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Neuromuscular Disorders : NMD
|
November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy
C Bruno, M DiRocco, L D Lamba, et al.
La Clinica Terapeutica
|
July 7, 2007
[HAV infection in patients with chronic hepatitis C]
G Bertino, A M Ardiri, M C Bruno, et al.
Molecular Cancer Research : MCR
|
August 26, 2018
A Role for Tryptophan-2,3-dioxygenase in CD8 T-cell Suppression and Evidence of Tryptophan Catabolism in Breast Cancer Patient Plasma
Lisa I Greene, Tullia C Bruno, Jessica L Christenson, et al.
Archives of Neurology
|
February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle disease
R Fernández, C Navarro, A L Andreu, et al.
Plos One
|
April 6, 2012
Phenotypic and functional properties of Helios+ regulatory T cells
Daniel J Zabransky, Christopher J Nirschl, Nicholas M Durham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 24, 2010
McArdle disease: a clinical review
R Quinlivan, J Buckley, M James, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 4, 2008
Phenotypic analysis of prostate-infiltrating lymphocytes reveals TH17 and Treg skewing
Karen Sandell Sfanos, Tullia C Bruno, Charles H Maris, et al.
La Clinica Terapeutica
|
May 1, 1997
[Comparative study of the modification of arterial pressure in adult and aged subjects treated with hemofiltration. Preliminary results]
G E Russo, S Giusti, E Vitaliano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 19, 2006
Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptor
Elaine M Sloand, Agnes S M Yong, Shakti Ramkissoon, et al.
American Journal of Human Genetics
|
August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
C Bruno, A Martinuzzi, Y Tang, et al.
Page
of 36
Search research articles
Search
Showing results (211-220 of 355) with videos related to
Sort By:
Page
of 36
Neuromuscular Disorders : NMD
|
November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy
C Bruno, M DiRocco, L D Lamba, et al.
La Clinica Terapeutica
|
July 7, 2007
[HAV infection in patients with chronic hepatitis C]
G Bertino, A M Ardiri, M C Bruno, et al.
Molecular Cancer Research : MCR
|
August 26, 2018
A Role for Tryptophan-2,3-dioxygenase in CD8 T-cell Suppression and Evidence of Tryptophan Catabolism in Breast Cancer Patient Plasma
Lisa I Greene, Tullia C Bruno, Jessica L Christenson, et al.
Archives of Neurology
|
February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle disease
R Fernández, C Navarro, A L Andreu, et al.
Plos One
|
April 6, 2012
Phenotypic and functional properties of Helios+ regulatory T cells
Daniel J Zabransky, Christopher J Nirschl, Nicholas M Durham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 24, 2010
McArdle disease: a clinical review
R Quinlivan, J Buckley, M James, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 4, 2008
Phenotypic analysis of prostate-infiltrating lymphocytes reveals TH17 and Treg skewing
Karen Sandell Sfanos, Tullia C Bruno, Charles H Maris, et al.
La Clinica Terapeutica
|
May 1, 1997
[Comparative study of the modification of arterial pressure in adult and aged subjects treated with hemofiltration. Preliminary results]
G E Russo, S Giusti, E Vitaliano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 19, 2006
Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptor
Elaine M Sloand, Agnes S M Yong, Shakti Ramkissoon, et al.
American Journal of Human Genetics
|
August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
C Bruno, A Martinuzzi, Y Tang, et al.
Page
of 36