首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
A family with E3δ40 mutations in the Parkin gene:: evidence for autosomal recessive inheritance of young onset benign parkinsonism rather than autosomal dominant inheritance
被引:0
|
作者
:
Sa, DS
论文数:
0
引用数:
0
h-index:
0
Sa, DS
Munhoz, RP
论文数:
0
引用数:
0
h-index:
0
Munhoz, RP
Rogaeva, E
论文数:
0
引用数:
0
h-index:
0
Rogaeva, E
Hyslop, PS
论文数:
0
引用数:
0
h-index:
0
Hyslop, PS
Farrer, MJ
论文数:
0
引用数:
0
h-index:
0
Farrer, MJ
Lang, AE
论文数:
0
引用数:
0
h-index:
0
Lang, AE
机构
:
来源
:
MOVEMENT DISORDERS
|
2002年
/ 17卷
关键词
:
D O I
:
暂无
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
P46
引用
收藏
页码:S30 / S30
页数:1
相关论文
共 13 条
[1]
Parkin gene mutation with an autosomal dominant inheritance - A family case report
Drobnis, A.
论文数:
0
引用数:
0
h-index:
0
Drobnis, A.
Scala, S. A.
论文数:
0
引用数:
0
h-index:
0
Scala, S. A.
Zani, J. W.
论文数:
0
引用数:
0
h-index:
0
Zani, J. W.
Apetauerova, D.
论文数:
0
引用数:
0
h-index:
0
Apetauerova, D.
MOVEMENT DISORDERS,
2012,
27
: S454
-
S454
[2]
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
Bonifati, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Bonifati, V
Lücking, CB
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Lücking, CB
Fabrizio, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Fabrizio, E
Periquet, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Periquet, M
Meco, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Meco, G
Brice, A
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
Brice, A
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
2001,
71
(04):
: 531
-
534
[3]
Mutations in the parkin gene are a common cause for autosomal recessive early onset parkinsonism in Europe
Brice, A
论文数:
0
引用数:
0
h-index:
0
Brice, A
Lücking, CB
论文数:
0
引用数:
0
h-index:
0
Lücking, CB
Abbas, N
论文数:
0
引用数:
0
h-index:
0
Abbas, N
Dürr, A
论文数:
0
引用数:
0
h-index:
0
Dürr, A
Ricard, S
论文数:
0
引用数:
0
h-index:
0
Ricard, S
Bonifati, V
论文数:
0
引用数:
0
h-index:
0
Bonifati, V
De Michele, G
论文数:
0
引用数:
0
h-index:
0
De Michele, G
Wood, NW
论文数:
0
引用数:
0
h-index:
0
Wood, NW
Gasser, T
论文数:
0
引用数:
0
h-index:
0
Gasser, T
Breteler, M
论文数:
0
引用数:
0
h-index:
0
Breteler, M
Harhangi, S
论文数:
0
引用数:
0
h-index:
0
Harhangi, S
Oostra, B
论文数:
0
引用数:
0
h-index:
0
Oostra, B
Filla, A
论文数:
0
引用数:
0
h-index:
0
Filla, A
Meco, G
论文数:
0
引用数:
0
h-index:
0
Meco, G
Denefle, P
论文数:
0
引用数:
0
h-index:
0
Denefle, P
Agid, Y
论文数:
0
引用数:
0
h-index:
0
Agid, Y
NEUROLOGY,
1999,
52
(06)
: A554
-
A555
[4]
Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
Maruyama, M
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Maruyama, M
Ikeuchi, T
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Ikeuchi, T
Saito, M
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Saito, M
Ishikawa, A
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Ishikawa, A
Yuasa, T
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Yuasa, T
Tanaka, H
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Tanaka, H
Hayashi, S
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Hayashi, S
Wakabayashi, K
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Wakabayashi, K
Takahashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Takahashi, H
Tsuji, S
论文数:
0
引用数:
0
h-index:
0
机构:
Niigata Univ, Inst Brain Res, Dept Neurol, Niigata 9518585, Japan
Tsuji, S
ANNALS OF NEUROLOGY,
2000,
48
(02)
: 245
-
250
[5]
Pseudo-autosomal dominant inheritance of PARK2:: two families with parkin gene mutations
Kobayashi, T
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Kobayashi, T
Matsumine, H
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Matsumine, H
Zhang, JL
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Zhang, JL
Imamichi, Y
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Imamichi, Y
Mizuno, Y
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Mizuno, Y
Hattori, N
论文数:
0
引用数:
0
h-index:
0
机构:
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
Hattori, N
JOURNAL OF THE NEUROLOGICAL SCIENCES,
2003,
207
(1-2)
: 11
-
17
[6]
Homozygous Exon 4 deletion in Parkin gene in a Korean family with autosomal recessive early onset parkinsonism
Kim, JS
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
Kim, JS
Lee, KS
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
Lee, KS
Kim, YI
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
Kim, YI
Lee, KH
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
Lee, KH
Kim, HT
论文数:
0
引用数:
0
h-index:
0
机构:
Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
Kim, HT
YONSEI MEDICAL JOURNAL,
2003,
44
(02)
: 336
-
339
[7]
A novel homozygous variant in ATL1 associated with early onset spastic paraplegia 3A: Further evidence for autosomal recessive inheritance
论文数:
引用数:
h-index:
机构:
Darouich, Sihem
Darouich, Samia
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tunis El Manar, Inst Super Sci Humaines Tunis, Tunis, Tunisia
Univ Tunis El Manar, Fac Med Tunis, Tunis, Tunisia
Darouich, Samia
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
2024,
194
(03)
[8]
Idiopathic torsion dystonia: Assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution
Leube, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Leube, B
Rudnicki, D
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Rudnicki, D
Ratzlaff, T
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Ratzlaff, T
Kessler, KR
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Kessler, KR
Benecke, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Benecke, R
Auburger, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
UNIV HOSP,DEPT NEUROL,D-40001 DUSSELDORF,GERMANY
Auburger, G
HUMAN MOLECULAR GENETICS,
1996,
5
(10)
: 1673
-
1677
[9]
Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient
Y. Sasaki
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Y. Sasaki
Mikiro Iseki
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Mikiro Iseki
Shinya Yamaguchi
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Shinya Yamaguchi
Yoshihiro Kurosawa
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Yoshihiro Kurosawa
Tetsuya Yamamoto
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Tetsuya Yamamoto
Yuji Moriwaki
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Yuji Moriwaki
Tsuyoshi Kenri
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Tsuyoshi Kenri
Tsuguo Sasaki
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Tsuguo Sasaki
Ryoko Yamashita
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Safety Research on Biologics,
Ryoko Yamashita
Human Genetics,
1998,
103
: 81
-
85
[10]
Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient
Sasaki, Y
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Sasaki, Y
Iseki, M
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Iseki, M
Yamaguchi, S
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Yamaguchi, S
Kurosawa, Y
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Kurosawa, Y
Yamamoto, T
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Yamamoto, T
Moriwaki, Y
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Moriwaki, Y
Kenri, T
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Kenri, T
Sasaki, T
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Sasaki, T
Yamashita, R
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Infect Dis, Dept Safety Res Biol, Tokyo 208, Japan
Yamashita, R
HUMAN GENETICS,
1998,
103
(01)
: 81
-
85
←
1
2
→