Salìh Kavukçu

Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

Anna Richards, Elizabeth J. Kemp, M. Kathryn Liszewski et al. · Proceedings of the National Academy of Sciences · 2003 · 407 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Nationwide and Long-Term Survey of Primary Glomerulonephritis in Japan as Observed in 1,850 Biopsied Cases

M. Brack, Carsten Schroeder, Margrit Fooke et al. · ˜The œNephron journals/Nephron journals · 1999 · 114 citations

Medicine, Nephrology, Pathology +15

Quality of life in children with chronic kidney disease (with child and parent assessments)

Necla Buyan, Mehmet Türkmen, İlmay Bilge et al. · Pediatric Nephrology · 2010 · 96 citations

Medicine, Nephrology, Pediatrics +14

Primary peritonitis in children with nephrotic syndrome: results of a 5-year multicenter study

Nermin Uncu, Mehmet Bülbül, Nurdan Yıldız et al. · European Journal of Pediatrics · 2009 · 67 citations

Medicine, Nephrology, Pediatrics +15

Clinical Course of Children With Nutcracker Syndrome

Demet Alaygut, Meral Torun Bayram, Alper Soylu et al. · Urology · 2013 · 65 citations

Medicine, Child Health, Pediatrics +6