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Neurology
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October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
A Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
G M Hadjigeorgiou, G P Comi, A Bordoni, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neurology
|
October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
R Del Bo, M Moggio, M Rango, et al.
European Journal of Neurology
|
December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
E Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology
|
May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
C Villa, E Venturelli, C Fenoglio, et al.
Journal of the Neurological Sciences
|
October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutations
R Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Medical Genetics
|
February 7, 2009
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum
C Crimella, A Arnoldi, F Crippa, et al.
Journal of Neurology
|
October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
M Sciacco, A Prelle, G P Comi, et al.
Molecular Biology and Evolution
|
February 10, 2012
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis
R Cagliani, F R Guerini, M Fumagalli, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 206) with videos related to
Sort By:
Page
of 21
Neurology
|
October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
A Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
G M Hadjigeorgiou, G P Comi, A Bordoni, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neurology
|
October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
R Del Bo, M Moggio, M Rango, et al.
European Journal of Neurology
|
December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
E Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology
|
May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
C Villa, E Venturelli, C Fenoglio, et al.
Journal of the Neurological Sciences
|
October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutations
R Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Medical Genetics
|
February 7, 2009
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum
C Crimella, A Arnoldi, F Crippa, et al.
Journal of Neurology
|
October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
M Sciacco, A Prelle, G P Comi, et al.
Molecular Biology and Evolution
|
February 10, 2012
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis
R Cagliani, F R Guerini, M Fumagalli, et al.
Page
of 21