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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 diseases
A 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 syndrome
J 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 myopathy
W F Arts, J Bethlem, K P Dingemans, et al.
Journal of the Neurological Sciences
|
November 1, 1971
Observations on central core disease
J 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 biopsies
F 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 myopathies
C Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology
|
October 7, 1977
Familial focal loss of cross striations
G 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 cultures
V Askanas, W K Engel, N B Reddy, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 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 diseases
A 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 syndrome
J 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 myopathy
W F Arts, J Bethlem, K P Dingemans, et al.
Journal of the Neurological Sciences
|
November 1, 1971
Observations on central core disease
J 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 biopsies
F 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 myopathies
C Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology
|
October 7, 1977
Familial focal loss of cross striations
G 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 cultures
V Askanas, W K Engel, N B Reddy, et al.
Page
of 2