SCOPUS 정보 검색 플랫폼

Volumn 253, Issue 3, 2006, Pages 396-398

Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene [9]

(10) Uchihara, T a Takeda, Y a Kobayashi, T b Kasuga, T a Ishikawa, K c Kirei, K c Mizusawa, H c Endo, T c Hirokawa, K c Kuroiwa, T c

a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE (Japan)

b Nakano General Hospital (Japan)

c TOKYO MEDICAL AND DENTAL UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIN 1;

AGED; ATAXIA; BULBAR PARALYSIS; CASE REPORT; CLINICAL FEATURE; DYSPHAGIA; ELECTROMYOGRAPHY; EXTRAPYRAMIDAL SYMPTOM; GAIT DISORDER; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LABORATORY TEST; LETTER; MALE; MOTOR NEURON DISEASE; MUSCLE ATROPHY; NEUROLOGIC EXAMINATION; PHENOTYPE; PRIORITY JOURNAL; SENSORY DYSFUNCTION; SPINOCEREBELLAR DEGENERATION;

AGED; BRAIN; GENOTYPE; HUMANS; MALE; REPETITIVE SEQUENCES, NUCLEIC ACID; SPINOCEREBELLAR ATAXIAS;

EID: 33644951730 PISSN: 03405354 EISSN: 14321459 Source Type: Journal
DOI: 10.1007/s00415-005-0980-z Document Type: Letter

Times cited : (6)

References (5)

1
- 0345391031
- Nuclear inclusions in spinocerebellar ataxia type 1
- Berl
- Duyckaerts C, Dürr A, Cancel G, Brice A (1999) Nuclear inclusions in spinocerebellar ataxia type 1. Acta Neuropathol (Berl) 97:201-207
- (1999) Acta Neuropathol , vol.97 , pp. 201-207
- Duyckaerts, C.¹ Dürr, A.² Cancel, G.³ Brice, A.⁴

2
- 0033111229
- Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations
- Paris
- Iwabuchi K, Tsuchiya K, Uchihara T, Yagishita S (1999) Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations. Rev Neurol (Paris) 155:255-270
- (1999) Rev Neurol , vol.155 , pp. 255-270
- Iwabuchi, K.¹ Tsuchiya, K.² Uchihara, T.³ Yagishita, S.⁴

3
- 0036786139
- Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion
- Koyano S, Iwabuchi K, Yagishita S, Kuroiwa Y, Uchihara T (2002) Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion. J Neurol Neurosurg. Psychiatry 73:453-455
- (2002) J Neurol Neurosurg Psychiatry , vol.73 , pp. 453-455
- Koyano, S.¹ Iwabuchi, K.² Yagishita, S.³ Kuroiwa, Y.⁴ Uchihara, T.⁵

4
- 0027164698
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
- Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY (1993) Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 4:221-226
- (1993) Nat Genet , vol.4 , pp. 221-226
- Orr, H.T.¹ Chung, M.Y.² Banfi, S.³ Kwiatkowski Jr., T.J.⁴ Servadio, A.⁵ Beaudet, A.L.⁶ McCall, A.E.⁷ Duvick, L.A.⁸ Ranum, L.P.⁹ Zoghbi, H.Y.¹⁰

5
- 0016396382
- Hereditary ataxia and HLA genotype
- Yakura H, Wakisaka A, Fujimoto S, Itakura K (1974) Hereditary ataxia and HLA genotype. N Engl J Med 291:154-155
- (1974) N Engl J Med , vol.291 , pp. 154-155
- Yakura, H.¹ Wakisaka, A.² Fujimoto, S.³ Itakura, K.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.