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Clinical Genetics
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July 18, 2002
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease
R Biancheri, E Verbeek, A Rossi, et al.
Communications in Agricultural and Applied Biological Sciences
|
March 11, 2005
Pesticides re-entry dermal exposure of workers in greenhouses
V Caffarelli, E Conte, A Correnti, et al.
Journal of Medical Genetics
|
April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intolerance
G Sebastio, R de Franchis, P Strisciuglio, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in Europe
S Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
C Bruno, C Minetti, Y Tang, et al.
Molecular Medicine (Cambridge, Mass.)
|
November 20, 2001
Interleukin-6 and glucocorticoids synergistically induce human immunodeficiency virus type-1 expression in chronically infected U1 cells by a long terminal repeat independent post-transcriptional mechanism
A L Kinter, P Biswas, M Alfano, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patients
R Gatti, P DiNatale, G R Villani, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
October 30, 2013
Predictors of effectiveness of multidisciplinary rehabilitation treatment on motor dysfunction in multiple sclerosis
G Liberatore, F Clarelli, A Nuara, et al.
Cephalalgia : an International Journal of Headache
|
September 25, 2007
Ethanol causes neurogenic vasodilation by TRPV1 activation and CGRP release in the trigeminovascular system of the guinea pig
P Nicoletti, M Trevisani, M Manconi, et al.
Genomics
|
January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome
G Palmieri, V Capra, G Romano, et al.
Page
of 24
Search research articles
Search
Showing results (211-220 of 239) with videos related to
Sort By:
Page
of 24
Clinical Genetics
|
July 18, 2002
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease
R Biancheri, E Verbeek, A Rossi, et al.
Communications in Agricultural and Applied Biological Sciences
|
March 11, 2005
Pesticides re-entry dermal exposure of workers in greenhouses
V Caffarelli, E Conte, A Correnti, et al.
Journal of Medical Genetics
|
April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intolerance
G Sebastio, R de Franchis, P Strisciuglio, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in Europe
S Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
C Bruno, C Minetti, Y Tang, et al.
Molecular Medicine (Cambridge, Mass.)
|
November 20, 2001
Interleukin-6 and glucocorticoids synergistically induce human immunodeficiency virus type-1 expression in chronically infected U1 cells by a long terminal repeat independent post-transcriptional mechanism
A L Kinter, P Biswas, M Alfano, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patients
R Gatti, P DiNatale, G R Villani, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
October 30, 2013
Predictors of effectiveness of multidisciplinary rehabilitation treatment on motor dysfunction in multiple sclerosis
G Liberatore, F Clarelli, A Nuara, et al.
Cephalalgia : an International Journal of Headache
|
September 25, 2007
Ethanol causes neurogenic vasodilation by TRPV1 activation and CGRP release in the trigeminovascular system of the guinea pig
P Nicoletti, M Trevisani, M Manconi, et al.
Genomics
|
January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome
G Palmieri, V Capra, G Romano, et al.
Page
of 24