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Adalberto Sessa

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)Gian Marco Ghiggeri, Gianluca Caridi, Umberto Magrini, et al.
Journal of Nephrology|August 6, 2004
Juvenile renal cell carcinoma as first manifestation of von Hippel-Lindau diseaseAntonio Granata, Adalberto Sessa, Marco Righetti, et al.
Lancet (London, England)|March 16, 2005
Blood-pressure control for renoprotection in patients with non-diabetic chronic renal disease (REIN-2): multicentre, randomised controlled trialPiero Ruggenenti, Annalisa Perna, Giacomina Loriga, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2005
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian familiesLaura Calabresi, Livia Pisciotta, Anna Costantin, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)Gian Marco Ghiggeri, Gianluca Caridi, Umberto Magrini, et al.
Journal of Nephrology|August 6, 2004
Juvenile renal cell carcinoma as first manifestation of von Hippel-Lindau diseaseAntonio Granata, Adalberto Sessa, Marco Righetti, et al.
Lancet (London, England)|March 16, 2005
Blood-pressure control for renoprotection in patients with non-diabetic chronic renal disease (REIN-2): multicentre, randomised controlled trialPiero Ruggenenti, Annalisa Perna, Giacomina Loriga, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2005
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian familiesLaura Calabresi, Livia Pisciotta, Anna Costantin, et al.
Pageof 2