Search research articles
Contact Us
Filters
Showing results (41-50 of 206) with videos related to
Page
of 21
Sort By:
Molecular and Cellular Biology
|
April 1, 1991
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria
A Chomyn, G Meola, N Bresolin, et al.
Neuromuscular Disorders : NMD
|
January 1, 1996
The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism
A Papadimitriou, G M Hadjigeorgiou, R Divari, et al.
Neuropsychologia
|
January 20, 2004
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins
F Fabbro, A Tavano, S Corti, et al.
American Journal of Human Genetics
|
June 1, 1994
Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers
A Chomyn, S T Lai, R Shakeley, et al.
Italian Journal of Neurological Sciences
|
February 1, 1989
Normal muscle mitochondrial function in Ramsay-Hunt syndrome
T Sacquegna, P Montagna, M Moggio, et al.
Cell Transplantation
|
October 19, 2000
Intramuscular migration of myoblasts transplanted after muscle pretreatment with metalloproteinases
Y Torrente, E El Fahime, N J Caron, et al.
FEBS Letters
|
October 7, 2006
High-resolution X-ray microtomography for three-dimensional visualization of human stem cell muscle homing
Y Torrente, M Gavina, M Belicchi, et al.
Minerva Pediatrica
|
March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]
M Bado, C Minetti, L Mallamaci, et al.
Neurology
|
June 1, 1985
Physiologic assessment of phosphoglycerate mutase deficiency: incremental exercise test
J T Kissel, W Beam, N Bresolin, et al.
Neurology Research International
|
August 9, 2011
Anti-MuSK-Positive Myasthenia Gravis in a Patient with Parkinsonism and Cognitive Impairment
S Lanfranconi, S Corti, P Baron, et al.
Page
of 21
Search research articles
Search
Showing results (41-50 of 206) with videos related to
Sort By:
Page
of 21
Molecular and Cellular Biology
|
April 1, 1991
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria
A Chomyn, G Meola, N Bresolin, et al.
Neuromuscular Disorders : NMD
|
January 1, 1996
The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism
A Papadimitriou, G M Hadjigeorgiou, R Divari, et al.
Neuropsychologia
|
January 20, 2004
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins
F Fabbro, A Tavano, S Corti, et al.
American Journal of Human Genetics
|
June 1, 1994
Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers
A Chomyn, S T Lai, R Shakeley, et al.
Italian Journal of Neurological Sciences
|
February 1, 1989
Normal muscle mitochondrial function in Ramsay-Hunt syndrome
T Sacquegna, P Montagna, M Moggio, et al.
Cell Transplantation
|
October 19, 2000
Intramuscular migration of myoblasts transplanted after muscle pretreatment with metalloproteinases
Y Torrente, E El Fahime, N J Caron, et al.
FEBS Letters
|
October 7, 2006
High-resolution X-ray microtomography for three-dimensional visualization of human stem cell muscle homing
Y Torrente, M Gavina, M Belicchi, et al.
Minerva Pediatrica
|
March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]
M Bado, C Minetti, L Mallamaci, et al.
Neurology
|
June 1, 1985
Physiologic assessment of phosphoglycerate mutase deficiency: incremental exercise test
J T Kissel, W Beam, N Bresolin, et al.
Neurology Research International
|
August 9, 2011
Anti-MuSK-Positive Myasthenia Gravis in a Patient with Parkinsonism and Cognitive Impairment
S Lanfranconi, S Corti, P Baron, et al.
Page
of 21