酪氨酸血症的诊断与治疗。 - Suppr

Suppr

超能文献

Diagnosis and treatment of tyrosinosis.

作者信息

Fairney A, Francis D, Ersser R S, Seakins J W, Cottom D

出版信息

Arch Dis Child. 1968 Oct;43(231):540-7. doi: 10.1136/adc.43.231.540.

DOI:10.1136/adc.43.231.540

PMID:5696464

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2020014/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b60d/2020014/725f3fe118a2/archdisch01560-0043-a.jpg

相似文献

Diagnosis and treatment of tyrosinosis.

Arch Dis Child. 1968 Oct;43(231):540-7. doi: 10.1136/adc.43.231.540.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

[Tyrosinosis].

Monatsschr Kinderheilkd (1902). 1969 Jan;117(1):31-2.

Tyrosinosis.

Acta Univ Carol Med Monogr. 1973;56:201-4.

[Tyrosinosis. Primary and secondary biochemical changes].

Z Kinderheilkd. 1972;113(3):193-204.

Observations on treatment in patients with tyrosyluria.

Can Med Assoc J. 1967 Oct 28;97(18):1089-95.

Dietary treatment of tyrosinosis.

J Am Diet Assoc. 1970 Apr;56(4):308-12.

Dietary treatment of infantile tyrosinemia.

Tohoku J Exp Med. 1968 Aug;95(4):337-44. doi: 10.1620/tjem.95.337.

Skin lesions in tyrosinosis: response to dietary treatment.

Br J Dermatol. 1973 Apr;88(4):335-40. doi: 10.1111/j.1365-2133.1973.tb07562.x.

[Tyrosinosis].

Presse Med (1893). 1968 Jun 1;76(27):138-9.

引用本文的文献

N-Acetyltyrosine as a Biomarker of Parenteral Nutrition Administration in First-Tier Newborn Screening Assays.

Int J Neonatal Screen. 2024 Dec 10;10(4):81. doi: 10.3390/ijns10040081.

N-acetyl-l-tyrosine is an intrinsic triggering factor of mitohormesis in stressed animals.

EMBO Rep. 2020 May 6;21(5):e49211. doi: 10.15252/embr.201949211. Epub 2020 Mar 2.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

Use of an amino acid mixture in treatment of phenylketonuria.

Arch Dis Child. 1970 Oct;45(243):640-50. doi: 10.1136/adc.45.243.640.

Neonatal hepatitis in premature infants simulating hereditary tyrosinosis.

Arch Dis Child. 1971 Jun;46(247):306-9. doi: 10.1136/adc.46.247.306.

Tyrosinosis: a new variant.

Can Med Assoc J. 1973 Feb 17;108(4):477 passim.

本文引用的文献

An inborn defect in the metabolism of tyrosine in infants on a normal diet.

Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320.

A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine.

Biochem J. 1932;26(4):917-40. doi: 10.1042/bj0260917.

Detection of heterozygotes for phenylketonuria.

Clin Chim Acta. 1960 Jul;5:471-6. doi: 10.1016/0009-8981(60)90054-1.

SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA.

JAMA. 1964 Apr 20;188:203-6. doi: 10.1001/jama.1964.03060290007001.

DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

Arch Dis Child. 1963 Oct;38(201):485-91. doi: 10.1136/adc.38.201.485.

Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.

Arch Dis Child. 1967 Dec;42(226):682-8. doi: 10.1136/adc.42.226.682.

Tyrosinaemia and tyrosyluria in infancy.

Dev Med Child Neurol. 1967 Oct;9(5):551-62. doi: 10.1111/j.1469-8749.1967.tb02324.x.

Paper chromatography of keto acid 2,4-dinitrophenylhydrazones.

J Chromatogr. 1967 Sep;30(1):273-5. doi: 10.1016/s0021-9673(00)84158-8.

Observations on treatment in patients with tyrosyluria.

Can Med Assoc J. 1967 Oct 28;97(18):1089-95.

Transient tyrosinemia of the newborn: dietary and clinical aspects.

Pediatrics. 1967 Mar;39(3):378-84.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

Diagnosis and treatment of tyrosinosis.

Arch Dis Child. 1968 Oct;43(231):540-7. doi: 10.1136/adc.43.231.540.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

[Tyrosinosis].

Monatsschr Kinderheilkd (1902). 1969 Jan;117(1):31-2.

Tyrosinosis.

Acta Univ Carol Med Monogr. 1973;56:201-4.

[Tyrosinosis. Primary and secondary biochemical changes].

Z Kinderheilkd. 1972;113(3):193-204.

Observations on treatment in patients with tyrosyluria.

Can Med Assoc J. 1967 Oct 28;97(18):1089-95.

Dietary treatment of tyrosinosis.

J Am Diet Assoc. 1970 Apr;56(4):308-12.

Dietary treatment of infantile tyrosinemia.

Tohoku J Exp Med. 1968 Aug;95(4):337-44. doi: 10.1620/tjem.95.337.

Skin lesions in tyrosinosis: response to dietary treatment.

Br J Dermatol. 1973 Apr;88(4):335-40. doi: 10.1111/j.1365-2133.1973.tb07562.x.

[Tyrosinosis].

Presse Med (1893). 1968 Jun 1;76(27):138-9.

引用本文的文献

N-Acetyltyrosine as a Biomarker of Parenteral Nutrition Administration in First-Tier Newborn Screening Assays.

Int J Neonatal Screen. 2024 Dec 10;10(4):81. doi: 10.3390/ijns10040081.

N-acetyl-l-tyrosine is an intrinsic triggering factor of mitohormesis in stressed animals.

EMBO Rep. 2020 May 6;21(5):e49211. doi: 10.15252/embr.201949211. Epub 2020 Mar 2.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

Use of an amino acid mixture in treatment of phenylketonuria.

Arch Dis Child. 1970 Oct;45(243):640-50. doi: 10.1136/adc.45.243.640.

Neonatal hepatitis in premature infants simulating hereditary tyrosinosis.

Arch Dis Child. 1971 Jun;46(247):306-9. doi: 10.1136/adc.46.247.306.

Tyrosinosis: a new variant.

Can Med Assoc J. 1973 Feb 17;108(4):477 passim.

本文引用的文献

An inborn defect in the metabolism of tyrosine in infants on a normal diet.

Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320.

A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine.

Biochem J. 1932;26(4):917-40. doi: 10.1042/bj0260917.

Detection of heterozygotes for phenylketonuria.

Clin Chim Acta. 1960 Jul;5:471-6. doi: 10.1016/0009-8981(60)90054-1.

SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA.

JAMA. 1964 Apr 20;188:203-6. doi: 10.1001/jama.1964.03060290007001.

DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

Arch Dis Child. 1963 Oct;38(201):485-91. doi: 10.1136/adc.38.201.485.

Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.

Arch Dis Child. 1967 Dec;42(226):682-8. doi: 10.1136/adc.42.226.682.

Tyrosinaemia and tyrosyluria in infancy.

Dev Med Child Neurol. 1967 Oct;9(5):551-62. doi: 10.1111/j.1469-8749.1967.tb02324.x.

Paper chromatography of keto acid 2,4-dinitrophenylhydrazones.

J Chromatogr. 1967 Sep;30(1):273-5. doi: 10.1016/s0021-9673(00)84158-8.

Observations on treatment in patients with tyrosyluria.

Can Med Assoc J. 1967 Oct 28;97(18):1089-95.

Transient tyrosinemia of the newborn: dietary and clinical aspects.

Pediatrics. 1967 Mar;39(3):378-84.