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[Enzyme activity determination in progressive muscular dystrophy. IV. Serum enzymatic kinetics in the preclinical stage of the Duchenne type during the 1st 2 years of life].

作者信息

Heyck H, Laudahn G, Carsten P M

出版信息

Klin Wochenschr. 1966 Jun 15;44(12):695-700. doi: 10.1007/BF01790793.

DOI:10.1007/BF01790793
PMID:5990806
Abstract
摘要

相似文献

1
[Enzyme activity determination in progressive muscular dystrophy. IV. Serum enzymatic kinetics in the preclinical stage of the Duchenne type during the 1st 2 years of life].[进行性肌营养不良症的酶活性测定。IV. 杜兴型在生命最初2年临床前期的血清酶动力学]
Klin Wochenschr. 1966 Jun 15;44(12):695-700. doi: 10.1007/BF01790793.
2
[Progressive muscle dystrophy. II. Enzyme activity chages in serum in progressive muscle dystrophy].[进行性肌营养不良。II. 进行性肌营养不良患者血清中的酶活性变化]
Wien Klin Wochenschr. 1971 Feb 19;83(7):109-13.
3
[Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].[关于假性肥大性肌营养不良症的研究贡献。I. 良性假性肥大性肌营养不良症]
Dtsch Z Nervenheilkd. 1969;196(2):92-115.
4
Biochemical aspects of genetically determined progressive muscular dystrophies.遗传性进行性肌营养不良的生化方面
Rev Roum Neurol. 1973;10(6):531-7.
5
[Changes in the enzyme activity of muscle tissue in progressive muscular dystrophy].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1970;70(1):72-6.
6
[Serum enzymatic activity in neuromuscular diseases].[神经肌肉疾病中的血清酶活性]
Neurol Neurochir Pol. 1975 Jan-Feb;9(1):1-5.
7
[Significance of enzyme variations in polytraumatic patients].[多发伤患者酶变异的意义]
Langenbecks Arch Chir. 1968;322:1111-3. doi: 10.1007/BF02454008.
8
DIAGNOSTIC AND PROGNOSTIC SIGNIFICANCE OF SERUM ENZYMES. I. MUSCULAR DYSTROPHY.血清酶的诊断和预后意义。I. 肌肉萎缩症
Arch Phys Med Rehabil. 1964 Mar;45:117-24.
9
[On the binding of muscle aldolase to coarsely dispersed particles in homogenates of stimulated muscle].[关于肌肉醛缩酶与受刺激肌肉匀浆中粗分散颗粒的结合]
Hoppe Seylers Z Physiol Chem. 1967 Jul;348(7):864-70.
10
Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities.隐匿性肌营养不良的诊断：血清氨基转移酶活性升高这一“偶然”发现的重要性。
J Pediatr. 1993 Feb;122(2):254-6. doi: 10.1016/s0022-3476(06)80126-5.

引用本文的文献

1
Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy.揭示杜氏肌营养不良症的胚胎起源。
WIREs Mech Dis. 2024 Nov-Dec;16(6):e1653. doi: 10.1002/wsbm.1653. Epub 2024 Oct 23.
2
Initial pulmonary respiration causes massive diaphragm damage and hyper-CKemia in Duchenne muscular dystrophy dog.初次肺呼吸会导致杜氏肌营养不良症犬的膈肌严重损伤和 CK 血症升高。
Sci Rep. 2013;3:2183. doi: 10.1038/srep02183.
3
Feasibility of neonatal screening for Duchenne muscular dystrophy.杜氏肌营养不良症新生儿筛查的可行性

本文引用的文献

1
Histopathological features of muscle in the preclinical stages of muscular dystrophy.肌肉营养不良临床前期阶段肌肉的组织病理学特征。
Brain. 1962 Mar;85:109-20. doi: 10.1093/brain/85.1.109.
2
Studies of enzymes in serum in muscular dystrophy. II. Diagnostic and prognostic significance in relatives of dystrophic persons.肌营养不良症患者血清中酶的研究。II. 对肌营养不良症患者亲属的诊断及预后意义。
Pediatrics. 1961 Dec;28:962-70.
3
Activity of glutamic-oxalacetic transminase and lactic dehydrogenase in cerebrospinal fluid and plasma of normal and abnormal newborn infants.
J Med Genet. 1982 Feb;19(1):1-3. doi: 10.1136/jmg.19.1.1.
4
[Contribution on progressive muscular dystrophy. V. Histological findings in the preclinical stage of Duchenne-type progressive muscular dystrophy].[关于进行性肌营养不良的研究。V. 杜兴型进行性肌营养不良临床前期的组织学发现]
Klin Wochenschr. 1966 Jul 15;44(14):813-8. doi: 10.1007/BF01711498.
5
[Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].[杜兴氏型进行性肌营养不良携带者血清中的肌酸磷酸激酶活性]
Humangenetik. 1969 Oct;8(2):115-33. doi: 10.1007/BF00295835.
6
[Limited anesthetic possibilities in patients with hereditary muscular diseases].[遗传性肌肉疾病患者麻醉选择有限]
Z Rechtsmed. 1973 Apr 30;72(2):128-39. doi: 10.1007/BF02077217.
7
Structural changes in the early stages of Duchenne muscular dystrophy.杜兴氏肌肉营养不良早期阶段的结构变化。
J Neurol Neurosurg Psychiatry. 1972 Aug;35(4):451-5. doi: 10.1136/jnnp.35.4.451.
8
Editorial: Screening of the newborn for Duchenne muscular dystrophy.社论：新生儿杜氏肌营养不良症筛查
Br Med J. 1975 May 24;2(5968):403-4. doi: 10.1136/bmj.2.5968.403.
9
Screening for Duchenne muscular dystrophy.杜氏肌营养不良症的筛查
Arch Dis Child. 1976 Apr;51(4):249-51. doi: 10.1136/adc.51.4.249.
正常和异常新生儿脑脊液及血浆中谷草转氨酶和乳酸脱氢酶的活性
Pediatrics. 1959 Sep;24:378-88.
4
A comparative study of fetal and maternal serum enzyme levels.
J Lab Clin Med. 1959 Sep;54:417-26.
5
[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE].[肌病的临床与生化研究。3. 具有相对良性病程的隐性X染色体连锁型肌营养不良症]
Klin Wochenschr. 1965 Feb 1;43:158-63. doi: 10.1007/BF01484508.
6
MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.肌肉萎缩症：知识领域的一些最新进展
Br Med J. 1964 May 16;1(5393):1271-4 CONTD. doi: 10.1136/bmj.1.5393.1271.
7
SOME DISEASES OF MUSCLE.肌肉的一些疾病。
Lancet. 1964 Feb 29;1(7331):447-52. doi: 10.1016/s0140-6736(64)90792-5.
8
MUSCULAR DYSTROPHY. REVIEW AND RECENT OBSERVATIONS.肌肉萎缩症。综述与近期观察
Am J Med. 1963 Nov;35:632-45. doi: 10.1016/0002-9343(63)90135-9.
9
SERUM ENZYME ACTIVITY IN LATE PREGNANCY, AT DELIVERY, AND DURING PUERPERIUM.
Scand J Clin Lab Invest. 1963;15:429-35. doi: 10.3109/00365516309079765.
10
Muscular dystrophy: current research in Newcastle upon Tyne.肌肉萎缩症：泰恩河畔纽卡斯尔的当前研究
Rev Can Biol. 1962 Sep-Dec;21:523-31.