Clinical and biochemical study of three patients with tyrosyluria.
作者信息
Sass-Kortsak A, Ficici S, Paunier L, Kooh S W, Fraser D, Jackson S H
出版信息
Can Med Assoc J. 1967 Oct 28;97(18):1056-8.
Abstract
摘要
相似文献
1
Clinical and biochemical study of three patients with tyrosyluria.
Can Med Assoc J. 1967 Oct 28;97(18):1056-8.
2
Hereditary tyrosinemia and tyrosyluria: clinical report of four patients.
Can Med Assoc J. 1967 Oct 28;97(18):1047-50.
3
Observations on treatment in patients with tyrosyluria.
Can Med Assoc J. 1967 Oct 28;97(18):1089-95.
4
Secondary metabolic derangements in patients with tyrosyluria.
Can Med Assoc J. 1967 Oct 28;97(18):1079-83.
5
The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis.
Can Med Assoc J. 1967 Oct 28;97(18):1073-5.
6
Tyrosinosis. I. Clinical, radiological and biochemical aspects.
Indian Pediatr. 1969 Jan;6(1):1-17.
7
Tyrosinaemia and tyrosyluria in infancy.
Dev Med Child Neurol. 1967 Oct;9(5):551-62. doi: 10.1111/j.1469-8749.1967.tb02324.x.
8
[Oculocutaneous albinism and tyrosinuria. Description of a clinical case].
Minerva Pediatr. 1983 Feb;35(3):99-103.
9
[Report on a case of hypertyrosinemia and tyrosinuria].
Minerva Pediatr. 1974 Feb 11;26(4):203-13.
10
[Hereditary tyrosinemia with tyrosiluria. Study of 44 cases in infants].
Union Med Can. 1968 Jun;97(6):762-72.
引用本文的文献
1
Hepatorenal tyrosinemia.
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(5):192-200. doi: 10.2183/pjab.88.192.
2
Recovery after dietary treatment of an infant with features of tyrosinosis.
Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.
3
Hereditary tyrosinemia in a French Canadian isolate.
Am J Hum Genet. 1969 Jan;21(1):36-45.
Zotero 插件