Jianhua Mao

NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.

Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis.

Lack of association between NPHS2 gene polymorphisms and sporadic IgA nephropathy.

Sibling cases of Henoch-Schönlein purpura in two families and review of literature.

Concurrence of Bartter syndrome and minimal change nephrotic syndrome.

Fluid management of hypernatraemic dehydration to prevent cerebral oedema: a retrospective case control study of 97 children in China.

Clinical outcomes in children with Henoch-Schönlein purpura nephritis grade IIIa or IIIb.

[Clinical application of tacrolimus with low-dose prednisone in 21 children with steroid-resistant nephrotic syndrome].

Treatment of tacrolimus or cyclosporine A in children with idiopathic nephrotic syndrome.

Rituximab followed by mycophenolate mofetil in children with IgM nephropathy.

[Management of fungal pyelonephritis with percutaneous pyelostomy in infants].

Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis.

Myo1e impairment results in actin reorganization, podocyte dysfunction, and proteinuria in zebrafish and cultured podocytes.

[Acute kidney injury induced by favism in children: a case report].

Overexpression of Myo1e in mouse podocytes enhances cellular endocytosis, migration, and adhesion.

Efficacy of triptolide for children with moderately severe Henoch-Schönlein purpura nephritis presenting with nephrotic range proteinuria: a prospective and controlled study in China.

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.

Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children.

Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing.

Relationship between immune parameters and organ involvement in children with Henoch-Schonlein purpura.

Henoch-Schönlein purpura nephritis in children: incidence, pathogenesis and management.

Clinical characteristics of concomitant nephrotic IgA nephropathy and minimal change disease in children.

24h Urinary Protein Levels and Urine Protein/Creatinine Ratios Could Probably Forecast the Pathological Classification of HSPN.

Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome.

The etiology of congenital nephrotic syndrome: current status and challenges.

The Value of Monitoring the Serum Concentration of Mycophenolate Mofetil in Children with Steroid-Dependent/Frequent Relapsing Nephrotic Syndrome.

Frosted Branch Angiitis in Pediatric Dyskeratosis Congenita: A Case Report.

Clinical Value of Assessing Cytokine Levels for the Differential Diagnosis of Bacterial Meningitis in a Pediatric Population.

Huaiqihuang may protect from proteinuria by resisting MPC5 podocyte damage via targeting p-ERK/CHOP pathway.

Haze is an important medium for the spread of rotavirus.

Haze is a risk factor contributing to the rapid spread of respiratory syncytial virus in children.

Clinical features and outcomes of diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis in children.

Dysregulation of calcium channels decreases parasecretion in pancreatic β-cells in rats born small for gestational age.

Molecular epidemiological study of enteroviruses associated with encephalitis in children from Hangzhou, China.

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.

Evaluation of TGF-β1 and MCP-1 expression and tubulointerstitial fibrosis in children with Henoch-Schönlein purpura nephritis and IgA nephropathy: A clinical correlation.

Clinical characteristics of children with hemolytic uremic syndrome in Hangzhou, China.

Evaluation of Mycophenolate Mofetil and Low-Dose Steroid Combined Therapy in Moderately Severe Henoch-Schönlein Purpura Nephritis.

Association between red blood cell distribution width and Henoch-Schonlein purpura nephritis.

Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress.

Encephalopathy in Henoch-Schönlein Purpura.

Association of TLR4 gene polymorphisms with childhood Henoch-Schönlein purpura in a Chinese population.

The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children.

Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.

Calcineurin inhibitors and nephrotoxicity in children.

Mycoplasma pneumoniae induces allergy by producing P1-specific immunoglobulin E.

The status quo and challenges of genetic diagnosis in children with steroid-resistant nephrotic syndrome.

Tempol Protects Against Acute Renal Injury by Regulating PI3K/Akt/mTOR and GSK3β Signaling Cascades and Afferent Arteriolar Activity.

Enhanced Renal Afferent Arteriolar Reactive Oxygen Species and Contractility to Endothelin-1 Are Associated with Canonical Wnt Signaling in Diabetic Mice.

Early prediction of acute kidney injury in children: known biomarkers but novel combination.

Platelet integrin αIIbβ3: signal transduction, regulation, and its therapeutic targeting.

