Progress in medical genetics. Volume 5 / edited by Arthur G. Steinberg and Alexander G. Bearn.
- Date:
- 1967
Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
Credit: Progress in medical genetics. Volume 5 / edited by Arthur G. Steinberg and Alexander G. Bearn. Source: Wellcome Collection.
155/168 page 143
![MI.SCrLAR DYSTROPHY 143 Senim creatine Phosphokinase and aldolase acñvity in neuromuscular disorders. 84th Ann. Meet Amer. Neurol. Assoc. Adantic Cin-. ——i —, —T. Walanabe. F. EbasJii, and S. EbashL 1964. C\-steine-stimulated serum creatine kmase in health and disease. J. Lab. Clin. Med. 64: 29^305. Pearce. G. W_ J. >L S. Pearce, and J. X. Walton. 1966. The Duchenne t>pe muscular dys¬ trophy: histopathological studies trf the carrier state. Biain 89: 109-120 Pearce. J. M. S.. R. J. Pennington, and J. N. Walton. 1964a. Serum enzyme studies in muscle disease 1П. Serum creatine kinase activity in relatives of patients with the Duchenne type of muscular dystrophy. J. Neurol. Neurosurg. Psychiat. 27: 181-185. —, and —. 1964b. Serum епг>тпе studies in muscle disease П. Serum creatine kinase activity in muscular dystrophy and in other myopathic and neuropathic disorders. ]. NeuroL Neurosurg. Psychiat. 27; 96-99. Pearson. C. NÍ. 1957. Serum enzymes in muscular dystrophy дпН certain other muscidar and neuromusciáar disease. New Eng. J. Med. 256: 1069-1075. —, S. R. Chowdhury, W. M. Fowler, M. H. Jones, and W. H. Griffith. 1961. Studies ot enzymes in serum in muscular dystrophy П. Diagnostic and prognostic signifacance in relatives ot dystrophic persons. Pediatrics 2S: 962-970. -—-, and W. M. Fowler. 1963. Hereditary non-progressive muscular dystrophy inducing arthrogry-posis syndrome. Brain 86: 75-88. —i —> and S. W. Wright. 1963. X-chromosome mosaicism in females with muscular dystrophy. Proc. Nat. Acad. Sci. 50: 24—31. —^ and A. S. Rose. i960. Myositb. The inflammatory disorders cf muscle. Res. Pubi. Ass. Xerv. Ment. Dis. 38: 422-47S. Penrose. L. S. 1947. The problem of anticipation in pedigrees of Dystrophia myotonica. .Ann. Eugen. 14: 125-132. —. 1961. Mutation. In: Recent .Advances in Human Genetics. L. S. Penrose, Ed. London: Churchill, pp. 1—18. Peterman, A. F., G. Lillington. and R. W. Jamplis. 1964. Progressive muscular dystrophy with ptosb and dysphagia. Arch. Neurol. 10: 38-41. Phihp. U.. J. N. Walton, and C. .\. B. Smith. 1956. Colour blindness and the Duchenne-type muscular dvstrophy. .\nn. Hum. Genet. 21: 155-158. Pruzanski, W. 1965. Consenitil malformations in myotonic dystrophy. .Acta Neurol. Scand. 41: 34-3^- Relkin, R. 1965. Arthrogryposis multiplex congenita. Report of two cases, review of literature. Amer. J. Med. 39: 87i-?76. Richter, R. В.. and E. M. Humphreys. 1955. Unusual myopathy: presentation of two cases with muscle biopsies. .Arch. Neurol. Psychiat. 73: 574-575. Richterich. R.. S. Rosin. U. .Aebi. and E. RossL 1963. Progressive muscular dv^strophy V. The identification of the carrier slate in the Duchenne type by serum creatine kinase determina¬ tion. -Amer. J. Hum. Genet. 15: 133-154. Rocthauwe, H. W„ and S. KowalewskL 1965. Klinische und biochemische Untersuchungen bei Myopathein II. Die Bedeutung der Serum-Kreatin-Phosphokinasc und der Serum- Aldolase für die Idendifizierung von Heterozygoten der recesar X-chromosomalen For¬ men der progressiven Muskeldystrophie (Typ Ша und b). Klin. Wschr. 43: 150-158. Schodand, D. I_ and L. P. Rowland. 1964. Muscular dystrophy. Features of ocular myopathy, distai myopathy and myotonic dystrophy. .Arch. Neurol. 10: 433-445.](https://iiif.wellcomecollection.org/image/b18033702_0156.JP2/full/800%2C/0/default.jpg)


