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Machado-Joseph disease, spinopontine atrophy, and SCA3 - Reply
被引:0
作者
:
Higgins, JJ
论文数:
0
引用数:
0
h-index:
0
Higgins, JJ
Polymeropoulos, MH
论文数:
0
引用数:
0
h-index:
0
Polymeropoulos, MH
机构
:
来源
:
NEUROLOGY
|
1997年
/ 48卷
/ 04期
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D O I
:
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中图分类号
:
R74 [神经病学与精神病学];
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页码:1138 / 1139
页数:2
相关论文
共 9 条
[1]
CLINICAL, NEUROPATHOLOGIC, AND GENETIC-STUDIES OF A LARGE SPINOCEREBELLAR ATAXIA TYPE-1 (SCA1) KINDRED - (CAG)(N) EXPANSION AND EARLY PREMONITORY SIGNS AND SYMPTOMS
GENIS, D
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
GENIS, D
MATILLA, T
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
MATILLA, T
VOLPINI, V
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
VOLPINI, V
ROSELL, J
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
ROSELL, J
DAVALOS, A
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
DAVALOS, A
FERRER, I
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
FERRER, I
MOLINS, A
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0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
MOLINS, A
ESTIVILL, X
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0
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[2]
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
Higgins, JJ
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h-index:
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机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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Nee, LE
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引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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Vasconcelos, O
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0
h-index:
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机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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引用数:
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h-index:
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机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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h-index:
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NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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Goldfarb, LG
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引用数:
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h-index:
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机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
Goldfarb, LG
Polymeropoulos, MH
论文数:
0
引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo
Ikeda, H
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h-index:
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机构:
KYOTO UNIV, FAC MED, DEPT PHARMACOL, KYOTO 60601, JAPAN
Ikeda, H
Yamaguchi, M
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h-index:
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KYOTO UNIV, FAC MED, DEPT PHARMACOL, KYOTO 60601, JAPAN
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h-index:
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KYOTO UNIV, FAC MED, DEPT PHARMACOL, KYOTO 60601, JAPAN
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KYOTO UNIV, FAC MED, DEPT PHARMACOL, KYOTO 60601, JAPAN
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KYOTO UNIV, FAC MED, DEPT PHARMACOL, KYOTO 60601, JAPAN
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Junck, L
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机构:
UNIV MICHIGAN,DEPT NEUROL,ANN ARBOR,MI
UNIV MICHIGAN,DEPT NEUROL,ANN ARBOR,MI
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MATILLA, T
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BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
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Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients
Silveira, I
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0
引用数:
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h-index:
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机构:
MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
Silveira, I
LopesCendes, I
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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引用数:
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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MONTREAL GEN HOSP, RES INST, MONTREAL, PQ H3G 1A4, CANADA
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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0
引用数:
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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0
引用数:
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
KARUBE, Y
SHIMAZAKI, H
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0
引用数:
0
h-index:
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
SHIMAZAKI, H
SOUTOME, M
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0
引用数:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
SOUTOME, M
ENDO, K
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0
引用数:
0
h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
ENDO, K
OHTA, S
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0
引用数:
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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KAGAWA, Y
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0
引用数:
0
h-index:
0
机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
KAGAWA, Y
KANAZAWA, I
论文数:
0
引用数:
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h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
KANAZAWA, I
MIZUNO, Y
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0
引用数:
0
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
MIZUNO, Y
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论文数:
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引用数:
0
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JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
YOSHIDA, M
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0
引用数:
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h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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0
引用数:
0
h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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0
引用数:
0
h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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0
引用数:
0
h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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机构:
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h-index:
0
机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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ONODERA, O
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0
引用数:
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h-index:
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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机构:
JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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←
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共 9 条
[1]
CLINICAL, NEUROPATHOLOGIC, AND GENETIC-STUDIES OF A LARGE SPINOCEREBELLAR ATAXIA TYPE-1 (SCA1) KINDRED - (CAG)(N) EXPANSION AND EARLY PREMONITORY SIGNS AND SYMPTOMS
GENIS, D
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
GENIS, D
MATILLA, T
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
MATILLA, T
VOLPINI, V
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
VOLPINI, V
ROSELL, J
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
ROSELL, J
DAVALOS, A
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
DAVALOS, A
FERRER, I
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
FERRER, I
MOLINS, A
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
MOLINS, A
ESTIVILL, X
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP PRINCEPS ESPANYA,NEUROPATHOL UNIT,LHOSP DEL LLOBREGAT,SPAIN
ESTIVILL, X
[J].
NEUROLOGY,
1995,
45
(01)
: 24
-
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[2]
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
Higgins, JJ
论文数:
0
引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
Higgins, JJ
Nee, LE
论文数:
0
引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
Nee, LE
Vasconcelos, O
论文数:
0
引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
Vasconcelos, O
Ide, SE
论文数:
0
引用数:
0
h-index:
0
机构:
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
Ide, SE
Lavedan, C
论文数:
0
引用数:
0
h-index:
0
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NIH,NATL CTR HUMAN GENOME RES,GENET DIS RES LAB,BETHESDA,MD 20892
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