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.
Abstract
摘要
相似文献
1
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
3
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。
Arch Dis Child. 1972 Oct;47(255):798-803. doi: 10.1136/adc.47.255.798.
4
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。
Gut. 1970 May;11(5):373-9. doi: 10.1136/gut.11.5.373.
5
Intestinal absorption and biopsy transport of peptides and amino acids in Hartnup disease.
Clin Sci. 1970 Dec;39(6):18P-19P. doi: 10.1042/cs039018pa.
6
Intestinal absorption of dipeptides and corresponding free amino acids in Hartnup disease.哈氏病中双肽及相应游离氨基酸的肠道吸收
Clin Sci. 1970 Jul;39(1):1P. doi: 10.1042/cs039001pa.
7
[Hartnup disease (author's transl)].[哈丁普病（作者译）]
Monatsschr Kinderheilkd (1902). 1973 Sep;121(9):571-83.
8
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
Sci Basis Med Annu Rev. 1971:161-77.
9
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
Pediatr Res. 1976 Apr;10(4):246-9. doi: 10.1203/00006450-197604000-00010.
10
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
Clin Sci Mol Med. 1974 Feb;46(2):15P. doi: 10.1042/cs046015p.
引用本文的文献
1
Diagnostic Approach to Abnormal Urine Colors: Lessons From a Case of Blue-Green Urine.异常尿液颜色的诊断方法：一例蓝绿色尿液病例的经验教训
Cureus. 2025 Apr 11;17(4):e82122. doi: 10.7759/cureus.82122. eCollection 2025 Apr.
2
Hartnup disease masked by kwashiorkor.夸希奥科病掩盖的哈特纳普病
J Health Popul Nutr. 2010 Aug;28(4):413-5. doi: 10.3329/jhpn.v28i4.6049.
3
Cellular transport of L-histidine in Hartnup disease.哈氏病中L-组氨酸的细胞转运
J Clin Invest. 1969 Aug;48(8):1552-9. doi: 10.1172/JCI106121.
4
Diagnosis and treatment of tyrosinosis.酪氨酸血症的诊断与治疗。
Arch Dis Child. 1968 Oct;43(231):540-7. doi: 10.1136/adc.43.231.540.
5
Studies on the origin of faecal amino acids in cystic fibrosis.囊性纤维化患者粪便氨基酸来源的研究。
Gut. 1970 Jul;11(7):600-9. doi: 10.1136/gut.11.7.600.
6
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。
Arch Dis Child. 1972 Oct;47(255):798-803. doi: 10.1136/adc.47.255.798.
7
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。
Gut. 1970 May;11(5):373-9. doi: 10.1136/gut.11.5.373.
8
Hartnup disease.哈丁普病
Biochem J. 1969 Feb;111(3):3P-4P. doi: 10.1042/bj1110003p.
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。
Am J Hum Genet. 1987 May;40(5):401-12.
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.
Zotero 插件