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The metabolic disorder in Hartnup disease.

作者信息

MILNE M D, CRAWFORD M A, GIRAO C B, LOUGHRIDGE L W

出版信息

Q J Med. 1960 Jul;29:407-21.

PMID:13770962
Abstract
摘要

相似文献

1
The metabolic disorder in Hartnup disease.哈丁普病中的代谢紊乱。
Q J Med. 1960 Jul;29:407-21.
2
[Proceedings: Pellagroid eruption and deep recurrent ataxia due to a tryptophan metabolism disorder].[会议论文：因色氨酸代谢紊乱导致的糙皮病样皮疹和深度复发性共济失调]
Pediatrie. 1975 Jul-Aug;30(5):539.
3
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. I. RESULTS OF INTRAVENOUS AND ORAL TRYPTOPHAN LOADING TESTS IN A CASE OF HARTNUP DISEASE.
Ann Paediatr. 1964;202:145-60.
4
Hartnup disease.哈特纳普病
Pediatrics. 1963 Jan;31:29-38.
5
[THE CLINICAL FORM OF HARTNUP'S DISEASE].
Acta Paediatr Belg. 1963;17:215-22.
6
Indole production in Hartnup disease.
Lancet. 1963 Jan 19;1(7273):126-8. doi: 10.1016/s0140-6736(63)91015-8.
7
Hartnup disease in psychiatric practice: clinical and biochemical features of three cases.精神科临床中的哈氏病：三例患者的临床及生化特征
J Neurol Neurosurg Psychiatry. 1960 Feb;23(1):40-5. doi: 10.1136/jnnp.23.1.40.
8
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. II. SOME OBSERVATIONS ON RATS ABOUT TRYPTOPHAN METABOLISM.
Ann Paediatr. 1964;202:253-62.
9
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS.
Ann Paediatr. 1964;202:321-31.
10
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.

引用本文的文献

1
Clinical and biochemical observations in two cases of hartnup disease.两例哈丁普病的临床与生化观察
Arch Dis Child. 1966 Aug;41(218):383-8. doi: 10.1136/adc.41.218.383.
2
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.
3
Clinical implications of recent advances in the physiology of motility and absorption.运动与吸收生理学最新进展的临床意义
Proc R Soc Med. 1961 Sep;54(9):775-7. doi: 10.1177/003591576105400923.
4
TRYPTOPHAN METABOLISM IN MAN.人体中的色氨酸代谢
J Clin Invest. 1964 Sep;43(9):1730-46. doi: 10.1172/JCI105048.
5
ABNORMAL TRYPTOPHAN METABOLISM IN PATIENTS WITH ADULT CELIAC DISEASE, WITH EVIDENCE FOR DEFICIENCY OF VITAMIN B6.成人乳糜泻患者色氨酸代谢异常，伴有维生素B6缺乏的证据。
J Clin Invest. 1964 May;43(5):894-903. doi: 10.1172/JCI104975.
6
RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA.健康及家族性高脯氨酸血症状态下脯氨酸、羟脯氨酸和甘氨酸的肾小管转运
J Clin Invest. 1964 Mar;43(3):374-85. doi: 10.1172/JCI104922.
7
[A CLINICAL PICTURE WITH POIKILODERMA-LIKE SKIN CHANGES, AMINOACIDURIA AND INDOLACETURIA. CONTRIBUTION TO DATA ON HARTNUP SYNDROME].[伴有类皮肤异色症样皮肤改变、氨基酸尿症和吲哚乙酸尿症的临床症状。对哈特纳普综合征数据的贡献]
Arch Klin Exp Dermatol. 1964 Jan 15;218:165-76.
8
CLINICAL AND BIOCHEMICAL FEATURES OF A CASE OF HARTNUP DISEASE.一例哈特纳普病的临床与生化特征
Br Med J. 1964 Feb 1;1(5378):282-5. doi: 10.1136/bmj.1.5378.282.
9
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.
10
Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.在北爱尔兰对智力落后个体的一项调查中检测到的代谢异常。
Arch Dis Child. 1962 Oct;37(195):505-13. doi: 10.1136/adc.37.195.505.