肝糖原贮积病。23例临床及实验室检查结果 - Suppr

Suppr

超能文献

Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases.

作者信息

Spencer-Peet J, Norman M E, Lake B D, McNamara J, Patrick A D

出版信息

Q J Med. 1971 Jan;40(157):95-114.

PMID:5282941

Abstract

摘要

相似文献

Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases.肝糖原贮积病。23例临床及实验室检查结果

Q J Med. 1971 Jan;40(157):95-114.

The hepatic glycogenoses.肝糖原贮积症

Lancet. 1971 Jun 26;1(7713):1339-40.

[Biochemistry and clinical picture of glycogenoses].[糖原贮积病的生物化学与临床表现]

Dtsch Med Wochenschr. 1969 Jul 4;94(27):1420-1. doi: 10.1055/s-0028-1110274.

[New possibilities of diagnosis and trial therapy of glycogenosis of type I].[I型糖原贮积症的诊断与试验性治疗的新可能性]

Pediatria (Napoli). 1969;77(3):360-70.

Hexose and protein tolerance tests in children with liver glycogenosis caused by a deficiency of the debranching enzyme system.脱支酶系统缺乏所致肝糖原累积症患儿的己糖和蛋白质耐量试验

Pediatrics. 1968 May;41(5):935-44.

[A case of glycogenosis with recurrent hypoglycemia without enzymatic deficiency on liver biopsy].[一例糖原贮积病伴反复低血糖，肝脏活检无酶缺乏]

Ann Pediatr (Paris). 1972 Jun-Jul;19(6):499-506.

[Liver glycogenosis with cirrhosis without enzyme deficiency].[无酶缺乏的肝硬化性肝糖原贮积症]

Arch Fr Pediatr. 1972 Jan;29(1):67-78.

Diphenylhydantoin treatment of glycogen storage diseases.二苯妥英治疗糖原贮积病。

Arch Intern Med. 1974 Sep;134(3):418-21.

[Glycogen disease in children].[儿童糖原贮积病]

Sov Zdravookhr Kirg. 1971 Sep-Oct;5:39-43.

The floppy infant syndrome in muscular glycogenosis.肌肉糖原贮积症中的松软婴儿综合征。

Padiatr Padol. 1972;7(4):365-71.

引用本文的文献

Dynamic Methods for Childhood Hypoglycemia Phenotyping: A Narrative Review.动态方法用于儿童低血糖表型分析：叙述性综述。

Front Endocrinol (Lausanne). 2022 Jun 17;13:858832. doi: 10.3389/fendo.2022.858832. eCollection 2022.

Cardiomyopathy of glycogen storage disease type III.Ⅲ型糖原贮积病性心肌病

Heart Vessels. 1993;8(3):155-9. doi: 10.1007/BF01744800.

Value of the glucagon test in screening for hepatic glycogen storage disease.胰高血糖素试验在肝糖原贮积病筛查中的价值。

Arch Dis Child. 1982 May;57(5):384-9. doi: 10.1136/adc.57.5.384.

Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twins.急性I型遗传性酪氨酸血症：对双胞胎的临床、生化及血液学研究

J Inherit Metab Dis. 1981;4(1):37-40. doi: 10.1007/BF02263580.

Growth and endocrine changes in the hepatic glycogenoses.肝糖原贮积症的生长与内分泌变化

Eur J Pediatr. 1982 May;138(3):226-30. doi: 10.1007/BF00441207.

Patterns of growth in the hepatic glycogenoses.肝糖原贮积症的生长模式。

Arch Dis Child. 1984 Jul;59(7):657-60. doi: 10.1136/adc.59.7.657.

Glycogen storage disease type Ib.Ⅰb型糖原贮积病

Eur J Pediatr. 1983 Sep;140(4):283-8. doi: 10.1007/BF00442664.

A new variant of glycogen storage disease type 1: probably due to a defect in the glucose-6-phosphate transport system.1型糖原贮积病的一种新变异型：可能由于6-磷酸葡萄糖转运系统缺陷所致。

J Inherit Metab Dis. 1980;2(3):45-9. doi: 10.1007/BF01801717.

The glycogen storage diseases.糖原贮积病

J Clin Pathol Suppl (R Coll Pathol). 1974;8:106-21.

Hepatic glycogen synthetase deficiency. Further studies on a family.肝糖原合成酶缺乏症。对一个家族的进一步研究。

Arch Dis Child. 1972 Aug;47(254):558-63. doi: 10.1136/adc.47.254.558.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验