H. Kaito

K. Nakanishi, N. Yoshikawa, K. Iijima, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Detection of a Transcript Abnormality in mRNA of the SLC12A3 Gene Extracted From Urinary Sediment Cells of a Patient With Gitelman's Syndrome

M. Matsuo, K. Nozu, K. Iijima, 2007, Pediatric Research.

FUNCTIONAL ASPECTS OF THE PANCREATIC LANGERHANS ISLETS IN STARVED ANIMALS BASED ON THE HISTOCHEMICAL AND ELECTRON MICROSCOPICAL OBSERVATION

H. Kaito, 1974 .

Leukocyte Differentiation by Histidine-Rich Glycoprotein/Stanniocalcin-2 Complex Regulates Murine Glioma Growth through Modulation of Antitumor Immunity

M. Essand, M. Welsh, B. Wollscheid, 2018, Molecular Cancer Therapeutics.

Regulatory T Cell and Nephrotic Syndrome

K. Iijima, H. Kaito, T. Ninchoji, 2012 .

ECTOPIC ACTH‐MSH PRODUCING CARCINOID TUMOR WITH MULTIPLE ENDOCRINE HYPERPLASIA IN A CHILD

F. Hazama, H. Kaito, M. Tsurusawa, 1978, Acta pathologica japonica.

A review of clinical characteristics and genetic backgrounds in Alport syndrome

K. Nakanishi, M. Nagata, K. Nozu, 2018, Clinical and Experimental Nephrology.

Treatment strategies and outcomes for Henoch–Schönlein nephritis: reply to Fujinaga et al.

H. Kaito, T. Ninchoji, 2012, Pediatric Nephrology.

A birth of bipartite exon by intragenic deletion

J. Královičová, I. Vořechovský, K. Nakanishi, 2017, Molecular genetics & genomic medicine.

Risk factors for developing severe clinical course in HUS patients: a national survey in Japan

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Cryptic exon activation in SLC12A3 in Gitelman syndrome

I. Vořechovský, K. Nakanishi, K. Nozu, 2016, Journal of Human Genetics.

Quartz Crystal Microbalance Measurement of Histidine-Rich Glycoprotein and Stanniocalcin-2 Binding to Each Other and to Inflammatory Cells

T. Aastrup, H. Kaito, C. Durall, 2022, Cells.

Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.

H. Fukuoka, S. Nishiumi, Masaru Yoshida, 2013, Early human development.

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

K. Nakanishi, K. Miyako, K. Nozu, 2018, Kidney international reports.

Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases

K. Nozu, K. Iijima, Y. Nozu, 2018, Clinical and Experimental Nephrology.

Molecular Background of Urate Transporter Genes in Patients with Exercise-Induced Acute Kidney Injury

K. Nakanishi, N. Yoshikawa, K. Nozu, 2013, American Journal of Nephrology.

Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.

Y. Takeshima, M. Matsuo, K. Nakanishi, 2008, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2010, Pediatric Nephrology.

Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene

T. Ariga, K. Nozu, K. Iijima, 2018, Clinical and Experimental Nephrology.

Kobe University Repository : Kernel タイトル Tit le The effect of aldosterone blockade in pat ients with Alport syndrome

H. Kaito, K. Yoshiya, K. Kanda, 2018 .

The effect of aldosterone blockade in patients with Alport syndrome

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2006, Pediatric Nephrology.

Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency.

M. Nishi, K. Nakanishi, H. Furuta, 2014, Endocrine journal.

Enamel-renal syndrome associated with hypokalaemic metabolic alkalosis and impaired renal concentration: a novel syndrome?

H. Nishio, M. Matsuo, K. Nozu, 2006, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes

M. Nangaku, T. Miyata, M. Matsuo, 2018, Journal of Human Genetics.

Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: medical therapy

K. Nakanishi, Takuhito Nagai, K. Iijima, 2014, Clinical and Experimental Nephrology.

Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome.

K. Nakanishi, T. Omori, K. Nozu, 2020, Kidney international.

Kobe University Repository : Kernel タイトル Tit le Natural History and Genotype-Phenotype Correlat ion in Female X-Linked Alport Syndrome

K. Nakanishi, N. Yoshikawa, K. Nozu, 2018 .

Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome

K. Nakanishi, N. Yoshikawa, K. Nozu, 2017, Kidney international reports.

Natural history of genetically proven autosomal recessive Alport syndrome

I. Vořechovský, M. Matsuo, K. Nakanishi, 2014, Pediatric Nephrology.

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome

K. Nakanishi, K. Nozu, K. Iijima, 2019, Molecular genetics & genomic medicine.

Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2008, Pediatric Nephrology.

