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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.
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.
Rivista Di Neurologia
|
July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]
G Meola, G Rotondo, M Velicogna, et al.
Cell Biochemistry and Biophysics
|
January 25, 2013
Low frequency pulsed electromagnetic field affects proliferation, tissue-specific gene expression, and cytokines release of human tendon cells
L de Girolamo, D Stanco, E Galliera, et al.
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA
|
June 25, 2014
In vitro functional response of human tendon cells to different dosages of low-frequency pulsed electromagnetic field
L de Girolamo, M Viganò, E Galliera, et al.
Journal of the Neurological Sciences
|
September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion
S Lucchiari, S Pagliarani, S Corti, et al.
Neurology
|
January 16, 2008
The hypocretin neurotransmission system in myotonic dystrophy type 1
E Ciafaloni, E Mignot, V Sansone, et al.
Human Molecular Genetics
|
October 9, 2001
Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2
A Mankodi, C R Urbinati, Q P Yuan, et al.
Annals of Neurology
|
October 23, 1997
Andersen's syndrome: a distinct periodic paralysis
V Sansone, R C Griggs, G Meola, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
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.
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.
Rivista Di Neurologia
|
July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]
G Meola, G Rotondo, M Velicogna, et al.
Cell Biochemistry and Biophysics
|
January 25, 2013
Low frequency pulsed electromagnetic field affects proliferation, tissue-specific gene expression, and cytokines release of human tendon cells
L de Girolamo, D Stanco, E Galliera, et al.
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA
|
June 25, 2014
In vitro functional response of human tendon cells to different dosages of low-frequency pulsed electromagnetic field
L de Girolamo, M Viganò, E Galliera, et al.
Journal of the Neurological Sciences
|
September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion
S Lucchiari, S Pagliarani, S Corti, et al.
Neurology
|
January 16, 2008
The hypocretin neurotransmission system in myotonic dystrophy type 1
E Ciafaloni, E Mignot, V Sansone, et al.
Human Molecular Genetics
|
October 9, 2001
Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2
A Mankodi, C R Urbinati, Q P Yuan, et al.
Annals of Neurology
|
October 23, 1997
Andersen's syndrome: a distinct periodic paralysis
V Sansone, R C Griggs, G Meola, et al.
Page
of 8