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Giacomo Colussi

Showing results (21-30 of 32) with videos related to

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Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|July 13, 2017
[Dialysis and cookers: a project for the empowerment of patients in managing their own chronic renal failure]Mara Cabibbe, Alberto Montoli, Franca Cassaro, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 20, 2017
Acquired Complement Regulatory Gene Mutations and Hematopoietic Stem Cell Transplant-Related Thrombotic MicroangiopathyGianluigi Ardissino, Stefania Salardi, Silvia Berra, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumorsFilomena Cetani, Elena Pardi, Simona Borsari, et al.
Human Molecular Genetics|October 23, 2003
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamicsLuca Rampoldi, Gianluca Caridi, Daniela Santon, et al.
Cell Transplantation|June 7, 2018
Long-term Effect of Islet Transplantation on Glycemic VariabilityFederico Bertuzzi, Luciano De Carlis, Mario Marazzi, et al.
Human Mutation|July 12, 2002
Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndromeMarie-Louise Syrén, Silvana Tedeschi, Laila Cesareo, et al.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2006
Sensitivity of fibroblast growth factor 23 measurements in tumor-induced osteomalaciaErik A Imel, Munro Peacock, Pisit Pitukcheewanont, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2022
Clinical and genetic characteristics of Dent's disease type 1 in EuropeCarla Burballa, Gerard Cantero-Recasens, Larisa Prikhodina, et al.
Kidney International|February 25, 2017
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosisViviana Palazzo, Aldesia Provenzano, Francesca Becherucci, et al.
Nature|January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalitiesLynn M Boyden, Murim Choi, Keith A Choate, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

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Pageof 4
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|July 13, 2017
[Dialysis and cookers: a project for the empowerment of patients in managing their own chronic renal failure]Mara Cabibbe, Alberto Montoli, Franca Cassaro, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 20, 2017
Acquired Complement Regulatory Gene Mutations and Hematopoietic Stem Cell Transplant-Related Thrombotic MicroangiopathyGianluigi Ardissino, Stefania Salardi, Silvia Berra, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumorsFilomena Cetani, Elena Pardi, Simona Borsari, et al.
Human Molecular Genetics|October 23, 2003
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamicsLuca Rampoldi, Gianluca Caridi, Daniela Santon, et al.
Cell Transplantation|June 7, 2018
Long-term Effect of Islet Transplantation on Glycemic VariabilityFederico Bertuzzi, Luciano De Carlis, Mario Marazzi, et al.
Human Mutation|July 12, 2002
Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndromeMarie-Louise Syrén, Silvana Tedeschi, Laila Cesareo, et al.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2006
Sensitivity of fibroblast growth factor 23 measurements in tumor-induced osteomalaciaErik A Imel, Munro Peacock, Pisit Pitukcheewanont, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2022
Clinical and genetic characteristics of Dent's disease type 1 in EuropeCarla Burballa, Gerard Cantero-Recasens, Larisa Prikhodina, et al.
Kidney International|February 25, 2017
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosisViviana Palazzo, Aldesia Provenzano, Francesca Becherucci, et al.
Nature|January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalitiesLynn M Boyden, Murim Choi, Keith A Choate, et al.
Pageof 4