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Journal of Inherited Metabolic Disease
|
January 1, 1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders
I Tein, D C De Vivo, D Ranucci, et al.
Archives of Neurology
|
March 1, 1973
Serum carnitine. An index of muscle destruction in man
S DiMauro, C Scott, A S Penn, et al.
Neurology
|
February 1, 1975
Hereditary carnitine deficiency of muscle
D H VanDyke, R C Griggs, W Markesbery, et al.
Neurology
|
May 1, 1994
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) gene
V V Ionasescu, M Hart, S DiMauro, et al.
Neurology
|
January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second case
M Zeviani, P Peterson, S Servidei, et al.
Muscle & Nerve
|
August 1, 1994
Ekbom's syndrome: lipomas, ataxia, and neuropathy with MERRF
P A Calabresi, G Silvestri, S DiMauro, et al.
Muscle & Nerve
|
October 1, 1985
Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency
C P Trevisan, H Reichmann, D C DeVivo, et al.
Biochemical and Biophysical Research Communications
|
April 28, 1989
Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome
C T Moraes, E A Schon, S DiMauro, et al.
The Journal of Clinical Investigation
|
November 1, 1987
Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VII
S Vora, S DiMauro, D Spear, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
February 1, 1989
Metabolic and functional adaptation of the diaphragm to training with resistive loads
S R Akabas, A R Bazzy, S DiMauro, et al.
Page
of 43
Search research articles
Search
Showing results (111-120 of 421) with videos related to
Sort By:
Page
of 43
Journal of Inherited Metabolic Disease
|
January 1, 1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders
I Tein, D C De Vivo, D Ranucci, et al.
Archives of Neurology
|
March 1, 1973
Serum carnitine. An index of muscle destruction in man
S DiMauro, C Scott, A S Penn, et al.
Neurology
|
February 1, 1975
Hereditary carnitine deficiency of muscle
D H VanDyke, R C Griggs, W Markesbery, et al.
Neurology
|
May 1, 1994
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) gene
V V Ionasescu, M Hart, S DiMauro, et al.
Neurology
|
January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second case
M Zeviani, P Peterson, S Servidei, et al.
Muscle & Nerve
|
August 1, 1994
Ekbom's syndrome: lipomas, ataxia, and neuropathy with MERRF
P A Calabresi, G Silvestri, S DiMauro, et al.
Muscle & Nerve
|
October 1, 1985
Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency
C P Trevisan, H Reichmann, D C DeVivo, et al.
Biochemical and Biophysical Research Communications
|
April 28, 1989
Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome
C T Moraes, E A Schon, S DiMauro, et al.
The Journal of Clinical Investigation
|
November 1, 1987
Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VII
S Vora, S DiMauro, D Spear, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
February 1, 1989
Metabolic and functional adaptation of the diaphragm to training with resistive loads
S R Akabas, A R Bazzy, S DiMauro, et al.
Page
of 43