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Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers
被引:23
作者:

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Antonini, A
论文数: 0 引用数: 0
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机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Volterrani, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Rossi, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Goldwurm, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Di Maria, E
论文数: 0 引用数: 0
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机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Kiferle, L
论文数: 0 引用数: 0
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机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Bonuccelli, U
论文数: 0 引用数: 0
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机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy

Murri, L
论文数: 0 引用数: 0
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机构: Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy
机构:
[1] Univ Pisa, Neurol Sect, Dept Neurosci, I-56126 Pisa, Italy
[2] Ist Clin Perfezionamento, Parkinson Inst, Milan, Italy
[3] Univ Pisa, Ctr Nucl Med, I-56100 Pisa, Italy
[4] Univ Genoa, Med Genet Sect, Dept Neurosci Ophthalmol & Genet, Genoa, Italy
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D O I:
10.1212/01.wnl.0000188821.51055.52
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
The authors studied four patients with parkinsonism carrying the fragile X premutation using SPECT with [I-23]FP-CIT. They found evidence of preserved presynaptic nigrostriatal function, suggesting that parkinsonism in the X fragile premutation might be related to postsynaptic dopaminergic changes or different neurotransmitter alterations.
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页码:1971 / 1973
页数:3
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机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, D-72086 Tubingen, Germany

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机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, D-72086 Tubingen, Germany

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机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, D-72086 Tubingen, Germany

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机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, D-72086 Tubingen, Germany

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h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Shen, H
论文数: 0 引用数: 0
h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Chandran, VR
论文数: 0 引用数: 0
h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Teoh, ML
论文数: 0 引用数: 0
h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Yih, Y
论文数: 0 引用数: 0
h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Pavanni, R
论文数: 0 引用数: 0
h-index: 0
机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Wong, MC
论文数: 0 引用数: 0
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机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore

Ng, IS
论文数: 0 引用数: 0
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机构: Singapore Gen Hosp, Natl Inst Neurosci, Dept Neurol, Singapore 169608, Singapore
[10]
Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia
[J].
Van Esch, H
;
Dom, R
;
Bex, D
;
Salden, I
;
Caeckebeke, J
;
Wibail, A
;
Borghgraef, M
;
Legius, E
;
Fryns, JP
;
Matthijs, G
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2005, 13 (01)
:121-123

Van Esch, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Dom, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Bex, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Salden, I
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Caeckebeke, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Wibail, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Borghgraef, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Legius, E
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h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Fryns, JP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium

Matthijs, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Gasthuisberg, Ctr Human Genet, B-3000 Louvain, Belgium