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Neuromuscular Disorders : NMD
|
May 1, 1996
Clinical heterogeneity of seronegative myasthenia gravis
A Evoli, A P Batocchi, M Lo Monaco, et al.
The Journal of Clinical Investigation
|
July 1, 1989
Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency
R G Haller, S F Lewis, R W Estabrook, et al.
Acta Neuropathologica
|
January 1, 1996
Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy
R Massa, R Lodi, B Barbiroli, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement
A Uncini, G Galluzzi, A Di Muzio, et al.
Urolithiasis
|
November 9, 2018
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation
M Bargagli, G Primiano, A Primiano, et al.
American Journal of Medical Genetics
|
December 1, 1988
Late onset scleroatonic familial myopathy (Ullrich disease): a study of two sibs
E Ricci, E Bertini, R Boldrini, et al.
Brain & Development
|
January 1, 1990
Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology study
E Bertini, E Ricci, R Boldrini, et al.
Neurology
|
October 1, 1991
Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome
E Ciafaloni, E Ricci, S Servidei, et al.
Neurology
|
August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Neurology
|
September 1, 1987
McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote
B Schmidt, S Servidei, A A Gabbai, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 146) with videos related to
Sort By:
Page
of 15
Neuromuscular Disorders : NMD
|
May 1, 1996
Clinical heterogeneity of seronegative myasthenia gravis
A Evoli, A P Batocchi, M Lo Monaco, et al.
The Journal of Clinical Investigation
|
July 1, 1989
Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency
R G Haller, S F Lewis, R W Estabrook, et al.
Acta Neuropathologica
|
January 1, 1996
Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy
R Massa, R Lodi, B Barbiroli, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement
A Uncini, G Galluzzi, A Di Muzio, et al.
Urolithiasis
|
November 9, 2018
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation
M Bargagli, G Primiano, A Primiano, et al.
American Journal of Medical Genetics
|
December 1, 1988
Late onset scleroatonic familial myopathy (Ullrich disease): a study of two sibs
E Ricci, E Bertini, R Boldrini, et al.
Brain & Development
|
January 1, 1990
Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology study
E Bertini, E Ricci, R Boldrini, et al.
Neurology
|
October 1, 1991
Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome
E Ciafaloni, E Ricci, S Servidei, et al.
Neurology
|
August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Neurology
|
September 1, 1987
McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote
B Schmidt, S Servidei, A A Gabbai, et al.
Page
of 15