MITOCHONDRIAL ABNORMALITIES OF LIVER IN PRIMARY ORNITHINE TRANSCARBAMYLASE DEFICIENCY

被引：29

作者：

SHAPIRO, JM

SCHAFFNER, F

TALLAN, HH

GAULL, GE

机构：

[1] CUNY MT SINAI SCH MED,DEPT MED,DIV LIVER DIS,NEW YORK,NY 10029

[2] CUNY MT SINAI SCH MED,DEPT PEDIAT,DIV HUMAN GENET,NEW YORK,NY 10029

[3] CUNY MT SINAI SCH MED,CTR CLIN RES,NEW YORK,NY 10029

[4] NEW YORK STATE INST BAS RES MENTAL RETARDAT,DEPT HUMAN DEV & NUTR,STATEN ISL,NY 10314

来源：

PEDIATRIC RESEARCH | 1980年 / 14卷 / 05期

关键词：

D O I：

10.1203/00006450-198005000-00006

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：735 / 739

页数：5

共 26 条

[1]

BELLINGER JF, 1971, CLIN CHEM, V17, P1132

[2]

BROWN GW, 1959, J BIOL CHEM, V234, P1769

[3] HEREDITARY HYPERAMMONAEMIA [J].

BRUTON, CJ ;

CORSELLIS, JA ;

RUSSELL, A .

BRAIN, 1970, 93 :423-+

[4] 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

[5]

COLOMBO JP, 1971, MONOGR PAEDIATR, V1, P55

[6] PERIODIC ATTACKS OF LETHARGY IN A BABY WITH AMMONIA INTOXICATION DUE TO A CONGENITAL DEFECT IN UREOGENESIS [J].

CORBEEL, LM ;

COLOMBO, JP ;

VANSANDE, M ;

WEBER, A .

ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (238) :681-&

[7] HYPERAMMONEMIA THROUGH DEFICIENCY OF ORNITHINE CARBAMYL TRANSFERASE [J].

FARRIAUX, JP ;

DHONDT, JL ;

CATHELIN.L ;

RATEL, J ;

FONTAINE, G .

ZEITSCHRIFT FUR KINDERHEILKUNDE, 1974, 118 (03) :231-247

[8]

FLEISHER LD, 1979, AM J HUM GENET, V31, P439

[9] METABOLIC AND GENETIC STUDIES OF A FAMILY WITH ORNITHINE TRANSCARBAMYLASE DEFICIENCY [J].

GOLDSTEIN, AS ;

HOOGENRAAD, NJ ;

JOHNSON, JD ;

FUKANAGA, K ;

SWIERCZEWSKI, E ;

CANN, HM ;

SUNSHINE, P .

PEDIATRIC RESEARCH, 1974, 8 (01) :5-12

[10] HYPERAMMONAEMIA DUE TO ORNITHINE TRANSCARBAMYLASE DEFICIENCY [J].

HOPKINS, IJ ;

CONNELLY, JF ;

DAWSON, AG ;

HIRD, FJR ;

MADDISON, TG .

ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (234) :143-&

← 1 2 3 →