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Cell Death and Differentiation
|
May 27, 2006
Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects
A Ciammola, J Sassone, L Alberti, et al.
Muscle & Nerve
|
June 1, 1993
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes
G Meola, J P Tremblay, V Sansone, et al.
Neurology
|
October 27, 1997
De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy
V Biousse, M D Brown, N J Newman, et al.
Behavioural Neurology
|
February 14, 2007
Persistent autobiographical amnesia: a case report
C Repetto, R Manenti, V Sansone, et al.
Basic and Applied Histochemistry
|
January 1, 1987
Human Schwann cells: cytochemical, ultrastructural and immunological studies in vivo and in vitro
E Scarpini, G Meola, P L Baron, et al.
Journal of Endocrinological Investigation
|
June 9, 2007
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency
R Lanzi, S C Previtali, V Sansone, et al.
European Journal of Histochemistry : EJH
|
December 29, 2015
Tibialis anterior muscle needle biopsy and sensitive biomolecular methods: a useful tool in myotonic dystrophy type 1
S Iachettini, R Valaperta, A Marchesi, et al.
Journal of Neurology
|
May 1, 1989
Muscle glucose-6-phosphate dehydrogenase deficiency
N Bresolin, L Bet, M Moggio, et al.
Neurology
|
September 25, 1999
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy
G Meola, V Sansone, D Perani, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 17, 2006
Italian guidelines for molecular analysis in myotonic dystrophies
A Botta, E Bonifazi, L Vallo, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 142) with videos related to
Sort By:
Page
of 15
Cell Death and Differentiation
|
May 27, 2006
Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects
A Ciammola, J Sassone, L Alberti, et al.
Muscle & Nerve
|
June 1, 1993
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes
G Meola, J P Tremblay, V Sansone, et al.
Neurology
|
October 27, 1997
De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy
V Biousse, M D Brown, N J Newman, et al.
Behavioural Neurology
|
February 14, 2007
Persistent autobiographical amnesia: a case report
C Repetto, R Manenti, V Sansone, et al.
Basic and Applied Histochemistry
|
January 1, 1987
Human Schwann cells: cytochemical, ultrastructural and immunological studies in vivo and in vitro
E Scarpini, G Meola, P L Baron, et al.
Journal of Endocrinological Investigation
|
June 9, 2007
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency
R Lanzi, S C Previtali, V Sansone, et al.
European Journal of Histochemistry : EJH
|
December 29, 2015
Tibialis anterior muscle needle biopsy and sensitive biomolecular methods: a useful tool in myotonic dystrophy type 1
S Iachettini, R Valaperta, A Marchesi, et al.
Journal of Neurology
|
May 1, 1989
Muscle glucose-6-phosphate dehydrogenase deficiency
N Bresolin, L Bet, M Moggio, et al.
Neurology
|
September 25, 1999
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy
G Meola, V Sansone, D Perani, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 17, 2006
Italian guidelines for molecular analysis in myotonic dystrophies
A Botta, E Bonifazi, L Vallo, et al.
Page
of 15