ULTRASTRUCTURE OF HEPATIC MITOCHONDRIA IN A CHILD WITH HYPERORNITHINEMIA, HYPERAMMONEMIA, AND HOMOCITRULLINURIA

被引：24

作者：

HAUST, MD

GATFIELD, PD

GORDON, BA

机构：

[1] UNIV WESTERN ONTARIO,DEPT PAEDIAT,LONDON N6A 5C1,ONTARIO,CANADA

[2] UNIV WESTERN ONTARIO,DEPT BIOCHEM,LONDON N6A 5C1,ONTARIO,CANADA

[3] ST THOMAS PSYCHIAT HOSP,LONDON,ONTARIO,CANADA

来源：

HUMAN PATHOLOGY | 1981年 / 12卷 / 03期

关键词：

D O I：

10.1016/S0046-8177(81)80121-9

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

引用

页码：212 / 223

页数：12

共 49 条

[1] CASE OF CARBAMYL PHOSPHATE SYNTHETASE DEFICIENCY [J].

ARASHIMA, S ;

MATSUDA, I .

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1972, 107 (02) :143-147

[2] TREATMENT OF CARBAMYL-PHOSPHATE SYNTHETASE DEFICIENCY WITH KETO ANALOGUES OF ESSENTIAL AMINO-ACIDS [J].

BATSHAW, M ;

BRUSILOW, S ;

WALSER, M .

NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (21) :1085-1090

[3]

BAUMGARTNER R, 1968, HELV PAEDIATR ACTA, V23, P77

[4] ARGININOSUCCINIC ACIDURIA - INVESTIGATION OF AN AFFECTED FAMILY [J].

BILLMEIER, GJ ;

MOLINARY, SV ;

WILROY, RS ;

DUENAS, DA ;

BRANNON, ME .

JOURNAL OF PEDIATRICS, 1974, 84 (01) :85-89

[5] HEREDITARY HYPERAMMONAEMIA [J].

BRUTON, CJ ;

CORSELLIS, JA ;

RUSSELL, A .

BRAIN, 1970, 93 :423-+

[6] L-LYSINE DEHYDROGENASE DEFICIENCY IN A PATIENT WITH CONGENITAL LYSINE INTOLERANCE [J].

BURGI, W ;

RICHTERICH, R ;

COLOMBO, JP .

NATURE, 1966, 211 (5051) :854-+

[7] ORNITHINE TRANSCARBAMYLASE DEFICIENCY - A CAUSE OF LETHAL NEONATAL HYPERAMMONEMIA IN MALES [J].

CAMPBELL, AG ;

ROSENBERG, LE ;

SNODGRASS, PJ ;

NUZUM, CT .

NEW ENGLAND JOURNAL OF MEDICINE, 1973, 288 (01) :1-6

[8]

CROME L, 1971, J MENT DEFIC RES, V15, P266

[9] NEUROPATHOLOGICAL OBSERVATIONS IN A PATIENT WITH CARBAMYLPHOSPHATE-SYNTHETASE DEFICIENCY AND IN 2 SIBS [J].

EBELS, EJ .

ARCHIVES OF DISEASE IN CHILDHOOD, 1972, 47 (251) :47-&

[10]

Farriaux J P, 1976, Acta Neurol Belg, V76, P26

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