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Lancet (London, England)
|
September 2, 1978
Myoglobinaemia in Duchenne muscular dystrophy patients and carriers: A new adjunct to carrier detection
B T Adornato, L J Kagen, W K Engel
Science (New York, N.Y.)
|
September 1, 1972
Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients
R I Roelofs, W K Engel, P B Chauvin
Science (New York, N.Y.)
|
June 11, 1971
Duchenne muscular dystrophy: functional ischemia reproduces its characteristic lesions
J R Mendell, W K Engel, E C Derrer
Neurology
|
March 1, 1977
Localization of technetium-99m diphosphonate in acutely injured muscle. Relationship to muscle calcium deposition
B A Siegel, W K Engel, E C Derrer
Annals of the New York Academy of Sciences
|
January 1, 1981
Splenic and total-body irradiation treatment of myasthenia gravis
W K Engel, A S Lichter, M C Dalakas
Neurology
|
December 1, 1976
Erythrocyte shape in Duchenne muscular dystrophy
D W Matheson, W K Engel, E C Derrer
Annals of Internal Medicine
|
April 1, 1975
Neuromuscular disease in secondary hyperparathyroidism
L E Mallette, B M Patten, W K Engel
Journal of Neurocytology
|
May 1, 1992
The influence of muscle contractile activity versus neural factors on morphologic properties of innervated cultured human muscle
Y C Park-Matsumoto, V Askanas, W K Engel
Folia Morphologica
|
March 13, 2008
Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy
S Wójcik, A Nogalska, W K Engel, et al.
The Journal of Biological Chemistry
|
August 5, 1992
The multiple ADP/ATP translocase genes are differentially expressed during human muscle development
J Lunardi, O Hurko, W K Engel, et al.
Page
of 19
Search research articles
Search
Showing results (71-80 of 189) with videos related to
Sort By:
Page
of 19
Lancet (London, England)
|
September 2, 1978
Myoglobinaemia in Duchenne muscular dystrophy patients and carriers: A new adjunct to carrier detection
B T Adornato, L J Kagen, W K Engel
Science (New York, N.Y.)
|
September 1, 1972
Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients
R I Roelofs, W K Engel, P B Chauvin
Science (New York, N.Y.)
|
June 11, 1971
Duchenne muscular dystrophy: functional ischemia reproduces its characteristic lesions
J R Mendell, W K Engel, E C Derrer
Neurology
|
March 1, 1977
Localization of technetium-99m diphosphonate in acutely injured muscle. Relationship to muscle calcium deposition
B A Siegel, W K Engel, E C Derrer
Annals of the New York Academy of Sciences
|
January 1, 1981
Splenic and total-body irradiation treatment of myasthenia gravis
W K Engel, A S Lichter, M C Dalakas
Neurology
|
December 1, 1976
Erythrocyte shape in Duchenne muscular dystrophy
D W Matheson, W K Engel, E C Derrer
Annals of Internal Medicine
|
April 1, 1975
Neuromuscular disease in secondary hyperparathyroidism
L E Mallette, B M Patten, W K Engel
Journal of Neurocytology
|
May 1, 1992
The influence of muscle contractile activity versus neural factors on morphologic properties of innervated cultured human muscle
Y C Park-Matsumoto, V Askanas, W K Engel
Folia Morphologica
|
March 13, 2008
Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy
S Wójcik, A Nogalska, W K Engel, et al.
The Journal of Biological Chemistry
|
August 5, 1992
The multiple ADP/ATP translocase genes are differentially expressed during human muscle development
J Lunardi, O Hurko, W K Engel, et al.
Page
of 19