Aldolase Activity in the Plasma or Serum of Normal Children and Families with Muscular Dystrophy

Overview

Journal Arch Dis Child

Specialty Pediatrics

Date 1963 Jun 1

PMID 14021638

Citations 7

Authors

B E Clayton

K M Wilson

C O Carter

Affiliations

Soon will be listed here.

Citing Articles

[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE].

ROTTHAUWE H, Kowalewski S Klin Wochenschr. 1965; 43:158-63.

PMID: 14258512 DOI: 10.1007/BF01484508.

CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.

Wilson K, Evans K, Carter C Br Med J. 1965; 1(5437):750-3.

PMID: 14248444 PMC: 2166169. DOI: 10.1136/bmj.1.5437.750.

[A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].

ROTTHAUWE H, Kowalewski S Humangenetik. 1966; 3(1):30-40.

PMID: 5986053 DOI: 10.1007/BF00273016.

Alpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophy.

Johnston H, Wilkinson J, WITHYCOMBE W, Raymond S J Clin Pathol. 1966; 19(3):250-6.

PMID: 5937610 PMC: 473248. DOI: 10.1136/jcp.19.3.250.

[Progressive muscular dystrophy. VII. Detection of heterozygotes of Duehenne muscular dystrophy by determining serum creatine kinase with localized work load in anoxia].

Wiesmann U, Moser H, Richterich R, Rossi E Klin Wochenschr. 1965; 43(19):1015-22.

PMID: 5881526 DOI: 10.1007/BF01746589.

References

LEYBURN P, Thomson W, Walton J . An investigation of the carrier state in the Duchenne type muscular dystrophy. Ann Hum Genet. 1961; 25:41-9. DOI: 10.1111/j.1469-1809.1961.tb01495.x. View

SCHAPIRA G, DREYFUS J, SCHAPIRA F, KRUH J . Glycogenolytic enzymes in human progressive muscular dystrophy. Am J Phys Med. 1955; 34(1):313-9. View

BECKER P . [Genetics of myopathy]. Dtsch Z Nervenheilkd. 1955; 173(5-6):482-98. View

SIBLEY J, FLEISHER G . The clinical significance of serum aldolase. Proc Staff Meet Mayo Clin. 1954; 29(23):591-603. View

Blyth H, Pugh R . Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance. Ann Hum Genet. 1959; 23(2):127-63. DOI: 10.1111/j.1469-1809.1958.tb01457.x. View