Haidong Fu

Department of Nephrology, Zhejiang University School of Medicine

Affiliated withZhejiang University School of Medicine

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 4	2023

Other Publications

Article	Year
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
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
Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis. World journal of pediatrics : WJP\| PubMed ID: 23677832	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
Interferon-gamma gene polymorphism +874 (a/t) in Chinese children with Henoch-Schonlein purpura. Iranian journal of allergy, asthma, and immunology\| PubMed ID: 24659122	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
Clinical characteristics of concomitant nephrotic IgA nephropathy and minimal change disease in children. Nephron\| PubMed ID: 25924689	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 Value of Monitoring the Serum Concentration of Mycophenolate Mofetil in Children with Steroid-Dependent/Frequent Relapsing Nephrotic Syndrome. Nephron\| PubMed ID: 26991496	2016
Association between IL17A and IL17F polymorphisms and risk of Henoch-Schonlein purpura in Chinese children. Rheumatology international\| PubMed ID: 27021337	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
Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review. World journal of pediatrics : WJP\| PubMed ID: 27351573	2016
Clinical features and outcomes of diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis in children. Clinics (Sao Paulo, Brazil)\| PubMed ID: 27652838	2016
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
Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review. Medicine\| PubMed ID: 29382012	2017
Analysis of 17 children with renal abscess. International journal of clinical and experimental pathology\| PubMed ID: 31934162	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
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
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
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
Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1. Acta physiologica (Oxford, England)\| PubMed ID: 33615732	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
Case Report: Membranoproliferative Glomerulonephritis, a Rare Clinical Manifestation of Abernethy Malformation Type II. Frontiers in pediatrics\| PubMed ID: 33816407	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
The immune cell landscape of peripheral blood mononuclear cells from PNS patients. Scientific reports\| PubMed ID: 34158604	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
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
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
The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome. Annals of translational medicine\| PubMed ID: 34734004	2021
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
Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome. Iranian journal of immunology : IJI\| PubMed ID: 35293350	2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia. JCI insight\| PubMed ID: 35472031	2022
Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients. Frontiers in genetics\| PubMed ID: 35559039	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
The interaction between cellular senescence and chronic kidney disease as a therapeutic opportunity. Frontiers in pharmacology\| PubMed ID: 36091755	2022
Psychological research of the children with chronic kidney disease and their guardians during the COVID-19 pandemic. Frontiers in public health\| PubMed ID: 36324445	2022
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
Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy. Kidney international reports\| PubMed ID: 36506238	2022
Benefits and risks of essential trace elements in chronic kidney disease: a narrative review. Annals of translational medicine\| PubMed ID: 36660676	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
Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome. European journal of clinical investigation\| PubMed ID: 36856027	2023
A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome. MedComm\| PubMed ID: 37180824	2023