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Clinical and genetic analysis of an Italian family with Machado-Joseph disease
被引:2
作者
:
Forleo, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Forleo, P
Cellini, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Cellini, E
Parnetti, L
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Parnetti, L
Murasecco, D
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Murasecco, D
Gallai, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Gallai, V
Nacmias, B
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Nacmias, B
Sorbi, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
Sorbi, S
机构
:
[1]
Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
[2]
Univ Perugia, Inst Mental & Nervous Dis, I-06100 Perugia, Italy
来源
:
JOURNAL OF NEUROLOGY
|
2001年
/ 248卷
/ 08期
关键词
:
D O I
:
10.1007/s004150170124
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
引用
收藏
页码:717 / 719
页数:3
相关论文
共 15 条
[1]
MACHADO-JOSEPH-AZOREAN DISEASE IN INDIA
[J].
BHARUCHA, NE
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHARUCHA, NE
;
BHARUCHA, EP
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHARUCHA, EP
;
BHABHA, SK
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHABHA, SK
.
ARCHIVES OF NEUROLOGY,
1986,
43
(02)
:142
-144
[2]
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes
[J].
Filla, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Filla, A
;
DeMichele, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
DeMichele, G
;
Campanella, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Campanella, G
;
Perretti, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Perretti, A
;
Santoro, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Santoro, L
;
论文数:
引用数:
h-index:
机构:
Serlenga, L
;
Ragno, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Ragno, M
;
Calabrese, O
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Calabrese, O
;
Castaldo, I
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Castaldo, I
;
DeJoanna, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
DeJoanna, G
;
Cocozza, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Cocozza, S
.
JOURNAL OF THE NEUROLOGICAL SCIENCES,
1996,
142
(1-2)
:140
-147
[3]
GALLAI V, 1973, RIV NEUROPSICHIATRIA, V19, P173
[4]
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
[J].
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
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
Lavedan, C
;
Goldfarb, LG
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
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
Polymeropoulos, MH
.
NEUROLOGY,
1996,
46
(01)
:208
-213
[5]
CAG EXPANSIONS IN A NOVEL GENE FOR MACHADO-JOSEPH DISEASE AT CHROMOSOME 14Q32.1
[J].
KAWAGUCHI, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAWAGUCHI, Y
;
OKAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
OKAMOTO, T
;
TANIWAKI, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
TANIWAKI, M
;
AIZAWA, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
AIZAWA, M
;
论文数:
引用数:
h-index:
机构:
INOUE, M
;
KATAYAMA, S
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KATAYAMA, S
;
KAWAKAMI, H
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAWAKAMI, H
;
论文数:
引用数:
h-index:
机构:
NAKAMURA, S
;
NISHIMURA, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
NISHIMURA, M
;
AKIGUCHI, I
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
AKIGUCHI, I
;
KIMURA, J
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KIMURA, J
;
NARUMIYA, S
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
NARUMIYA, S
;
KAKIZUKA, A
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAKIZUKA, A
.
NATURE GENETICS,
1994,
8
(03)
:221
-228
[6]
Machado-Joseph Disease in an American-Italian Family
[J].
Livingstone, Ian R.
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Livingstone, Ian R.
;
Sequeiros, Jorge
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Sequeiros, Jorge
.
JOURNAL OF NEUROGENETICS,
1984,
1
(02)
:185
-188
[7]
Machado-Joseph disease presenting as severe generalised dystonia in a German patient
[J].
Münchau, A
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Münchau, A
;
Dressler, D
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Dressler, D
;
Bhatia, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Bhatia, KP
;
Vogel, P
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Vogel, P
;
Zühlke, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Zühlke, C
.
JOURNAL OF NEUROLOGY,
1999,
246
(09)
:840
-842
[8]
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I:: SCA1 and SCA2 are the most common genotypes
[J].
Pareyson, D
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Pareyson, D
;
Gellera, C
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Gellera, C
;
Castellotti, B
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Castellotti, B
;
Antonelli, A
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Antonelli, A
;
Riggio, MC
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Riggio, MC
;
Mazzucchelli, F
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Mazzucchelli, F
;
Girotti, F
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Girotti, F
;
Pietrini, V
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Pietrini, V
;
Mariotti, C
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Mariotti, C
;
Di Donato, S
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Di Donato, S
.
JOURNAL OF NEUROLOGY,
1999,
246
(05)
:389
-393
[9]
JOSEPH DISEASE IN A NON-PORTUGUESE FAMILY
[J].
SAKAI, T
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
SAKAI, T
;
OHTA, M
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
OHTA, M
;
ISHINO, H
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
ISHINO, H
.
NEUROLOGY,
1983,
33
(01)
:74
-80
[10]
MATHADO-JOSEPH DISEASE MUTATIONS AS THE GENETIC-BASIS OF MOST SPINOCEREBELLAR ATAXIAS IN GERMANY
[J].
SCHOLS, L
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
SCHOLS, L
;
AMOIRIDIS, G
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
AMOIRIDIS, G
;
LANGKAFEL, M
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
LANGKAFEL, M
;
BUTTNER, T
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
BUTTNER, T
;
PRZUNTEK, H
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
PRZUNTEK, H
;
RIESS, O
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RIESS, O
;
VIEIRASAECKER, AMM
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
VIEIRASAECKER, AMM
;
EPPLEN, JT
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
EPPLEN, JT
.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
1995,
59
(04)
:449
-450
←
1
2
→
共 15 条
[1]
MACHADO-JOSEPH-AZOREAN DISEASE IN INDIA
[J].
