Kazumoto Iijima


Ontology type: schema:Person     


Person Info

NAME

Kazumoto

SURNAME

Iijima

Publications in SciGraph latest 50 shown

  • 2019-05 Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study) in PEDIATRIC NEPHROLOGY
  • 2019-02 A review of clinical characteristics and genetic backgrounds in Alport syndrome in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2019-02 TGFBI-associated corneal dystrophy and nephropathy: a novel syndrome? in CEN CASE REPORTS
  • 2019-02 Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome in JOURNAL OF NEPHROLOGY
  • 2019-01 Clinical spectrum of male patients with OFD1 mutations in JOURNAL OF HUMAN GENETICS
  • 2018-12-24 Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-12-18 Rituximab therapy for refractory steroid-resistant nephrotic syndrome in children in PEDIATRIC NEPHROLOGY
  • 2018-12 Recent Advances in Genetic Aspects and Treatments for Steroid-Sensitive Nephrotic Syndrome in Children in CURRENT PEDIATRICS REPORTS
  • 2018-12 Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicenter double-blind, randomized, placebo-controlled trial (JSKDC07) in BMC NEPHROLOGY
  • 2018-12 The utility of urinary CD80 as a diagnostic marker in patients with renal diseases in SCIENTIFIC REPORTS
  • 2018-12 Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment in NATURE COMMUNICATIONS
  • 2018-12 Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial) in BMC NEPHROLOGY
  • 2018-11 Combination therapy with or without warfarin and dipyridamole for severe childhood IgA nephropathy: an RCT in PEDIATRIC NEPHROLOGY
  • 2018-10-26 The prescription rates of glucagon for hypoglycemia by pediatricians and physicians are low in Japan in ENDOCRINE
  • 2018-09 Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials in PEDIATRIC NEPHROLOGY
  • 2018-08 Clinical features in a series of 258 Japanese pediatric patients with thrombotic microangiopathy in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-08 Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-08 Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome in JOURNAL OF HUMAN GENETICS
  • 2018-08 Ensuring safe drug administration to pediatric patients with renal dysfunction: a multicenter study in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-06 Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes in JOURNAL OF HUMAN GENETICS
  • 2018-05 ETV6–ABL1 fusion combined with monosomy 7 in childhood B-precursor acute lymphoblastic leukemia in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2018-05 Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome in JOURNAL OF HUMAN GENETICS
  • 2018-05 Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-Analysis in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2018-05 Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease in JOURNAL OF HUMAN GENETICS
  • 2018 Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period in NONE
  • 2017-12 Diagnostic strategy for inherited hypomagnesemia in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-12 An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis in BMC NEPHROLOGY
  • 2017-12 Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children’s primary emergency medical center in ENVIRONMENTAL HEALTH AND PREVENTIVE MEDICINE
  • 2017-11-30 The smallest de novo 20q11.2 microdeletion causing intellectual disability and dysmorphic features in HUMAN GENOME VARIATION
  • 2017-11 Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab in PEDIATRIC NEPHROLOGY
  • 2017-11 A case of mild phenotype Alport syndrome caused by COL4A3 mutations in CEN CASE REPORTS
  • 2017-10 Female X-linked Alport syndrome with somatic mosaicism in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-10 Clinical characteristics and long-term outcome of diarrhea-associated hemolytic uremic syndrome: a single center experience in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-09 Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome in JOURNAL OF HUMAN GENETICS
  • 2017-09 Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome in JOURNAL OF HUMAN GENETICS
  • 2017-09 Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases in JOURNAL OF HUMAN GENETICS
  • 2017-08 High incidence of idiopathic nephrotic syndrome in East Asian children: a nationwide survey in Japan (JP-SHINE study) in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-07 Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis in JOURNAL OF HUMAN GENETICS
  • 2017-04 Rituximab for nephrotic syndrome in children in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-03 IgA nephropathy with presentation of nephrotic syndrome at onset in children in PEDIATRIC NEPHROLOGY
  • 2017-02 Cryptic exon activation in SLC12A3 in Gitelman syndrome in JOURNAL OF HUMAN GENETICS
  • 2017-02 Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2016-12 Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2 in HUMAN GENOME VARIATION
  • 2016-12 Transcutaneous bilirubin monitoring predicts unexplained late-onset hemolysis in a very low birthweight infant in BMC RESEARCH NOTES
  • 2016-12 A 12p13 GRIN2B deletion is associated with developmental delay and macrocephaly in HUMAN GENOME VARIATION
  • 2016-12 Gestational age-dependency of height and body mass index trajectories during the first 3 years in Japanese small-for-gestational age children in SCIENTIFIC REPORTS
  • 2016-12 An unusual case of congenital cytomegalovirus infection-related retinopathy in BMC OPHTHALMOLOGY
  • 2016-10 X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2016-09 Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits in PEDIATRIC NEPHROLOGY
  • 2016-09 Fluorescent protein-based detection of unconjugated bilirubin in newborn serum in SCIENTIFIC REPORTS
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