Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Rodo O. von Vigier"'
Autor:
Christina Nießl, Anne-Laure Boulesteix, Jun Oh, Katja Palm, Peter Schlingmann, Simone Wygoda, Dieter Haffner, Elke Wühl, Burkhard Tönshoff, Anja Buescher, Heiko Billing, Bernd Hoppe, Matthias Zirngibl, Matthias Kettwig, Kristina Moeller, Birgit Acham-Roschitz, Klaus Arbeiter, Martin Bald, Marcus Benz, Matthias Galiano, Ulrike John-Kroegel, Guenter Klaus, Daniela Marx-Berger, Katja Moser, Dirk Mueller, Ludwig Patzer, Martin Pohl, Barbara Seitz, Ulrike Treikauskas, Rodo O. von Vigier, William Allen Gahl, Katharina Hohenfellner
Infantile nephropathic cystinosis, due to impaired transport of cystine out of lysosomes, occurs with an incidence of 1 in 100–200,000 live births. It is characterized by renal Fanconi syndrome in the first year of life and glomerular dysfunction p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f153907d5bb7c1cde126a1c1be60a4b3
https://www.ncbi.nlm.nih.gov/pubmed/35835062
https://www.ncbi.nlm.nih.gov/pubmed/35835062
Autor:
Erik Harms, Susanne Bechtold, Nadine Herzig, Malcolm Lewis, Justine Bacchetta, William A. Gahl, Alexey Tsygin, Ewa Elenberg, Fernando Santos, Oliver Greil, Noelle Cassidy, Karl P. Schlingmann, Neveen A. Soliman, Atif Awan, Gema Ariceta, Frank Rauch, Dieter Haffner, Elena Levtchenko, Aude Servais, Jozef Zustin, Bernd Hoppe, Rezan Topaloglu, Galina Nesterova, Koenraad Veys, Carsten Bergmann, Ulrike Treikauskas, Christian Koeppl, Geroges Deschenes, Katharina Hohenfellner, Clodagh Sweeney, Guenther Steidle, Rodo O. von Vigier
Publikováno v:
Journal of Inherited Metabolic Disease
Cystinosis is an autosomal recessive storage disease due to impaired transport of cystine out of lysosomes. Since the accumulation of intracellular cystine affects all organs and tissues, the management of cystinosis requires a specialized multidisci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c24db0ff1f1e1c5291d9fb8fc4ad9d
https://doi.org/10.1002/jimd.12134
https://doi.org/10.1002/jimd.12134
Autor:
Christoph Berger, Rodo O. von Vigier, Ulrich Heininger, Philipp Agyeman, Julia Bielicki, Thomas J. Neuhaus, Christoph Rudin, Lisa Kottanattu, Anita Niederer-Loher, Johannes Trueck, Sandra A. Asner, Christian R Kahlert, Petra Zimmermann, Guido F. Laube, Michael Buettcher, Klara M. Posfay-Barbe, Rita Gobet, Christa Relly, Nicole Ritz, Patrick M. Meyer Sauteur, Sandra Shavit, Paolo Paioni, Franziska Zucol
The article “Swiss consensus recommendations on urinary tract infections in children”
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::280c6bf22cdd07aa9f26c0d3ce664465
https://doi.org/10.5167/uzh-192847
https://doi.org/10.5167/uzh-192847
Publikováno v:
Praxis. 106:519-526
Zusammenfassung. Hintergrund: Die Wirksamkeit der peroralen antibiotischen Therapie bei Säuglingen und Kleinkindern mit akuter Pyelonephritis wurde unlängst gezeigt; systematische Daten über die Häufigkeit limitierender Faktoren dieser Therapiefo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::915e44d5e1889c4131ede51e9163bb9f
https://doi.org/10.1024/1661-8157/a002676
https://doi.org/10.1024/1661-8157/a002676
Publikováno v:
Trück, Johannes; Laube, Guido F; von Vigier, Rodo O; Goetschel, Philippe (2010). Gout in pediatric renal transplant recipients. Pediatric nephrology, 25(12), pp. 2535-8. Berlin: Springer 10.1007/s00467-010-1599-6
Clinical gout has rarely been described after pediatric renal transplantation (RTx), although asymptomatic hyperuricemia is common in these patients. We describe three male pediatric patients who presented with gouty arthritis 7-8.5 years following R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dc586b99716641f2924afd29943121e
