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

Overview

Journal Klin Wochenschr

Specialty General Medicine

Date 1965 Feb 1

PMID 14258512

Citations 5

Authors

H W ROTTHAUWE

S Kowalewski

Affiliations

Soon will be listed here.

Citing Articles

[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].

HEYCK H, LAUDAHN G, CARSTEN P Klin Wochenschr. 1966; 44(12):695-700.

PMID: 5990806 DOI: 10.1007/BF01790793.

[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.

[Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].

Radu H, Stenzel K Dtsch Z Nervenheilkd. 1969; 196(2):92-115.

PMID: 5800957

[Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].

BARTHELMAI W, Dikbas G, Wullner S Humangenetik. 1969; 8(2):115-33.

PMID: 5365581 DOI: 10.1007/BF00295835.

[New data on the genetics and classification of muscular dystrophies].

BECKER P Humangenetik. 1972; 17(1):1-22.

PMID: 4567289

References

Chung C, Morton N . Discrimination of genetic entities in muscular dystrophy. Am J Hum Genet. 1959; 11:339-59. PMC: 1932040. View

Aebi U, Richterich R, STILLHART H, COLOMBO J, Rossi E . [Progressive muscular dystrophy. III. Serum enzymes in muscular dystrophy in childhood]. Helv Paediatr Acta. 1961; 16:543-64. 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

Dubowitz V . Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. Brain. 1960; 83:432-9. DOI: 10.1093/brain/83.3.432. View

Walton J, Nattrass F . On the classification, natural history and treatment of the myopathies. Brain. 1954; 77(2):169-231. DOI: 10.1093/brain/77.2.169. View

BECKER P, KIENER F . [A new x-chromosomal muscular dystrophy]. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1955; 193(4):427-48. DOI: 10.1007/BF00343141. View

Morton N, Chung C . Formal genetics of muscular dystrophy. Am J Hum Genet. 1959; 11:360-79. PMC: 1932041. View

BECKER P, Lenz F . [Estimation of mutation rate in muscular dystrophy]. Z Mensch Vererb Konstitutionsl. 1955; 33(1):42-56. View

Clayton B, Wilson K, Carter C . Aldolase activity in the plasma or serum of normal children and families with muscular dystrophy. Arch Dis Child. 1963; 38:208-14. PMC: 2019036. DOI: 10.1136/adc.38.199.208. View

10.

Walton J, RACE R, PHILIP U . On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies. Ann Hum Genet. 1955; 20(1):1-38. DOI: 10.1111/j.1469-1809.1955.tb01274.x. View

11.

ROTTHAUWE H, ZURUKZOGLU-SKLAVOUNOU S, HAMMANN H . [Research on the methodology of activity determination of creatine phosphokinase]. Klin Wochenschr. 1961; 39:1269-75. DOI: 10.1007/BF01481966. View

12.

BECKER P . Two families of benign sex-linked recessive muscular dystrophy. Rev Can Biol. 1962; 21:551-66. View