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Developmental Neuroscience
|
January 1, 1991
The clinical aspects of adult hexosaminidase deficiencies
A Federico, S Palmeri, A Malandrini, et al.
Journal of the Neurological Sciences
|
December 1, 1996
Increased apoptotic response to 2-deoxy-D-ribose in ataxia-telangiectasia
C Battisti, P Formichi, S A Tripodi, 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.
Acta Neurologica
|
May 1, 1973
[Hunter's disease: study of a family from the plain of Paestum]
S Carlomagno, A Federico, L Pinto, 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.
Journal of Submicroscopic Cytology and Pathology
|
May 7, 2002
Nemaline myopathy: description of an adult onset case
F Ginanneschi, M Mondelli, A Malandrini, et al.
Experimental Gerontology
|
September 9, 2000
Enhanced 2-deoxy-D-ribose-induced-apoptosis, a phenotype of lymphocytes from old donors, is not observed in the Werner syndrome
C Battisti, P Formichi, S A Tripodi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 17, 2018
A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up
A R Pati, C Battisti, I Taglia, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Retinochoroidal atrophy in two adult patients with Angelman syndrome
A Rufa, M T Dotti, A Orrico, et al.
Page
of 42
Search research articles
Search
Showing results (191-200 of 419) with videos related to
Sort By:
Page
of 42
Developmental Neuroscience
|
January 1, 1991
The clinical aspects of adult hexosaminidase deficiencies
A Federico, S Palmeri, A Malandrini, et al.
Journal of the Neurological Sciences
|
December 1, 1996
Increased apoptotic response to 2-deoxy-D-ribose in ataxia-telangiectasia
C Battisti, P Formichi, S A Tripodi, 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.
Acta Neurologica
|
May 1, 1973
[Hunter's disease: study of a family from the plain of Paestum]
S Carlomagno, A Federico, L Pinto, 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.
Journal of Submicroscopic Cytology and Pathology
|
May 7, 2002
Nemaline myopathy: description of an adult onset case
F Ginanneschi, M Mondelli, A Malandrini, et al.
Experimental Gerontology
|
September 9, 2000
Enhanced 2-deoxy-D-ribose-induced-apoptosis, a phenotype of lymphocytes from old donors, is not observed in the Werner syndrome
C Battisti, P Formichi, S A Tripodi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 17, 2018
A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up
A R Pati, C Battisti, I Taglia, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Retinochoroidal atrophy in two adult patients with Angelman syndrome
A Rufa, M T Dotti, A Orrico, et al.
Page
of 42