Faculty Information - Kanda Shiyouichirou

（Last updated : 2024-03-08 15:53:18）

Kanda Shiyouichirou
Department School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine Department of Obstetrics and Gynecology, Division of Obstetrics

Position

■ Books

1.	Chapter contribution	autosomal dominant tubulointerstitial kidney disease「多発性嚢胞腎～進化する治療最前線～」 2015/08
2.	Chapter contribution	bardet-biedl syndrome「多発性嚢胞腎～進化する治療最前線～ 1」 2015/08
3.	Chapter contribution	ciliopathy「多発性嚢胞腎～進化する治療最前線～」 2015/08
4.	Chapter contribution	glomerulocystic kidney disease「多発性嚢胞腎～進化する治療最前線～」 2015/08
5.	Chapter contribution	Joubert syndrome and Joubert syndrome related disorders「多発性嚢胞腎～進化する治療最前線～」 2015/08
6.	Chapter contribution	Meckel-Gruber syndrome「多発性嚢胞腎～進化する治療最前線～」 2015/08
7.	Chapter contribution	multicystic dysplastic kidney「多発性嚢胞腎～進化する治療最前線～」 2015/08
8.	Chapter contribution	multilocular renal cyst「多発性嚢胞腎～進化する治療最前線～」 2015/08
9.	Chapter contribution	nephronophthisis「多発性嚢胞腎～進化する治療最前線～」 2015/08
10.	Chapter contribution	oral-facial-digital syndrome [OFD] type 1「多発性嚢胞腎～進化する治療最前線～」 2015/08
11.	Chapter contribution	von Hippel-Lindau disease「多発性嚢胞腎～進化する治療最前線～」 2015/08
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■ Published papers

1.	Original article	A multi-institutional study found a possible role of anti-nephrin antibodies in post-transplant focal segmental glomerulosclerosis recurrence. 2024
2.	Original article	Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome. 2023/02
3.	Original article	Urinary extracellular vesicles signature for diagnosis of kidney disease 2022/11
4.	Original article	Circulating nephrin autoantibodies and posttransplant recurrence of primary focal segmental glomerulosclerosis. 2022/04/26
5.	Original article	Response to steroid and immunosuppressive therapies may predict post-transplant recurrence of steroid- resistant nephrotic syndrome 2022
6.	Original article	A case of early onset cystinuria in a 4-month-old girl 2021/10/20
7.	Original article	Response to steroid and immunosuppressive therapies may predict post-transplant recurrence of steroid-resistant nephrotic syndrome 2021/06
8.	Original article	Cancer After Pediatric Kidney Transplantation: A Long-term Single-center Experience in JapanTransplantation Direct 2021
9.	Original article	Renal hypoplasia can be the cause of membranous nephropathy-like lesions. 2020/05
10.	Original article	Deletion in the Cobalamin Synthetase W Domain-Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract 2020/01
11.	Original article	Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells. 2018/02
12.	Original article	M-type phospholipase A2 receptor (PLA2R) glomerular staining in pediatric idiopathic membranous nephropathy 2017/04
13.	Original article	New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation 2016/02
14.	Original article	SPECT/CT to diagnose pleuroperitoneal communication-associated hydrothorax in peritoneal dialysis 2015/04
15.	Original article	Epithelial protein lost in neoplasm modulates platelet-derived growth factor-mediated adhesion and motility of mesangial cells 2014/04
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■ Academic conference presentation

1.	Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome. 2022/10/07
2.	Cancer after pediatric kidney transplantation: a long-term single-center experience in Japan 2018/02/24
3.	Genital organ anomalies in female pediatric patients with congenital anomalies of the kidney and urinary tract. 2017/10/07
4.	Nation-wide survey of genetic disorders with low molecular weight proteinuria proposal of Japanese diagnostic criteria 2017/06/02
5.	A case of congenital nephrotic syndrome with a heterozygous WT1 mutation complicated by bilateral multiple renal cysts mimicking polycystic kidney disease 2017/04/08
6.	Proliferative glomerulonephritis with monoclonal IgG deposits in pediatric patients: a possible differential diagnosis of pediatric membranoploliferative glomerulonephritis. 2016/11/18
7.	NODAT in a pediatric patient with a novel mutation of HNF1B 2016/04/09
8.	A Family Case of Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome with a Novel Mutation of GATA3 2015/11/06
9.	New-Onset Diabetes after Transplantation in a Pediatric Patient with Congenital Anomalies of the Kidney and Urinary Tract The Role of Hepatocyte Nuclear Facter 2015/11/06
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