Yuko Shima

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

Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome

K. Nakanishi, N. Yoshikawa, A. Tanaka, 2021, Clinical and Experimental Nephrology.

Interprovincial differences in the achievement of K/DOQI targets of mineral metabolism in Canada

K. Nakanishi, N. Yoshikawa, K. Nozu, 2010 .

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

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

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.

Endoplasmic reticulum stress with low-dose cyclosporine in frequently relapsing nephrotic syndrome

K. Nakanishi, N. Yoshikawa, K. Nozu, 2013, Pediatric 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.

A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndrome

K. Nakanishi, K. Nozu, K. Iijima, 2020, CEN Case Reports.

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

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

Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome

M. Matsuo, K. Nakanishi, K. Nozu, 2021, Kidney international reports.

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.

First Japanese case of Pierson syndrome with mutations in LAMB2

K. Nakanishi, N. Yoshikawa, K. Iijima, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.

M. Nagasaki, K. Tokunaga, K. Nakanishi, 2018, Journal of the American Society of Nephrology : JASN.

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

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

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.

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.

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

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

Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial)

K. Nakanishi, S. Ito, N. Yoshikawa, 2018, BMC Nephrology.

Improved renal survival in Japanese children with IgA nephropathy

K. Nakanishi, N. Yoshikawa, K. Nozu, 2008, Pediatric Nephrology.

Central Hypothyroidism in Infants Who Were Born to Mothers With Thyrotoxicosis Before 32 Weeks' Gestation: 3 Cases

T. Okutani, Yuko Shima, Megumi Yoshiyama, 2005, 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.

Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing

M. Matsuo, K. Nakanishi, H. Awano, 2021, Kidney International Reports.

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

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

Molecular mechanisms determining severity in patients with Pierson syndrome

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

Clinical spectrum of male patients with OFD1 mutations

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

Aberrant Smad3 phosphoisoforms in cyst-lining epithelial cells in the cpk mouse, a model of autosomal recessive polycystic kidney disease.

S. Nagao, K. Nakanishi, Hisahide Takahashi, 2017, American journal of physiology. Renal physiology.

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.

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.

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

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

Membranous nephropathy associated with thyroid-peroxidase antigen

K. Nakanishi, N. Yoshikawa, K. Nozu, 2009, Pediatric Nephrology.

A case of membranous nephropathy secondary to asymptomatic Graves’ disease

Marenao Tanaka, M. Furuhashi, N. Moniwa, 2022, CEN Case Reports.

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.

Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population

M. Matsuo, K. Nakanishi, N. Okamoto, 2022, Journal of Human Genetics.

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.

Serine Protease Inhibitor Kazal Type I (SPINK1) Mutation: A Risk Factor for Early-onset Chronic Pancreatitis?

Mitsuyoshi Suzuki, Yuko Shima, Taketsugu Hama, 2018, Journal of pediatric gastroenterology and nutrition.

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.

Elizabethkingia meningoseptica : Emergent bacteria causing pneumonia in a critically ill child

K. Nakanishi, N. Yoshikawa, K. Iijima, 2013 .

Neoplasms in three patients following Kawasaki disease

N. Yoshikawa, Yuko Shima, Hiroyuki Suzuki, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6‐year clinical course

M. Nishi, H. Furuta, Asako Doi, 2019, Journal of diabetes investigation.

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

K. Nakanishi, K. Nozu, K. Iijima, 2020, Scientific Reports.

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.

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

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

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).

Defining renal remission in an international cohort of 248 children and adolescents with lupus nephritis.

A. Bagga, S. Ito, Avinash Jain, 2021, Rheumatology.

Increased chymase-positive mast cells in children with crescentic glomerulonephritis

K. Nakanishi, N. Yoshikawa, K. Nozu, 2009, Pediatric Nephrology.

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

Clinical spectrum of male patients with OFD1 mutations

K. Nakanishi, K. Nozu, K. Iijima, 2018, 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.

Histologic and Clinical Factors Associated with Kidney Outcomes in IgA Vasculitis Nephritis

C. Zeng, L. Peruzzi, D. Maixnerova, 2024, Clinical journal of the American Society of Nephrology : CJASN.

IPNA clinical practice recommendations for the diagnosis and management of children with IgA nephropathy and IgA vasculitis nephritis.

H. Trimarchi, M. Mantan, K. Gibson, 2024, Pediatric nephrology.