Search Results - "LEUMANN, Ernst"

Renal replacement therapy in children and adolescents by Leumann, Ernst

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Children with Steroid-sensitive Nephrotic Syndrome Come of Age: Long-term Outcome by Rüth, Eva-Maria, Kemper, Markus J., Leumann, Ernst P., Laube, Guido F., Neuhaus, Thomas J.

“…Long-term outcome of steroid-sensitive idiopathic nephrotic syndrome (SSNS) in children is usually considered benign, although data on follow-up into adulthood…”
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Xanthinuria type I: a rare cause of urolithiasis by Arikyants, Nina, Sarkissian, Ashot, Hesse, Albrecht, Eggermann, Thomas, Leumann, Ernst, Steinmann, Beat

“…Xanthinuria type I is a rare disorder of purine metabolism caused by xanthine oxidoreductase or dehydrogenase (XDH) deficiency. We report a family with two…”
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Obituary of Andreas Fanconi, 12 August 1928–5 October 2022 by Leumann, Ernst, Neuhaus, Thomas Jacob

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Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis by RUF, Rainer, RENSING, Cornelia, LEUMANN, Ernst, ANTIGNAC, Corinne, RIZZONI, Gianfranco, FILLER, Guido, BRANDIS, Matthias, WEBER, James L, HILDEBRANDT, Friedhelm, TOPALOGLU, Rezan, GUAY-WOODFORD, Lisa, KLEIN, Cornelia, VOLLMER, Martin, OTTO, Edgar, BEEKMANN, Frank, HALLER, Maria, WIEDENSOHLER, Alexander

“…Primary distal renal tubular acidosis (dRTA) type I is a hereditary renal tubular disorder, which is characterized by impaired renal acid secretion resulting…”
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Deceased donor kidney transplanted in childhood functioning well after 52 years by Spartà, Giuseppina, Hadaya, Karine, Paunier, Luc, Girardin, Eric, Leumann, Ernst

“…Background Kidney transplantation in children in 1970 was considered by many to be unethical, as long-term survival was minimal. It was therefore risky at the…”
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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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Renal Chloride Channel, CLCN5, Mutations in Dent's Disease by Cox, Jeremy P. D., Yamamoto, Katsusuke, Christie, Paul T., Wooding, Carol, Feest, Terry, Flinter, Frances A., Goodyer, Paul R., Leumann, Ernst, Neuhaus, Thomas, Reid, Christopher, Williams, Paul F., Wrong, Oliver, Thakker, Rajesh V.

“…Dent's disease is an X‐linked renal tubular disorder characterized by low‐molecular‐weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and…”
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The primary hyperoxalurias by LEUMANN, Ernst, HOPPE, Bernd

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Native kidney biopsies in Armenian and Swiss children: high prevalence of amyloidosis in Yerevan and of IgA nephropathy in Zurich by Laube, Guido F., Sarkissian, Ashot, Nazaryan, Helen, Spartà, Giuseppina, Sanamyan, Armen, Babloyan, Ara, Leumann, Ernst, Gaspert, Ariana

“…The spectrum of pathology in native kidney biopsies varies considerably between different countries. Based on similar biopsy policy and joint workup, biopsy…”
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P01 ‐ Sensitisation pattern to inhalant allergens in Armenian children by Baghdasaryan, Astghik, Sarkissian, Ashot, Leumann, Ernst, Lauener, Roger

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

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Primary hyperoxaluria type 1: is genotyping clinically helpful? by Leumann, Ernst, Hoppe, Bernd

“…There is some controversy about the value of mutation analysis in the management of primary hyperoxaluria type 1 (PH1). About 50 different mutations of the…”
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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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What is new in primary hyperoxaluria? by Leumann, Ernst, Hoppe, Bernd

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

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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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Persistent and transient distal renal tubular acidosis with bicarbonate wasting by Leumann, E P, Steinmann, B

“…Bicarbonate titration studies were performed on two patients with bicarbonate wasting distal renal tubular acidosis (RTA; patients 1 and 2) and on three…”
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Immunization in children with chronic renal failure by LAUBE, Guido F, BERGER, Christoph, GOETSCHEL, Philippe, LEUMANN, Ernst, NEUHAUS, Thomas J

“…Infections jeopardize children on immunosuppression after organ transplantation. Immunization is protective in healthy children. The aims of this study were to…”
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