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Genomics
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April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation
M Piccini, F Vitelli, M Bruttini, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
Immunolocalization of several laminin chains in the normal human central and peripheral nervous system
M Villanova, C Sewry, A Malandrini, et al.
Neuromuscular Disorders : NMD
|
May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency
M Villanova, A Malandrini, R Biancotti, et al.
Neurology
|
May 1, 1997
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy
A Malandrini, P Carrera, G Ciacci, et al.
The Journal of Rheumatology
|
May 17, 2000
Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases
A Malandrini, E Selvi, M Villanova, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities
A Malandrini, S Cesaretti, M Mulinari, et al.
Neurology
|
August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy
B A Minassian, R Aiyar, S Alic, et al.
Neurology
|
August 28, 2002
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL
A Malandrini, F Albani, S Palmeri, et al.
European Neurology
|
February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological study
S Palmeri, M Villanova, A Malandrini, et al.
Transplantation Proceedings
|
December 23, 2018
Oil Red O Is a Useful Tool to Assess Donor Liver Steatosis on Frozen Sections During Transplantation
G Riva, M Villanova, L Cima, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 85) with videos related to
Sort By:
Page
of 9
Genomics
|
April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation
M Piccini, F Vitelli, M Bruttini, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
Immunolocalization of several laminin chains in the normal human central and peripheral nervous system
M Villanova, C Sewry, A Malandrini, et al.
Neuromuscular Disorders : NMD
|
May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency
M Villanova, A Malandrini, R Biancotti, et al.
Neurology
|
May 1, 1997
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy
A Malandrini, P Carrera, G Ciacci, et al.
The Journal of Rheumatology
|
May 17, 2000
Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases
A Malandrini, E Selvi, M Villanova, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities
A Malandrini, S Cesaretti, M Mulinari, et al.
Neurology
|
August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy
B A Minassian, R Aiyar, S Alic, et al.
Neurology
|
August 28, 2002
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL
A Malandrini, F Albani, S Palmeri, et al.
European Neurology
|
February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological study
S Palmeri, M Villanova, A Malandrini, et al.
Transplantation Proceedings
|
December 23, 2018
Oil Red O Is a Useful Tool to Assess Donor Liver Steatosis on Frozen Sections During Transplantation
G Riva, M Villanova, L Cima, et al.
Page
of 9