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Alessandro Rubinacci

Showing results (41-50 of 46) with videos related to

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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 hemodialysisAnnalisa 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 insufficiencyAisha 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 genesMichela 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 modelIlaria 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 densityIan 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 HypophosphatasiaJair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 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 hemodialysisAnnalisa 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 insufficiencyAisha 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 genesMichela 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 modelIlaria 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 densityIan 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 HypophosphatasiaJair Tenorio, Ignacio Álvarez, Leyre Riancho-Zarrabeitia, et al.
Pageof 5