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J Bethlem

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Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1971
Diagnostic value of electrophoretical isoenzyme determination of L-lactate dehydrogenase in affected quadriceps muscle of patients with neuromuscular diseasesA E Meijer, J Bethlem, G K Van Wijngaarden
Journal of the Neurological Sciences|March 1, 1973
The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndromeJ Bethlem, G K van Wijngaarden, J de Jong
Archives of Neurology|July 1, 1970
Centronuclear myopathy with type I fiber atrophy and "myotubes"J Bethlem, G K van Wijngaarden, M Mumenthaler, et al.
Archives of Neurology|February 1, 1978
Investigations on the inheritance of nemaline myopathyW F Arts, J Bethlem, K P Dingemans, et al.
Journal of the Neurological Sciences|November 1, 1971
Observations on central core diseaseJ Bethlem, G K van Wijngaarden, A E Meijer, et al.
Journal of the Neurological Sciences|November 1, 1974
Fibre hybrids in type groups. An investigation of human muscle biopsiesF G Jennekens, A E Meijer, J Bethlem, et al.
Neurology|November 1, 1976
Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathiesC Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology|October 7, 1977
Familial focal loss of cross striationsG K van Wijngaarden, J Bethlem, K P Dingemans, et al.
Archives of Neurology|October 1, 1979
X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue culturesV Askanas, W K Engel, N B Reddy, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1971
Diagnostic value of electrophoretical isoenzyme determination of L-lactate dehydrogenase in affected quadriceps muscle of patients with neuromuscular diseasesA E Meijer, J Bethlem, G K Van Wijngaarden
Journal of the Neurological Sciences|March 1, 1973
The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndromeJ Bethlem, G K van Wijngaarden, J de Jong
Archives of Neurology|July 1, 1970
Centronuclear myopathy with type I fiber atrophy and "myotubes"J Bethlem, G K van Wijngaarden, M Mumenthaler, et al.
Archives of Neurology|February 1, 1978
Investigations on the inheritance of nemaline myopathyW F Arts, J Bethlem, K P Dingemans, et al.
Journal of the Neurological Sciences|November 1, 1971
Observations on central core diseaseJ Bethlem, G K van Wijngaarden, A E Meijer, et al.
Journal of the Neurological Sciences|November 1, 1974
Fibre hybrids in type groups. An investigation of human muscle biopsiesF G Jennekens, A E Meijer, J Bethlem, et al.
Neurology|November 1, 1976
Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathiesC Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology|October 7, 1977
Familial focal loss of cross striationsG K van Wijngaarden, J Bethlem, K P Dingemans, et al.
Archives of Neurology|October 1, 1979
X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue culturesV Askanas, W K Engel, N B Reddy, et al.
Pageof 2