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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 Series
Manon 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 survey
Benjamin 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 survey
Benjamin 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 Therapies
Julien 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 clone
Samih H Nasr, Christopher P Larsen, Christophe Sirac, et al.
Kidney International
|
July 30, 2025
Management recommendations for kidney transplantation in patients with plasma cell dyscrasia
Naoka 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 survey
Benjamin Terrier, Fabrice Carrat, Evguenia Krastinova, et al.
Kidney International Reports
|
January 18, 2018
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary Glomerulonephritis
Samih 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-microglobulin
Sophie 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 profile
Sophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, et al.
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of 17
Search research articles
Search
Showing results (141-150 of 165) with videos related to
Sort By:
Page
of 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 Series
Manon 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 survey
Benjamin 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 survey
Benjamin 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 Therapies
Julien 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 clone
Samih H Nasr, Christopher P Larsen, Christophe Sirac, et al.
Kidney International
|
July 30, 2025
Management recommendations for kidney transplantation in patients with plasma cell dyscrasia
Naoka 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 survey
Benjamin Terrier, Fabrice Carrat, Evguenia Krastinova, et al.
Kidney International Reports
|
January 18, 2018
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary Glomerulonephritis
Samih 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-microglobulin
Sophie 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 profile
Sophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, et al.
Page
of 17