Detalhe da pesquisa
1.
A proteomic atlas of kidney amyloidosis provides insights into disease pathogenesis.
Kidney Int
; 105(3): 484-495, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38096952
2.
Pathological characteristics of light chain crystalline podocytopathy.
Kidney Int
; 103(3): 616-626, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36581019
3.
Light Chain-Only Immunotactoid Glomerulopathy: A Case Report.
Am J Kidney Dis
; 81(5): 611-615, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328099
4.
The characteristics of patients with kidney light chain deposition disease concurrent with light chain amyloidosis.
Kidney Int
; 101(1): 152-163, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34767832
5.
Immunoglobulin-Negative DNAJB9-Associated Fibrillary Glomerulonephritis: A Report of 9 Cases.
Am J Kidney Dis
; 77(3): 454-458, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32711071
6.
The novel form of amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1 (EFEMP1) preferentially affects the lower gastrointestinal tract of elderly femalesa.
Histopathology
; 78(3): 459-463, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33020971
7.
Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell clone.
Kidney Int
; 97(3): 589-601, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32001067
8.
Amyloidosis in surgically resected atrial appendages: a study of 345 consecutive cases with clinical implications.
Mod Pathol
; 33(5): 764-774, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31723241
9.
DnaJ Heat Shock Protein Family B Member 9 Is a Novel Biomarker for Fibrillary GN.
J Am Soc Nephrol
; 29(1): 51-56, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29097623
10.
Congophilic Fibrillary Glomerulonephritis: A Case Series.
Am J Kidney Dis
; 72(3): 325-336, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29866458
11.
Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.
J Am Soc Nephrol
; 28(2): 439-445, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27297947
12.
Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype.
J Am Soc Nephrol
; 28(2): 431-438, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28049649
13.
Clinical, biopsy, and mass spectrometry findings of renal gelsolin amyloidosis.
Kidney Int
; 91(4): 964-971, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28139293
14.
Clinicopathologic and proteomic characteristics of intratubular cytoplasmic AL amyloidosis.
Kidney Int
; 102(4): 926-929, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35964797
15.
Characterization of C3 in C3 glomerulopathy.
Nephrol Dial Transplant
; 32(3): 459-465, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27507892
16.
Complement activation in pauci-immune necrotizing and crescentic glomerulonephritis: results of a proteomic analysis.
Nephrol Dial Transplant
; 32(suppl_1): i139-i145, 2017 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391334
17.
Clinical, biopsy, and mass spectrometry characteristics of renal apolipoprotein A-IV amyloidosis.
Kidney Int
; 90(3): 658-64, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262366
18.
Leukocyte chemotactic factor 2 amyloidosis (ALECT2) is a common form of renal amyloidosis among Egyptians.
Mod Pathol
; 29(4): 416-20, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26867784
19.
Leukocyte cell-derived chemotaxin 2 (LECT2)-associated amyloidosis is a frequent cause of hepatic amyloidosis in the United States.
Blood
; 123(10): 1479-82, 2014 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24415538
20.
Spatiotemporal phosphoprotein distribution and associated cytokine response of a traumatic injury.
Cytokine
; 79: 12-22, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26702931