Department of Nephrology,
The Children's Hospital,
Department of Nephrology, The Children's Hospital
Jianhua Mao has not added Biography.
If you are Jianhua Mao and would like to personalize this page please email our Author Liaison for assistance.
NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.
Pediatric research Jan, 2007 | Pubmed ID: 17211152
Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis.
Archives of dermatological research Jun, 2007 | Pubmed ID: 17393177
Lack of association between NPHS2 gene polymorphisms and sporadic IgA nephropathy.
Nephrology (Carlton, Vic.) Aug, 2007 | Pubmed ID: 17635752
Sibling cases of Henoch-Schönlein purpura in two families and review of literature.
Pediatric dermatology , 2008 | Pubmed ID: 18577056
Concurrence of Bartter syndrome and minimal change nephrotic syndrome.
Chinese medical journal Aug, 2009 | Pubmed ID: 19781336
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 Jun, 2010 | Pubmed ID: 20412412
Clinical outcomes in children with Henoch-Schönlein purpura nephritis grade IIIa or IIIb.
Pediatric nephrology (Berlin, Germany) Jul, 2011 | Pubmed ID: 21387156
[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 Nov, 2011 | Pubmed ID: 22336304
Treatment of tacrolimus or cyclosporine A in children with idiopathic nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) Nov, 2012 | Pubmed ID: 22714672
Rituximab followed by mycophenolate mofetil in children with IgM nephropathy.
Indian pediatrics Oct, 2012 | Pubmed ID: 23144102
[Management of fungal pyelonephritis with percutaneous pyelostomy in infants].
Zhonghua er ke za zhi = Chinese journal of pediatrics Dec, 2012 | Pubmed ID: 23324153
Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis.
World journal of pediatrics : WJP May, 2013 | Pubmed ID: 23677832
Myo1e impairment results in actin reorganization, podocyte dysfunction, and proteinuria in zebrafish and cultured podocytes.
PloS one , 2013 | Pubmed ID: 23977349
[Acute kidney injury induced by favism in children: a case report].
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi Aug, 2013 | Pubmed ID: 23978025
Overexpression of Myo1e in mouse podocytes enhances cellular endocytosis, migration, and adhesion.
Journal of cellular biochemistry Feb, 2014 | Pubmed ID: 24339252
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 , 2013 | Pubmed ID: 24455682
Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.
BMC pediatrics Mar, 2014 | Pubmed ID: 24628802
Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children.
Pediatric nephrology (Berlin, Germany) Feb, 2015 | Pubmed ID: 25034499
Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing.
Nephrology (Carlton, Vic.) Jan, 2015 | Pubmed ID: 25312783
Relationship between immune parameters and organ involvement in children with Henoch-Schonlein purpura.
PloS one , 2014 | Pubmed ID: 25514176
Henoch-Schönlein purpura nephritis in children: incidence, pathogenesis and management.
World journal of pediatrics : WJP Feb, 2015 | Pubmed ID: 25557596
Clinical characteristics of concomitant nephrotic IgA nephropathy and minimal change disease in children.
Nephron , 2015 | Pubmed ID: 25924689
24h Urinary Protein Levels and Urine Protein/Creatinine Ratios Could Probably Forecast the Pathological Classification of HSPN.
PloS one , 2015 | Pubmed ID: 25996387
Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome.
Nephrology (Carlton, Vic.) Jan, 2016 | Pubmed ID: 26697959
The etiology of congenital nephrotic syndrome: current status and challenges.
World journal of pediatrics : WJP May, 2016 | Pubmed ID: 26961288
The Value of Monitoring the Serum Concentration of Mycophenolate Mofetil in Children with Steroid-Dependent/Frequent Relapsing Nephrotic Syndrome.
Nephron , 2016 | Pubmed ID: 26991496
Frosted Branch Angiitis in Pediatric Dyskeratosis Congenita: A Case Report.
Medicine Mar, 2016 | Pubmed ID: 27015183
Clinical Value of Assessing Cytokine Levels for the Differential Diagnosis of Bacterial Meningitis in a Pediatric Population.
