[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene

被引：13

作者：

Cossu, G

Cella, C

Melis, M

Antonini, A

Floris, GL

Ruffini, L

Spissu, A

机构：

[1] AOB S Michele Gen Hosp, Dept Neurosci, I-09134 Cagliari, Sardinia, Italy

[2] AOB S Michele Gen Hosp, Dept Nucl Med, I-09134 Cagliari, Sardinia, Italy

[3] Reg Ctr Multiple Sclerosis, Cagliari, Sardinia, Italy

[4] Ist Clin Perfezionamento, Parkinson Ctr, Milan, Italy

来源：

NEUROLOGY | 2005年 / 64卷 / 01期

关键词：

D O I：

10.1212/01.WNL.0000148577.62644.77

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：167 / 168

页数：3

共 7 条

[1]

HALLERVORDEN-SPATZ DISEASE - CLINICAL AND MRI STUDY OF 11 CASES DIAGNOSED IN LIFE [J].

ANGELINI, L ;

NARDOCCI, N ;

RUMI, V ;

ZORZI, C ;

STRADA, L ;

SAVOIARDO, M .

JOURNAL OF NEUROLOGY, 1992, 239 (08) :417-425

[2]

123I-Ioflupane/SPECT binding to striatal dopamine transporter (DAT) uptake in patients with Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy [J].

Antonini, A ;

Benti, R ;

De Notaris, R ;

Tesei, S ;

Zecchinelli, A ;

Sacilotto, G ;

Meucci, N ;

Canesi, M ;

Mariani, C ;

Pezzoli, G ;

Gerundini, P .

NEUROLOGICAL SCIENCES, 2003, 24 (03) :149-150

[3]

Booij J, 1999, J NUCL MED, V40, P753

[4]

Hallervorden Spatz syndrome (pantothenate kinase associated neurodegeneration) in two Sardinian brother with homozygous mutation in PANK 2 gene [J].

Cossu, G ;

Melis, M ;

Floris, G ;

Hayflick, SJ ;

Spissu, A .

JOURNAL OF NEUROLOGY, 2002, 249 (11) :1599-1600

[5]

Diagnosis of Hallervorden-Spatz disease using MRI, 123I-beta-CIT-SPECT and 123I-IBZM-SPECT [J].

Hermann, W ;

Reuter, M ;

Barthel, H ;

Dietrich, J ;

Georgi, P ;

Wagner, A .

EUROPEAN NEUROLOGY, 2000, 43 (03) :187-188

[6]

Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration [J].

Thomas, M ;

Hayflick, SJ ;

Jankovic, J .

MOVEMENT DISORDERS, 2004, 19 (01) :36-42

[7]

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome [J].

Zhou, B ;

Westaway, SK ;

Levinson, B ;

Johnson, MA ;

Gitschier, J ;

Hayflick, SJ .

NATURE GENETICS, 2001, 28 (04) :345-349

← 1 →