Clin. Exp. Nephrol. 2020 Jan 31
Identification of children with chronic kidney disease through school urinary screening using urinary protein/creatinine ratio measurement: an observational study.
Kajiwara N, Hayashi K, Fujiwara M, Nakayama H, Ozaki Y
School urinary screening has been performed in Japan. ...
Read More
Source: PubMed
BMC Nephrol
Diagnostic and treatment challenge of unrecognized subacute bacterial endocarditis associated with ANCA-PR3 positive immunocomplex glomerulonephritis: a case report and literature review.
Bele D, Kojc N, Perše M, Cerne Cercek A, Lindic J, Aleš Rigler A, Veceric-Haler Ž
Diagnosis and treatment of either ANCA disease or silent infection-related glomerulonephritis is complicated and is a huge treatment challenge when ov ...
Read More
Source: PubMed
PLoS ONE
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD.
Ibrahim ST, Chinnadurai R, Ali I, Payne D, Rice GI, Newman WG, Algohary E, Adam AG, Kalra PA
The R102G variant in complement 3 (C3) results in two allotypic variants: C3 fast (C3F) and C3 slow (C3S). C3F presents at increased frequency in pati ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell clone.
Nasr SH, Larsen CP, Sirac C, Theis JD, Domenger C, Chauvet S, Javaugue V, Hogan JJ, Said SM, Dasari S, Vrana JA, McPhail ED, Cornell LD, Vilaine E, Massy ZA, Boffa JJ, Buob D, Toussaint S, Guincestre T, Touchard G, D'Agati VD, Leung N, Bridoux F
IgG (mainly IgG3) is the most commonly involved isotype in proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID). Here we ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Serum amyloid P deposition is a sensitive and specific feature of membranous-like glomerulopathy with masked IgG kappa deposits.
Larsen CP, Sharma SG, Caza TN, Kenan DJ, Storey AJ, Edmondson RD, Herzog C, Arthur JM
Membranous-like glomerulopathy with masked IgG kappa deposits (MGMID) is a recently described pattern of glomerulonephritis with a unique histopatholo ...
Read More
Source: PubMed
Clin. Exp. Nephrol. 2020 Jan 31
Identification of children with chronic kidney disease through school urinary screening using urinary protein/creatinine ratio measurement: an observational study.
Kajiwara N, Hayashi K, Fujiwara M, Nakayama H, Ozaki Y
School urinary screening has been performed in Japan. ...
Read More
Source: PubMed
BMC Nephrol
Diagnostic and treatment challenge of unrecognized subacute bacterial endocarditis associated with ANCA-PR3 positive immunocomplex glomerulonephritis: a case report and literature review.
Bele D, Kojc N, Perše M, Cerne Cercek A, Lindic J, Aleš Rigler A, Veceric-Haler Ž
Diagnosis and treatment of either ANCA disease or silent infection-related glomerulonephritis is complicated and is a huge treatment challenge when ov ...
Read More
Source: PubMed
PLoS ONE
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD.
Ibrahim ST, Chinnadurai R, Ali I, Payne D, Rice GI, Newman WG, Algohary E, Adam AG, Kalra PA
The R102G variant in complement 3 (C3) results in two allotypic variants: C3 fast (C3F) and C3 slow (C3S). C3F presents at increased frequency in pati ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell clone.
Nasr SH, Larsen CP, Sirac C, Theis JD, Domenger C, Chauvet S, Javaugue V, Hogan JJ, Said SM, Dasari S, Vrana JA, McPhail ED, Cornell LD, Vilaine E, Massy ZA, Boffa JJ, Buob D, Toussaint S, Guincestre T, Touchard G, D'Agati VD, Leung N, Bridoux F
IgG (mainly IgG3) is the most commonly involved isotype in proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID). Here we ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Serum amyloid P deposition is a sensitive and specific feature of membranous-like glomerulopathy with masked IgG kappa deposits.
Larsen CP, Sharma SG, Caza TN, Kenan DJ, Storey AJ, Edmondson RD, Herzog C, Arthur JM
Membranous-like glomerulopathy with masked IgG kappa deposits (MGMID) is a recently described pattern of glomerulonephritis with a unique histopatholo ...
Read More
Source: PubMed
Clin. Exp. Nephrol. 2020 Jan 31
Identification of children with chronic kidney disease through school urinary screening using urinary protein/creatinine ratio measurement: an observational study.
Kajiwara N, Hayashi K, Fujiwara M, Nakayama H, Ozaki Y
School urinary screening has been performed in Japan. ...
Read More
Source: PubMed
BMC Nephrol
Diagnostic and treatment challenge of unrecognized subacute bacterial endocarditis associated with ANCA-PR3 positive immunocomplex glomerulonephritis: a case report and literature review.
Bele D, Kojc N, Perše M, Cerne Cercek A, Lindic J, Aleš Rigler A, Veceric-Haler Ž
Diagnosis and treatment of either ANCA disease or silent infection-related glomerulonephritis is complicated and is a huge treatment challenge when ov ...
Read More
Source: PubMed
PLoS ONE
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD.
Ibrahim ST, Chinnadurai R, Ali I, Payne D, Rice GI, Newman WG, Algohary E, Adam AG, Kalra PA
The R102G variant in complement 3 (C3) results in two allotypic variants: C3 fast (C3F) and C3 slow (C3S). C3F presents at increased frequency in pati ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell clone.
Nasr SH, Larsen CP, Sirac C, Theis JD, Domenger C, Chauvet S, Javaugue V, Hogan JJ, Said SM, Dasari S, Vrana JA, McPhail ED, Cornell LD, Vilaine E, Massy ZA, Boffa JJ, Buob D, Toussaint S, Guincestre T, Touchard G, D'Agati VD, Leung N, Bridoux F
IgG (mainly IgG3) is the most commonly involved isotype in proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID). Here we ...
Read More
Source: PubMed
Kidney Int. 2019 Nov 09
Serum amyloid P deposition is a sensitive and specific feature of membranous-like glomerulopathy with masked IgG kappa deposits.
Larsen CP, Sharma SG, Caza TN, Kenan DJ, Storey AJ, Edmondson RD, Herzog C, Arthur JM
Membranous-like glomerulopathy with masked IgG kappa deposits (MGMID) is a recently described pattern of glomerulonephritis with a unique histopatholo ...
Read More
Source: PubMed
