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The International Journal of Pediatric Nephrology|June 1, 1983
A case of hemolytic uremic syndrome with high concentration of circulating immune complex in the initial stageA Furuse, S Hattori, I Matsuda
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.
The International Journal of Pediatric Nephrology|September 1, 1984
A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidismM Hiramatsu, S Karashima, S Hattori, et al.
Clinical Nephrology|August 1, 1987
Asymptomatic low molecular weight proteinuria: studies in five patientsT Murakami, H Kawakami, S Matsuyama, et al.
Nephron|January 1, 1983
Glomerular IgA1 and IgA2 deposits in IgA nephropathiesT Murakami, A Furuse, S Hattori, et al.
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.
European Journal of Pediatrics|October 1, 1983
Circulating immune complex in the mucocutaneous lymph node syndromeA Furuse, I Matsuda
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.
European Journal of Pediatrics|July 3, 1978
Methylmalonic acidemiaI Matsuda, T Terashima, J Yamamoto, et al.
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