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McArdle's disease: successful symptomatic therapy by high dose oral administration of ribose.

作者信息

Wagner D R, Zöllner N

机构信息

Medizinische Poliklinik, Universität München.

出版信息

Klin Wochenschr. 1991 Jan 22;69(2):92. doi: 10.1007/BF01666823.

DOI:10.1007/BF01666823
PMID:1902882
Abstract
摘要

相似文献

1
McArdle's disease: successful symptomatic therapy by high dose oral administration of ribose.麦卡德尔病:通过高剂量口服核糖进行成功的对症治疗。
Klin Wochenschr. 1991 Jan 22;69(2):92. doi: 10.1007/BF01666823.
2
Lactate production in McArdle's disease.麦克尔憩室病中的乳酸生成
Postgrad Med J. 1977 Mar;53(617):161-4. doi: 10.1136/pgmj.53.617.161.
3
Increased ammonia production during forearm ischemic work test in McArdle's disease.
Klin Wochenschr. 1981 Dec 1;59(23):1319-20. doi: 10.1007/BF01711182.
4
Metabolism of branched-chain amino acids and ammonia during exercise: clues from McArdle's disease.运动期间支链氨基酸和氨的代谢:来自麦克尔憩室病的线索。
Int J Sports Med. 1990 May;11 Suppl 2:S101-13. doi: 10.1055/s-2007-1024861.
5
Changes in arterial K+ and ventilation during exercise in normal subjects and subjects with McArdle's syndrome.正常受试者和患有麦卡德尔综合征的受试者在运动过程中动脉血钾和通气的变化。
J Physiol. 1990 Oct;429:339-48. doi: 10.1113/jphysiol.1990.sp018260.
6
Pharmacological and nutritional treatment for McArdle's disease (Glycogen Storage Disease type V).麦克尔憩室病(糖原贮积病Ⅴ型)的药物和营养治疗
Cochrane Database Syst Rev. 2004(3):CD003458. doi: 10.1002/14651858.CD003458.pub2.
7
Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.麦克尔憩室病或线粒体肌病患者的运动不耐受
Eur J Med. 1992 Dec;1(8):457-63.
8
A double blind, placebo controlled, crossover trial of D-ribose in McArdle's disease.
J Neurol Sci. 1996 Mar;136(1-2):174-7. doi: 10.1016/0022-510x(95)00320-2.
9
Exercise and recovery ventilatory and VO2 responses of patients with McArdle's disease.麦克尔迪氏病患者运动及恢复过程中的通气和摄氧量反应
J Appl Physiol (1985). 1990 Apr;68(4):1393-8. doi: 10.1152/jappl.1990.68.4.1393.
10
Mcardle's disease. A case report.麦卡德尔病。病例报告。
Turk J Pediatr. 1996 Jul-Sep;38(3):355-9.

引用本文的文献

1
Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V).麦克尔病(糖原贮积病Ⅴ型)的药物和营养治疗
Cochrane Database Syst Rev. 2014 Nov 12;2014(11):CD003458. doi: 10.1002/14651858.CD003458.pub5.
2
Effects of therapeutic ribose levels on human lymphocyte proliferation in vitro.治疗性核糖水平对人淋巴细胞体外增殖的影响。
Clin Investig. 1993 Oct;71(10):770-3. doi: 10.1007/BF00190316.
3
The oxidative pentose phosphate pathway in the heart: regulation, physiological significance, and clinical implications.

本文引用的文献

1
[Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].[肌肉活检在代谢性肌病中的诊断意义。II. 临床生物化学]
Klin Wochenschr. 1984 Jul 16;62(14):651-8. doi: 10.1007/BF01716461.
2
Hypoxanthine and Mcardle disease: a clue to metabolic stress in the working forearm.次黄嘌呤与麦卡德尔病:工作中前臂代谢应激的线索
Muscle Nerve. 1983 Mar-Apr;6(3):204-6. doi: 10.1002/mus.880060307.
3
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiency.伴有肌腺苷酸脱氨酶缺乏的麦克尔氏病:一种复合酶缺乏症的观察
心脏中的氧化戊糖磷酸途径:调节、生理意义及临床意义
Basic Res Cardiol. 1992 Jul-Aug;87(4):303-16. doi: 10.1007/BF00796517.
Neurology. 1987 Jun;37(6):1039-42. doi: 10.1212/wnl.37.6.1039.
4
Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine.肌腺苷酸脱氨酶缺乏症和麦卡德尔病的缺血运动试验:血浆腺苷、肌苷和次黄嘌呤的测定
Clin Sci (Lond). 1986 Apr;70(4):399-401. doi: 10.1042/cs0700399.
5
Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose.肌腺苷酸脱氨酶缺乏症:高剂量口服核糖成功进行症状性治疗。
Klin Wochenschr. 1986 Dec 15;64(24):1281-90. doi: 10.1007/BF01785710.