Medicine Mar, 2016 | Pubmed ID: 27043692
Huaiqihuang may protect from proteinuria by resisting MPC5 podocyte damage via targeting p-ERK/CHOP pathway.
Bosnian journal of basic medical sciences Aug, 2016 | Pubmed ID: 27186971
Haze is an important medium for the spread of rotavirus.
Environmental pollution (Barking, Essex : 1987) Sep, 2016 | Pubmed ID: 27289527
Haze is a risk factor contributing to the rapid spread of respiratory syncytial virus in children.
Environmental science and pollution research international Oct, 2016 | Pubmed ID: 27439752
Clinical features and outcomes of diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis in children.
Clinics (Sao Paulo, Brazil) Sep, 2016 | Pubmed ID: 27652838
Dysregulation of calcium channels decreases parasecretion in pancreatic β-cells in rats born small for gestational age.
Growth factors (Chur, Switzerland) Dec, 2016 | Pubmed ID: 27681688
Molecular epidemiological study of enteroviruses associated with encephalitis in children from Hangzhou, China.
Medicine Oct, 2016 | Pubmed ID: 27749541
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) Jul, 2017 | Pubmed ID: 28204945
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) Feb, 2017 | Pubmed ID: 28273242
Clinical characteristics of children with hemolytic uremic syndrome in Hangzhou, China.
World journal of pediatrics : WJP Apr, 2017 | Pubmed ID: 28353273
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 May, 2017 | Pubmed ID: 28515415
Association between red blood cell distribution width and Henoch-Schonlein purpura nephritis.
Medicine Jun, 2017 | Pubmed ID: 28591051
Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress.
Molecular medicine reports Aug, 2017 | Pubmed ID: 28627684
Encephalopathy in Henoch-Schönlein Purpura.
Indian pediatrics Aug, 2017 | Pubmed ID: 28891482
Association of TLR4 gene polymorphisms with childhood Henoch-Schönlein purpura in a Chinese population.
Rheumatology international Nov, 2017 | Pubmed ID: 28905155
The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children.
Clinical rheumatology Dec, 2017 | Pubmed ID: 28963667
Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.
Medicine Nov, 2017 | Pubmed ID: 29382012
Calcineurin inhibitors and nephrotoxicity in children.
World journal of pediatrics : WJP Apr, 2018 | Pubmed ID: 29532435
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 07, 2018 | Pubmed ID: 29555351
The status quo and challenges of genetic diagnosis in children with steroid-resistant nephrotic syndrome.
World journal of pediatrics : WJP Apr, 2018 | Pubmed ID: 29644498
Tempol Protects Against Acute Renal Injury by Regulating PI3K/Akt/mTOR and GSK3β Signaling Cascades and Afferent Arteriolar Activity.
Kidney & blood pressure research , 2018 | Pubmed ID: 29870982
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 , 2018 | Pubmed ID: 29870994
Early prediction of acute kidney injury in children: known biomarkers but novel combination.
World journal of pediatrics : WJP Dec, 2018 | Pubmed ID: 30112669
Platelet integrin αIIbβ3: signal transduction, regulation, and its therapeutic targeting.
Journal of hematology & oncology Mar, 2019 | Pubmed ID: 30845955
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 Jul, 2019 | Pubmed ID: 30874715
An imbalance of T cell subgroups exists in children with sepsis.
Microbes and infection , 2019 | Pubmed ID: 31009807
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Clinical genetics Nov, 2019 | Pubmed ID: 31328266
Protein phosphatase 2A modulates podocyte maturation and glomerular functional integrity in mice.
Cell communication and signaling : CCS Aug, 2019 | Pubmed ID: 31387591
Impact of and polymorphisms on tacrolimus exposure and response in pediatric primary nephrotic syndrome.
Pharmacogenomics Oct, 2019 | Pubmed ID: 31588879
Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
Clinical genetics Mar, 2020 | Pubmed ID: 31674016
Haze facilitates sensitization to house dust mites in children.
Environmental geochemistry and health Jul, 2020 | Pubmed ID: 31858358
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 Feb, 2020 | Pubmed ID: 31862313
[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 Jun, 2019 | Pubmed ID: 31901041
Clinical features and genetic findings in Chinese children with distal renal tubular acidosis.