Relationships of Cadmium, Lead, and Mercury Levels With Albuminuria in US Adults: Results From the National Health and Nutrition Examination Survey Database, 2009-2012.

An imbalance of T cell subgroups exists in children with sepsis.

Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.

Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice.

Impact of and polymorphisms on tacrolimus exposure and response in pediatric primary nephrotic syndrome.

Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.

Haze facilitates sensitization to house dust mites in children.

Population pharmacokinetic study of tacrolimus in pediatric patients with primary nephrotic syndrome: A comparison of linear and nonlinear Michaelis-Menten pharmacokinetic model.

[Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families].

Clinical features and genetic findings in Chinese children with distal renal tubular acidosis.

Overexpression of Myo1e promotes albumin endocytosis by mouse glomerular podocytes mediated by Dynamin.

Epidemiological analysis of COVID-19 and practical experience from China.

Dent disease: classification, heterogeneity and diagnosis.

The pathogenesis and treatment of the `Cytokine Storm' in COVID-19.

Severe vaso-occlusive lupus retinopathy in the early stage of a pediatric patient with systemic lupus erythematosus: a case report.

Non-apoptotic cell death induced by opening the large conductance mechanosensitive channel MscL in hepatocellular carcinoma HepG2 cells.

[Principles and suggestions on biosafety protection of biological specimen preservation during prevalence of COVID-19].

Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).

IPDN-China promotes the development of pediatric dialysis in China.

Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.

Crosstalk between coronavirus disease 2019 and cardiovascular disease and its treatment.

Clinically applicable 53-Gene prognostic assay predicts chemotherapy benefit in gastric cancer: A multicenter study.

The Roles of Base Modifications in Kidney Cancer.

SARS-CoV-2 effects on the renin-angiotensin-aldosterone system, therapeutic implications.

Clinical and genetic characteristics of concomitant Mucopolysaccharidosis type IVA and neurogenic bladder in children: two case reports and literature review.

Multiple bladder diverticula with Williams-Beuren syndrome: a case report.

Host genetics and gut microbiota cooperatively contribute to azoxymethane-induced acute toxicity in Collaborative Cross mice.

CT and MRI imaging analysis of nontuberculous mycobacterium infection in bone and joint.

Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1.

Glomerular podocyte dysfunction in inherited renal tubular disease.

Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough?

Immunopathogenesis of idiopathic nephrotic syndrome in children: two sides of the coin.

Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.

Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report.

Efficacy and safety of Huaiqihuang granule as adjuvant treatment for primary nephrotic syndrome in children: a meta-analysis and systematic review.

The immune cell landscape of peripheral blood mononuclear cells from PNS patients.

DNA demethylase Tet2 suppresses cisplatin-induced acute kidney injury.

Correlation between infections with different glycoprotein H genotypes of human cytomegalovirus in children and hepatitis.

Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease.

Renoprotection with sodium-glucose cotransporter-2 inhibitors in children: Knowns and unknowns.

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 gene.

Coronavirus disease 2019 vaccine for children in China: when to start? Mandatory or voluntary?

Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies.

Tolvaptan in Pediatric Autosomal Dominant Polycystic Kidney Disease: From Here to Where?

PP2A protects podocytes against Adriamycin-induced injury and epithelial-to-mesenchymal transition via suppressing JIP4/p38-MAPK pathway.

Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.

Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.

New-onset and relapsing glomerular diseases related to COVID-19 vaccination.

Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study.

Rotavirus and adenovirus infections in children during COVID-19 outbreak in Hangzhou, China.

The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome.

Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in and .

Genetic Variations and Clinical Features of -Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study.

Mosaic in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.

rhADAMTS13 reduces oxidative stress by cleaving VWF in ischaemia/reperfusion-induced acute kidney injury.

Incident changes in the prevalence of respiratory virus among children during COVID-19 pandemic in Hangzhou, China.

Booster vaccination strategy: Necessity, immunization objectives, immunization strategy, and safety.

Hyperuricemia and Associated Factors in Children with Chronic Kidney Disease: A Cross-Sectional Study.

Autoimmune Podocytopathies: A Novel Sub-Group of Diseases from Childhood Idiopathic Nephrotic Syndrome.

