Detalhe da pesquisa
1.
Artificial intelligence-assisted quantification and assessment of whole slide images for pediatric kidney disease diagnosis.
Bioinformatics
; 40(1)2024 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38058211
2.
Are children with IgA nephropathy different from adult patients?
Pediatr Nephrol
; 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38578470
3.
Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy.
Pediatr Res
; 94(2): 747-755, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36864281
4.
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Kidney Int
; 102(3): 604-612, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35643375
5.
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Kidney Int
; 102(3): 592-603, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35483523
6.
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with OCRL Mutations.
Genet Res (Camb)
; 2022: 1473260, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35919034
7.
New-onset and relapsing glomerular diseases related to COVID-19 vaccination.
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 50(4): 524-528, 2021 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34704408
8.
Epigenetic modifier trichostatin A enhanced osteogenic differentiation of mesenchymal stem cells by inhibiting NF-κB (p65) DNA binding and promoted periodontal repair in rats.
J Cell Physiol
; 235(12): 9691-9701, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32399963
9.
Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.
BMC Pediatr
; 20(1): 327, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32616040
10.
Fat mass and obesity-associated (FTO) protein regulates adult neurogenesis.
Hum Mol Genet
; 26(13): 2398-2411, 2017 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28398475
11.
Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.
BMC Pediatr
; 14: 73, 2014 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24628802
12.
Role of mitochondrial dysfunction in kidney disease: Insights from the cGAS-STING signaling pathway.
Chin Med J (Engl)
; 137(9): 1044-1053, 2024 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38445370
13.
A Child With Concomitant Neuroblastoma and IgA Nephropathy: A Case Report and Literature Review.
Cureus
; 16(5): e60089, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38736768
14.
Artificial intelligence in renal pathology: Current status and future.
Biomol Biomed
; 23(2): 225-234, 2023 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36378066
15.
Rapid detection of telomerase expression of neuroblastoma in paraffin-embedded tissue: combination of in situ hybridisation and quantitative PCR.
Pathology
; 55(7): 958-965, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37741703
16.
Tolvaptan in Pediatric Autosomal Dominant Polycystic Kidney Disease: From Here to Where?
Kidney Dis (Basel)
; 7(5): 343-349, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34604341
17.
Primary IgA nephropathy with nephrotic-range proteinuria in Chinese children.
Medicine (Baltimore)
; 100(21): e26050, 2021 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34032732
18.
Case Report: Membranoproliferative Glomerulonephritis, a Rare Clinical Manifestation of Abernethy Malformation Type II.
Front Pediatr
; 9: 647364, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33816407
19.
Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.
Front Pediatr
; 9: 544925, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33996672
20.
The important roles and molecular mechanisms of annexin A2 autoantibody in children with nephrotic syndrome.
Ann Transl Med
; 9(18): 1452, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34734004