International journal of clinical and experimental pathology , 2018 | Pubmed ID: 31949730
Overexpression of Myo1e promotes albumin endocytosis by mouse glomerular podocytes mediated by Dynamin.
PeerJ , 2020 | Pubmed ID: 32211226
Epidemiological analysis of COVID-19 and practical experience from China.
Journal of medical virology Jul, 2020 | Pubmed ID: 32237160
Dent disease: classification, heterogeneity and diagnosis.
World journal of pediatrics : WJP Feb, 2021 | Pubmed ID: 32248351
The pathogenesis and treatment of the `Cytokine Storm' in COVID-19.
The Journal of infection Jun, 2020 | Pubmed ID: 32283152
Severe vaso-occlusive lupus retinopathy in the early stage of a pediatric patient with systemic lupus erythematosus: a case report.
Medicine Apr, 2020 | Pubmed ID: 32312013
Non-apoptotic cell death induced by opening the large conductance mechanosensitive channel MscL in hepatocellular carcinoma HepG2 cells.
Biomaterials Aug, 2020 | Pubmed ID: 32361391
[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 May, 2020 | Pubmed ID: 32391660
Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).
BMC nephrology May, 2020 | Pubmed ID: 32393202
IPDN-China promotes the development of pediatric dialysis in China.
Pediatric nephrology (Berlin, Germany) Nov, 2020 | Pubmed ID: 32529322
Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.
BMC pediatrics Jul, 2020 | Pubmed ID: 32616040
Crosstalk between coronavirus disease 2019 and cardiovascular disease and its treatment.
ESC heart failure Dec, 2020 | Pubmed ID: 32935928
Clinically applicable 53-Gene prognostic assay predicts chemotherapy benefit in gastric cancer: A multicenter study.
EBioMedicine Nov, 2020 | Pubmed ID: 33069062
The Roles of Base Modifications in Kidney Cancer.
Frontiers in oncology , 2020 | Pubmed ID: 33282735
SARS-CoV-2 effects on the renin-angiotensin-aldosterone system, therapeutic implications.
Acta physiologica (Oxford, England) Apr, 2021 | Pubmed ID: 33350096
Clinical and genetic characteristics of concomitant Mucopolysaccharidosis type IVA and neurogenic bladder in children: two case reports and literature review.
BMC pediatrics Jan, 2021 | Pubmed ID: 33407246
Multiple bladder diverticula with Williams-Beuren syndrome: a case report.
Translational pediatrics Dec, 2020 | Pubmed ID: 33457309
Host genetics and gut microbiota cooperatively contribute to azoxymethane-induced acute toxicity in Collaborative Cross mice.
Archives of toxicology Mar, 2021 | Pubmed ID: 33458792
CT and MRI imaging analysis of nontuberculous mycobacterium infection in bone and joint.
Minerva medica Aug, 2022 | Pubmed ID: 33576200
Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1.
Acta physiologica (Oxford, England) May, 2021 | Pubmed ID: 33615732
Glomerular podocyte dysfunction in inherited renal tubular disease.
World journal of pediatrics : WJP Jun, 2021 | Pubmed ID: 33625696
Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough?
Journal of the American Society of Nephrology : JASN Apr, 2021 | Pubmed ID: 33649100
Immunopathogenesis of idiopathic nephrotic syndrome in children: two sides of the coin.
World journal of pediatrics : WJP Apr, 2021 | Pubmed ID: 33660135
Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.
Frontiers in pediatrics , 2021 | Pubmed ID: 33996672
Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report.
The Journal of international medical research May, 2021 | Pubmed ID: 34039074
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 Jun, 2021 | Pubmed ID: 34075551
The immune cell landscape of peripheral blood mononuclear cells from PNS patients.
Scientific reports Jun, 2021 | Pubmed ID: 34158604
DNA demethylase Tet2 suppresses cisplatin-induced acute kidney injury.
Cell death discovery Jun, 2021 | Pubmed ID: 34226503
Correlation between infections with different glycoprotein H genotypes of human cytomegalovirus in children and hepatitis.
