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Tetsuo Ashizawa

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Adriana Moro; Mariana Moscovich; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa; Torben C Bezerra; Hélio A G Teive
Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids.
Misti White; Guangbin Xia; Rui Gao; Karen McFarland; Partha S Sarkar; Maki Wakamiya; Tetsuo Ashizawa
Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model.
Hélio A G Teive; Lineu C Werneck; Walter Oleschko Arruda; Iscia Lopes-Cendes; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa
Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.

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2013: Adriana Moro; Mariana Moscovich; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa; Torben C Bezerra; Hélio A G Teive
Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids.
Arquivos de neuro-psiquiatria 2013;71(1):66.
2012: Misti White; Guangbin Xia; Rui Gao; Karen McFarland; Partha S Sarkar; Maki Wakamiya; Tetsuo Ashizawa
Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: a toxic RNA gain-of-function model.
Journal of neuroscience research 2012;90(3):706-14.
2012: Hélio A G Teive; Lineu C Werneck; Walter Oleschko Arruda; Iscia Lopes-Cendes; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa
Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Clinics (São Paulo, Brazil) 2012;67(5):443-9.
2011: Hélio A G Teive; Lineu César Werneck; Walter Oleschko Arruda; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa
Spinocerebellar ataxia type 10 - A review.
Parkinsonism & related disorders 2011;17(9):655-61.
2011: Hélio A G Teive; Renato P Munhoz; Tetsuo Ashizawa
Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol.
Arquivos de neuro-psiquiatria 2011;69(5):841.
2011: Hélio A G Teive; Walter Oleschko Arruda; Salmo Raskin; Renato P Munhoz; Jorge A A Zavala; Lineu César Werneck; Tetsuo Ashizawa
Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2011;18(3):437-8.
2010: Hélio A G Teive; Renato P Munhoz; Salmo Raskin; Walter Oleschko Arruda; Luciano de Paola; Lineu César Werneck; Tetsuo Ashizawa
Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.
Movement disorders : official journal of the Movement Disorder Society 2010;25(16):2875-8.
2010: Misti C White; Rui Gao; Weidong Xu; Santi M Mandal; Jung G Lim; Tapas K Hazra; Maki Wakamiya; Sharon F Edwards; Salmo Raskin; Hélio A G Teive; Huda Y Zoghbi; Partha S Sarkar; Tetsuo Ashizawa
Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.
PLoS genetics 2010;6(6):e1000984.
2008: Rui Gao; Tohru Matsuura; Mary Coolbaugh; Christine Zühlke; Koichiro Nakamura; Astrid Rasmussen; Michael J Siciliano; Tetsuo Ashizawa; Xi Lin
Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17.
European journal of human genetics : EJHG 2008;16(2):215-22.
2007: Hélio A G Teive; Walter Oleschko Arruda; Salmo Raskin; Tetsuo Ashizawa; Lineu César Werneck
The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene.
Arquivos de neuro-psiquiatria 2007;65(4A):965-8.
2007: Astrid Rasmussen; Irene De Biase; Marcela Fragoso-Benítez; Marco Antonio Macías-Flores; Petra Yescas; Adriana Ochoa; Tetsuo Ashizawa; Maria E Alonso; Sanjay I Bidichandani
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
Annals of neurology 2007;61(6):607-10.
2007: Elisa Alonso; Leticia Martínez-Ruano; Irene De Biase; Christopher Mader; Adriana Ochoa; Petra Yescas; Roxana Gutiérrez; Misti White; Luís Ruano; Marcela Fragoso-Benítez; Tetsuo Ashizawa; Sanjay I Bidichandani; Astrid Rasmussen
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Movement disorders : official journal of the Movement Disorder Society 2007;22(7):1050-3.
2007: Salmo Raskin; Tetsuo Ashizawa; Hélio A G Teive; Walter Oleschko Arruda; Ping Fang; Rui Gao; Misti C White; Lineu César Werneck; Benjamin B Roa
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
Archives of neurology 2007;64(4):591-4.
