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Neurology
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December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
A Fogli, C Dionisi-Vici, F Deodato, et al.
Minerva Pediatrica
|
October 15, 1987
[Recurrent intracranial hemorrhage in a nursing infant with congenital factor VII deficiency. Survival and follow-up after neurosurgical intervention]
C Miano, A Donfrancesco, A Lombardi, et al.
Muscle & Nerve
|
February 1, 1997
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)
G Silvestri, E Bertini, S Servidei, et al.
American Journal of Medical Genetics
|
February 1, 1993
Presymptomatic diagnosis of SMA III by genotype analysis
C Brahe, S Zappata, I Velonà, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle
M Sabatelli, E Bertini, E Ricci, et al.
The Journal of Urology
|
February 1, 1986
The natural history of traumatic branch renal artery injury
J E Bertini, S M Flechner, P Miller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1994
High dose immunoglobulin IV treatment in adrenoleukodystrophy
M Cappa, E Bertini, P del Balzo, et al.
Acta Neuropathologica
|
January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study
E Bertini, C Bosman, E Ricci, et al.
Neuroscience
|
June 28, 2011
Effect of protein glutathionylation on neuronal cytoskeleton: a potential link to neurodegeneration
B Carletti, C Passarelli, M Sparaco, et al.
Neurology
|
April 13, 2012
Increased muscle expression of interleukin-17 in Duchenne muscular dystrophy
L De Pasquale, A D'Amico, M Verardo, et al.
Page
of 21
Search research articles
Search
Showing results (41-50 of 205) with videos related to
Sort By:
Page
of 21
Neurology
|
December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
A Fogli, C Dionisi-Vici, F Deodato, et al.
Minerva Pediatrica
|
October 15, 1987
[Recurrent intracranial hemorrhage in a nursing infant with congenital factor VII deficiency. Survival and follow-up after neurosurgical intervention]
C Miano, A Donfrancesco, A Lombardi, et al.
Muscle & Nerve
|
February 1, 1997
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)
G Silvestri, E Bertini, S Servidei, et al.
American Journal of Medical Genetics
|
February 1, 1993
Presymptomatic diagnosis of SMA III by genotype analysis
C Brahe, S Zappata, I Velonà, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle
M Sabatelli, E Bertini, E Ricci, et al.
The Journal of Urology
|
February 1, 1986
The natural history of traumatic branch renal artery injury
J E Bertini, S M Flechner, P Miller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1994
High dose immunoglobulin IV treatment in adrenoleukodystrophy
M Cappa, E Bertini, P del Balzo, et al.
Acta Neuropathologica
|
January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study
E Bertini, C Bosman, E Ricci, et al.
Neuroscience
|
June 28, 2011
Effect of protein glutathionylation on neuronal cytoskeleton: a potential link to neurodegeneration
B Carletti, C Passarelli, M Sparaco, et al.
Neurology
|
April 13, 2012
Increased muscle expression of interleukin-17 in Duchenne muscular dystrophy
L De Pasquale, A D'Amico, M Verardo, et al.
Page
of 21