BHARUCHA, NE
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHARUCHA, NE
;
BHARUCHA, EP
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHARUCHA, EP
;
BHABHA, SK
论文数:
0
引用数:
0
h-index:
0
机构:
SETH GS MED COLL,BOMBAY,INDIA
BHABHA, SK
.
ARCHIVES OF NEUROLOGY,
1986,
43
(02)
:142
-144
[2]
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes
[J].
Filla, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Filla, A
;
DeMichele, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
DeMichele, G
;
Campanella, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Campanella, G
;
Perretti, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Perretti, A
;
Santoro, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Santoro, L
;
论文数:
引用数:
h-index:
机构:
Serlenga, L
;
Ragno, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Ragno, M
;
Calabrese, O
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Calabrese, O
;
Castaldo, I
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Castaldo, I
;
DeJoanna, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
DeJoanna, G
;
Cocozza, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV NAPLES FEDERICO II,DEPT CLIN NEUROPHYSIOL,I-80131 NAPLES,ITALY
Cocozza, S
.
JOURNAL OF THE NEUROLOGICAL SCIENCES,
1996,
142
(1-2)
:140
-147
[3]
GALLAI V, 1973, RIV NEUROPSICHIATRIA, V19, P173
[4]
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
[J].
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
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
Lavedan, C
;
Goldfarb, LG
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
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
Polymeropoulos, MH
.
NEUROLOGY,
1996,
46
(01)
:208
-213
[5]
CAG EXPANSIONS IN A NOVEL GENE FOR MACHADO-JOSEPH DISEASE AT CHROMOSOME 14Q32.1
[J].
KAWAGUCHI, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAWAGUCHI, Y
;
OKAMOTO, T
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
OKAMOTO, T
;
TANIWAKI, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
TANIWAKI, M
;
AIZAWA, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
AIZAWA, M
;
论文数:
引用数:
h-index:
机构:
INOUE, M
;
KATAYAMA, S
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KATAYAMA, S
;
KAWAKAMI, H
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAWAKAMI, H
;
论文数:
引用数:
h-index:
机构:
NAKAMURA, S
;
NISHIMURA, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
NISHIMURA, M
;
AKIGUCHI, I
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
AKIGUCHI, I
;
KIMURA, J
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KIMURA, J
;
NARUMIYA, S
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
NARUMIYA, S
;
KAKIZUKA, A
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 60601,JAPAN
KAKIZUKA, A
.
NATURE GENETICS,
1994,
8
(03)
:221
-228
[6]
Machado-Joseph Disease in an American-Italian Family
[J].
Livingstone, Ian R.
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Livingstone, Ian R.
;
Sequeiros, Jorge
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Dept Med, Moore Clin,Div Med Genet, Baltimore, MD 21205 USA
Sequeiros, Jorge
.
JOURNAL OF NEUROGENETICS,
1984,
1
(02)
:185
-188
[7]
Machado-Joseph disease presenting as severe generalised dystonia in a German patient
[J].
Münchau, A
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Münchau, A
;
Dressler, D
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Dressler, D
;
Bhatia, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Bhatia, KP
;
Vogel, P
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Vogel, P
;
Zühlke, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol, London WC1N 3BG, England
Zühlke, C
.
JOURNAL OF NEUROLOGY,
1999,
246
(09)
:840
-842
[8]
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I:: SCA1 and SCA2 are the most common genotypes
[J].
Pareyson, D
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Pareyson, D
;
Gellera, C
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Gellera, C
;
Castellotti, B
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Castellotti, B
;
Antonelli, A
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Antonelli, A
;
Riggio, MC
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Riggio, MC
;
Mazzucchelli, F
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Mazzucchelli, F
;
Girotti, F
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Girotti, F
;
Pietrini, V
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Pietrini, V
;
Mariotti, C
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Mariotti, C
;
Di Donato, S
论文数:
0
引用数:
0
h-index:
0
机构:
Ist Neurol C Besta, Dept Biochem & Genet, I-20133 Milan, Italy
Di Donato, S
.
JOURNAL OF NEUROLOGY,
1999,
246
(05)
:389
-393
[9]
JOSEPH DISEASE IN A NON-PORTUGUESE FAMILY
[J].
SAKAI, T
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
SAKAI, T
;
OHTA, M
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
OHTA, M
;
ISHINO, H
论文数:
0
引用数:
0
h-index:
0
机构:
SHIMANE MED UNIV,DEPT PSYCHIAT,IZUMO,SHIMANE 693,JAPAN
ISHINO, H
.
NEUROLOGY,
1983,
33
(01)
:74
-80
[10]
MATHADO-JOSEPH DISEASE MUTATIONS AS THE GENETIC-BASIS OF MOST SPINOCEREBELLAR ATAXIAS IN GERMANY
[J].
SCHOLS, L
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
SCHOLS, L
;
AMOIRIDIS, G
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
AMOIRIDIS, G
;
LANGKAFEL, M
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
LANGKAFEL, M
;
BUTTNER, T
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
BUTTNER, T
;
PRZUNTEK, H
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
PRZUNTEK, H
;
RIESS, O
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RIESS, O
;
VIEIRASAECKER, AMM
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
VIEIRASAECKER, AMM
;
EPPLEN, JT
论文数:
0
引用数:
0
h-index:
0
机构:
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
RUHR UNIV BOCHUM,DEPT MOLEC HUMAN GENET,W-4630 BOCHUM,GERMANY
EPPLEN, JT
.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
1995,
59
(04)
:449
-450
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