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Silvana Tedeschi

Showing results (1-10 of 37) with videos related to

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Acta Bio-Medica : Atenei Parmensis|April 2, 2004
Hypokalemia and hypomagnesemia of hereditary renal tubular origin. Bartter and Gitelman syndromesAlberto Bettinelli, Silvana Tedeschi
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Complement System as a New Target for Hematopoietic Stem Cell Transplantation-Related Thrombotic MicroangiopathyGianluigi Ardissino, Valentina Capone, Silvana Tedeschi, et al.
Case Reports in Pediatrics|March 13, 2018
Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes InsipidusGianluca Vergine, Elena Fabbri, Annalisa Pedini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 28, 2002
Bartter syndrome type 3: an unusual cause of nephrolithiasisGiacomo Colussi, Maria Elisabetta De Ferrari, Silvana Tedeschi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidusMilena Brugnara, Rossella Gaudino, Silvana Tedeschi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|August 20, 2017
ResponseGianluigi Ardissino, Silvana Tedeschi, Marco Zecca, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 12, 2010
Long-term follow-up of patients with Bartter syndrome type I and IIElena Puricelli, Alberto Bettinelli, Nicolò Borsa, et al.
Pediatric Nephrology (Berlin, Germany)|September 1, 2004
Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter diseaseCristina Malafronte, Nicolò Borsa, Silvana Tedeschi, et al.
Prenatal Diagnosis|October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombinationAntonio Percesepe, Maurizio Ferrari, Domenico Coviello, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 25, 2014
Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 casesGianluigi Ardissino, Sara Testa, Ilaria Possenti, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Acta Bio-Medica : Atenei Parmensis|April 2, 2004
Hypokalemia and hypomagnesemia of hereditary renal tubular origin. Bartter and Gitelman syndromesAlberto Bettinelli, Silvana Tedeschi
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Complement System as a New Target for Hematopoietic Stem Cell Transplantation-Related Thrombotic MicroangiopathyGianluigi Ardissino, Valentina Capone, Silvana Tedeschi, et al.
Case Reports in Pediatrics|March 13, 2018
Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes InsipidusGianluca Vergine, Elena Fabbri, Annalisa Pedini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 28, 2002
Bartter syndrome type 3: an unusual cause of nephrolithiasisGiacomo Colussi, Maria Elisabetta De Ferrari, Silvana Tedeschi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidusMilena Brugnara, Rossella Gaudino, Silvana Tedeschi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|August 20, 2017
ResponseGianluigi Ardissino, Silvana Tedeschi, Marco Zecca, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 12, 2010
Long-term follow-up of patients with Bartter syndrome type I and IIElena Puricelli, Alberto Bettinelli, Nicolò Borsa, et al.
Pediatric Nephrology (Berlin, Germany)|September 1, 2004
Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter diseaseCristina Malafronte, Nicolò Borsa, Silvana Tedeschi, et al.
Prenatal Diagnosis|October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombinationAntonio Percesepe, Maurizio Ferrari, Domenico Coviello, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 25, 2014
Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 casesGianluigi Ardissino, Sara Testa, Ilaria Possenti, et al.
Pageof 4