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The New England Journal of Medicine
|
November 23, 1972
Renal failure in McArdle's disease
W J Bank, S DiMauro, L P Rowland
Transactions of the American Neurological Association
|
January 1, 1977
McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
S DiMauro, S Arnold, A Miranda, et al.
Archives of Neurology
|
August 1, 1972
Myosin from normal and dystrophic human muscle. Immunochemical and electrophoretic studies
A S Penn, R A Cloak, L P Rowland
Annals of Neurology
|
January 1, 1978
McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme
S DiMauro, S Arnold, A Miranda, et al.
Neurology
|
February 1, 1970
Muscular dystrophy in young girls
A S Penn, R P Lisak, L P Rowland
Muscle & Nerve
|
January 1, 1978
Infiltrating lipoma: a cause of monomelic hypertrophy
M R Fetell, P E Duffy, L P Rowland
Archives of Neurology
|
April 1, 1972
Drugs, coma, and myoglobinuria
A S Penn, L P Rowland, D W Fraser
Muscle & Nerve. Supplement
|
January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overview
S DiMauro, S Tsujino, S Shanske, et al.
Archives of Neurology
|
July 1, 1974
Reversible forms of motor neuron disease. Lead "neuritis"
J A Boothby, P V DeJesus, L P Rowland
Archives of Biochemistry and Biophysics
|
May 1, 1971
Binding of enzymes of glycogen metabolism to glycogen in skeletal muscle
S DiMauro, W Trojaborg, P Gambetti, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 189) with videos related to
Sort By:
Page
of 19
The New England Journal of Medicine
|
November 23, 1972
Renal failure in McArdle's disease
W J Bank, S DiMauro, L P Rowland
Transactions of the American Neurological Association
|
January 1, 1977
McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
S DiMauro, S Arnold, A Miranda, et al.
Archives of Neurology
|
August 1, 1972
Myosin from normal and dystrophic human muscle. Immunochemical and electrophoretic studies
A S Penn, R A Cloak, L P Rowland
Annals of Neurology
|
January 1, 1978
McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme
S DiMauro, S Arnold, A Miranda, et al.
Neurology
|
February 1, 1970
Muscular dystrophy in young girls
A S Penn, R P Lisak, L P Rowland
Muscle & Nerve
|
January 1, 1978
Infiltrating lipoma: a cause of monomelic hypertrophy
M R Fetell, P E Duffy, L P Rowland
Archives of Neurology
|
April 1, 1972
Drugs, coma, and myoglobinuria
A S Penn, L P Rowland, D W Fraser
Muscle & Nerve. Supplement
|
January 1, 1995
Biochemistry and molecular genetics of human glycogenoses: an overview
S DiMauro, S Tsujino, S Shanske, et al.
Archives of Neurology
|
July 1, 1974
Reversible forms of motor neuron disease. Lead "neuritis"
J A Boothby, P V DeJesus, L P Rowland
Archives of Biochemistry and Biophysics
|
May 1, 1971
Binding of enzymes of glycogen metabolism to glycogen in skeletal muscle
S DiMauro, W Trojaborg, P Gambetti, et al.
Page
of 19