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European Journal of Pediatrics|May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?R Gitzelmann, M A Spycher, S Adank, et al.The Journal of Biological Chemistry|January 25, 1989
Decreased thermal denaturation temperature of osteogenesis imperfecta mutant collagen is independent of post-translational overmodifications of lysine and hydroxylysineV H Rao, B Steinmann, W de Wet, et al.Life Sciences|January 1, 1994
Protracted high-dose interferon gamma therapy for chronic experimental nephropathyF Ginevri, E Bergamaschi, A Mutti, et al.Nephron|January 1, 1989
Endogenous albumin as a marker of renal selectivity in steroid-unresponsive nephrotic syndromeF Ginevri, G M Ghiggeri, G Candiano, et al.Advances in Peritoneal Dialysis. Conference on Peritoneal Dialysis|January 1, 1996
Protein and calorie intake, nitrogen losses, and nitrogen balance in children undergoing chronic peritoneal dialysisA Canepa, F Perfumo, A Carrea, et al.Klinische Monatsblatter Fur Augenheilkunde|December 1, 1986
[Infantile cataract, hypertrophic cardiomyopathy and lactic acidosis following minor muscular exertion--a little known metabolic disease]S Lalive d'Epinay, S Rampini, U Arbenz, et al.American Journal of Medical Genetics|January 31, 1998
Retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia (RHYNS): a new syndrome?M Di Rocco, P Picco, A Arslanian, et al.American Journal of Medical Genetics. Part A|September 19, 2009
Mandibuloacral dysplasia type A in childhoodL Garavelli, M R D'Apice, F Rivieri, et al.Kidney International|April 1, 1992
Nutritional status and muscle amino acids in children with end-stage renal failureA Canepa, J C Divino Filho, A M Forsberg, et al.Nature Genetics|November 14, 1997
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndromeR Santer, R Schneppenheim, A Dombrowski, et al.Pageof 31