Jianhua Mao

Department of Nephrology, Zhejiang University School of Medicine

Affiliated withZhejiang University School of Medicine The Children's Hospital, Zhejiang University School of Medicine

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 4	2023
Publication title Cited by 2	2023

Other Publications

Article	Year
NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome. Pediatric research\| PubMed ID: 17211152	2007
Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis. Archives of dermatological research\| PubMed ID: 17393177	2007
Lack of association between NPHS2 gene polymorphisms and sporadic IgA nephropathy. Nephrology (Carlton, Vic.)\| PubMed ID: 17635752	2007
Sibling cases of Henoch-Schönlein purpura in two families and review of literature. Pediatric dermatology\| PubMed ID: 18577056	2008
Concurrence of Bartter syndrome and minimal change nephrotic syndrome. Chinese medical journal\| PubMed ID: 19781336	2009
Fluid management of hypernatraemic dehydration to prevent cerebral oedema: a retrospective case control study of 97 children in China. Journal of paediatrics and child health\| PubMed ID: 20412412	2010
Clinical outcomes in children with Henoch-Schönlein purpura nephritis grade IIIa or IIIb. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 21387156	2011
[Clinical application of tacrolimus with low-dose prednisone in 21 children with steroid-resistant nephrotic syndrome]. Zhonghua er ke za zhi = Chinese journal of pediatrics\| PubMed ID: 22336304	2011
Treatment of tacrolimus or cyclosporine A in children with idiopathic nephrotic syndrome. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 22714672	2012
Rituximab followed by mycophenolate mofetil in children with IgM nephropathy. Indian pediatrics\| PubMed ID: 23144102	2012
[Management of fungal pyelonephritis with percutaneous pyelostomy in infants]. Zhonghua er ke za zhi = Chinese journal of pediatrics\| PubMed ID: 23324153	2012
Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis. World journal of pediatrics : WJP\| PubMed ID: 23677832	2013
Myo1e impairment results in actin reorganization, podocyte dysfunction, and proteinuria in zebrafish and cultured podocytes. PloS one\| PubMed ID: 23977349	2013
[Acute kidney injury induced by favism in children: a case report]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi\| PubMed ID: 23978025	2013
Overexpression of Myo1e in mouse podocytes enhances cellular endocytosis, migration, and adhesion. Journal of cellular biochemistry\| PubMed ID: 24339252	2014
Efficacy of triptolide for children with moderately severe Henoch-Schönlein purpura nephritis presenting with nephrotic range proteinuria: a prospective and controlled study in China. BioMed research international\| PubMed ID: 24455682	2013
Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review. BMC pediatrics\| PubMed ID: 24628802	2014
Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 25034499	2015
Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing. Nephrology (Carlton, Vic.)\| PubMed ID: 25312783	2015
Relationship between immune parameters and organ involvement in children with Henoch-Schonlein purpura. PloS one\| PubMed ID: 25514176	2014
Henoch-Schönlein purpura nephritis in children: incidence, pathogenesis and management. World journal of pediatrics : WJP\| PubMed ID: 25557596	2015
Clinical characteristics of concomitant nephrotic IgA nephropathy and minimal change disease in children. Nephron\| PubMed ID: 25924689	2015
24h Urinary Protein Levels and Urine Protein/Creatinine Ratios Could Probably Forecast the Pathological Classification of HSPN. PloS one\| PubMed ID: 25996387	2015
Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome. Nephrology (Carlton, Vic.)\| PubMed ID: 26697959	2016
The etiology of congenital nephrotic syndrome: current status and challenges. World journal of pediatrics : WJP\| PubMed ID: 26961288	2016
The Value of Monitoring the Serum Concentration of Mycophenolate Mofetil in Children with Steroid-Dependent/Frequent Relapsing Nephrotic Syndrome. Nephron\| PubMed ID: 26991496	2016
Frosted Branch Angiitis in Pediatric Dyskeratosis Congenita: A Case Report. Medicine\| PubMed ID: 27015183	2016
