Hartnup disease.
作者信息
Milne M D
出版信息
Biochem J. 1969 Feb;111(3):3P-4P. doi: 10.1042/bj1110003p.
Abstract
摘要
相似文献
1
Hartnup disease.哈丁普病
Biochem J. 1969 Feb;111(3):3P-4P. doi: 10.1042/bj1110003p.
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Treatment of Hartnup disease with nicotinic acid.用烟酸治疗哈特纳普病。
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Hartnup disease.哈特纳普病
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[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
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[Pathologic deviations of tryptophan metabolism and their biochemical examination].
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Tryptophan load and uptake of tryptophan by leukocytes in Hartnup disease.哈特纳普病中色氨酸负荷与白细胞对色氨酸的摄取
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8
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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9
Circumvention of defective neutral amino acid transport in Hartnup disease using tryptophan ethyl ester.利用色氨酸乙酯规避哈特纳普病中缺陷性中性氨基酸转运
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10
Maternal Hartnup disorder.母亲患哈特纳普病。
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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
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.
3
HARTNUP DISEASE IN TWO SIBLINGS. CLINICAL OBSERVATIONS AND BIOCHEMICAL STUDIES.两名同胞患哈氏病。临床观察与生化研究
Ann Paediatr Fenn. 1964;10:42-56.
4
Stature and nutrition in cystinuria and Hartnup disease.胱氨酸尿症和哈特纳普病中的身高与营养状况。
Br Med J. 1963 Mar 2;1(5330):590-2. doi: 10.1136/bmj.1.5330.590.
5
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.
6
The metabolic disorder in Hartnup disease.哈丁普病中的代谢紊乱。
Q J Med. 1960 Jul;29:407-21.
7
[Photodermatosis with aminoaciduria, indolaceturia & cerebral manifestations (Hartnup syndrome)].
Klin Wochenschr. 1958 Oct 1;36(19):893-7. doi: 10.1007/BF01485009.
8
A case of Hartnup disease.一例哈特纳普病。
Arch Dis Child. 1958 Apr;33(168):114-7. doi: 10.1136/adc.33.168.114.
9
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.
10
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.
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