Y. Hashimura

发表

Validity of the Oxford classification of IgA nephropathy in children

K. Nakanishi, N. Yoshikawa, K. Iijima, 2012, Pediatric Nephrology.

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.

K. Nakanishi, N. Yoshikawa, K. Nozu, 2014, Kidney international.

Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

H. Kanegane, T. Miyawaki, M. Matsuo, 2009, Pediatric Nephrology.

Renal condition in IPEX Syndrome

H. Kanegane, T. Miyawaki, M. Matsuo, 2009 .

Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase

Yasuhisa Fujii, A. Hata, T. Ariga, 2019, The Lancet.

Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo‐obstruction in a neonate

Y. Takeshima, H. Yokozaki, A. Ohtake, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

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

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

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.

Natural history of genetically proven autosomal recessive Alport syndrome

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

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

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

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.

The case of a hemodialysis patient with hemophilia A

M. Fujisawa, H. Fujii, S. Goto, 2016 .

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.

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.

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

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

Two cases of atypical membranoproliferative glomerulonephritis showing opposite clinical course

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

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

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

Segmental membranous nephropathy with severe IgG3 deposition

T. Uchiyama, N. Yoshikawa, Atsushi Kondo, 2018, Pediatrics international : official journal of the Japan Pediatric Society.

307. EFFICACY OF PRIMARY TREATMENT WITH IMMUNOGLOBULIN PLUS CYCLOSPORINE FOR PREVENTION OF CORONARY ARTERY ABNORMALITIES IN KAWASAKI DISEASE PATIENTS PREDICTED TO BE AT INCREASED RISK OF IVIG NON- RESPONSE (KAICA STUDY): A CONTROLLED, PHASE 3, RANDOMISED, OPEN-LABEL, BLINDED-ENDPOINTS TRIAL

T. Ariga, S. Kurotobi, S. Takatsuki, 2019, Rheumatology.

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 .

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

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