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Clinical Kidney Journal
|
September 9, 2020
Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis
Annalisa Terranegra, Teresa Arcidiacono, Lorenza Macrina, et al.
Blood
|
July 28, 2009
ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiency
Aisha V Sauer, Emanuela Mrak, Raisa Jofra Hernandez, et al.
Plos One
|
October 23, 2009
Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes
Michela Traglia, Cinzia Sala, Corrado Masciullo, et al.
Blood
|
September 18, 2010
Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model
Ilaria Visigalli, Stefania Delai, Letterio S Politi, et al.
The New England Journal of Medicine
|
March 1, 2002
Intravenous zoledronic acid in postmenopausal women with low bone mineral density
Ian R Reid, Jacques P Brown, Peter Burckhardt, et al.
American Journal of Medical Genetics. Part A
|
January 28, 2017
Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia
Jair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
Page
of 5
Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Clinical Kidney Journal
|
September 9, 2020
Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis
Annalisa Terranegra, Teresa Arcidiacono, Lorenza Macrina, et al.
Blood
|
July 28, 2009
ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiency
Aisha V Sauer, Emanuela Mrak, Raisa Jofra Hernandez, et al.
Plos One
|
October 23, 2009
Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes
Michela Traglia, Cinzia Sala, Corrado Masciullo, et al.
Blood
|
September 18, 2010
Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model
Ilaria Visigalli, Stefania Delai, Letterio S Politi, et al.
The New England Journal of Medicine
|
March 1, 2002
Intravenous zoledronic acid in postmenopausal women with low bone mineral density
Ian R Reid, Jacques P Brown, Peter Burckhardt, et al.
American Journal of Medical Genetics. Part A
|
January 28, 2017
Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia
Jair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
Page
of 5