.
- Germline mutational dynamics in myotonic Dystrophy type 1 males: allele length and age effects.
- Atypical Friedreich Ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
- Clinical phenotype of Brazilian families with spinocerebellar Ataxia 10.
- SCA10 and ATTCT repeat expansion: clinical features and molecular aspects.
- Reduced penetrance of intermediate size alleles in spinocerebellar Ataxia type 10.
- Suppression of experimental Myasthenia gravis by monoclonal antibodies against MHC peptide region involved in presentation of a pathogenic T-cell epitope.
- Autosomal dominant cerebellar Ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
Schools
Keio Gijuku University School of Medicine
Allegheny Genl Hospital
Baylor College Of Med
UF Health The University of Florida Academic Health Center Director McKnight Brain Institute
Conditions Treated
- Anterior Horn Disease
- Ataxia
- Chronic Inflammatory Demyelinating Polyneuritis
- Convulsions
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Doctors Specialties
- Neurology
Accepted Insurances
Awards
- America's Top Doctors
- CMS Meaningful Use Stage 1 Certification
Education
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Baylor College of Medicine -
Allegheny General Hospital - Western Pennsylvania Hospital -
Keio Gujuku University School of Medicine
Hospital
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UF Health Shands Hospital
Drug Facts
| NPI NUMBER | 1093873754 | |
| NPPES Provider LastName | ASHIZAWA | |
| NPPES Provider FirstName | TETSUO | |
| NPPES Provider ZIPCode | 326103003 | |
| NPPES Provider State | FL | |
| Specialty Description | Nephrology | |
| Total Claim Count | 44.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1093873754 |
| Last Name Of The Provider | ASHIZAWA |
| First Name Of The Provider | TETSUO |
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