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European Journal of Neurology
|
September 23, 2008
CSF levels of beta-amyloid 1-42, tau and phosphorylated tau protein in CADASIL
P Formichi, L Parnetti, E Radi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 30, 2005
Typical pathological changes of CADASIL in the optic nerve
A Rufa, A Malandrini, M T Dotti, et al.
European Neurology
|
October 13, 2006
Inclusion body myopathy-like changes in a family with cerebellar atrophy, mental retardation and abnormal pupils
S Gambelli, M T Dotti, A Malandrini, et al.
The Journal of Laryngology and Otology
|
May 25, 2006
Auditory neuropathy in a patient with mitochondrial myopathy and multiple mtDNA deletions
F Forli, M Mancuso, A Santoro, et al.
European Journal of Neurology
|
April 29, 2015
Pendular nystagmus, palatal tremor and progressive ataxia in GM2-gangliosidosis
E Pretegiani, F Rosini, P Federighi, et al.
Journal of the Neurological Sciences
|
May 20, 1998
Vitamin E serum levels in Rett syndrome
P Formichi, C Battisti, M T Dotti, et al.
American Journal of Medical Genetics
|
August 26, 1998
Mosaicism for full mutation and normal-sized allele of the FMR1 gene: a new case
A Orrico, L Galli, M T Dotti, et al.
European Journal of Neurology
|
July 31, 2007
First report of a Romanian CADASIL patient following immigration to Italy
F Pescini, S Bianchi, M T Dotti, et al.
Journal of Inherited Metabolic Disease
|
January 9, 2015
Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis
M Brienza, G Fiermonte, C Cambieri, et al.
Human Genetics
|
April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation
Silvia Bianchi, M T Dotti, N De Stefano, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 144) with videos related to
Sort By:
Page
of 15
European Journal of Neurology
|
September 23, 2008
CSF levels of beta-amyloid 1-42, tau and phosphorylated tau protein in CADASIL
P Formichi, L Parnetti, E Radi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 30, 2005
Typical pathological changes of CADASIL in the optic nerve
A Rufa, A Malandrini, M T Dotti, et al.
European Neurology
|
October 13, 2006
Inclusion body myopathy-like changes in a family with cerebellar atrophy, mental retardation and abnormal pupils
S Gambelli, M T Dotti, A Malandrini, et al.
The Journal of Laryngology and Otology
|
May 25, 2006
Auditory neuropathy in a patient with mitochondrial myopathy and multiple mtDNA deletions
F Forli, M Mancuso, A Santoro, et al.
European Journal of Neurology
|
April 29, 2015
Pendular nystagmus, palatal tremor and progressive ataxia in GM2-gangliosidosis
E Pretegiani, F Rosini, P Federighi, et al.
Journal of the Neurological Sciences
|
May 20, 1998
Vitamin E serum levels in Rett syndrome
P Formichi, C Battisti, M T Dotti, et al.
American Journal of Medical Genetics
|
August 26, 1998
Mosaicism for full mutation and normal-sized allele of the FMR1 gene: a new case
A Orrico, L Galli, M T Dotti, et al.
European Journal of Neurology
|
July 31, 2007
First report of a Romanian CADASIL patient following immigration to Italy
F Pescini, S Bianchi, M T Dotti, et al.
Journal of Inherited Metabolic Disease
|
January 9, 2015
Enlarging brain xanthomas in a patient with cerebrotendinous xanthomatosis
M Brienza, G Fiermonte, C Cambieri, et al.
Human Genetics
|
April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation
Silvia Bianchi, M T Dotti, N De Stefano, et al.
Page
of 15