Peroxisomal disorders: Overview

被引:34
作者
Moser, HW
Moser, AB
机构
[1] JOHNS HOPKINS UNIV, DEPT NEUROL, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, DEPT PEDIAT, BALTIMORE, MD 21205 USA
来源
PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE | 1996年 / 804卷
关键词
D O I
10.1111/j.1749-6632.1996.tb18634.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
引用
收藏
页码:427 / 441
页数:15
相关论文
共 100 条
[1]  
ASSIES J, 1994, ADV T ADDISONS DISEA, P191
[2]   A 2-YEAR TRIAL OF OLEIC AND ERUCIC ACIDS (LORENZO OIL) AS TREATMENT FOR ADRENOMYELONEUROPATHY [J].
AUBOURG, P ;
ADAMSBAUM, C ;
LAVALLARDROUSSEAU, MC ;
ROCCHICCIOLI, F ;
CARTIER, N ;
JAMBAQUE, I ;
JAKOBEZAK, C ;
LEMAITRE, A ;
BOUREAU, F ;
WOLF, C ;
BOUGNERES, PF .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (11) :745-752
[3]   REVERSAL OF EARLY NEUROLOGIC AND NEURORADIOLOGICAL MANIFESTATIONS OF X-LINKED ADRENOLEUKODYSTROPHY BY BONE-MARROW TRANSPLANTATION [J].
AUBOURG, P ;
BLANCHE, S ;
JAMBAQUE, I ;
ROCCHICCIOLI, F ;
KALIFA, G ;
NAUDSAUDREAU, C ;
ROLLAND, MO ;
DEBRE, M ;
CHAUSSAIN, JL ;
GRISCELLI, C ;
FISCHER, A ;
BOUGNERES, PF .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1860-1866
[4]  
AUBOURG P, 1982, ARCH FR PEDIATR, V39, P663
[5]  
BAZAN NG, 1989, INHERITED ENV INDUCE, P191
[6]   ATYPICAL RIBOFLAVIN-RESPONSIVE GLUTARIC ACIDURIA, AND DEFICIENT PEROXISOMAL GLUTARYL-COA OXIDASE ACTIVITY - A NEW PEROXISOMAL DISORDER [J].
BENNETT, MJ ;
POLLITT, RJ ;
GOODMAN, SI ;
HALE, DE ;
VAMECQ, J .
JOURNAL OF INHERITED METABOLIC DISEASE, 1991, 14 (02) :165-173
[7]  
BJORKHEM I, 1986, J LIPID RES, V27, P786
[8]  
BOWEN P, 1964, B JOHNS HOPKINS HOSP, V114, P402
[9]   GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS [J].
BRUL, S ;
WESTERVELD, A ;
STRIJLAND, A ;
WANDERS, RJA ;
SCHRAM, AW ;
HEYMANS, HSA ;
SCHUTGENS, RBH ;
VANDENBOSCH, H ;
TAGER, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) :1710-1715
[10]   BILE-ACID ANALYSES IN PSEUDO-ZELLWEGER SYNDROME - CLUES TO THE DEFECT IN PEROXISOMAL BETA-OXIDATION [J].
CLAYTON, PT ;
LAKE, BD ;
HJELM, M ;
STEPHENSON, JBP ;
BESLEY, GTN ;
WANDERS, RJA ;
SCHRAM, AW ;
TAGER, JM ;
SCHUTGENS, RBH ;
LAWSON, AM .
JOURNAL OF INHERITED METABOLIC DISEASE, 1988, 11 :165-168