Identifizierung heterozygoter Genträgerinnen der rasch progredienten recessiv X-chromosomalen Muskeldystrophie (Typ Duchenne)
- 1 January 1973
- journal article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 115 (4) , 333-342
- https://doi.org/10.1007/bf00438745
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- PREGNANCY AND SERUM-C.P.K. LEVELS IN POTENTIAL CARRIERS OF " SEVERE " X-LINKED MUSCULAR DYSTROPHYThe Lancet, 1971
- Die Erfassung von Konduktorinnen der progressiven Muskeldystrophie Typ Duchenne mittels Diskriminanzanalyse verschiedener SerumenzymaktivitätenKlinische Wochenschrift, 1969
- Studies of healthy relatives of patients with Duchenne muscular dystrophyJournal of the Neurological Sciences, 1968
- Studies of the carrier state in the Duchenne type of muscular dystrophy. I. Effect of exercise on serum creatine kinase activity.Journal of Neurology, Neurosurgery & Psychiatry, 1967
- Creatine Phosphokinase in Neuromuscular DiseaseArchives of Neurology, 1967
- THE VALUE OF SERUM ENZYME DETERMINATIONS IN THE IDENTIFICATION OF DYSTROPHIC CARRIERSAnnals of the New York Academy of Sciences, 1966
- A histochemical study of developing human skeletal muscleNeurology, 1966
- Myopathic changes in a muscular dystrophy carrierJournal of Neurology, Neurosurgery & Psychiatry, 1963
- CLINICAL MANIFESTATIONS IN TWO CARRIERS OF DUCHENNE MUSCULAR DYSTROPHYThe Lancet, 1963
- Progressive Muscular DystrophyEnzymologia Biologica Et Clinica, 1961