A case of mild phenotype Alport syndrome caused by COL4A3 mutations

T. Nishino, H. Mukae, Y. Obata, 2017, CEN Case Reports.

Renal transplantations from parents to siblings with autosomal recessive Alport syndrome caused by a rearrangement in an intronic antisense Alu element in the COL4A3 gene led to different outcomes

H. Rakugi, N. Ichimaru, N. Nonomura, 2013, CEN Case Reports.

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

R. Mori, Y. Ohashi, K. Nakanishi, 2014, The Lancet.

Diagnostic strategy for inherited hypomagnesemia

K. Nakanishi, K. Nozu, K. Iijima, 2017, Clinical and Experimental Nephrology.

Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onset

K. Nakanishi, N. Yoshikawa, K. Nozu, 2015, Pediatric Nephrology.

Pretransplantation combined therapy with plasmapheresis and rituximab in a second living‐related kidney transplant pediatric recipient with a very high risk for focal segmental glomerulosclerosis recurrence

Yuko Kajiho, M. Hattori, K. Nozu, 2012, Pediatric transplantation.

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry

K. Nozu, K. Iijima, H. Kaito, 2018, Case Reports in Nephrology and Dialysis.

Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

K. Nakanishi, T. Omori, K. Nozu, 2021, Scientific Reports.

ABO‐incompatible renal transplantation in Epstein syndrome

S. Ito, K. Matsuoka, Eriko Kikuchi, 2010, Clinical transplantation.

Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics

K. Nakanishi, N. Yoshikawa, K. Nozu, 2015, Genetics in Medicine.

Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: general therapy

K. Nakanishi, Takuhito Nagai, K. Iijima, 2015, Clinical and Experimental Nephrology.

A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment

E. Ota, R. Mori, S. Ito, 2014, Kidney international.

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

S. Mane, D. Lowy, K. Nakayama, 2018, Nature Communications.

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.

M. Nagasaki, K. Tokunaga, M. Matsuo, 2020, Kidney international.

The "bronze baby" syndrome: postmortem data.

C. F. Clark, H. Kaito, Y. Hamamoto, 1976, The Journal of pediatrics.

Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease

K. Nakanishi, K. Nozu, K. Iijima, 2018, Journal of Human Genetics.

Clinical and genetic variability of PAX2-related disorder in the Japanese population

S. Ito, K. Nozu, K. Iijima, 2020, Journal of Human Genetics.

An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis

M. Matsuo, K. Nakanishi, K. Nozu, 2017, BMC Nephrology.

In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation

Y. Takeshima, M. Matsuo, K. Nakanishi, 2009, Human Genetics.

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay

M. Matsuo, K. Nakanishi, K. Nozu, 2019, Scientific Reports.

X-linked Alport syndrome caused by splicing mutations in COL4A5.

I. Vořechovský, Y. Makita, K. Nakanishi, 2014, Clinical journal of the American Society of Nephrology : CJASN.

Prognosis and pathological characteristics of five children with non‐Shiga toxin‐mediated hemolytic uremic syndrome

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Molecular mechanisms determining severity in patients with Pierson syndrome

K. Nakanishi, M. Nagata, N. Yoshikawa, 2020, Journal of Human Genetics.

A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome.

M. Matsuo, K. Nakanishi, H. Awano, 2017, European journal of medical genetics.

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2007, Journal of Medical Genetics.

Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome

M. Matsuo, K. Asanuma, M. Hattori, 2019, Journal of Human Genetics.

Rituximab treatment combined with methylprednisolone pulse therapy and immunosuppressants for childhood steroid-resistant nephrotic syndrome

S. Ito, K. Iijima, H. Kaito, 2014, Pediatric Nephrology.

Successful treatment of collapsing focal segmental glomerulosclerosis with a combination of rituximab, steroids and ciclosporin

S. Ito, M. Nagata, K. Matsuoka, 2010, Pediatric Nephrology.

Clinicopathological characteristics and renal outcomes of childhood-onset lupus nephritis with acute kidney injury: A multicenter study

K. Nakanishi, N. Yoshikawa, K. Nozu, 2019, Modern rheumatology.

Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2011, Pediatric Nephrology.

M-Type Phospholipase A2 Receptor Staining in Children with Idiopathic Membranous Nephropathy: PLA2R Staining in Children with IMN

N. Yoshikawa, T. Nakagawa, K. Nozu, 2019, The Open Urology & Nephrology Journal.

Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity

K. Nakanishi, N. Yoshikawa, K. Nozu, 2022, Pediatric Nephrology.

Two cases of atypical membranoproliferative glomerulonephritis showing opposite clinical course

K. Nakanishi, N. Yoshikawa, K. Nozu, 2012, CEN Case Reports.

Long-term follow-up of juvenile acute nonproliferative glomerulitis (JANG)

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2007, Pediatric Nephrology.

A novel technique of catheter placement with fibrin glue to prevent pericatheter leakage and to enable no break-in period in peritoneal dialysis.

K. Nozu, K. Iijima, H. Kaito, 2015, Journal of Pediatric Urology.

Recurrent EIARF and PRES With Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2011, Pediatrics.

Clinical characteristics and long-term outcome of diarrhea-associated hemolytic uremic syndrome: a single center experience

K. Nakanishi, N. Yoshikawa, K. Nozu, 2017, Clinical and Experimental Nephrology.

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2010, The Journal of clinical endocrinology and metabolism.

