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Frank Bridoux

Showing results (141-150 of 165) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2022
Complement Activation and Thrombotic Microangiopathy Associated With Monoclonal Gammopathy: A National French Case SeriesManon Martins, Frank Bridoux, Jean Michel Goujon, et al.
Autoimmunity Reviews|January 15, 2014
Predictors of early relapse in patients with non-infectious mixed cryoglobulinemia vasculitis: results from the French nationwide CryoVas surveyBenjamin Terrier, Isabelle Marie, David Launay, et al.
Blood|April 5, 2012
Management of noninfectious mixed cryoglobulinemia vasculitis: data from 242 cases included in the CryoVas surveyBenjamin Terrier, Evguenia Krastinova, Isabelle Marie, et al.
Kidney International Reports|July 9, 2025
Kidney Outcomes in Patients With Hereditary Transthyretin Amyloid Nephropathy Treated With Transthyretin Stabilizers And Gene-Silencer TherapiesJulien Dang, Justine Solignac, Sophie Ferlicot, et al.
Kidney International|February 1, 2020
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell cloneSamih H Nasr, Christopher P Larsen, Christophe Sirac, et al.
Kidney International|July 30, 2025
Management recommendations for kidney transplantation in patients with plasma cell dyscrasiaNaoka Murakami, Christopher D Blosser, Allison B Webber, et al.
Annals of the Rheumatic Diseases|May 16, 2012
Prognostic factors of survival in patients with non-infectious mixed cryoglobulinaemia vasculitis: data from 242 cases included in the CryoVas surveyBenjamin Terrier, Fabrice Carrat, Evguenia Krastinova, et al.
Kidney International Reports|January 18, 2018
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary GlomerulonephritisSamih H Nasr, Julie A Vrana, Surendra Dasari, et al.
The New England Journal of Medicine|June 15, 2012
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulinSophie Valleix, Julian D Gillmore, Frank Bridoux, et al.
Nature Communications|January 22, 2016
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profileSophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2022
Complement Activation and Thrombotic Microangiopathy Associated With Monoclonal Gammopathy: A National French Case SeriesManon Martins, Frank Bridoux, Jean Michel Goujon, et al.
Autoimmunity Reviews|January 15, 2014
Predictors of early relapse in patients with non-infectious mixed cryoglobulinemia vasculitis: results from the French nationwide CryoVas surveyBenjamin Terrier, Isabelle Marie, David Launay, et al.
Blood|April 5, 2012
Management of noninfectious mixed cryoglobulinemia vasculitis: data from 242 cases included in the CryoVas surveyBenjamin Terrier, Evguenia Krastinova, Isabelle Marie, et al.
Kidney International Reports|July 9, 2025
Kidney Outcomes in Patients With Hereditary Transthyretin Amyloid Nephropathy Treated With Transthyretin Stabilizers And Gene-Silencer TherapiesJulien Dang, Justine Solignac, Sophie Ferlicot, et al.
Kidney International|February 1, 2020
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell cloneSamih H Nasr, Christopher P Larsen, Christophe Sirac, et al.
Kidney International|July 30, 2025
Management recommendations for kidney transplantation in patients with plasma cell dyscrasiaNaoka Murakami, Christopher D Blosser, Allison B Webber, et al.
Annals of the Rheumatic Diseases|May 16, 2012
Prognostic factors of survival in patients with non-infectious mixed cryoglobulinaemia vasculitis: data from 242 cases included in the CryoVas surveyBenjamin Terrier, Fabrice Carrat, Evguenia Krastinova, et al.
Kidney International Reports|January 18, 2018
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary GlomerulonephritisSamih H Nasr, Julie A Vrana, Surendra Dasari, et al.
The New England Journal of Medicine|June 15, 2012
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulinSophie Valleix, Julian D Gillmore, Frank Bridoux, et al.
Nature Communications|January 22, 2016
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profileSophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, et al.
Pageof 17