Detection of carriers of benign X-linked muscular dystrophy.
作者信息
Emery A E, Clack E R, Simon S, Taylor J L
出版信息
Br Med J. 1967 Dec 2;4(5578):522-3. doi: 10.1136/bmj.4.5578.522.
Abstract
摘要
相似文献
1
Detection of carriers of benign X-linked muscular dystrophy.良性X连锁肌营养不良携带者的检测
Br Med J. 1967 Dec 2;4(5578):522-3. doi: 10.1136/bmj.4.5578.522.
2
The detection of female carriers of pseudohypertrophic muscular dystrophy.假肥大型肌营养不良女性携带者的检测
Proc Aust Assoc Neurol. 1968;5(3):545-51.
3
X-linked muscular dystrophy, benign form with contractures.
Birth Defects Orig Artic Ser. 1971 Feb;7(2):113-5.
4
Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.利用肌酸激酶检测严重X连锁型肌营养不良症携带者。
Br Med J. 1976 Sep 4;2(6035):577-9. doi: 10.1136/bmj.2.6035.577.
5
The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.良性（贝克型）X连锁肌营养不良症携带者的检测
J Med Genet. 1975 Jun;12(2):131-4. doi: 10.1136/jmg.12.2.131.
6
Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.良性（贝克型）X连锁肌营养不良症基因座与蓝色盲基因座之间的连锁关系。
J Med Genet. 1974 Dec;11(4):317-20. doi: 10.1136/jmg.11.4.317.
7
[An unusual form of benign hereditary recessive x-chromosomal muscular dystrophy].[一种罕见的良性遗传性隐性X染色体型肌营养不良症]
Monatsschr Kinderheilkd (1902). 1970 Jun;118(6):410.
8
Variability of serum creatine phosphokinase activity in normal women and carriers of the gene for Duchenne muscular dystrophy.正常女性及杜氏肌营养不良症基因携带者血清肌酸磷酸激酶活性的变异性
Neurology. 1973 Dec;23(12):1316-23. doi: 10.1212/wnl.23.12.1316.
9
The detection of carriers of X-linked muscular dystrophy genes. A review of some methods studied in Newcastle upon Tyne.X连锁型肌营养不良基因携带者的检测。对在泰恩河畔纽卡斯尔研究的一些方法的综述。
J Neurol Sci. 1971 Aug;13(4):459-74. doi: 10.1016/0022-510x(71)90008-6.
10
Pregnancy and serum C.P.K. levels in potential carriers of severe X-linked muscular dystrophy.严重X连锁肌营养不良症潜在携带者的妊娠情况及血清肌酸磷酸激酶水平
Lancet. 1971 Apr 24;1(7704):855-6. doi: 10.1016/s0140-6736(71)91520-0.
引用本文的文献
1
Hand fracture epidemiology and etiology in children-time trends in Malmö, Sweden, during six decades.儿童手部骨折的流行病学和病因学——瑞典马尔默六十年间的时间趋势。
J Orthop Surg Res. 2019 Jul 12;14(1):213. doi: 10.1186/s13018-019-1248-0.
2
The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.杜氏和贝克型肌营养不良症的临床与分子遗传学研究方法：最新方案
J Med Genet. 1997 Oct;34(10):805-12. doi: 10.1136/jmg.34.10.805.
3
[Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].
Humangenetik. 1971;11(4):328-35. doi: 10.1007/BF00278661.
4
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.贝克肌营养不良症（BMD）与克兰费尔特综合征：家系中BMD表现型变异的一种可能原因。
J Med Genet. 1989 Apr;26(4):251-4. doi: 10.1136/jmg.26.4.251.
5
The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.良性（贝克型）X连锁肌营养不良症携带者的检测
J Med Genet. 1975 Jun;12(2):131-4. doi: 10.1136/jmg.12.2.131.
本文引用的文献
1
ACTIVATION OF CREATINE PHOSPHOKINASE BY SULFHYDRYL COMPOUNDS IN NORMAL AND MUSCULAR DYSTROPHY SERA.
Proc Soc Exp Biol Med. 1965 Mar;118:662-4. doi: 10.3181/00379727-118-29933.
2
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
A method for the estimation of serum creatine kinase and its use in comparing creatine kinase and aldolase activity in normal and pathological sera.一种血清肌酸激酶的估算方法及其在比较正常和病理血清中肌酸激酶与醛缩酶活性方面的应用。
Clin Chim Acta. 1962 Sep;7:597-603. doi: 10.1016/0009-8981(62)90137-7.
4
Creatine and creatine kinase measurement.肌酸和肌酸激酶测量。
J Biol Chem. 1959 Dec;234:3201-4.
5
Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.儿童期肌营养不良；遗传学方面；利兹地区临床类型及其遗传的实地研究。
Ann Hum Genet. 1959 Apr;23(2):127-63. doi: 10.1111/j.1469-1809.1958.tb01457.x.
6
[Genetics of myopathy].[肌病的遗传学]
Dtsch Z Nervenheilkd. 1955;173(5-6):482-98.
7
[A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].[一种良性X染色体遗传性肌营养不良症。I. 症状携带者的检查]
Humangenetik. 1966;3(1):17-29. doi: 10.1007/BF00273015.
8
Unusual type of benign x-linked muscular dystrophy.罕见类型的良性X连锁肌营养不良症。
J Neurol Neurosurg Psychiatry. 1966 Aug;29(4):338-42. doi: 10.1136/jnnp.29.4.338.
9
Hereditary myopathies.遗传性肌病
Clin Orthop Relat Res. 1964 Mar-Apr;33:164-73.
10
X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression.X连锁隐性假肥大型肌营养不良，起病较晚且进展缓慢。
N Engl J Med. 1965 Nov 11;273(20):1062-70. doi: 10.1056/NEJM196511112732002.
Zotero 插件