Fortuitous detection of a sporadic carrier of Duchenne's muscular dystrophy.
作者信息
Hanson J W, Zellweger H, Afifi A K, McCormick W F
出版信息
Humangenetik. 1968;6(1):34-9. doi: 10.1007/BF00287152.
PMID:5699892
Abstract
摘要
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Fortuitous detection of a sporadic carrier of Duchenne's muscular dystrophy.偶然发现一名杜氏肌营养不良症的散发携带者。
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[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.
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CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.携带三种肌肉萎缩症基因的女性的肌酸激酶水平。
Br Med J. 1965 Mar 20;1(5437):750-3. doi: 10.1136/bmj.1.5437.750.
3
CYSTEINE-STIMULATED SERUM CREATINE KINASE IN HEALTH AND DISEASE.健康与疾病状态下的半胱氨酸刺激血清肌酸激酶
J Lab Clin Med. 1964 Aug;64:299-305.
4
SERUM ENZYME STUDIES IN MUSCLE DISEASE. I. VARIATIONS IN SERUM CREATINE KINASE ACTIVITY IN NORMAL INDIVIDUALS.肌肉疾病中的血清酶研究。I. 正常个体血清肌酸激酶活性的变化。
J Neurol Neurosurg Psychiatry. 1964 Feb;27(1):1-4. doi: 10.1136/jnnp.27.1.1.
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Benign congenital muscular dystrophy: a special form of congenital hypotonia.良性先天性肌营养不良：先天性肌张力低下的一种特殊形式。
Clin Pediatr (Phila). 1967 Nov;6(11):655-63. doi: 10.1177/000992286700601113.
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Creatine phosphokinase in neuromuscular disease. Patients and families.神经肌肉疾病中的肌酸磷酸激酶。患者及家属。
Arch Neurol. 1967 May;16(5):529-35. doi: 10.1001/archneur.1967.00470230081011.
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The Duchenne type muscular dystrophy: histopathological studies of the carrier state.杜兴型肌营养不良症：携带者状态的组织病理学研究。
Brain. 1966 Mar;89(1):109-20. doi: 10.1093/brain/89.1.109.
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Statistical characteristics and normal values of four serum enzymes, glutamic oxalacetic transaminase, glutamic pyruvic transaminase, aldolase, and creatine phosphokinase.
Enzymol Biol Clin (Basel). 1966;6(1):10-24. doi: 10.1159/000457839.
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The muscular dystrophies in Iowa.爱荷华州的肌营养不良症
J Iowa Med Soc. 1968 Mar;58(3):251-60.
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Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.肢带型肌营养不良症：临床表现及临床前期疾病的检测
Pediatrics. 1968 Feb;41(2):495-502.
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