酪氨酸血症（酪氨酸病）的饮食治疗。关于携带者状态可能识别的说明。 - Suppr

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超能文献

Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state.

作者信息

Gentz J, Lindblad B, Lindstedt S, Levy L, Shasteen W, Zetterstrom R

出版信息

Am J Dis Child. 1967 Jan;113(1):31-7. doi: 10.1001/archpedi.1967.02090160081006.

DOI:10.1001/archpedi.1967.02090160081006

PMID:6015903

Abstract

摘要

相似文献

Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state.酪氨酸血症（酪氨酸病）的饮食治疗。关于携带者状态可能识别的说明。

Am J Dis Child. 1967 Jan;113(1):31-7. doi: 10.1001/archpedi.1967.02090160081006.

Dietary treatment of tyrosinosis.酪氨酸血症的饮食治疗。

Am J Dis Child. 1967 Jan;113(1):38-40. doi: 10.1001/archpedi.1967.02090160088007.

Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity.

J Pediatr. 1972 Jun;80(6):994-1004. doi: 10.1016/s0022-3476(72)80013-1.

Tyrosinosis: a patient without liver or renal disease.

Pediatrics. 1971 Sep;48(3):393-400.

Long-term dietary treatment of tyrosinosis.酪氨酸血症的长期饮食治疗。

J Pediatr. 1968 May;72(5):620-7. doi: 10.1016/s0022-3476(68)80004-6.

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.

Recovery after dietary treatment of an infant with features of tyrosinosis.对一名具有酪氨酸血症特征的婴儿进行饮食治疗后的恢复情况。

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate.法裔加拿大一个地理隔离群体中的遗传性酪氨酸血症和酪氨酸尿症。

Am J Dis Child. 1967 Jan;113(1):41-6. doi: 10.1001/archpedi.1967.02090160091008.

Tyrosinosis: a new variant.酪氨酸血症：一种新的变异型。

Can Med Assoc J. 1973 Feb 17;108(4):477 passim.

[Tyrosinosis: effect of diet on the tubular reabsorption of phosphorus].[酪氨酸血症：饮食对磷肾小管重吸收的影响]

Arch Fr Pediatr. 1973 May;30(5):560-1.

引用本文的文献

Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report.I型遗传性酪氨酸血症小鼠模型的治疗试验：进展报告。

J Inherit Metab Dis. 1998 Aug;21(5):518-31. doi: 10.1023/a:1005462804271.

Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone.遗传性酪氨酸血症与血红素生物合成途径。琥珀酰丙酮对δ-氨基乙酰丙酸脱水酶活性的深度抑制。

J Clin Invest. 1983 Mar;71(3):625-34. doi: 10.1172/jci110809.

Recovery after dietary treatment of an infant with features of tyrosinosis.对一名具有酪氨酸血症特征的婴儿进行饮食治疗后的恢复情况。

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

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.

Hereditary tyrosinemia. Formation of succinylacetone-amino acid adducts.遗传性酪氨酸血症。琥珀酰丙酮 - 氨基酸加合物的形成。

J Exp Med. 1985 Sep 1;162(3):1060-74. doi: 10.1084/jem.162.3.1060.

Liver transplantation in a 23-year-old tyrosinaemia patient: effects on the renal tubular dysfunction.一名23岁酪氨酸血症患者的肝移植：对肾小管功能障碍的影响

J Inherit Metab Dis. 1986;9(2):216-24. doi: 10.1007/BF01799465.

Determinants of nocturnal enuresis in homozygous sickle cell disease.纯合子镰状细胞病夜间遗尿的决定因素。

Arch Dis Child. 1990 Jun;65(6):615-8. doi: 10.1136/adc.65.6.615.

Evidence for the possible formation of a toxic tyrosine metabolite by the liver microsomal drug metabolizing system.肝脏微粒体药物代谢系统可能形成有毒酪氨酸代谢物的证据。

Naunyn Schmiedebergs Arch Pharmacol. 1976;292(1):79-86. doi: 10.1007/BF00506493.

A syndrome of hereditary tyrosinemia in mink (Mustela vison Schreb.).水貂（鼬属水貂）遗传性酪氨酸血症综合征。

Can J Comp Med. 1979 Jul;43(3):333-40.

On the enzymic defects in hereditary tyrosinemia.关于遗传性酪氨酸血症中的酶缺陷

Proc Natl Acad Sci U S A. 1977 Oct;74(10):4641-5. doi: 10.1073/pnas.74.10.4641.

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