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European Journal of Histochemistry : EJH
|
August 18, 2009
Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies
R Cardani, E Mancinelli, M Giagnacovo, et al.
Acta Neurologica Belgica
|
May 1, 1982
Immunological properties of myosin in myotonic dystrophy
P Volpe, E Damiani, A Margreth, et al.
American Journal of Hematology
|
May 1, 1982
Phosphofructokinase (PFK) deficiency due to a catalytically inactive mutant M-type subunit
A Zenella, M Mariani, G Meola, et al.
Chemotherapy
|
October 1, 1973
Comparative investigations of the enzyme-inducing activity of rifampicin and barbiturates in man
V Nitti, A Ninni, G Meola, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Proximal myotonic myopathy: report on italian families and literature review
G Meola, V Sansone, E Vitelli, et al.
European Journal of Histochemistry : EJH
|
September 8, 2010
Routinely frozen biopsies of human skeletal muscle are suitable for morphological and immunocytochemical analyses at transmission electron microscopy
M Giagnacovo, R Cardani, G Meola, et al.
Basic and Applied Histochemistry
|
January 1, 1989
Nile red simultaneous staining of intracellular lipids and membrane network in human muscle cultures
I Santilli, A Prelle, L Geremia, et al.
European Journal of Histochemistry : EJH
|
February 19, 2005
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy
R Cardani, E Mancinelli, V Sansone, et al.
Recenti Progressi in Medicina
|
December 1, 1989
[Mitochondrial encephalomyopathy]
G Scarlato, N Bresolin, M Moggio, et al.
European Journal of Histochemistry : EJH
|
August 22, 2006
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
R Cardani, E Mancinelli, G Rotondo, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 142) with videos related to
Sort By:
Page
of 15
European Journal of Histochemistry : EJH
|
August 18, 2009
Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies
R Cardani, E Mancinelli, M Giagnacovo, et al.
Acta Neurologica Belgica
|
May 1, 1982
Immunological properties of myosin in myotonic dystrophy
P Volpe, E Damiani, A Margreth, et al.
American Journal of Hematology
|
May 1, 1982
Phosphofructokinase (PFK) deficiency due to a catalytically inactive mutant M-type subunit
A Zenella, M Mariani, G Meola, et al.
Chemotherapy
|
October 1, 1973
Comparative investigations of the enzyme-inducing activity of rifampicin and barbiturates in man
V Nitti, A Ninni, G Meola, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Proximal myotonic myopathy: report on italian families and literature review
G Meola, V Sansone, E Vitelli, et al.
European Journal of Histochemistry : EJH
|
September 8, 2010
Routinely frozen biopsies of human skeletal muscle are suitable for morphological and immunocytochemical analyses at transmission electron microscopy
M Giagnacovo, R Cardani, G Meola, et al.
Basic and Applied Histochemistry
|
January 1, 1989
Nile red simultaneous staining of intracellular lipids and membrane network in human muscle cultures
I Santilli, A Prelle, L Geremia, et al.
European Journal of Histochemistry : EJH
|
February 19, 2005
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy
R Cardani, E Mancinelli, V Sansone, et al.
Recenti Progressi in Medicina
|
December 1, 1989
[Mitochondrial encephalomyopathy]
G Scarlato, N Bresolin, M Moggio, et al.
European Journal of Histochemistry : EJH
|
August 22, 2006
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
R Cardani, E Mancinelli, G Rotondo, et al.
Page
of 15