Pediatrics and neonatology 11, 2021 | Pubmed ID: 34348886
Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease.
Stem cell research Aug, 2021 | Pubmed ID: 34365103
Renoprotection with sodium-glucose cotransporter-2 inhibitors in children: Knowns and unknowns.
Nephrology (Carlton, Vic.) Feb, 2022 | Pubmed ID: 34545979
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.
Stem cell research Oct, 2021 | Pubmed ID: 34547705
Coronavirus disease 2019 vaccine for children in China: when to start? Mandatory or voluntary?
Chinese medical journal Sep, 2021 | Pubmed ID: 34561329
Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies.
Clinical immunology (Orlando, Fla.) Nov, 2021 | Pubmed ID: 34600127
Tolvaptan in Pediatric Autosomal Dominant Polycystic Kidney Disease: From Here to Where?
Kidney diseases (Basel, Switzerland) Sep, 2021 | Pubmed ID: 34604341
PP2A protects podocytes against Adriamycin-induced injury and epithelial-to-mesenchymal transition via suppressing JIP4/p38-MAPK pathway.
Cytotechnology Oct, 2021 | Pubmed ID: 34629746
Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.
Children (Basel, Switzerland) Oct, 2021 | Pubmed ID: 34682152
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.
BMC medical genomics Oct, 2021 | Pubmed ID: 34696790
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 Aug, 2021 | Pubmed ID: 34704408
Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study.
World journal of pediatrics : WJP Dec, 2021 | Pubmed ID: 34716893
Rotavirus and adenovirus infections in children during COVID-19 outbreak in Hangzhou, China.
Translational pediatrics Sep, 2021 | Pubmed ID: 34733668
The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome.
Annals of translational medicine Sep, 2021 | Pubmed ID: 34734004
Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in and .
Frontiers in medicine , 2021 | Pubmed ID: 34778325
Genetic Variations and Clinical Features of -Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study.
Frontiers in medicine , 2021 | Pubmed ID: 34859019
Mosaic in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.
Frontiers in medicine , 2021 | Pubmed ID: 34977057
rhADAMTS13 reduces oxidative stress by cleaving VWF in ischaemia/reperfusion-induced acute kidney injury.
Acta physiologica (Oxford, England) Mar, 2022 | Pubmed ID: 34989474
Incident changes in the prevalence of respiratory virus among children during COVID-19 pandemic in Hangzhou, China.
The Journal of infection Apr, 2022 | Pubmed ID: 35016902
Booster vaccination strategy: Necessity, immunization objectives, immunization strategy, and safety.
Journal of medical virology Jun, 2022 | Pubmed ID: 35028946
Hyperuricemia and Associated Factors in Children with Chronic Kidney Disease: A Cross-Sectional Study.
Children (Basel, Switzerland) Dec, 2021 | Pubmed ID: 35053631
Autoimmune Podocytopathies: A Novel Sub-Group of Diseases from Childhood Idiopathic Nephrotic Syndrome.
Journal of the American Society of Nephrology : JASN Mar, 2022 | Pubmed ID: 35064050
Impact of Sampling Time Variability on Tacrolimus Dosage Regimen in Pediatric Primary Nephrotic Syndrome: Single-Center, Prospective, Observational Study.
Frontiers in pharmacology , 2021 | Pubmed ID: 35069185
Recent advances and clinical application in point-of-care testing of SARS-CoV-2.
Journal of medical virology May, 2022 | Pubmed ID: 35080017
Application experience of a rapid nucleic acid detection system for COVID-19.
Microbes and infection Jun, 2022 | Pubmed ID: 35093551
Urinary Sediment mRNA Level of CREBBP and CYBA in Children With Steroid-Resistant Nephrotic Syndrome.
Frontiers in immunology , 2021 | Pubmed ID: 35173708
Renoprotective Role of Hypoxia-Inducible Factors and the Mechanism.
Kidney diseases (Basel, Switzerland) Jan, 2022 | Pubmed ID: 35224006
Circular RNA circDVL1 inhibits clear cell renal cell carcinoma progression through the miR-412-3p/PCDH7 axis.
