HEREDITARY HYPERAMMONAEMIA

被引：61

作者：

BRUTON, CJ

CORSELLIS, JA

RUSSELL, A

机构：

来源：

BRAIN | 1970年 / 93卷

关键词：

D O I：

10.1093/brain/93.2.423

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：423 / +

页数：1

共 17 条

[1]

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[2]

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[3] 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-&

[4] HYPERAMMONAEMIA - A DEFICIENCY OF LIVER ORNITHINE TRANSCARBAMYLASE - OCCURRENCE IN MOTHER AND CHILD [J].

LEVIN, B ;

ABRAHAM, JM ;

OBERHOLZER, VG ;

BURGESS, EA .

ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (234) :152-+

[5] HYPERAMMONAEMIA - A VARIANT TYPE OF DEFICIENCY OF LIVER ORNITHINE TRANSCARBAMYLASE [J].

LEVIN, B ;

DOBBS, RH ;

BURGESS, EA ;

PALMER, T .

ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (234) :162-&

[6]

LEVIN B, 1969, LANCET, V2, P170

[7] EPISODIC STUPOR ASSOCIATED WITH AN ECK FISTULA IN THE HUMAN WITH PARTICULAR REFERENCE TO THE METABOLISM OF AMMONIA [J].

MCDERMOTT, WV ;

ADAMS, RD .

JOURNAL OF CLINICAL INVESTIGATION, 1954, 33 (01) :1-9

[8]

READ AE, 1967, Q J MED, V36, P135

[9]

Rett A, 1968, Wien Med Wochenschr, V118, P311

[10]

Rett A., 1966, WIENER MED WOCHENSCH, V116, P723

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