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Erica Daina

Showing results (11-20 of 39) with videos related to

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Pediatric Nephrology (Berlin, Germany)|June 5, 2012
Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutationParaskevas Iatropoulos, Erica Daina, Caterina Mele, et al.
Nephron|September 18, 2024
Lysinuric Protein Intolerance: Not Only a Disorder for Pediatric Nephrologists - Case ReportMiriam Rigoldi, Caterina Mele, Matteo Breno, et al.
The Annals of Thoracic Surgery|January 17, 2004
Left main stem patch plasty and aortic root homograft in Takayasu's diseaseMarco L S Matteucci, Maria Iascone, Amando Gamba, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 21, 2007
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic backgroundElena Bresin, Erica Daina, Marina Noris, et al.
Nephron|April 22, 2015
A multidrug, antiproteinuric approach to alport syndrome: a ten-year cohort studyErica Daina, Paolo Cravedi, Mirella Alpa, et al.
Nephron|February 13, 2020
Morphofunctional Effects of C5 Convertase Blockade in Immune Complex-Mediated Membranoproliferative Glomerulonephritis: Report of Two Cases with Evidence of Terminal Complement ActivationCamillo Carrara, Manuel Alfredo Podestà, Mauro Abbate, et al.
Journal of the American Society of Nephrology : JASN|February 7, 2001
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Human Molecular Genetics|October 30, 2003
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the diseaseJessica Caprioli, Federica Castelletti, Sara Bucchioni, et al.
Nephron|November 5, 2023
Functional Magnetic Resonance Imaging to Monitor Disease Progression: A Prospective Study in Patients with Primary Membranoproliferative GlomerulonephritisGiulia Villa, Erica Daina, Paolo Brambilla, et al.
Thrombosis and Haemostasis|February 5, 2009
Rituximab as pre-emptive treatment in patients with thrombotic thrombocytopenic purpura and evidence of anti-ADAMTS13 autoantibodiesElena Bresin, Sara Gastoldi, Erica Daina, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Pediatric Nephrology (Berlin, Germany)|June 5, 2012
Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutationParaskevas Iatropoulos, Erica Daina, Caterina Mele, et al.
Nephron|September 18, 2024
Lysinuric Protein Intolerance: Not Only a Disorder for Pediatric Nephrologists - Case ReportMiriam Rigoldi, Caterina Mele, Matteo Breno, et al.
The Annals of Thoracic Surgery|January 17, 2004
Left main stem patch plasty and aortic root homograft in Takayasu's diseaseMarco L S Matteucci, Maria Iascone, Amando Gamba, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 21, 2007
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic backgroundElena Bresin, Erica Daina, Marina Noris, et al.
Nephron|April 22, 2015
A multidrug, antiproteinuric approach to alport syndrome: a ten-year cohort studyErica Daina, Paolo Cravedi, Mirella Alpa, et al.
Nephron|February 13, 2020
Morphofunctional Effects of C5 Convertase Blockade in Immune Complex-Mediated Membranoproliferative Glomerulonephritis: Report of Two Cases with Evidence of Terminal Complement ActivationCamillo Carrara, Manuel Alfredo Podestà, Mauro Abbate, et al.
Journal of the American Society of Nephrology : JASN|February 7, 2001
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, et al.
Human Molecular Genetics|October 30, 2003
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the diseaseJessica Caprioli, Federica Castelletti, Sara Bucchioni, et al.
Nephron|November 5, 2023
Functional Magnetic Resonance Imaging to Monitor Disease Progression: A Prospective Study in Patients with Primary Membranoproliferative GlomerulonephritisGiulia Villa, Erica Daina, Paolo Brambilla, et al.
Thrombosis and Haemostasis|February 5, 2009
Rituximab as pre-emptive treatment in patients with thrombotic thrombocytopenic purpura and evidence of anti-ADAMTS13 autoantibodiesElena Bresin, Sara Gastoldi, Erica Daina, et al.
Pageof 4