http://doc.rero.ch/record/320673/files/467_2010_Article_1599.pdf
http://doc.rero.ch/record/320673/files/467_2010_Article_1599.pdf
Autor:
Urs B. Schaad, Bettina Essers, Christoph Aebi, Rodo O. von Vigier, André P. Burnens, Stefano G. E. Somaruga, Mario G. Bianchetti, Francesco M. Lanfranchini
Publikováno v:
Essers, Bettina; Burnens, André P.; Lanfranchini, Francesco M.; Somaruga, Stefano G. E.; von Vigier, Rodo O.; Schaad, Urs B.; Aebi, Christoph; Bianchetti, Mario G. (2000). Acute Community-Acquired Diarrhea Requiring Hospital Admission in Swiss Children. Clinical infectious diseases, 31(1), pp. 192-196. The University of Chicago Press 10.1086/313901
In order to ascertain the prevalence of agents that cause childhood diarrheal illness, stool specimens of 312 consecutive children with community-acquired diarrhea requiring admission were evaluated. Pathogens were detected in 166 (53%) of the 312 ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30dd84f2a3fe2c4b30392fa654dc8db4
http://doc.rero.ch/record/301260/files/31-1-192.pdf
http://doc.rero.ch/record/301260/files/31-1-192.pdf
Autor:
Rodo O. von Vigier, Carmen Casaulta Aebischer, Anita C. Truttmann, Alberto Bettinelli, Mario G. Bianchetti, Bendicht Wermuth, Karin Zindler‐Schmocker
Publikováno v:
von Vigier, Rodo O.; Truttmann, Anita C.; Zindler-Schmocker, Karin; Bettinelli, Alberto; Casaulta Aebischer, Carmen; Wermuth, Bendicht; Bianchetti, Mario G. (2000). Aminoglycosides and renal magnesium homeostasis in humans. Nephrology, dialysis, transplantation, 15(6), pp. 822-826. Oxford University Press 10.1093/ndt/15.6.822
complication of aminoglycosides, which is mostly asso- ciated with acute renal failure, has been documented Background. The use of aminoglycosides has been linked with hypomagnesaemia in scattered reports. The in scattered anecdotal reports (1-5). Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d766f5808092e02e6b2c37beafd5d05a
http://doc.rero.ch/record/298748/files/150822.pdf
http://doc.rero.ch/record/298748/files/150822.pdf
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 58:404-408
OBJECTIVES: Premature babies require supplementation with calcium and phosphorus to prevent metabolic bone disease of prematurity. To guide mineral supplementation, two methods of monitoring urinary excretion of calcium and phosphorus are used: urina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5320c92cacd9cb9101740b09bfe896a4
https://doi.org/10.1097/mpg.0000000000000244
https://doi.org/10.1097/mpg.0000000000000244
Publikováno v:
Journal of the American Society of Nephrology. 19:1331-1341
Despite identification of the genes responsible for autosomal dominant polycystic kidney disease (PKD) and autosomal recessive PKD (ARPKD), the precise functions of their cystoprotein products remain unknown. Recent data suggested that multimeric cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7628ae8ea98b517564b4cd754af7dee9
https://doi.org/10.1681/asn.2007060665
https://doi.org/10.1681/asn.2007060665
Autor:
Stefanie Weber, Eberhard Kuwertz-Bröking, Tomáš Seeman, Hammad O. Alshaya, Velibor Tasic, André Schaller, Rodo O. von Vigier, Daniel A. Goodenough, Jörg Dötsch, Sabina Gallati, Katalin Dittrich, Jianghui Hou, Amira Peco-Antic, Martin Konrad, Jameela A. Kari
Publikováno v:
Journal of the American Society of Nephrology. 19:171-181
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive tubular disorder caused by CLDN16 mutations. CLDN16 encodes the renal tight junction protein claudin-16, which is important for the paracellular re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8633bb699e2a07f059b45e15f445cd67
https://doi.org/10.1681/asn.2007060709
https://doi.org/10.1681/asn.2007060709