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S Karashima

Showing results (11-20 of 23) with videos related to

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Kidney International|January 20, 1999
Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuriaH Nakazato, J Yoshimuta, S Karashima, et al.
The Japanese Journal of Surgery|November 1, 1986
Primary malignant thymoma in a 6-year-old boyK Shibata, Y Koga, T Onitsuka, et al.
Nihon Jinzo Gakkai Shi|July 1, 1992
[Clinicopathological survey of persistent hypocomplementemic glomerulonephritis in children; correlation of DPGN and MPGN type I]S Hattori, M Hiramatsu, T Ushijima, et al.
American Journal of Nephrology|January 1, 1985
Clinicopathological correlation of IgA nephropathy in childrenS Hattori, S Karashima, A Furuse, et al.
Surgery Today|January 1, 1993
Right common iliac arterio-intestinal fistula caused by tubercular peritonitis: report of a caseI Iwamoto, Y Takechi, H Tomoe, et al.
Clinical Nephrology|April 5, 2000
Membranoproliferative glomerulonephritis in congenital portosystemic shunt without liver cirrhosisS Karashima, S Hattori, H Nakazato, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1995
Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblastsH Nakazato, S Hattori, T Ushijima, et al.
Diabetes, Obesity & Metabolism|September 29, 2011
Protective effects of mineralocorticoid receptor blockade against neuropathy in experimental diabetic ratsH Takata, Y Takeda, A Zhu, et al.
Kidney International|November 5, 1997
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuriaH Nakazato, S Hattori, A Furuse, et al.
Genomics|December 1, 1996
Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2)R Hoshide, Y Ikeda, S Karashima, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Kidney International|January 20, 1999
Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuriaH Nakazato, J Yoshimuta, S Karashima, et al.
The Japanese Journal of Surgery|November 1, 1986
Primary malignant thymoma in a 6-year-old boyK Shibata, Y Koga, T Onitsuka, et al.
Nihon Jinzo Gakkai Shi|July 1, 1992
[Clinicopathological survey of persistent hypocomplementemic glomerulonephritis in children; correlation of DPGN and MPGN type I]S Hattori, M Hiramatsu, T Ushijima, et al.
American Journal of Nephrology|January 1, 1985
Clinicopathological correlation of IgA nephropathy in childrenS Hattori, S Karashima, A Furuse, et al.
Surgery Today|January 1, 1993
Right common iliac arterio-intestinal fistula caused by tubercular peritonitis: report of a caseI Iwamoto, Y Takechi, H Tomoe, et al.
Clinical Nephrology|April 5, 2000
Membranoproliferative glomerulonephritis in congenital portosystemic shunt without liver cirrhosisS Karashima, S Hattori, H Nakazato, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1995
Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblastsH Nakazato, S Hattori, T Ushijima, et al.
Diabetes, Obesity & Metabolism|September 29, 2011
Protective effects of mineralocorticoid receptor blockade against neuropathy in experimental diabetic ratsH Takata, Y Takeda, A Zhu, et al.
Kidney International|November 5, 1997
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuriaH Nakazato, S Hattori, A Furuse, et al.
Genomics|December 1, 1996
Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2)R Hoshide, Y Ikeda, S Karashima, et al.
Pageof 3