Impact of Sampling Time Variability on Tacrolimus Dosage Regimen in Pediatric Primary Nephrotic Syndrome: Single-Center, Prospective, Observational Study.

Recent advances and clinical application in point-of-care testing of SARS-CoV-2.

Application experience of a rapid nucleic acid detection system for COVID-19.

Urinary Sediment mRNA Level of CREBBP and CYBA in Children With Steroid-Resistant Nephrotic Syndrome.

Renoprotective Role of Hypoxia-Inducible Factors and the Mechanism.

Circular RNA circDVL1 inhibits clear cell renal cell carcinoma progression through the miR-412-3p/PCDH7 axis.

Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome.

Strategies and safety considerations of booster vaccination in COVID-19.

Multiplex detection of eight different viral enteropathogens in clinical samples, combining RT-PCR technology with melting curve analysis.

Epithelial-mesenchymal transition in organ fibrosis development: current understanding and treatment strategies.

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Identification of a 12-Gene Signature and Hub Genes Involved in Kidney Wilms Tumor Integrated Bioinformatics Analysis.

Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients.

Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy.

Evaluation of a Novel Simulation Curriculum With the Segmented Model in Pediatric Cardiovascular Education.

A critical role of the podocyte cytoskeleton in the pathogenesis of glomerular proteinuria and autoimmune podocytopathies.

The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study.

A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells.

Management of multiple magnetic foreign body ingestion in pediatric patients.

Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review.

Robot-Assisted Resection of Intestinal Duplication in Children.

Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations.

Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.

Vasculitis after COVID-19 Vaccination.

Pediatric membranous nephropathy: In the novel antigens era.

The interaction between cellular senescence and chronic kidney disease as a therapeutic opportunity.

Corrigendum: Impact of sampling time variability on tacrolimus dosage regimen in pediatric primary nephrotic syndrome: Single-center, prospective, observational study.

Integrated analysis of immune- and apoptosis-related lncRNA-miRNA-mRNA regulatory network in children with Henoch Schönlein purpura nephritis.

Nonpharmaceutical interventions for COVID-19 disrupt the dynamic balance between influenza A virus and human immunity.

Glomerular diseases after immune checkpoint inhibitors use: What do We know so far?

COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients.

T-cell and B-cell repertoire diversity are selectively skewed in children with idiopathic nephrotic syndrome revealed by high-throughput sequencing.

Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy.

Serum IL-12p40: A novel biomarker for early prediction of minimal change disease relapse following glucocorticoids therapy.

Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review.

Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation.

Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study.

Benefits and risks of essential trace elements in chronic kidney disease: a narrative review.

Lumasiran for primary hyperoxaluria type 1: What we have learned?

Advances in imaging techniques to assess kidney fibrosis.

Roxadustat: Do we know all the answers?

Comprehensive mapping of B lymphocyte immune dysfunction in idiopathic nephrotic syndrome children.

Cysteine Pathogenic Variants of PMM2 Are Sensitive to Environmental Stress with Loss of Structural Stability.

Association between social supports and negative emotions among pediatric residents in China: The chain-mediating role of psychological resilience and burnout.

Prominent Staining of MYCN Immunohistochemistry Predicts a Poor Prognosis in Non-Amplified Neuroblastoma.

Machine learning models for predicting steroid-resistant of nephrotic syndrome.

Structure, signal transduction, activation, and inhibition of integrin αIIbβ3.

Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.

A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients.

Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy.

Multiple functions of stress granules in viral infection at a glance.

Genetic Architecture of Childhood Kidney and Urological Diseases in China.

Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis.

Correlation between Toll-like Receptor Gene Polymorphisms and Idiopathic Nephrotic Syndrome in Chinese Children.

A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome.

Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with N215S mutation: Case report and literature review.

Dihydromyricetin attenuates cisplatin-induced acute kidney injury by reducing oxidative stress, inflammation and ferroptosis.

A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations.

Low skeletal muscle mass as an early sign in children with fabry disease.

Cysteine mutations impair the structural stability of phosphomannomutase 2 (PMM2) in glycosylation-associated metabolic disorders.

Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1.

Rapid detection of telomerase expression of neuroblastoma in paraffin-embedded tissue: combination of in situ hybridisation and quantitative PCR.