Detalles de la búsqueda
1.
Value of the modified semiquantitative classification in predicting outcomes in children with Henoch-Schönlein purpura nephritis.
Nephrology (Carlton)
; 28(9): 495-505, 2023 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-37323118
2.
Clinical manifestations, prognosis, and treat-to-target assessment of pediatric lupus nephritis.
Pediatr Nephrol
; 37(2): 367-376, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34379208
3.
Thromboelastography Detects Possible Coagulation Disturbance in Pediatric Patients with Portal Cavernoma.
Transfus Med Hemother
; 47(2): 135-143, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-32355473
4.
Inflammation Induces Lipid Deposition in Kidneys by Downregulating Renal PCSK9 in Mice with Adriamycin-Induced Nephropathy.
Med Sci Monit
; 25: 5327-5335, 2019 Jul 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-31317882
5.
Indirect-comparison meta-analysis of treatment options for patients with refractory Kawasaki disease.
BMC Pediatr
; 19(1): 158, 2019 05 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31101091
6.
CD36 Promotes Podocyte Apoptosis by Activating the Pyrin Domain-Containing-3 (NLRP3) Inflammasome in Primary Nephrotic Syndrome.
Med Sci Monit
; 24: 6832-6839, 2018 Sep 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-30258045
7.
Endoplasmic reticulum stress participates in inflammation-accelerated, lipid-mediated injury of human glomerular mesangial cells.
Nephrology (Carlton)
; 22(3): 234-242, 2017 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26890338
8.
Comparison of different genetic testing modalities applied in paediatric patients with steroid-resistant nephrotic syndrome.
Ital J Pediatr
; 50(1): 85, 2024 Apr 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-38654395
9.
A genomic association study revealing subphenotypes of childhood steroid-sensitive nephrotic syndrome in a larger genomic sequencing cohort.
Genes Dis
; 11(4): 101126, 2024 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-38560502
10.
Validation of the children international IgA nephropathy prediction tool based on data in Southwest China.
Front Pediatr
; 11: 1183562, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37425278
11.
Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases.
Front Pediatr
; 11: 1183013, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37063683
12.
Molecular characteristics of circulating B cells and kidney cells at the single-cell level in special types of primary membranous nephropathy.
Clin Kidney J
; 16(12): 2639-2651, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-38046035
13.
Cell-type-specific molecular characterization of cells from circulation and kidney in IgA nephropathy with nephrotic syndrome.
Front Immunol
; 14: 1231937, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37908345
14.
Functional urination or defecation disorders may be warning signs of attention-deficit/hyperactivity disorder among children in rural China.
J Affect Disord
; 316: 63-70, 2022 11 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35981625
15.
A novel FOXP3 mutation in a Chinese child with IPEX-associated membranous nephropathy.
Mol Genet Genomic Med
; 10(6): e1945, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35434975
16.
Detection of De Novo PAX2 Variants and Phenotypes in Chinese Population: A Single-Center Study.
Front Genet
; 13: 799562, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35444690
17.
Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases.
Front Pediatr
; 10: 1030191, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36843884
18.
Association between HLA alleles and sub-phenotype of childhood steroid-sensitive nephrotic syndrome.
World J Pediatr
; 18(2): 109-119, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34973118
19.
Psychological research of the children with chronic kidney disease and their guardians during the COVID-19 pandemic.
Front Public Health
; 10: 922678, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36324445
20.
Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome.
Genes Dis
; 9(6): 1662-1673, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-36157477