Clinical Value of Assessing Cytokine Levels for the Differential Diagnosis of Bacterial Meningitis in a Pediatric Population. Medicine\| PubMed ID: 27043692	2016
Huaiqihuang may protect from proteinuria by resisting MPC5 podocyte damage via targeting p-ERK/CHOP pathway. Bosnian journal of basic medical sciences\| PubMed ID: 27186971	2016
Haze is an important medium for the spread of rotavirus. Environmental pollution (Barking, Essex : 1987)\| PubMed ID: 27289527	2016
Haze is a risk factor contributing to the rapid spread of respiratory syncytial virus in children. Environmental science and pollution research international\| PubMed ID: 27439752	2016
Clinical features and outcomes of diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis in children. Clinics (Sao Paulo, Brazil)\| PubMed ID: 27652838	2016
Dysregulation of calcium channels decreases parasecretion in pancreatic β-cells in rats born small for gestational age. Growth factors (Chur, Switzerland)\| PubMed ID: 27681688	2016
Molecular epidemiological study of enteroviruses associated with encephalitis in children from Hangzhou, China. Medicine\| PubMed ID: 27749541	2016
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 28204945	2017
Evaluation of TGF-β1 and MCP-1 expression and tubulointerstitial fibrosis in children with Henoch-Schönlein purpura nephritis and IgA nephropathy: A clinical correlation. Clinics (Sao Paulo, Brazil)\| PubMed ID: 28273242	2017
Clinical characteristics of children with hemolytic uremic syndrome in Hangzhou, China. World journal of pediatrics : WJP\| PubMed ID: 28353273	2017
Evaluation of Mycophenolate Mofetil and Low-Dose Steroid Combined Therapy in Moderately Severe Henoch-Schönlein Purpura Nephritis. Medical science monitor : international medical journal of experimental and clinical research\| PubMed ID: 28515415	2017
Association between red blood cell distribution width and Henoch-Schonlein purpura nephritis. Medicine\| PubMed ID: 28591051	2017
Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress. Molecular medicine reports\| PubMed ID: 28627684	2017
Encephalopathy in Henoch-Schönlein Purpura. Indian pediatrics\| PubMed ID: 28891482	2017
Association of TLR4 gene polymorphisms with childhood Henoch-Schönlein purpura in a Chinese population. Rheumatology international\| PubMed ID: 28905155	2017
The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children. Clinical rheumatology\| PubMed ID: 28963667	2017
Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review. Medicine\| PubMed ID: 29382012	2017
Calcineurin inhibitors and nephrotoxicity in children. World journal of pediatrics : WJP\| PubMed ID: 29532435	2018
Mycoplasma pneumoniae induces allergy by producing P1-specific immunoglobulin E. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology\| PubMed ID: 29555351	2018
The status quo and challenges of genetic diagnosis in children with steroid-resistant nephrotic syndrome. World journal of pediatrics : WJP\| PubMed ID: 29644498	2018
Tempol Protects Against Acute Renal Injury by Regulating PI3K/Akt/mTOR and GSK3β Signaling Cascades and Afferent Arteriolar Activity. Kidney & blood pressure research\| PubMed ID: 29870982	2018
Enhanced Renal Afferent Arteriolar Reactive Oxygen Species and Contractility to Endothelin-1 Are Associated with Canonical Wnt Signaling in Diabetic Mice. Kidney & blood pressure research\| PubMed ID: 29870994	2018
Early prediction of acute kidney injury in children: known biomarkers but novel combination. World journal of pediatrics : WJP\| PubMed ID: 30112669	2018
Platelet integrin αIIbβ3: signal transduction, regulation, and its therapeutic targeting. Journal of hematology & oncology\| PubMed ID: 30845955	2019
Relationships of Cadmium, Lead, and Mercury Levels With Albuminuria in US Adults: Results From the National Health and Nutrition Examination Survey Database, 2009-2012. American journal of epidemiology\| PubMed ID: 30874715	2019
An imbalance of T cell subgroups exists in children with sepsis. Microbes and infection\| PubMed ID: 31009807	2019
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system. Clinical genetics\| PubMed ID: 31328266	2019
Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice. Cell communication and signaling : CCS\| PubMed ID: 31387591	2019
Impact of and polymorphisms on tacrolimus exposure and response in pediatric primary nephrotic syndrome. Pharmacogenomics\| PubMed ID: 31588879	2019
Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease. Clinical genetics\| PubMed ID: 31674016	2020
Haze facilitates sensitization to house dust mites in children. Environmental geochemistry and health\| PubMed ID: 31858358	2020
Population pharmacokinetic study of tacrolimus in pediatric patients with primary nephrotic syndrome: A comparison of linear and nonlinear Michaelis-Menten pharmacokinetic model. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences\| PubMed ID: 31862313	2020
[Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families]. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences\| PubMed ID: 31901041	2019
Clinical features and genetic findings in Chinese children with distal renal tubular acidosis. International journal of clinical and experimental pathology\| PubMed ID: 31949730	2018
Overexpression of Myo1e promotes albumin endocytosis by mouse glomerular podocytes mediated by Dynamin. PeerJ\| PubMed ID: 32211226	2020
Epidemiological analysis of COVID-19 and practical experience from China. Journal of medical virology\| PubMed ID: 32237160	2020
Dent disease: classification, heterogeneity and diagnosis. World journal of pediatrics : WJP\| PubMed ID: 32248351	2021
The pathogenesis and treatment of the `Cytokine Storm' in COVID-19. The Journal of infection\| PubMed ID: 32283152	2020
Severe vaso-occlusive lupus retinopathy in the early stage of a pediatric patient with systemic lupus erythematosus: a case report. Medicine\| PubMed ID: 32312013	2020
Non-apoptotic cell death induced by opening the large conductance mechanosensitive channel MscL in hepatocellular carcinoma HepG2 cells. Biomaterials\| PubMed ID: 32361391	2020
[Principles and suggestions on biosafety protection of biological specimen preservation during prevalence of COVID-19]. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences\| PubMed ID: 32391660	2020
Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq). BMC nephrology\| PubMed ID: 32393202	2020
IPDN-China promotes the development of pediatric dialysis in China. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 32529322	2020
Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review. BMC pediatrics\| PubMed ID: 32616040	2020
Crosstalk between coronavirus disease 2019 and cardiovascular disease and its treatment. ESC heart failure\| PubMed ID: 32935928	2020
Clinically applicable 53-Gene prognostic assay predicts chemotherapy benefit in gastric cancer: A multicenter study. EBioMedicine\| PubMed ID: 33069062	2020
The Roles of Base Modifications in Kidney Cancer. Frontiers in oncology\| PubMed ID: 33282735	2020
SARS-CoV-2 effects on the renin-angiotensin-aldosterone system, therapeutic implications. Acta physiologica (Oxford, England)\| PubMed ID: 33350096	2021
Clinical and genetic characteristics of concomitant Mucopolysaccharidosis type IVA and neurogenic bladder in children: two case reports and literature review. BMC pediatrics\| PubMed ID: 33407246	2021
Multiple bladder diverticula with Williams-Beuren syndrome: a case report. Translational pediatrics\| PubMed ID: 33457309	2020
Host genetics and gut microbiota cooperatively contribute to azoxymethane-induced acute toxicity in Collaborative Cross mice. Archives of toxicology\| PubMed ID: 33458792	2021
CT and MRI imaging analysis of nontuberculous mycobacterium infection in bone and joint. Minerva medica\| PubMed ID: 33576200	2022
Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1. Acta physiologica (Oxford, England)\| PubMed ID: 33615732	2021
Glomerular podocyte dysfunction in inherited renal tubular disease. World journal of pediatrics : WJP\| PubMed ID: 33625696	2021
Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough? Journal of the American Society of Nephrology : JASN\| PubMed ID: 33649100	2021
Immunopathogenesis of idiopathic nephrotic syndrome in children: two sides of the coin. World journal of pediatrics : WJP\| PubMed ID: 33660135	2021
Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome. Frontiers in pediatrics\| PubMed ID: 33996672	2021
Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report. The Journal of international medical research\| PubMed ID: 34039074	2021
Efficacy and safety of Huaiqihuang granule as adjuvant treatment for primary nephrotic syndrome in children: a meta-analysis and systematic review. World journal of pediatrics : WJP\| PubMed ID: 34075551	2021
The immune cell landscape of peripheral blood mononuclear cells from PNS patients. Scientific reports\| PubMed ID: 34158604	2021
DNA demethylase Tet2 suppresses cisplatin-induced acute kidney injury. Cell death discovery\| PubMed ID: 34226503	2021
Correlation between infections with different glycoprotein H genotypes of human cytomegalovirus in children and hepatitis. Pediatrics and neonatology\| PubMed ID: 34348886	2021
Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease. Stem cell research\| PubMed ID: 34365103	2021
Renoprotection with sodium-glucose cotransporter-2 inhibitors in children: Knowns and unknowns. Nephrology (Carlton, Vic.)\| PubMed ID: 34545979	2022
Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 ge... Stem cell research\| PubMed ID: 34547705	2021
Coronavirus disease 2019 vaccine for children in China: when to start? Mandatory or voluntary? Chinese medical journal\| PubMed ID: 34561329	2021
Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies. Clinical immunology (Orlando, Fla.)\| PubMed ID: 34600127	2021
Tolvaptan in Pediatric Autosomal Dominant Polycystic Kidney Disease: From Here to Where? Kidney diseases (Basel, Switzerland)\| PubMed ID: 34604341	2021
PP2A protects podocytes against Adriamycin-induced injury and epithelial-to-mesenchymal transition via suppressing JIP4/p38-MAPK pathway. Cytotechnology\| PubMed ID: 34629746	2021
Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report. Children (Basel, Switzerland)\| PubMed ID: 34682152	2021
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort. BMC medical genomics\| PubMed ID: 34696790	2021
New-onset and relapsing glomerular diseases related to COVID-19 vaccination. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences\| PubMed ID: 34704408	2021
Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study. World journal of pediatrics : WJP\| PubMed ID: 34716893	2021
Rotavirus and adenovirus infections in children during COVID-19 outbreak in Hangzhou, China. Translational pediatrics\| PubMed ID: 34733668	2021
The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome. Annals of translational medicine\| PubMed ID: 34734004	2021
Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in and . Frontiers in medicine\| PubMed ID: 34778325	2021
Genetic Variations and Clinical Features of -Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study. Frontiers in medicine\| PubMed ID: 34859019	2021
Mosaic in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes. Frontiers in medicine\| PubMed ID: 34977057	2021
rhADAMTS13 reduces oxidative stress by cleaving VWF in ischaemia/reperfusion-induced acute kidney injury. Acta physiologica (Oxford, England)\| PubMed ID: 34989474	2022
Incident changes in the prevalence of respiratory virus among children during COVID-19 pandemic in Hangzhou, China. The Journal of infection\| PubMed ID: 35016902	2022
Booster vaccination strategy: Necessity, immunization objectives, immunization strategy, and safety. Journal of medical virology\| PubMed ID: 35028946	2022
Hyperuricemia and Associated Factors in Children with Chronic Kidney Disease: A Cross-Sectional Study. Children (Basel, Switzerland)\| PubMed ID: 35053631	2021
Autoimmune Podocytopathies: A Novel Sub-Group of Diseases from Childhood Idiopathic Nephrotic Syndrome. Journal of the American Society of Nephrology : JASN\| PubMed ID: 35064050	2022
Impact of Sampling Time Variability on Tacrolimus Dosage Regimen in Pediatric Primary Nephrotic Syndrome: Single-Center, Prospective, Observational Study. Frontiers in pharmacology\| PubMed ID: 35069185	2021
Recent advances and clinical application in point-of-care testing of SARS-CoV-2. Journal of medical virology\| PubMed ID: 35080017	2022
