Metabolic syndromes with dermatologic manifestations.
作者信息
Irons M, Levy H L
出版信息
Clin Rev Allergy. 1986 Feb;4(1):101-24. doi: 10.1007/BF02991190.
PMID:3516355
Abstract
摘要
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本文引用的文献
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The effects of a phenylalanine-free and phenylalanine-poor diet in phenylpyruvic oligophrenis.无苯丙氨酸和低苯丙氨酸饮食对苯丙酮尿性智力发育不全的影响。
Exp Med Surg. 1954;12(1):114-7. doi: 10.1159/000382329.
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Argininosuccinicaciduria: the hair abnormality revisited.精氨琥珀酸尿症：对毛发异常的再探讨。
Am J Dis Child. 1980 Nov;134(11):1095-6. doi: 10.1001/archpedi.1980.02130230073023.
4
Studies of phenylketonurics with dermatitis.对患有皮炎的苯丙酮尿症患者的研究。
J Am Acad Dermatol. 1981 Mar;4(3):284-90. doi: 10.1016/s0190-9622(81)70029-x.
5
Prolidase deficiency: an inborn error of metabolism with major dermatological manifestations.脯氨酰肽酶缺乏症：一种具有主要皮肤表现的先天性代谢紊乱疾病。
Dermatologica. 1982 May;164(5):293-304. doi: 10.1159/000250106.
6
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.尿素合成先天性缺陷的治疗：激活废氮合成与排泄的替代途径。
N Engl J Med. 1982 Jun 10;306(23):1387-92. doi: 10.1056/NEJM198206103062303.
7
Phenotypic variation in biotinidase deficiency.生物素酶缺乏症的表型变异。
J Pediatr. 1983 Aug;103(2):233-7. doi: 10.1016/s0022-3476(83)80351-5.
8
Deficient biotinidase activity in late-onset multiple carboxylase deficiency.迟发性多种羧化酶缺乏症中的生物素酶活性不足
N Engl J Med. 1983 Jan 20;308(3):161. doi: 10.1056/NEJM198301203080321.
9
Prolidase deficiency with iminodipeptiduria: biochemical investigations and first results of attempted therapy.伴有亚氨基二肽尿症的脯氨酰寡肽酶缺乏症：生化研究及尝试性治疗的初步结果
J Inherit Metab Dis. 1981;4(2):77-8. doi: 10.1007/BF02263599.
10
Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.尿素合成先天性代谢缺陷患儿的神经学转归。尿素循环酶病的转归。
N Engl J Med. 1984 Jun 7;310(23):1500-5. doi: 10.1056/NEJM198406073102304.
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