（Last updated : 2024-03-08 15:53:18）
  神田　祥一郎
   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
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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 Link
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
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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
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