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases

K. Nozu, K. Iijima, H. Kaito, 2018, Scientific Reports.

Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia

S. Ito, K. Iijima, H. Kaito, 2014, European Journal of Pediatrics.

Acute renal failure due to obstructive uric acid stones associated with acute gastroenteritis

M. Matsuo, K. Nozu, K. Iijima, 2009, Pediatric Nephrology.

Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome

K. Nakanishi, S. Ito, Hidefumi Nakamura, 2021, Journal of the American Society of Nephrology : JASN.

Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis

S. Ito, K. Matsuoka, N. Yoshikawa, 2022, Kidney360.

Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.

M. Matsuo, K. Nakanishi, M. Kawano, 2018, Journal of the American Society of Nephrology : JASN.

Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema

H. Fuchs, Wei Liu, Liqun He, 2017, Scientific Reports.

[Cobb syndrome (cutaneomeningospinal angiomatosis). The first case reported in Japan].

H. Kaito, S. Mochio, N. Hashimoto, 1989, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay

M. Matsuo, K. Nakanishi, K. Nozu, 2020, Molecular genetics & genomic medicine.

A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism

M. Matsuo, K. Nozu, K. Iijima, 2007, Pediatric Nephrology.

Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits

K. Nakanishi, K. Asanuma, K. Nozu, 2016, Pediatric Nephrology.

Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits

M. Matsuo, K. Nozu, K. Iijima, 2017, Nephron.

Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis

I. Vořechovský, K. Nakanishi, M. Yanagita, 2017, Journal of Human Genetics.

Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes

M. Nangaku, T. Miyata, M. Matsuo, 2018, Journal of Human Genetics.

A patient report with focal segmental glomelular sclerosis and severe interstitial fibrosis 8 years after the onset of hemolyticuremic syndrome

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2009 .

Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome

K. Nozu, K. Iijima, H. Kaito, 2018, Journal of Human Genetics.

SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations.

K. Nozu, K. Iijima, H. Kaito, 2013, The Kobe journal of medical sciences.

Kobe University Repository : Kernel タイトル Tit le SLC 26 A 3 Gene Analysis in Pat ients with Bart ter and Gitelman Syndromes and the Clinical

K. Nozu, K. Iijima, H. Kaito, 2019 .

Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome

K. Nozu, K. Iijima, H. Kaito, 2018, Journal of Human Genetics.

Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis.

K. Nakanishi, N. Yoshikawa, K. Nozu, 2023, Pediatric nephrology.

Nephrotic-range proteinuria in an infant with thin basement membrane nephropathy

K. Nakanishi, N. Yoshikawa, K. Iijima, 2013, CEN Case Reports.

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

K. Nakanishi, N. Yoshikawa, K. Nozu, 2020, Scientific Reports.

Alport-like glomerular basement membrane changes with renal-coloboma syndrome

K. Nakanishi, K. Iijima, H. Kaito, 2012, Pediatric Nephrology.

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene

M. Matsuo, K. Nozu, K. Iijima, 2009, BMC nephrology.

Female X-linked Alport syndrome with somatic mosaicism

K. Nakanishi, K. Nozu, K. Iijima, 2017, Clinical and Experimental Nephrology.

Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR

M. Matsuo, K. Nakanishi, N. Yoshikawa, 2007, Pediatric Research.

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY

I. Vořechovský, K. Nakanishi, K. Nozu, 2014, Molecular genetics & genomic medicine.

International cohort of 382 children with lupus nephritis – presentation, treatment and outcome at 24 months

A. Bagga, Avinash Jain, H. Kaito, 2023, Pediatric nephrology (Berlin, West).

Combined Alport syndrome and Klinefelter syndrome

K. Nozu, K. Iijima, H. Kaito, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

R. Mori, Y. Ohashi, K. Nakanishi, 2014, The Lancet.

Kobe University Repository : Kernel タイトル Tit le A review of clinical characterist ics and genet ic backgrounds in Alport syndrome

K. Nakanishi, M. Nagata, K. Nozu, 2020 .

Underestimation of kidney function due to poorly controlled 21‐hydroxylase deficiency

K. Iijima, H. Kaito, Yosuke Inaguma, 2023, Pediatrics international : official journal of the Japan Pediatric Society.

K. Nakanishi, N. Yoshikawa, D. Tokuhara, 2023, Pediatric nephrology.

Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome

M. Matsuo, K. Asanuma, M. Hattori, 2019, Journal of Human Genetics.

Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome

K. Nakanishi, N. Yoshikawa, K. Nozu, 2015, European Journal of Human Genetics.

Role of Iron in Children With Immunoglobulin A Nephropathy and Macrohematuria-Induced Acute Kidney Injury

K. Nozu, H. Kaito, Tomohiko Yamamura, 2024, Kidney International Reports.

Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1

K. Nakanishi, K. Nozu, K. Iijima, 2016, Clinical and Experimental Nephrology.