糖原贮积病 - Suppr

Suppr

超能文献

Glycogen storage diseases.

作者信息

Van Hoof F, Hue L, De Barsy T, Jacquemin P, Devos P, Hers H G

出版信息

Biochimie. 1972;54(5):745-52. doi: 10.1016/s0300-9084(72)80177-9.

DOI:10.1016/s0300-9084(72)80177-9

PMID:4347397

Abstract

摘要

相似文献

Glycogen storage diseases.糖原贮积病

Biochimie. 1972;54(5):745-52. doi: 10.1016/s0300-9084(72)80177-9.

Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidase.庞贝病中的酶替代：使用纯化的人酸性α-葡萄糖苷酶的尝试。

Birth Defects Orig Artic Ser. 1973 Mar;9(2):184-90.

Enzymes of glycogen metabolism in human skin with particular reference to differential diagnosis of the glycogen storage diseases.人类皮肤中糖原代谢的酶，特别涉及糖原贮积病的鉴别诊断。

Clin Sci. 1971 Mar;40(3):261-9. doi: 10.1042/cs0400261.

Alpha-glucosidase administration: experiences in two patients with glycogen storage disease compared with animal experiments.

Birth Defects Orig Artic Ser. 1973 Mar;9(2):191-4.

A technique for the enzymatic diagnosis of glycogen storage disease on very small tissue specimens.一种用于在非常小的组织样本上进行糖原贮积病酶学诊断的技术。

Acta Paediatr Scand. 1968 Mar;57(2):105-9. doi: 10.1111/j.1651-2227.1968.tb04660.x.

Administration of a mixture of fungal glucosidases to a patient with type II glycogenosis (Pompe's disease).向一名患有II型糖原贮积病（庞贝氏病）的患者施用真菌糖苷酶混合物。

Pediatrics. 1968 Oct;42(4):672-6.

Branching enzyme-deficiency glycogenosis: studies in therapy.分支酶缺乏性糖原贮积症：治疗研究

Arch Dis Child. 1968 Jun;43(229):347-52. doi: 10.1136/adc.43.229.347.

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.

Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex.用α-葡萄糖苷酶-低密度脂蛋白复合物对庞贝病进行酶替代治疗。

Birth Defects Orig Artic Ser. 1980;16(1):415-23.

[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.

引用本文的文献

Glycogenosis type Ib. Further evidence for a membrane disease.Ⅰb型糖原贮积病。膜疾病的进一步证据。

Eur J Pediatr. 1981 Feb;135(3):325. doi: 10.1007/BF00442112.

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.

Some aspects of the cellular biochemistry of lysosomal and related glycosidases.溶酶体及相关糖苷酶的细胞生物化学的某些方面。

Mol Cell Biochem. 1973 Dec 15;2(2):169-77. doi: 10.1007/BF01795471.

Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses.肝磷酸化酶缺乏症。它与其他肝糖原贮积症的鉴别。

Arch Dis Child. 1974 Mar;49(3):186-91. doi: 10.1136/adc.49.3.186.

Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Acta Neuropathol. 1973 Feb 19;23(3):229-44. doi: 10.1007/BF00687878.

Soluble neutral and acid maltases in the suckling-rat intestine. The effect of cortisol and development.乳鼠肠道中的可溶性中性和酸性麦芽糖酶。皮质醇与发育的影响。

Biochem J. 1974 Nov;144(2):281-92. doi: 10.1042/bj1440281.

The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases.定量细胞化学分析在代谢疾病快速产前检测和体细胞遗传学研究中的应用。

Histochem J. 1974 Sep;6(5):491-509. doi: 10.1007/BF01003266.

Inhibition of gluconeogenesis by hypoglycin in the rat. Evidence for inhibition of glucose-6-phosphatase in vivo.低血糖素对大鼠糖异生的抑制作用。体内葡萄糖-6-磷酸酶受抑制的证据。

Biochem J. 1986 Dec 15;240(3):765-9. doi: 10.1042/bj2400765.

Incidence of glycogen storage disease in the German Federal Republic.德意志联邦共和国糖原贮积病的发病率。

Z Kinderheilkd. 1975 Aug 11;120(2):79-85. doi: 10.1007/BF00445157.

The effects of hypoglycin on glucose metabolism in the rat. A kinetic study in vivo and [U-14C,2-3H]glucose.降血糖素对大鼠葡萄糖代谢的影响。一项使用[U-14C,2-3H]葡萄糖的体内动力学研究。

Biochem J. 1978 Feb 15;170(2):337-42. doi: 10.1042/bj1700337.

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