2006: M Wakamiya; T Matsuura; Y Liu; G C Schuster; R Gao; W Xu; P S Sarkar; Xi Lin; Tetsuo Ashizawa
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
Neurology 2006;67(4):607-13.
2006: Maria de Haro; Ismael Al-Ramahi; Beatrice De Gouyon; Lubna Ukani; Alberto Rosa; Nuno André Faustino; Tetsuo Ashizawa; Thomas A Cooper; Juan Botas
MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
Human molecular genetics 2006;15(13):2138-45.
2006: Masaaki Waragai; Shinichiro Nagamitsu; Weidong Xu; Yu Jiang Li; Xi Lin; Tetsuo Ashizawa
Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit.
Journal of neuroscience research 2006;83(7):1170-8.
2006: Tohru Matsuura; Ping Fang; Christopher E Pearson; Parul Jayakar; Tetsuo Ashizawa; Benjamin B Roa; David L Nelson
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
American journal of human genetics 2006;78(1):125-9.
2005: Xi Lin; Tetsuo Ashizawa
Recent progress in spinocerebellar ataxia type-10 (SCA10).
Cerebellum (London, England) 2005;4(1):37-42.
2004: Rajesh Sharma; Irene De Biase; Mariluz Gómez; Martin B Delatycki; Tetsuo Ashizawa; Sanjay I Bidichandani
Friedreich ataxia in carriers of unstable borderline GAA triplet-repeat alleles.
Annals of neurology 2004;56(6):898-901.
2004: Hélio A G Teive; Benjamin B Roa; Salmo Raskin; Ping Fang; Walter Oleschko Arruda; Y Correa Neto; R Gao; Lineu César Werneck; Tetsuo Ashizawa
Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
Neurology 2004;63(8):1509-12.
2004: Madhavi Thomas; Tetsuo Ashizawa; Joseph Jankovic
Minocycline in Huntington's disease: a pilot study.
Movement disorders : official journal of the Movement Disorder Society 2004;19(6):692-5.
2004: Tohru Matsuura; Ping Fang; Xi Lin; Mehrdad Khajavi; Kuniko Tsuji; Astrid Rasmussen; Raji P Grewal; Madhureeta Achari; Maria E Alonso; Stef pulst; Huda Y Zoghbi; David L Nelson; Benjamin B Roa; Tetsuo Ashizawa
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.
American journal of human genetics 2004;74(6):1216-24.
2004: Vera I Hashem; Malgorzata J Pytlos; Elzbieta A Klysik; Kuniko Tsuji; Mehrdad Khajavi; Merhdad Khajav; Tetsuo Ashizawa; Richard R Sinden
Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients.
Nucleic acids research 2004;32(21):6334-46.
2004: Vladimir N Potaman; Elena A Oussatcheva; Yuri L Lyubchenko; Luda S Shlyakhtenko; S I Bidichandani; Tetsuo Ashizawa; Richard R Sinden
Length-dependent structure formation in Friedreich ataxia (GAA)n*(TTC)n repeats at neutral pH.
Nucleic acids research 2004;32(3):1224-31.
2003: Tetsuo Ashizawa
[Recent changes in the neurology residency program in the United States].
Rinshō shinkeigaku = Clinical neurology 2003;43(11):854-6.
2003: Alberto L Rosa; Joseph Jankovic; Tetsuo Ashizawa
Screening for mutations in the MECP2 (Rett syndrome) gene in Gilles de la Tourette syndrome.
Archives of neurology 2003;60(4):502-3.
2003: Vladimir N Potaman; John J Bissler; Vera I Hashem; Elena A Oussatcheva; Lu Lu; Luda S Shlyakhtenko; Yuri L Lyubchenko; Tohru Matsuura; Tetsuo Ashizawa; Michael Leffak; Craig J Benham; Richard R Sinden
Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats.
