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American Journal of Medical Genetics|June 24, 1998
4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girlsK Imamura, H Tonoki, K Wakui, et al.Nephron|January 1, 1991
Urinary excretion of terminal complement complexes in glomerular diseaseY Kusunoki, Y Akutsu, N Itami, et al.Pediatric Research|March 1, 1992
Inherited copper toxicity in Long-Evans cinnamon rats exhibiting spontaneous hepatitis: a model of Wilson's diseaseT Okayasu, H Tochimaru, T Hyuga, et al.Kidney International|November 1, 1992
IgA nephropathy in patients with congenital C9 deficiencyK Yoshioka, T Takemura, N Akano, et al.The American Journal of Pathology|May 1, 1994
Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibodyK Yoshioka, S Hino, T Takemura, et al.Nihon Jinzo Gakkai Shi|January 20, 1999
[Standard versus long-term prednisolone with sairei-to for initial therapy in childhood steroid-responsive nephrotic syndrome: a prospective controlled study]N Yoshikawa, H Ito, Y Takekoshi, et al.Journal of Medical Genetics|May 23, 1998
Oral-facial-digital syndrome type IX in a patient with Dandy-Walker malformationK Nagai, M Nagao, M Nagao, et al.Journal of the American Society of Nephrology : JASN|January 16, 1999
A controlled trial of combined therapy for newly diagnosed severe childhood IgA nephropathy. The Japanese Pediatric IgA Nephropathy Treatment Study GroupN Yoshikawa, H Ito, T Sakai, et al.Nihon Jinzo Gakkai Shi|July 1, 1997
[A prospective controlled study of sairei-to in childhood IgA nephropathy with focal/minimal mesangial proliferation. Japanese Pediatric IgA Nephropathy Treatment Study Group]N Yoshikawa, H Ito, T Sakai, et al.Pageof 3