International journal of biological sciences , 2022 | Pubmed ID: 35280687
Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome.
Iranian journal of immunology : IJI Mar, 2022 | Pubmed ID: 35293350
Strategies and safety considerations of booster vaccination in COVID-19.
Bosnian journal of basic medical sciences Jun, 2022 | Pubmed ID: 35366790
Multiplex detection of eight different viral enteropathogens in clinical samples, combining RT-PCR technology with melting curve analysis.
Virology journal Apr, 2022 | Pubmed ID: 35392937
Epithelial-mesenchymal transition in organ fibrosis development: current understanding and treatment strategies.
Burns & trauma , 2022 | Pubmed ID: 35402628
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.
JCI insight Jun, 2022 | Pubmed ID: 35472031
Identification of a 12-Gene Signature and Hub Genes Involved in Kidney Wilms Tumor Integrated Bioinformatics Analysis.
Frontiers in oncology , 2022 | Pubmed ID: 35480093
Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients.
Frontiers in genetics , 2022 | Pubmed ID: 35559039
Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy.
Neurobiology of disease Aug, 2022 | Pubmed ID: 35568100
Evaluation of a Novel Simulation Curriculum With the Segmented Model in Pediatric Cardiovascular Education.
Frontiers in public health , 2022 | Pubmed ID: 35669747
A critical role of the podocyte cytoskeleton in the pathogenesis of glomerular proteinuria and autoimmune podocytopathies.
Acta physiologica (Oxford, England) Aug, 2022 | Pubmed ID: 35716094
The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study.
Frontiers in medicine , 2022 | Pubmed ID: 35755072
A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells.
STAR protocols Sep, 2022 | Pubmed ID: 35834385
Management of multiple magnetic foreign body ingestion in pediatric patients.
BMC pediatrics Jul, 2022 | Pubmed ID: 35879696
Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review.
Frontiers in pediatrics , 2022 | Pubmed ID: 35899130
Robot-Assisted Resection of Intestinal Duplication in Children.
Journal of laparoendoscopic & advanced surgical techniques. Part A Dec, 2022 | Pubmed ID: 35904972
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations.
Genetics research , 2022 | Pubmed ID: 35919034
Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.
Laboratory medicine Jan, 2023 | Pubmed ID: 35964233
Vasculitis after COVID-19 Vaccination.
Current rheumatology reviews , 2023 | Pubmed ID: 35980076
Pediatric membranous nephropathy: In the novel antigens era.
Frontiers in immunology , 2022 | Pubmed ID: 36016931
The interaction between cellular senescence and chronic kidney disease as a therapeutic opportunity.
Frontiers in pharmacology , 2022 | Pubmed ID: 36091755
Corrigendum: Impact of sampling time variability on tacrolimus dosage regimen in pediatric primary nephrotic syndrome: Single-center, prospective, observational study.
Frontiers in pharmacology , 2022 | Pubmed ID: 36313378
Integrated analysis of immune- and apoptosis-related lncRNA-miRNA-mRNA regulatory network in children with Henoch Schönlein purpura nephritis.
Translational pediatrics Oct, 2022 | Pubmed ID: 36345450
Nonpharmaceutical interventions for COVID-19 disrupt the dynamic balance between influenza A virus and human immunity.
Journal of medical virology Jan, 2023 | Pubmed ID: 36367115
Glomerular diseases after immune checkpoint inhibitors use: What do We know so far?
Renal failure Dec, 2022 | Pubmed ID: 36420664
COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients.
Vaccines Nov, 2022 | Pubmed ID: 36423007
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 Mar, 2023 | Pubmed ID: 36449136
Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy.
Kidney international reports Dec, 2022 | Pubmed ID: 36506238
Serum IL-12p40: A novel biomarker for early prediction of minimal change disease relapse following glucocorticoids therapy.
Frontiers in medicine , 2022 | Pubmed ID: 36507530
Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review.
Frontiers in pediatrics , 2022 | Pubmed ID: 36523395
Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation.
Pediatric research Jul, 2023 | Pubmed ID: 36539574
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 Dec, 2022 | Pubmed ID: 36549658
Benefits and risks of essential trace elements in chronic kidney disease: a narrative review.
