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Diabetes Care
|
June 1, 1988
Early detection of neurological involvement in IDDM and NIDDM. Multimodal evoked potentials versus metabolic control
G Pozzessere, P A Rizzo, E Valle, et al.
Minerva Cardioangiologica
|
November 1, 1983
[The heart-brain relationship: role of cardiopathy and hypertension in the natural history of localized acute cerebral vasculopathy]
L Allori, M Servi, M Bartolo, et al.
American Journal of Human Genetics
|
June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I
C Jodice, P Malaspina, F Persichetti, et al.
Diabetes Research (Edinburgh, Scotland)
|
January 1, 1989
A longitudinal study of multimodal evoked potentials in diabetes mellitus
G Pozzessere, P A Rizzo, E Valle, et al.
Archives of Gerontology and Geriatrics
|
February 24, 2007
Drug adverse events and drop-out risk: a clinical case
R M Scoyni, L Aiello, I Trani, et al.
Acta Neuropathologica
|
August 1, 1996
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy
A Malandrini, P Carrera, S Palmeri, et al.
Neuromuscular Disorders : NMD
|
August 30, 2001
Respiratory chain defects in hereditary spastic paraplegias
F Piemonte, C Casali, R Carrozzo, et al.
Neurology
|
April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family
C Casali, G M Fabrizi, F M Santorelli, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
Diabetes Care
|
June 1, 1988
Early detection of neurological involvement in IDDM and NIDDM. Multimodal evoked potentials versus metabolic control
G Pozzessere, P A Rizzo, E Valle, et al.
Minerva Cardioangiologica
|
November 1, 1983
[The heart-brain relationship: role of cardiopathy and hypertension in the natural history of localized acute cerebral vasculopathy]
L Allori, M Servi, M Bartolo, et al.
American Journal of Human Genetics
|
June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I
C Jodice, P Malaspina, F Persichetti, et al.
Diabetes Research (Edinburgh, Scotland)
|
January 1, 1989
A longitudinal study of multimodal evoked potentials in diabetes mellitus
G Pozzessere, P A Rizzo, E Valle, et al.
Archives of Gerontology and Geriatrics
|
February 24, 2007
Drug adverse events and drop-out risk: a clinical case
R M Scoyni, L Aiello, I Trani, et al.
Acta Neuropathologica
|
August 1, 1996
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy
A Malandrini, P Carrera, S Palmeri, et al.
Neuromuscular Disorders : NMD
|
August 30, 2001
Respiratory chain defects in hereditary spastic paraplegias
F Piemonte, C Casali, R Carrozzo, et al.
Neurology
|
April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family
C Casali, G M Fabrizi, F M Santorelli, et al.
Page
of 9