Planet Of The Apes Coloring Book - c2433

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Lancet II: 475-478 Bodaghi E, Zaman T (1978) Familial nephropathy associated with bone anomaly, degenerative retinitis and congenital liver fibrosis (Abstr) 12th annual meeting of the European Society for Pediatric Nephrology, Israel 1978 Bodaghi E, Zaman T, Kheradpir MH (1980) Familial nephropathy associated with congenital liver firbrosis, degenerative retinitis and cone-shaped epiphysis. Int J Pediatr Nephrol 1:153-156 Biochis H, Passwell J, David R, Miller H (1973) Congenital hepatic fibrosis and nephrononphthisis.

Waldherr R, Gubler MC, Levy M, Broyer M, Habib R (1978)The significance of pure mesangial proliferation in idiopathic nephrotic syndrome. Clin Nephrol 10:171-179 Waldherr R, Scharer K, Muller-Wiefel DE, Seelig HP (1979) Neue klinische und patho-anatomische Aspekte bei der fokalen und segmentalen Sklerose/Hyalinose. In: Olbing H (ed) Nierenbiopsie bei Kindern. Springer, Berlin, Heidelberg, New York, pp 91-99 White RHR, Mills RJ, Beetham R, Raine DN (1975) The significance of variation in the selectivity of proteinuria.

T \~ \ o 0,5 o 2 4 6 8 , 12 YEARS Fig. 1. Protein clearances (ClgG/Ctransferrin) in children with focal segmental sclerosis. Abscissa = years after apparent onset. Serial values of individual patients are interconnected.. 5 mg/dl; P, isolated proteinuria; interrupted Zine (T), transplantation 24 . B8 had the same frequency in FSGS as in controls (18 %), being less frequent than in atopic MC (38 %) (9). 1. 5 mg/dl) this proportion was much higher (85 %i results of 105 protein clearance determinations i'n 35 patients).

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