Molecular basis of the neurodegenerative disorders

被引：319

作者：

Martin, JB ^{[1
]}

机构：

[1] Harvard Univ, Sch Med, Boston, MA 02115 USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1999年 / 340卷 / 25期

关键词：

D O I：

10.1056/NEJM199906243402507

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1970 / 1980

页数：11

共 98 条

[1] Ubiquitin, cellular inclusions and their role in neurodegeneration [J].

Alves-Rodrigues, A ;

Gregori, L ;

Figueiredo-Pereira, ME .

TRENDS IN NEUROSCIENCES, 1998, 21 (12) :516-520

[2] Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin [J].

Babcock, M ;

deSilva, D ;

Oaks, R ;

DavisKaplan, S ;

Jiralerspong, S ;

Montermini, L ;

Pandolfo, M ;

Kaplan, J .

SCIENCE, 1997, 276 (5319) :1709-1712

[3] IDENTIFICATION AND CHARACTERIZATION OF THE GENE CAUSING TYPE-1 SPINOCEREBELLAR ATAXIA [J].

BANFI, S ;

SERVADIO, A ;

CHUNG, MY ;

KWIATKOWSKI, TJ ;

MCCALL, AE ;

DUVICK, LA ;

SHEN, Y ;

ROTH, EJ ;

ORR, HT ;

ZOGHBI, HY .

NATURE GENETICS, 1994, 7 (04) :513-520

[4] CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients [J].

Benson, KF ;

Horwitz, M ;

Wolff, J ;

Friend, K ;

Thompson, E ;

White, S ;

Richards, RI ;

Raskind, WH ;

Bird, TD .

HUMAN MOLECULAR GENETICS, 1998, 7 (11) :1779-1786

[5] Alpha-2 macroglobulin is genetically associated with Alzheimer disease [J].

Blacker, D ;

Wilcox, MA ;

Laird, NM ;

Rodes, L ;

Horvath, SM ;

Go, RCP ;

Perry, R ;

Watson, B ;

Bassett, SS ;

McInnis, MG ;

Albert, MS ;

Hyman, BT ;

Tanzi, RE .

NATURE GENETICS, 1998, 19 (04) :357-360

[6] Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I [J].

Brahe, C ;

Clermont, O ;

Zappata, S ;

Tiziano, F ;

Melki, J ;

Neri, G .

HUMAN MOLECULAR GENETICS, 1996, 5 (12) :1971-1976

[7]

BROWN RH, 1998, MOL NEUROLOGY, P223

[8]

BRUN A, 1994, J NEUROL NEUROSUR PS, V57, P416

[9] Apoptosis in degenerative diseases of the basal ganglia [J].

Burke, RE .

NEUROSCIENTIST, 1998, 4 (04) :301-311

[10] Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion [J].

Campuzano, V ;

Montermini, L ;

Molto, MD ;

Pianese, L ;

Cossee, M ;

Cavalcanti, F ;

Monros, E ;

Rodius, F ;

Duclos, F ;

Monticelli, A ;

Zara, F ;

Canizares, J ;

Koutnikova, H ;

Bidichandani, SI ;

Gellera, C ;

Brice, A ;

Trouillas, P ;

DeMichele, G ;

Filla, A ;

DeFrutos, R ;

Palau, F ;

Patel, PI ;

DiDonato, S ;

Mandel, JL ;

Cocozza, S ;

Koenig, M ;

Pandolfo, M .

SCIENCE, 1996, 271 (5254) :1423-1427

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