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CITRULLINURIA.

作者信息

MCMURRAY W C, RATHBUN J C, MOHYUDDIN F, KOEGLER S J

出版信息

Pediatrics. 1963 Sep;32:347-57.

PMID:14063512

Abstract

摘要

相似文献

CITRULLINURIA.

Pediatrics. 1963 Sep;32:347-57.

[CITRULLINURIA].

Pediatrie. 1963;18:847-9.

AN OCCURRENCE OF ARGININOSUCCINIC ACIDURIA.

Pediatrics. 1964 Feb;33:280-3.

RENAL TUBULAR DISORDERS.

Dis Mon. 1964 Oct;89:SUPPL 1964:1+. doi: 10.1016/s0011-5029(64)80012-2.

HOMOCYSTINURIA.

Proc R Soc Med. 1963 Nov;56(11):996-7. doi: 10.1177/003591576305601127.

HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE.

Pediatrics. 1964 Mar;33:413-20.

HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.

Arch Dis Child. 1963 Oct;38(201):425-36. doi: 10.1136/adc.38.201.425.

CITRULLINURIA.

Rev Neuropsiquiatr. 1964 Sep;27:287-93.

[EVALUATION OF AMINOACIDURIA IN CHILDHOOD].

Pediatria (Napoli). 1964 Oct 31;72:1061-70.

DISORDERS OF AMINO ACID TRANSPORT.

Ann Intern Med. 1965 Apr;62:847-51. doi: 10.7326/0003-4819-62-4-847.

引用本文的文献

Hyperammonaemia due to ornithine transcarbamylase deficiency.

Arch Dis Child. 1969 Apr;44(234):143-8. doi: 10.1136/adc.44.234.143.

Two hypomorphic alleles of mouse Ass1 as a new animal model of citrullinemia type I and other hyperammonemic syndromes.

Am J Pathol. 2010 Oct;177(4):1958-68. doi: 10.2353/ajpath.2010.100118. Epub 2010 Aug 19.

DISORDERS OF AMINO-ACID TRANSPORT.

Br Med J. 1964 Feb 8;1(5379):327-36. doi: 10.1136/bmj.1.5379.327.

Neonatal screening for citrullinaemia.

Eur J Pediatr. 2003 Jun;162(6):417-20. doi: 10.1007/s00431-003-1177-z. Epub 2003 Apr 8.

Chronic vomiting in a case of citrullinaemia detected after treatment by total parenteral nutrition.

Gut. 1984 May;25(5):531-3. doi: 10.1136/gut.25.5.531.

Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemia.

J Inherit Metab Dis. 1983;6(1):36-9. doi: 10.1007/BF02391191.

[Thin-layer chromatography of acid-and ether-soluble dinitrophenyl amino acids in the urine].

Klin Wochenschr. 1965 Nov 15;43(22):1202-8. doi: 10.1007/BF01746182.

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Arch Dis Child. 1969 Apr;44(234):152-61. doi: 10.1136/adc.44.234.152.

Amino acid metabolism during prolonged starvation.

J Clin Invest. 1969 Mar;48(3):584-94. doi: 10.1172/JCI106017.

Hyperaminoaciduria in childhood.

Indian J Pediatr. 1966 Feb;33(217):56-62. doi: 10.1007/BF02803758.

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相似文献

CITRULLINURIA.

Pediatrics. 1963 Sep;32:347-57.

[CITRULLINURIA].

Pediatrie. 1963;18:847-9.

AN OCCURRENCE OF ARGININOSUCCINIC ACIDURIA.

Pediatrics. 1964 Feb;33:280-3.

RENAL TUBULAR DISORDERS.

Dis Mon. 1964 Oct;89:SUPPL 1964:1+. doi: 10.1016/s0011-5029(64)80012-2.

HOMOCYSTINURIA.

Proc R Soc Med. 1963 Nov;56(11):996-7. doi: 10.1177/003591576305601127.

HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE.

Pediatrics. 1964 Mar;33:413-20.

HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.

Arch Dis Child. 1963 Oct;38(201):425-36. doi: 10.1136/adc.38.201.425.

CITRULLINURIA.

Rev Neuropsiquiatr. 1964 Sep;27:287-93.

[EVALUATION OF AMINOACIDURIA IN CHILDHOOD].

Pediatria (Napoli). 1964 Oct 31;72:1061-70.

DISORDERS OF AMINO ACID TRANSPORT.

Ann Intern Med. 1965 Apr;62:847-51. doi: 10.7326/0003-4819-62-4-847.

引用本文的文献

Hyperammonaemia due to ornithine transcarbamylase deficiency.

Arch Dis Child. 1969 Apr;44(234):143-8. doi: 10.1136/adc.44.234.143.

Two hypomorphic alleles of mouse Ass1 as a new animal model of citrullinemia type I and other hyperammonemic syndromes.

Am J Pathol. 2010 Oct;177(4):1958-68. doi: 10.2353/ajpath.2010.100118. Epub 2010 Aug 19.

DISORDERS OF AMINO-ACID TRANSPORT.

Br Med J. 1964 Feb 8;1(5379):327-36. doi: 10.1136/bmj.1.5379.327.

Neonatal screening for citrullinaemia.

Eur J Pediatr. 2003 Jun;162(6):417-20. doi: 10.1007/s00431-003-1177-z. Epub 2003 Apr 8.

Chronic vomiting in a case of citrullinaemia detected after treatment by total parenteral nutrition.

Gut. 1984 May;25(5):531-3. doi: 10.1136/gut.25.5.531.

Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemia.

J Inherit Metab Dis. 1983;6(1):36-9. doi: 10.1007/BF02391191.

[Thin-layer chromatography of acid-and ether-soluble dinitrophenyl amino acids in the urine].

Klin Wochenschr. 1965 Nov 15;43(22):1202-8. doi: 10.1007/BF01746182.

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Arch Dis Child. 1969 Apr;44(234):152-61. doi: 10.1136/adc.44.234.152.

Amino acid metabolism during prolonged starvation.

J Clin Invest. 1969 Mar;48(3):584-94. doi: 10.1172/JCI106017.

Hyperaminoaciduria in childhood.

Indian J Pediatr. 1966 Feb;33(217):56-62. doi: 10.1007/BF02803758.