Search Results - "Leumann, E"

The primary hyperoxalurias by LEUMANN, Ernst, HOPPE, Bernd

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POS-772 50 YEARS FUNCTIONING RENAL GRAFT PERFORMED IN CHILDHOOD by Sparta, G., Hadaya, K., Luc, P., Girardin, E., Leumann, E.

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Diagnostic and therapeutic strategies in hyperoxaluria: a plea for early intervention by Hoppe, Bernd, Leumann, Ernst

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Changing pattern of primary hyperoxaluria in Switzerland by Kopp, N, Leumann, E

“…The clinical course of primary hyperoxaluria (PH) is greatly variable and diagnosis is often delayed. Little is known about the overall occurrence and current…”
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Pediatric urolithiasis in Armenia : a study of 198 patients observed from 1991 to 1999 by SARKISSIAN, Ashot, BABLOYAN, Ara, ARIKYANTS, Nina, HESSE, Albrecht, BLAU, Nenad, LEUMANN, Ernst

“…To study prospectively the risk factors and etiology of urolithiasis in all stone patients aged <15 years admitted from 1991 to 1999 to the Arabkir hospital in…”
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New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels by MULDERS, S. M, KNOERS, N. V. A. M, VAN LIEBURG, A. F, MONNENS, L. A. H, LEUMANN, E, WOHL, E, SCHOBER, E, RIJSS, J. P. L, VAN OS, C. H, DEEN, P. M. T

“…Nephrogenic diabetes insipidus (NDI) is characterized by the inability of the kidney to concentrate urine in response to vasopressin. The autosomal recessive…”
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Urinary oxalate excretion in urolithiasis and nephrocalcinosis by Neuhaus, Thomas J, Belzer, Tanja, Blau, Nenad, Hoppe, Bernd, Sidhu, Harmeet, Leumann, Ernst

“…AIMS To investigate urinary oxalate excretion in children with urolithiasis and/or nephrocalcinosis and to classify hyperoxaluria (HyOx). METHODS A total of…”
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Heterogeneity of atypical haemolytic uraemic syndromes by Neuhaus, Thomas J, Calonder, Seraina, Leumann, Ernst P

“…Atypical, non-diarrhoea associated haemolytic uraemic syndrome (D−HUS) is a heterogeneous disorder with a generally poor outcome, although this view has now…”
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Heparin-induced thrombocytopenia type II on hemodialysis : switch to danaparoid by NEUHAUS, T. J, GOETSCHEL, P, SCHMUGGE, M, LEUMANN, E

“…We report two pediatric patients with end-stage renal failure who developed heparin-induced thrombocytopenia type II (HIT II) on hemodialysis (HD). Both…”
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A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severity by Hoppe, B, Danpure, C J, Rumsby, G, Fryer, P, Jennings, P R, Blau, N, Schubiger, G, Neuhaus, T, Leumann, E

“…Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused by a deficiency of alanine:glyoxylate aminotransferase (encoded by the AGXT…”
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Efficacy of oral citrate administration in primary hyperoxaluria by Leumann, E, Hoppe, B, Neuhaus, T, Blau, N

“…Urinary citrate is a potent inhibitor of calcium oxalate (CaOx) crystallization, but oral citrate has rarely been used in patients with primary hyperoxaluria…”
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The boy with massive glucosuria by Sarkissian, Ashot, Santer, René, Steinmann, Beat, Amaryan, Gayane, Leumann, Ernst

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Pyelonephritis and vesicoureteral reflux after renal transplantation in young children by Neuhaus, T J, Schwöbel, M, Schlumpf, R, Offner, G, Leumann, E, Willi, U

“…We assessed morbidity and risk factors of pyelonephritis in children after renal transplantation. Between 1986 and 1995, 41 children underwent transplantation…”
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An epidemic of acute postinfectious glomerulonephritis in Armenia by Sarkissian, Ashot, Papazian, Marina, Azatian, Gayane, Arikiants, Nina, Babloyan, Ara, Leumann, Ernst

“…AIM To evaluate the presentation and course of acute postinfectious glomerulonephritis (APGN), which has increased dramatically in Armenia after serious…”
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Renal-hepatic-pancreatic dysplasia : an autosomal recessive disorder with renal and hepatic failure by NEUHAUS, T. J, SENNHAUSER, F, BRINER, J, VAN DAMME, B, LEUMANN, E. P

“…We report two brothers with renal dysplasia and congenital hepatic fibrosis. One patient died shortly after birth of lung hypoplasia. The second developed…”
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Urinary saturation and nephrocalcinosis in preterm infants: effect of parenteral nutrition by Hoppe, B, Hesse, A, Neuhaus, T, Fanconi, S, Forster, I, Blau, N, Leumann, E

“…Urinary lithogenic and inhibitory factors were studied in 27 preterm infants; 16 had total parenteral nutrition (TPN) and 11 had breastmilk with an additional…”
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Long-term low-dose cyclosporin A in steroid dependent nephrotic syndrome of childhood by NEUHAUS, T. J, BURGER, H. R, KLINGLER, M, FANCONI, A, LEUMANN, E. P

“…Therapy of steroid-dependent idiopathic nephrotic syndrome is often unsatisfactory. Since 1986 we have treated nine children (six male and three female), aged…”
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Acute renal failure in paediatric patients : the role of continuous haemofiltration by FANCONI, S, LEUMANN, E. P

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Prenatal sonographic diagnosis of autosomal recessive polycystic kidney disease (ARPKD) during the early second trimester by Wisser, J, Hebisch, G, Froster, U, Zerres, K, Stallmach, T, Leumann, E, Schinzel, A, Huch, A

“…Autosomal recessive polycystic kidney disease (ARPKD) is a rare hereditary disease with a high neonatal mortality. Currently, prenatal diagnosis is possible…”
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Familial progressive tubulo-interstitial nephropathy and cholestatic liver disease: a newly recognized entity? by NEUHAUS, T. J, STALLMACH, T, LEUMANN, E, ALTORFER, J, BRAEGGER, C. P

“…We describe two siblings (female and male) with progressive tubulo-interstitial nephropathy and cholestatic liver disease. The main characteristics were…”
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