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Journal of the Neurological Sciences
|
May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
N Checcarelli, A Prelle, M Moggio, et al.
Neurology
|
October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features
D Biral, E Damiani, E Scarpini, et al.
Neurology
|
October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain
R Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics
|
April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy
O Musumeci, A L Andreu, S Shanske, et al.
American Journal of Medical Genetics
|
April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area
S Lucchiari, I Fogh, A Prelle, et al.
Human Gene Therapy
|
December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expression
A Fassati, A Bardoni, M Sironi, et al.
European Neurology
|
January 1, 1993
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism
G Vita, A Toscano, G Mileto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 19, 2008
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
R Virgilio, S Corti, P Agazzi, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 8, 2008
Stem cell therapy in stroke
F Locatelli, A Bersano, E Ballabio, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophin
A Prelle, M Moggio, G P Comi, et al.
Page
of 21
Search research articles
Search
Showing results (101-110 of 206) with videos related to
Sort By:
Page
of 21
Journal of the Neurological Sciences
|
May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
N Checcarelli, A Prelle, M Moggio, et al.
Neurology
|
October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features
D Biral, E Damiani, E Scarpini, et al.
Neurology
|
October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain
R Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics
|
April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy
O Musumeci, A L Andreu, S Shanske, et al.
American Journal of Medical Genetics
|
April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area
S Lucchiari, I Fogh, A Prelle, et al.
Human Gene Therapy
|
December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expression
A Fassati, A Bardoni, M Sironi, et al.
European Neurology
|
January 1, 1993
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism
G Vita, A Toscano, G Mileto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 19, 2008
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
R Virgilio, S Corti, P Agazzi, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 8, 2008
Stem cell therapy in stroke
F Locatelli, A Bersano, E Ballabio, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophin
A Prelle, M Moggio, G P Comi, et al.
Page
of 21