Literature DB >> 479899

Haemophilic neuromyopathy.

C R Defaria, S E De Melo-Souza, E D Pinheiro.   

Abstract

Twenty haemophilic patients were examined neurologically and found to have varying degrees of muscle atrophy. The pathogenesis of the atrophy was investigated by electromyography, serum muscle enzyme levels, and muscle biopsies. In most cases the EMG showed such abnormalities as reduced numbers of functioning motor units and "myopathic" motor unit potentials. Serum enzyme levels were frequently raised, and type 2 fibre atrophy was found in the three patients who underwent muscle biopsy. These findings suggest the presence of neuromyopathic involvement in haemophilic patients.

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Year:  1979        PMID: 479899      PMCID: PMC490273          DOI: 10.1136/jnnp.42.7.600

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  4 in total

1.  NEUROPATHY IN HEMOPHILIA.

Authors:  A SILVERSTEIN
Journal:  JAMA       Date:  1964-11-09       Impact factor: 56.272

2.  Haemophilia syndromes. A survey of 267 patients.

Authors:  J F WILKINSON; F NOUR-ELDIN; M C ISRAELS; K E BARRETT
Journal:  Lancet       Date:  1961-10-28       Impact factor: 79.321

3.  Haemophilia. A study of its laboratory, clinical, genetic and social aspects based on known haemophiliacs in Finland.

Authors:  E IKKALA
Journal:  Scalpel (Brux)       Date:  1960

4.  Electrophysiological estimation of the number of motor units within a human muscle.

Authors:  A J McComas; P R Fawcett; M J Campbell; R E Sica
Journal:  J Neurol Neurosurg Psychiatry       Date:  1971-04       Impact factor: 10.154

  4 in total

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