Journal of molecular biology 2003;326(4):1095-111.
2003: Xi Lin; Tetsuo Ashizawa
SCA10 and ATTCT repeat expansion: clinical features and molecular aspects.
Cytogenetic and genome research 2003;100(1-4):184-8.
2002: Rajesh Sharma; Saeeda Bhatti; Mariluz Gomez; Rhonda M Clark; Cynthia Murray; Tetsuo Ashizawa; Sanjay I Bidichandani
The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions.
Human molecular genetics 2002;11(18):2175-87.
2002: Raji P Grewal; Madhureeta Achari; Tohru Matsuura; Alberto Durazo; Emilio Tayag; Lan Zu; Stef pulst; Tetsuo Ashizawa
Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.
Archives of neurology 2002;59(8):1285-90.
2002: Minako Oshima; Philip R Deitiker; Tetsuo Ashizawa; M Zouhair Atassi
Vaccination with a MHC class II peptide attenuates cellular and humoral responses against tAChR and suppresses clinical EAMG.
Autoimmunity 2002;35(3):183-90.
2002: Tohru Matsuura; Laura P W Ranum; V Volpini; M Pandolfo; H Sasaki; K Tashiro; Kei Watase; Huda Y Zoghbi; Tetsuo Ashizawa
Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.
Neurology 2002;58(6):983-4.
2002: P-Y Xu; R Liang; Joseph Jankovic; Christine Hunter; Y-X Zeng; Tetsuo Ashizawa; Dejian Lai; Wei-Dong Le
Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease.
Neurology 2002;58(6):881-4.
2002: Tohru Matsuura; Tetsuo Ashizawa
Spinocerebellar ataxia type 10: a disease caused by a large ATTCT repeat expansion.
Advances in experimental medicine and biology 2002;516():79-97.
2002: Shinichiro Nagamitsu; Tetsuo Ashizawa
Myotonic dystrophies.
Advances in neurology 2002;88():293-314.
2001: Tetsuo Ashizawa; Tohru Matsuura
[Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].
Rinshō shinkeigaku = Clinical neurology 2001;41(12):1120-2.
2001: Astrid Rasmussen; T Matsuura; L Ruano; Petra Yescas; Adriana Ochoa; Tetsuo Ashizawa; Elisa Alonso
Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
Annals of neurology 2001;50(2):234-9.
2001: EK Tan; Shinichiro Nagamitsu; Tohru Matsuura; Mehrdad Khajavi; Joseph Jankovic; William G Ondo; Tetsuo Ashizawa
Alcohol dehydrogenase polymorphism and Parkinson's disease.
Neuroscience letters 2001;305(1):70-2.
2001: Mehrdad Khajavi; Ana M Tari; N B Patel; Kuniko Tsuji; Doris R Siwak; Marvin L Meistrich; N H Terry; Tetsuo Ashizawa
"Mitotic drive" of expanded CTG repeats in myotonic dystrophy type 1 (DM1).
Human molecular genetics 2001;10(8):855-63.
2001: Nikolai A Timchenko; Zong-Jin Cai; Alana L Welm; S Reddy; Tetsuo Ashizawa; Lubov T Timchenko
RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1.
The Journal of biological chemistry 2001;276(11):7820-6.
2001: E K Tan; Tetsuo Ashizawa
Genetic testing in spinocerebellar ataxias: defining a clinical role.
Archives of neurology 2001;58(2):191-5.
2000: Shinichiro Nagamitsu; Tohru Matsuura; Mehrdad Khajavi; R Armstrong; Clifton L Gooch; Yadollah Harati; Tetsuo Ashizawa
A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.
Neurology 2000;55(11):1697-703.