Application experience of a rapid nucleic acid detection system for COVID-19. Microbes and infection\| PubMed ID: 35093551	2022
Urinary Sediment mRNA Level of CREBBP and CYBA in Children With Steroid-Resistant Nephrotic Syndrome. Frontiers in immunology\| PubMed ID: 35173708	2021
Renoprotective Role of Hypoxia-Inducible Factors and the Mechanism. Kidney diseases (Basel, Switzerland)\| PubMed ID: 35224006	2022
Circular RNA circDVL1 inhibits clear cell renal cell carcinoma progression through the miR-412-3p/PCDH7 axis. International journal of biological sciences\| PubMed ID: 35280687	2022
Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome. Iranian journal of immunology : IJI\| PubMed ID: 35293350	2022
Strategies and safety considerations of booster vaccination in COVID-19. Bosnian journal of basic medical sciences\| PubMed ID: 35366790	2022
Multiplex detection of eight different viral enteropathogens in clinical samples, combining RT-PCR technology with melting curve analysis. Virology journal\| PubMed ID: 35392937	2022
Epithelial-mesenchymal transition in organ fibrosis development: current understanding and treatment strategies. Burns & trauma\| PubMed ID: 35402628	2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia. JCI insight\| PubMed ID: 35472031	2022
Identification of a 12-Gene Signature and Hub Genes Involved in Kidney Wilms Tumor Integrated Bioinformatics Analysis. Frontiers in oncology\| PubMed ID: 35480093	2022
Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients. Frontiers in genetics\| PubMed ID: 35559039	2022
Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy. Neurobiology of disease\| PubMed ID: 35568100	2022
Evaluation of a Novel Simulation Curriculum With the Segmented Model in Pediatric Cardiovascular Education. Frontiers in public health\| PubMed ID: 35669747	2022
A critical role of the podocyte cytoskeleton in the pathogenesis of glomerular proteinuria and autoimmune podocytopathies. Acta physiologica (Oxford, England)\| PubMed ID: 35716094	2022
The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study. Frontiers in medicine\| PubMed ID: 35755072	2022
A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells. STAR protocols\| PubMed ID: 35834385	2022
Management of multiple magnetic foreign body ingestion in pediatric patients. BMC pediatrics\| PubMed ID: 35879696	2022
Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review. Frontiers in pediatrics\| PubMed ID: 35899130	2022
Robot-Assisted Resection of Intestinal Duplication in Children. Journal of laparoendoscopic & advanced surgical techniques. Part A\| PubMed ID: 35904972	2022
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations. Genetics research\| PubMed ID: 35919034	2022
Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population. Laboratory medicine\| PubMed ID: 35964233	2023
Vasculitis after COVID-19 Vaccination. Current rheumatology reviews\| PubMed ID: 35980076	2023
Pediatric membranous nephropathy: In the novel antigens era. Frontiers in immunology\| PubMed ID: 36016931	2022
The interaction between cellular senescence and chronic kidney disease as a therapeutic opportunity. Frontiers in pharmacology\| PubMed ID: 36091755	2022
Corrigendum: Impact of sampling time variability on tacrolimus dosage regimen in pediatric primary nephrotic syndrome: Single-center, prospective, observational study. Frontiers in pharmacology\| PubMed ID: 36313378	2022
Integrated analysis of immune- and apoptosis-related lncRNA-miRNA-mRNA regulatory network in children with Henoch Schönlein purpura nephritis. Translational pediatrics\| PubMed ID: 36345450	2022
Nonpharmaceutical interventions for COVID-19 disrupt the dynamic balance between influenza A virus and human immunity. Journal of medical virology\| PubMed ID: 36367115	2023
Glomerular diseases after immune checkpoint inhibitors use: What do We know so far? Renal failure\| PubMed ID: 36420664	2022
COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients. Vaccines\| PubMed ID: 36423007	2022
T-cell and B-cell repertoire diversity are selectively skewed in children with idiopathic nephrotic syndrome revealed by high-throughput sequencing. World journal of pediatrics : WJP\| PubMed ID: 36449136	2023
Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy. Kidney international reports\| PubMed ID: 36506238	2022
Serum IL-12p40: A novel biomarker for early prediction of minimal change disease relapse following glucocorticoids therapy. Frontiers in medicine\| PubMed ID: 36507530	2022
Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review. Frontiers in pediatrics\| PubMed ID: 36523395	2022
Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation. Pediatric research\| PubMed ID: 36539574	2023
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association\| PubMed ID: 36549658	2022
Benefits and risks of essential trace elements in chronic kidney disease: a narrative review. Annals of translational medicine\| PubMed ID: 36660676	2022
Lumasiran for primary hyperoxaluria type 1: What we have learned? Frontiers in pediatrics\| PubMed ID: 36704142	2022
Advances in imaging techniques to assess kidney fibrosis. Renal failure\| PubMed ID: 36723057	2023
Roxadustat: Do we know all the answers? Biomolecules & biomedicine\| PubMed ID: 36724056	2023
Comprehensive mapping of B lymphocyte immune dysfunction in idiopathic nephrotic syndrome children. Clinical and translational medicine\| PubMed ID: 36740447	2023
Cysteine Pathogenic Variants of PMM2 Are Sensitive to Environmental Stress with Loss of Structural Stability. Oxidative medicine and cellular longevity\| PubMed ID: 36743691	2023
Association between social supports and negative emotions among pediatric residents in China: The chain-mediating role of psychological resilience and burnout. Frontiers in public health\| PubMed ID: 36755738	2022
Prominent Staining of MYCN Immunohistochemistry Predicts a Poor Prognosis in Non-Amplified Neuroblastoma. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society\| PubMed ID: 36775958	2023
Machine learning models for predicting steroid-resistant of nephrotic syndrome. Frontiers in immunology\| PubMed ID: 36776850	2023
Structure, signal transduction, activation, and inhibition of integrin αIIbβ3. Thrombosis journal\| PubMed ID: 36782235	2023
Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome. European journal of clinical investigation\| PubMed ID: 36856027	2023
A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients. Clinical immunology (Orlando, Fla.)\| PubMed ID: 36863601	2023
Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy. Pediatric research\| PubMed ID: 36864281	2023
Multiple functions of stress granules in viral infection at a glance. Frontiers in microbiology\| PubMed ID: 36937261	2023
Genetic Architecture of Childhood Kidney and Urological Diseases in China. Phenomics (Cham, Switzerland)\| PubMed ID: 36939782	2021
Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis. Clinical journal of the American Society of Nephrology : CJASN\| PubMed ID: 37099456	2023
Correlation between Toll-like Receptor Gene Polymorphisms and Idiopathic Nephrotic Syndrome in Chinese Children. Current medical science\| PubMed ID: 37115397	2023
A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome. MedComm\| PubMed ID: 37180824	2023
Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with N215S mutation: Case report and literature review. Heliyon\| PubMed ID: 37205992	2023
Dihydromyricetin attenuates cisplatin-induced acute kidney injury by reducing oxidative stress, inflammation and ferroptosis. Toxicology and applied pharmacology\| PubMed ID: 37328118	2023
A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations. Vaccines\| PubMed ID: 37376434	2023
Low skeletal muscle mass as an early sign in children with fabry disease. Orphanet journal of rare diseases\| PubMed ID: 37480128	2023
Cysteine mutations impair the structural stability of phosphomannomutase 2 (PMM2) in glycosylation-associated metabolic disorders. Genes & diseases\| PubMed ID: 37492729	2023
Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1. iScience\| PubMed ID: 37599822	2023
Rapid detection of telomerase expression of neuroblastoma in paraffin-embedded tissue: combination of in situ hybridisation and quantitative PCR. Pathology\| PubMed ID: 37741703	2023