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Giacomo Colussi

Showing results (11-20 of 32) with videos related to

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Blood Purification|May 6, 2019
Single Session and Weekly Beta 2-Microglobulin Removal with Different Dialytic Procedures: Comparison between High-Flux Standard Bicarbonate Hemodialysis, Post-Dilution Hemodiafiltration, Short Frequent Hemodialysis with NxStage Technology and Automated Peritoneal DialysisChiara Carla Maria Brunati, Francesca Gervasi, Mara Cabibbe, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 1, 2017
[Home Daily Hemodialysis with NxStage System One: monocentric italian casistic results]Chiara Brunati, Franca Cassaro, Laura Cretti, et al.
Plos One|May 30, 2020
A simple method for the calculation of dialysis Kt factor as a quantitative measure of removal efficiency of uremic retention solutes: Applicability to high-dialysate vs low-dialysate volume technologiesGiacomo Colussi, Chiara Carla Maria Brunati, Francesca Gervasi, et al.
Journal of Transplantation|June 5, 2018
Renal Transplants from Older Deceased Donors: Use of Preimplantation Biopsy and Differential Allocation to Dual or Single Kidney Transplant according to Histological Score Has No Advantages over Allocation to Single Kidney Transplant by Simple Clinical IndicationCostanza Casati, Valeriana Giuseppina Colombo, Marialuisa Perrino, et al.
BMC Nephrology|October 14, 2018
Home hemodialysis treatment and outcomes: retrospective analysis of the Knowledge to Improve Home Dialysis Network in Europe (KIHDNEy) cohortShashidhar Cherukuri, Maria Bajo, Giacomo Colussi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 3, 2010
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestorMarie-Louise Syrén, Nicolò Borsa Ghiringhelli, Alberto Bettinelli, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 20, 2007
A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of kappa light chainsJoakim Bergström, Maria Cristina Patrosso, Giacomo Colussi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 16, 2013
Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failureGiacomo Colussi, Liat Ganon, Silvana Penco, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 19, 2007
A thiazide test for the diagnosis of renal tubular hypokalemic disordersGiacomo Colussi, Alberto Bettinelli, Silvana Tedeschi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 7, 2002
Autosomal dominant hypocalcemia caused by a novel mutation in the loop 2 region of the human calcium receptor extracellular domainJianxin Hu, Stefano Mora, Giacomo Colussi, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Blood Purification|May 6, 2019
Single Session and Weekly Beta 2-Microglobulin Removal with Different Dialytic Procedures: Comparison between High-Flux Standard Bicarbonate Hemodialysis, Post-Dilution Hemodiafiltration, Short Frequent Hemodialysis with NxStage Technology and Automated Peritoneal DialysisChiara Carla Maria Brunati, Francesca Gervasi, Mara Cabibbe, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 1, 2017
[Home Daily Hemodialysis with NxStage System One: monocentric italian casistic results]Chiara Brunati, Franca Cassaro, Laura Cretti, et al.
Plos One|May 30, 2020
A simple method for the calculation of dialysis Kt factor as a quantitative measure of removal efficiency of uremic retention solutes: Applicability to high-dialysate vs low-dialysate volume technologiesGiacomo Colussi, Chiara Carla Maria Brunati, Francesca Gervasi, et al.
Journal of Transplantation|June 5, 2018
Renal Transplants from Older Deceased Donors: Use of Preimplantation Biopsy and Differential Allocation to Dual or Single Kidney Transplant according to Histological Score Has No Advantages over Allocation to Single Kidney Transplant by Simple Clinical IndicationCostanza Casati, Valeriana Giuseppina Colombo, Marialuisa Perrino, et al.
BMC Nephrology|October 14, 2018
Home hemodialysis treatment and outcomes: retrospective analysis of the Knowledge to Improve Home Dialysis Network in Europe (KIHDNEy) cohortShashidhar Cherukuri, Maria Bajo, Giacomo Colussi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 3, 2010
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestorMarie-Louise Syrén, Nicolò Borsa Ghiringhelli, Alberto Bettinelli, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 20, 2007
A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of kappa light chainsJoakim Bergström, Maria Cristina Patrosso, Giacomo Colussi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 16, 2013
Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failureGiacomo Colussi, Liat Ganon, Silvana Penco, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 19, 2007
A thiazide test for the diagnosis of renal tubular hypokalemic disordersGiacomo Colussi, Alberto Bettinelli, Silvana Tedeschi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 7, 2002
Autosomal dominant hypocalcemia caused by a novel mutation in the loop 2 region of the human calcium receptor extracellular domainJianxin Hu, Stefano Mora, Giacomo Colussi, et al.
Pageof 4