2000: Tohru Matsuura; T Yamagata; Daniel L Burgess; A Rasmussen; Raji P Grewal; Kei Watase; Mehrdad Khajavi; AE McCall; Caleb F Davis; Lan Zu; Madhureeta Achari; Stef pulst; E Alonso; Jeffrey L Noebels; David L Nelson; Huda Y Zoghbi; Tetsuo Ashizawa
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Nature genetics 2000;26(2):191-4.
2000: EK Tan; Mehrdad Khajavi; J I Thornby; Shinichiro Nagamitsu; Joseph Jankovic; Tetsuo Ashizawa
Variability and validity of polymorphism association studies in Parkinson's disease.
Neurology 2000;55(4):533-8.
2000: N Nakayashiki; Minako Oshima; Philip R Deitiker; Tetsuo Ashizawa; M Zouhair Atassi
Suppression of experimental myasthenia gravis by monoclonal antibodies against MHC peptide region involved in presentation of a pathogenic T-cell epitope.
Journal of neuroimmunology 2000;105(2):131-44.
2000: EK Tan; Tohru Matsuura; Shinichiro Nagamitsu; Mehrdad Khajavi; Joseph Jankovic; Tetsuo Ashizawa
Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?
Neurology 2000;54(5):1195-8.
2000: Philip R Deitiker; Tetsuo Ashizawa; M Zouhair Atassi
Antigen mimicry in autoimmune disease. Can immune responses to microbial antigens that mimic acetylcholine receptor act as initial triggers of Myasthenia gravis?
Human immunology 2000;61(3):255-65.
2000: Daniel L Burgess; Tohru Matsuura; Tetsuo Ashizawa; Jeffrey L Noebels
Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.
Epilepsia 2000;41(1):24-7.
1999: Sanjay I Bidichandani; Smita M Purandare; E E Taylor; G Gumin; H Machkhas; Yadollah Harati; Richard A Gibbs; Tetsuo Ashizawa; Pragna I Patel
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence.
Human molecular genetics 1999;8(13):2425-36.
1999: Tohru Matsuura; Madhureeta Achari; Mehrdad Khajavi; L L Bachinski; Huda Y Zoghbi; Tetsuo Ashizawa
Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.
Annals of neurology 1999;45(3):407-11.
1998: C S Benton; R de Silva; S L Rutledge; S Bohlega; Tetsuo Ashizawa; Huda Y Zoghbi
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype.
Neurology 1998;51(4):1081-6.
1998: Sanjay I Bidichandani; Tetsuo Ashizawa; Pragna I Patel
The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.
American journal of human genetics 1998;62(1):111-21.
1997: Tetsuo Ashizawa
[Instability of myotonic dystrophy CTG trinucleotide repeat].
Rinshō shinkeigaku = Clinical neurology 1997;37(12):1151.
1997: Olga Zhuchenko; J Bailey; Penelope E Bonnen; Tetsuo Ashizawa; David Wayne Stockton; Christopher I Amos; William B Dobyns; S H Subramony; Huda Y Zoghbi; Cheng Chi Lee
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
Nature genetics 1997;15(1):62-9.
1996: Raye L Alford; Tetsuo Ashizawa; Joseph Jankovic; CT Caskey; Carolyn S (Sue) Richards
Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease.
American journal of medical genetics 1996;66(3):281-6.
1996: Tetsuo Ashizawa; Darren G Monckton; S Vaishnav; B J Patel; A Voskova; CT Caskey
Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.
Genomics 1996;36(1):47-53.
1996: Tetsuo Ashizawa; Joseph Jankovic
Cervical dystonia as the initial presentation of Huntington's disease.
Movement disorders : official journal of the Movement Disorder Society 1996;11(4):457-9.
1995: L S Tokgozoglu; Tetsuo Ashizawa; A Pacifico; R M Armstrong; Henry F Epstein; W A Zoghbi
Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion.
JAMA : the journal of the American Medical Association 1995;274(10):813-9.
1995: Joseph Jankovic; J Beach; Tetsuo Ashizawa
Emotional and functional impact of DNA testing on patients with symptoms of Huntington's disease.