Annals of translational medicine Dec, 2022 | Pubmed ID: 36660676
Lumasiran for primary hyperoxaluria type 1: What we have learned?
Frontiers in pediatrics , 2022 | Pubmed ID: 36704142
Advances in imaging techniques to assess kidney fibrosis.
Renal failure Dec, 2023 | Pubmed ID: 36723057
Roxadustat: Do we know all the answers?
Biomolecules & biomedicine May, 2023 | Pubmed ID: 36724056
Comprehensive mapping of B lymphocyte immune dysfunction in idiopathic nephrotic syndrome children.
Clinical and translational medicine Feb, 2023 | Pubmed ID: 36740447
Cysteine Pathogenic Variants of PMM2 Are Sensitive to Environmental Stress with Loss of Structural Stability.
Oxidative medicine and cellular longevity , 2023 | Pubmed ID: 36743691
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 , 2022 | Pubmed ID: 36755738
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 , 2023 | Pubmed ID: 36775958
Machine learning models for predicting steroid-resistant of nephrotic syndrome.
Frontiers in immunology , 2023 | Pubmed ID: 36776850
Structure, signal transduction, activation, and inhibition of integrin αIIbβ3.
Thrombosis journal Feb, 2023 | Pubmed ID: 36782235
Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.
European journal of clinical investigation Jul, 2023 | Pubmed ID: 36856027
A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients.
Clinical immunology (Orlando, Fla.) Apr, 2023 | Pubmed ID: 36863601
Urinary epidermal growth factor predicts complete remission of proteinuria in Chinese children with IgA nephropathy.
Pediatric research Aug, 2023 | Pubmed ID: 36864281
Multiple functions of stress granules in viral infection at a glance.
Frontiers in microbiology , 2023 | Pubmed ID: 36937261
Genetic Architecture of Childhood Kidney and Urological Diseases in China.
Phenomics (Cham, Switzerland) Jun, 2021 | Pubmed ID: 36939782
Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis.
Clinical journal of the American Society of Nephrology : CJASN Apr, 2023 | Pubmed ID: 37099456
Correlation between Toll-like Receptor Gene Polymorphisms and Idiopathic Nephrotic Syndrome in Chinese Children.
Current medical science Jun, 2023 | Pubmed ID: 37115397
A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome.
MedComm Jun, 2023 | Pubmed ID: 37180824
Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with N215S mutation: Case report and literature review.
Heliyon May, 2023 | Pubmed ID: 37205992
Dihydromyricetin attenuates cisplatin-induced acute kidney injury by reducing oxidative stress, inflammation and ferroptosis.
Toxicology and applied pharmacology Aug, 2023 | Pubmed ID: 37328118
A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations.
Vaccines May, 2023 | Pubmed ID: 37376434
Low skeletal muscle mass as an early sign in children with fabry disease.
Orphanet journal of rare diseases Jul, 2023 | Pubmed ID: 37480128
Cysteine mutations impair the structural stability of phosphomannomutase 2 (PMM2) in glycosylation-associated metabolic disorders.
Genes & diseases Sep, 2023 | Pubmed ID: 37492729
Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1.
iScience Aug, 2023 | Pubmed ID: 37599822
Rapid detection of telomerase expression of neuroblastoma in paraffin-embedded tissue: combination of in situ hybridisation and quantitative PCR.
Pathology Sep, 2023 | Pubmed ID: 37741703
Langping Gao*,1,2,
Yue Wang*,3,
Gang Wang4,
Hangdi Wu2,
Qingtao Yan1,
Jingjing Wang1,
Fei Liu1,
Haidong Fu1,
Wei Li5,
Lidan Hu1,
Jianhua Mao1,2
1Department of Nephrology, The Children's Hospital, Zhejiang University School of Medicine,
2, Zhejiang University School of Medicine,
3, Hubei Normal University,
4National Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing University School of Medicine,
5Clinical Laboratory, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health
关于 JoVE
版权所属 © 2024 MyJoVE 公司版权所有,本公司不涉及任何医疗业务和医疗服务。