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

作者信息

Seakins J W, Ersser R S

出版信息

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

DOI:10.1136/adc.42.226.682
PMID:6073838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2019892/
Abstract
摘要

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Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.氨基酸负荷对一名具有哈特纳普病生化特征的健康婴儿的影响。
Arch Dis Child. 1967 Dec;42(226):682-8. doi: 10.1136/adc.42.226.682.
2
Absorption of amino acids and the dipeptide, carnosine, from the gut in normal subjects and a case of Hartnup disease.正常受试者及一例哈特纳普病患者肠道对氨基酸和二肽肌肽的吸收情况。
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Absorption of amino acids and peptides in a child with a variant of Hartnup disease and coexistent coeliac disease.患有哈丁普病变体并伴有乳糜泻的儿童对氨基酸和肽的吸收情况。
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Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease.对一名Hartnup病患者氨基酸和二肽肠道吸收情况的研究。
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Intestinal absorption and biopsy transport of peptides and amino acids in Hartnup disease.
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6
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7
[Hartnup disease (author's transl)].[哈丁普病（作者译）]
Monatsschr Kinderheilkd (1902). 1973 Sep;121(9):571-83.
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Transport of amino acids and peptides in the gut and the kidney.肠道和肾脏中氨基酸及肽的转运
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Intestinal absorption of amino acids and peptides in Hartnup disorder.哈丁普病中氨基酸和肽的肠道吸收
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Proceedings: Absorption of amino acids and peptides in Hartnup disease.论文集：哈特纳普病中氨基酸和肽的吸收
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Cellular transport of L-histidine in Hartnup disease.哈氏病中L-组氨酸的细胞转运
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7
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8
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9
The Hartnup phenotype: Mendelian transport disorder, multifactorial disease.哈丁普表型：孟德尔式转运障碍，多因素疾病。
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本文引用的文献

1
The intestinal absorption defect in cystinuria.胱氨酸尿症中的肠道吸收缺陷。
Gut. 1961 Dec;2(4):323-37. doi: 10.1136/gut.2.4.323.
2
An inborn defect in the metabolism of tyrosine in infants on a normal diet.正常饮食的婴儿体内酪氨酸代谢的先天性缺陷。
Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320.
3
Detection of heterozygotes for phenylketonuria.苯丙酮尿症杂合子的检测。
Clin Chim Acta. 1960 Jul;5:471-6. doi: 10.1016/0009-8981(60)90054-1.
4
HARTNUP DISEASE: A GENETIC MODIFICATION OF INTESTINAL AND RENAL TRANSPORT OF CERTAIN NEUTRAL ALPHA-AMINO ACIDS.哈丁普病：某些中性α-氨基酸肠道和肾脏转运的一种基因改变。
N Engl J Med. 1965 Sep 2;273:530-2. doi: 10.1056/NEJM196509022731005.
5
ABSORPTION FROM THE SMALL INTESTINE.来自小肠的吸收
Sci Basis Med Annu Rev. 1963:171-96.
6
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS.
Ann Paediatr. 1964;202:321-31.
7
DISORDERS OF AMINO-ACID TRANSPORT.氨基酸转运障碍
Br Med J. 1964 Feb 8;1(5379):327-36. doi: 10.1136/bmj.1.5379.327.
8
Renal clearances of amino acids in normal adults and in patients with aminoaciduria.正常成年人及氨基酸尿症患者的氨基酸肾清除率。
Biochem J. 1960 Mar;74(3):550-61. doi: 10.1042/bj0740550.
9
The metabolic disorder in Hartnup disease.哈丁普病中的代谢紊乱。
Q J Med. 1960 Jul;29:407-21.
10
Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.遗传性糙皮病样皮疹伴暂时性小脑共济失调、持续性肾性氨基酸尿及其他奇异生化特征。
Lancet. 1956 Sep 1;271(6940):421-8. doi: 10.1016/s0140-6736(56)91914-6.