Journal of medical genetics 1995;32(7):516-8.
1995: Joseph Jankovic; Tetsuo Ashizawa
Tourettism associated with Huntington's disease.
Movement disorders : official journal of the Movement Disorder Society 1995;10(1):103-5.
1995: L J Wong; Tetsuo Ashizawa; Darren G Monckton; CT Caskey; Carolyn S (Sue) Richards
Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.
American journal of human genetics 1995;56(1):114-22.
1995: Darren G Monckton; L J Wong; Tetsuo Ashizawa; CT Caskey
Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses.
Human molecular genetics 1995;4(1):1-8.
1994: Tetsuo Ashizawa; L J Wong; Carolyn S (Sue) Richards; CT Caskey; Joseph Jankovic
CAG repeat size and clinical presentation in Huntington's disease.
Neurology 1994;44(6):1137-43.
1994: Tetsuo Ashizawa; M Anvret; M Baiget; J M Barceló; H Brunner; A M Cobo; Bruno Dallapiccola; R G Fenwick; U Grandell; H Harley
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.
American journal of human genetics 1994;54(3):414-23.
1994: Tetsuo Ashizawa; P W Dunne; P A Ward; W K Seltzer; Carolyn S (Sue) Richards
Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring.
Neurology 1994;44(1):120-2.
1993: Tetsuo Ashizawa; J R Dubel; Yadollah Harati
Somatic instability of CTG repeat in myotonic dystrophy.
Neurology 1993;43(12):2674-8.
1993: Y H Fu; D L Friedman; S Richards; J A Pearlman; Richard A Gibbs; Antonio Pizzuti; Tetsuo Ashizawa; M Benjamin Perryman; G Scarlato; R G Fenwick
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.
Science (New York, N.Y.) 1993;260(5105):235-8.
1992: P W Dunne; S W Wang; Tetsuo Ashizawa; M Benjamin Perryman; Henry F Epstein
cDNA surveying of specific tissue expression of human chromosome 19 sequences.
Genomics 1992;14(2):263-9.
1992: Tetsuo Ashizawa; J R Dubel; P W Dunne; C J Dunne; Y H Fu; Antonio Pizzuti; CT Caskey; E Boerwinkle; M Benjamin Perryman; Henry F Epstein
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.
Neurology 1992;42(10):1877-83.
1992: Tetsuo Ashizawa; C J Dunne; J R Dubel; M Benjamin Perryman; Henry F Epstein; E Boerwinkle; J Fielding Hejtmancik
Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings.
Neurology 1992;42(10):1871-7.
1992: J R Dubel; R M Armstrong; M Benjamin Perryman; Henry F Epstein; Tetsuo Ashizawa
Phenotypic expression of the myotonic dystrophy gene in monozygotic twins.
Neurology 1992;42(9):1815-7.
1992: Y H Fu; Antonio Pizzuti; R G Fenwick; J King; S Rajnarayan; P W Dunne; J Dubel; G A Nasser; Tetsuo Ashizawa; P de Jong
An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
Science (New York, N.Y.) 1992;255(5049):1256-8.
1992: Tetsuo Ashizawa; J Fielding Hejtmancik; J Liu; M Benjamin Perryman; Henry F Epstein; D D Koch
Diagnostic value of ophthalmologic findings in myotonic dystrophy: comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms.
American journal of medical genetics 1992;42(1):55-60.
1988: M Benjamin Perryman; J Fielding Hejtmancik; Tetsuo Ashizawa; R Armstrong; S C Lin; Robert Roberts; Henry F Epstein
NcoI and TaqI RFLPs for human M creatine kinase (CKM)
Nucleic acids research 1988;16(17):8744.
1988: S S Stewart; Tetsuo Ashizawa; A W Dudley; J W Goldberg; M D Lidsky
Cerebral vasculitis in relapsing polychondritis.
Neurology 1988;38(1):150-2.