HISTOCHEMICAL, ULTRASTRUCTURAL AND BIOCHEMICAL-STUDY OF MUSCLE MITOCHONDRIA IN LEBERS HEREDITARY OPTIC ATROPHY

被引：11

作者：

FEDERICO, A

MANNESCHI, L

MELONI, M

ALESSANDRINI, C

BARDELLI, AM

DOTTI, MT

SABATELLI, P

机构：

[1] UNIV SIENA,CTR STUDIO ENCEFALO NEURO MIOPATTIE GENET,I-53100 SIENA,ITALY

[2] UNIV SIENA,IST ISTOL & EMBRIOL GEN,I-53100 SIENA,ITALY

[3] UNIV SIENA,IST SCI OFTALMOL,I-53100 SIENA,ITALY

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1988年 / 11卷

关键词：

D O I：

10.1007/BF01804233

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：193 / 197

页数：5

共 8 条

[1] RHODANESE-MEDIATED SULFUR TRANSFER TO SUCCINATE-DEHYDROGENASE [J].

BONOMI, F ;

PAGANI, S ;

CERLETTI, P ;

CANNELLA, C .

EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 72 (01) :17-24

[2] DECREASED THIOSULFATE SULFUR TRANSFERASE (RHODANESE) IN LEBERS HEREDITARY OPTIC ATROPHY [J].

CAGIANUT, B ;

SCHNEBLI, HP ;

RHYNER, K ;

FURRER, J .

KLINISCHE WOCHENSCHRIFT, 1984, 62 (18) :850-854

[3] BIOCHEMICAL DIFFERENCE BETWEEN INTERMYOFIBRILLAR AND SUBSARCOLEMMAL MITOCHONDRIA FROM HUMAN-MUSCLE [J].

FEDERICO, A ;

MANNESCHI, L ;

PAOLINI, E .

JOURNAL OF INHERITED METABOLIC DISEASE, 1987, 10 :242-246

[4]

NIKOSKELAINEN E, 1984, LANCET, V2, P1474

[5] LEBERS DISEASE AND DYSTONIA - A MITOCHONDRIAL DISEASE [J].

NOVOTNY, EJ ;

SINGH, G ;

WALLACE, DC ;

DORFMAN, LJ ;

LOUIS, A ;

SOGG, RL ;

STEINMAN, L .

NEUROLOGY, 1986, 36 (08) :1053-1060

[6] LEBERS DISEASE WITH SPASTIC PARAPLEGIA AND PERIPHERAL NEUROPATHY - CASE-REPORT WITH NERVE BIOPSY STUDY [J].

PAGES, M ;

PAGES, AM .

EUROPEAN NEUROLOGY, 1983, 22 (03) :181-185

[7] NORMAL RHODANESE ACTIVITY IN LEUKOCYTES FROM LEBER PATIENTS - ENZYME CHARACTERIZATION AND ACTIVITY LEVELS [J].

PALLINI, R ;

MARTELLI, P ;

BARDELLI, AM ;

GUAZZI, GC ;

FEDERICO, A .

NEUROLOGY, 1987, 37 (12) :1878-1880

[8] DEFICIENCY OF THIOSULFATE SULFURTRANSFERASE (RHODANESE) IN LEBERS HEREDITARY OPTIC NEUROPATHY [J].

POOLE, CJM ;

KIND, PRN .

BRITISH MEDICAL JOURNAL, 1986, 292 (6530) :1229-1230

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