Kandai Nozu

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Publications in SciGraph latest 50 shown

  • 2022-05-12 Long use of continuous positive airway pressure protects against the development of treatment-requiring retinopathy of prematurity in SCIENTIFIC REPORTS
  • 2022-03-25 The association between prehospital vital signs of children and their critical clinical outcomes at hospitals in SCIENTIFIC REPORTS
  • 2022-03-05 Prognostic effects of treatment protocols for febrile convulsive status epilepticus in children in BMC NEUROLOGY
  • 2022-02-09 Efficacy of combination therapy for childhood complicated focal IgA nephropathy in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2022-02-09 Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2022-02-03 Clinical, pathological, and genetic characteristics of cases with asymptomatic proteinuria not manifesting nephrotic syndrome at onset: a single-center retrospective study in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2022-01-11 Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity in PEDIATRIC NEPHROLOGY
  • 2021-11-13 A disease-causing variant of COL4A5 in a Chinese family with Alport syndrome: a case series in BMC NEPHROLOGY
  • 2021-10-15 BCS1L mutations produce Fanconi syndrome with developmental disability in JOURNAL OF HUMAN GENETICS
  • 2021-09-28 Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-09-26 A digest of the Evidence-Based Clinical Practice Guideline for Nephrotic Syndrome 2020 in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-09-18 Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-08-30 Contradiction between genetic analysis and diuretic loading test in type I Bartter syndrome: a case report in BMC NEPHROLOGY
  • 2021-08-09 Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases in SCIENTIFIC REPORTS
  • 2021-07-12 Correction to: Risk factors for post-nephrectomy hypotension in pediatric patients in PEDIATRIC NEPHROLOGY
  • 2021-06-18 Spontaneous regression of arterial pseudoaneurysm after kidney biopsy in CEN CASE REPORTS
  • 2021-06-14 X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-05-14 Risk factors for post-nephrectomy hypotension in pediatric patients in PEDIATRIC NEPHROLOGY
  • 2021-03-20 Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-03-17 Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2021-03-15 Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1 in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-01-21 An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing in CEN CASE REPORTS
  • 2020-10-13 A woman with a dual genetic diagnosis of autosomal dominant tubulointerstitial kidney disease and KBG syndrome in CEN CASE REPORTS
  • 2020-10-04 Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy in PEDIATRIC NEPHROLOGY
  • 2020-09-09 FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child in CEN CASE REPORTS
  • 2020-08-24 Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature in BMC NEPHROLOGY
  • 2020-08-20 Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases in SCIENTIFIC REPORTS
  • 2020-08-17 A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy in HUMAN GENOME VARIATION
  • 2020-07-28 Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1 in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2020-07-18 Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2 in PEDIATRIC NEPHROLOGY
  • 2020-07-14 Onset mechanism of a female patient with Dent disease 2 in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2020-07-06 A different clinical manifestation in a Japanese family with autosomal dominant distal renal tubular acidosis caused by SLC4A1 mutation in CEN CASE REPORTS
  • 2020-07-04 A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndrome in CEN CASE REPORTS
  • 2020-06-26 Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experience in CEN CASE REPORTS
  • 2020-06-02 Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 in NATURE COMMUNICATIONS
  • 2020-04-15 Gastrointestinal symptoms as an extended clinical feature of Pierson syndrome: a case report and review of the literature in BMC MEDICAL GENOMICS
  • 2020-04-06 Bardet–Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations in CEN CASE REPORTS
  • 2020-03-30 How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2020-03-16 Clinical and genetic variability of PAX2-related disorder in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2020-01-28 Crescentic IgA nephropathy in children in PEDIATRIC NEPHROLOGY
  • 2020-01-21 Molecular mechanisms determining severity in patients with Pierson syndrome in JOURNAL OF HUMAN GENETICS
  • 2020-01-14 Comprehensive genetic diagnosis of Japanese patients with severe proteinuria in SCIENTIFIC REPORTS
  • 2019-11-08 Combination of furosemide and fludrocortisone as a loading test for diagnosis of distal renal tubular acidosis in a pediatric case in CEN CASE REPORTS
  • 2019-09-19 A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease in CEN CASE REPORTS
  • 2019-09-03 Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay in SCIENTIFIC REPORTS
  • 2019-08-02 Study protocol: multicenter double-blind, randomized, placebo-controlled trial of rituximab for the treatment of childhood-onset early-stage uncomplicated frequently relapsing or steroid-dependent nephrotic syndrome (JSKDC10 trial) in BMC NEPHROLOGY
  • 2019-07-09 A case report of thin basement membrane nephropathy accompanied by sporadic glomerulocystic kidney disease in BMC NEPHROLOGY
  • 2019-06-24 A girl with CLOVES syndrome with a recurrent PIK3CA somatic mutation and pancreatic steatosis in HUMAN GENOME VARIATION
  • 2019-05-27 Clinical characteristics of HNF1B-related disorders in a Japanese population in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2019-04-23 Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome in JOURNAL OF HUMAN GENETICS
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