Penetrating observations of dystonia

被引：2

作者：

Bird, TD ^{[1
]}

机构：

[1] Univ Washington, Vet Adm Med Ctr, Seattle, WA 98195 USA

来源：

ANNALS OF NEUROLOGY | 1998年 / 44卷 / 03期

关键词：

D O I：

10.1002/ana.410440302

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：299 / 300

页数：2

共 12 条

[1] Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families [J].

Almasy, L ;

Bressman, SB ;

Raymond, D ;

Kramer, PL ;

Greene, PE ;

Heiman, GA ;

Ford, B ;

Yount, J ;

deLeon, D ;

Chouinard, S ;

SaundersPullman, R ;

Brin, MF ;

Kapoor, RP ;

Jones, AC ;

Shen, H ;

Fahn, S ;

Risch, NJ ;

Nygaard, TG .

ANNALS OF NEUROLOGY, 1997, 42 (04) :670-673

[2] IDIOPATHIC DYSTONIA AMONG ASHKENAZI JEWS - EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE [J].

BRESSMAN, SB ;

DELEON, D ;

BRIN, MF ;

RISCH, N ;

BURKE, RE ;

GREENE, PE ;

SHALE, H ;

FAHN, S .

ANNALS OF NEUROLOGY, 1989, 26 (05) :612-620

[3] The metabolic topography of idiopathic torsion dystonia [J].

Eidelberg, D ;

Moeller, JR ;

Ishikawa, T ;

Dhawan, V ;

Spetsieris, P ;

Przedborski, S ;

Fahn, S .

BRAIN, 1995, 118 :1473-1484

[4] Functional brain networks in DYT1 dystonia [J].

Eidelberg, D ;

Moeller, JR ;

Antonini, A ;

Kazumata, K ;

Nakamura, T ;

Dhawan, V ;

Spetsieris, P ;

deLeon, D ;

Bressman, SB ;

Fahn, S .

ANNALS OF NEUROLOGY, 1998, 44 (03) :303-312

[5] Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia [J].

Furukawa, Y ;

Lang, AE ;

Trugman, JM ;

Bird, TD ;

Hunter, A ;

Sadeh, M ;

Tagawa, T ;

St George-Hyslop, PH ;

Guttman, M ;

Morris, LW ;

Hornykiewicz, O ;

Shimadzu, M ;

Kish, SJ .

NEUROLOGY, 1998, 50 (04) :1015-1020

[6] HEREDITARY PROGRESSIVE DYSTONIA WITH MARKED DIURNAL FLUCTUATION CAUSED BY MUTATIONS IN THE GTP CYCLOHYDROLASE-I GENE [J].

ICHINOSE, H ;

OHYE, T ;

TAKAHASHI, E ;

SEKI, N ;

HORI, T ;

SEGAWA, M ;

NOMURA, Y ;

ENDO, K ;

TANAKA, H ;

TSUJI, S ;

FUJITA, K ;

NAGATSU, T .

NATURE GENETICS, 1994, 8 (03) :236-242

[7] RECESSIVELY INHERITED L-DOPA-RESPONSIVE DYSTONIA CAUSED BY A POINT MUTATION (Q381K) IN THE TYROSINE-HYDROXYLASE GENE [J].

KNAPPSKOG, PM ;

FLATMARK, T ;

MALLET, J ;

LUDECKE, B ;

BARTHOLOME, K .

HUMAN MOLECULAR GENETICS, 1995, 4 (07) :1209-1212

[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 [J].

Leube, B ;

Rudnicki, D ;

Ratzlaff, T ;

Kessler, KR ;

Benecke, R ;

Auburger, G .

HUMAN MOLECULAR GENETICS, 1996, 5 (10) :1673-1677

[9] The early-onset torsion dystonia gene (DYT1) encodes an ATP binding protein [J].

Ozelius, LJ ;

Hewett, JW ;

Page, CE ;

Bressman, SB ;

Kramer, PL ;

Shalish, C ;

deLeon, D ;

Brin, MF ;

Raymond, D ;

Corey, DP ;

Fahn, S ;

Risch, NJ ;

Buckler, AJ ;

Gusella, JF ;

Breakefield, XO .

NATURE GENETICS, 1997, 17 (01) :40-48

[10] COMPLEX SEGREGATION ANALYSIS OF DYSTONIA PEDIGREES SUGGESTS AUTOSOMAL DOMINANT INHERITANCE [J].

PAULS, DL ;

KORCZYN, AD .

NEUROLOGY, 1990, 40 (07) :1107-1110

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