Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Nicolas, Gürtler"'
Autor:
Nicolas Gürtler, Michael Osthoff, Florian Rueter, Daniel Wüthrich, Lukas Zimmerli, Adrian Egli, Stefano Bassetti
Publikováno v:
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Infective endocarditis (IE) caused by gram-negative bacilli is rare. However, the incidence of this severe infection is rising because of the increasing number of persons at risk, such as patients with immunosuppression or with ca
Externí odkaz:
https://doaj.org/article/403b961ea0b643a6a1944b586651a77c
Autor:
Nina Lenherr, John Christodoulou, John Duley, Doreen Dobritzsch, Lynette Fairbanks, Alexandre N. Datta, Isabel Filges, Nicolas Gürtler, Jeroen Roelofsen, André B.P. van Kuilenburg, Claudia Kemper, Erin E. West, Gabor Szinnai, Martina Huemer
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100709- (2021)
Arts syndrome or phosphoribosyl-pyrophosphate-synthetase-1 (PRPS1) deficiency is caused by loss-of-function mutations in the PRPS1 gene (Xq22.3). PRPS1 is an initial and essential step for the synthesis of the nucleotides of purines, pyrimidines, and
Externí odkaz:
https://doaj.org/article/5a14f9f7c4834064a3a5b611e8e50b24
Autor:
Nicolas Gürtler, Andrea Erba, Céline Giehl, Sarah Tschudin-Sutter, Stefano Bassetti, Michael Osthoff
Publikováno v:
Swiss Medical Weekly, Vol 149, Iss 4142 (2019)
AIMS OF THE STUDY Inappropriate use of antimicrobials is associated with the emergence of antimicrobial resistance and adverse events. Antimicrobial stewardship programmes may both optimise treatment of infections and reduce antimicrobial resistance
Externí odkaz:
https://doaj.org/article/dd96249bbcbe49dfa1ed1f28f44d13ba
Publikováno v:
Otology & Neurotology.
Autor:
Nicolas Gürtler, Claudine Gysin, Nevenka Schmid, Claudia Pieren, Mattheus Vischer, Stefan Schumacher, Peter Oppermann, Daniel Leuba, Dorothée Veraguth
Publikováno v:
Swiss Medical Weekly, Vol 147, Iss 0910 (2017)
BACKGROUND The introduction of newborn hearing screening has led to earlier identification of children with congenital sensorineural hearing loss (SNHL). Aetiological clarification offers several benefits. There is currently a lack of agreement on w
Externí odkaz:
https://doaj.org/article/8464c8bf856d40dc863335bc8a3c3ff2
Publikováno v:
European Archives of Oto-Rhino-Laryngology. 279:1203-1210
To review long-term outcomes for chronic otitis media with and without cholesteatoma in staged canal-wall-up tympanoplasty with temporary silastic sheeting and to compare hearing and recurrence results with the literature. Retrospective data analysis
Autor:
Adam F. Cohen, Philip Lambrechtse, Simone Heuscher, Yael Gilgen, Ernst Jan Bos, Andrew Atkinson, Johannes N. van den Anker, Tatjana Welzel, Victoria C. Ziesenitz, Nicolas Gürtler
Publikováno v:
European Journal of Pediatrics. 180:527-533
An observational prospective feasibility study in which children received a tracker 2 weeks before a tonsillectomy and were required to wear it until four weeks postoperatively. The parents used a diary to log the estimated steps of their child. As p
Autor:
Anne Sophie Rebillat, Marie Goulet, Darawan Rinchai, Tanwir Habib, Vincent Bondet, Martine Conte, Anne Puel, Clotilde Mircher, Xiao-Fei Kong, Luyan Liu, Puthen V. Jithesh, Arnold Munnich, Laurent Abel, Damien Chaussabel, Stanislas Lyonnet, Jean-Laurent Casanova, Mohammed Elanbari, Emilie Nonnotte, Jacinta Bustamante, Mélanie Migaud, Nicolas Gürtler, Lisa Worley, Stuart G. Tangye, Aimé Ravel, Cindy S. Ma, Darragh Duffy, Stéphanie Boisson-Dupuis
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2020, Online ahead of print, ⟨10.1007/s10875-020-00803-9⟩
J Clin Immunol
Journal of Clinical Immunology, 2020, Online ahead of print, ⟨10.1007/s10875-020-00803-9⟩
Journal of Clinical Immunology, Springer Verlag, 2020, Online ahead of print, ⟨10.1007/s10875-020-00803-9⟩
J Clin Immunol
Journal of Clinical Immunology, 2020, Online ahead of print, ⟨10.1007/s10875-020-00803-9⟩
International audience; Down syndrome (DS) is characterized by the occurrence of three copies of human chromosome 21 (HSA21). HSA21 contains a cluster of four interferon receptor (IFN-R) genes: IFNAR1, IFNAR2, IFNGR2, and IL10RB. DS patients often de
Publikováno v:
Der Internist. 61:513-517
This article presents the case of a 75-year-old male patient, who underwent a percutaneous abscess puncture of a liver abscess. A few days after the puncture and drainage there was a sudden onset of right upper quadrant abdominal pain accompanied by
Autor:
Claudia Kemper, Doreen Dobritzsch, Jeroen Roelofsen, Alexandre N. Datta, Gabor Szinnai, John A. Duley, Nina Lenherr, Nicolas Gürtler, Isabel Filges, John Christodoulou, Erin E. West, Lynette D. Fairbanks, André B.P. van Kuilenburg, Martina Huemer
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss, Pp 100709-(2021)
Molecular genetics and metabolism reports, 26:100709. Elsevier BV
Molecular Genetics and Metabolism Reports
Molecular genetics and metabolism reports, 26:100709. Elsevier BV
Molecular Genetics and Metabolism Reports
Arts syndrome or phosphoribosyl-pyrophosphate-synthetase-1 (PRPS1) deficiency is caused by loss-of-function mutations in the PRPS1 gene (Xq22.3). PRPS1 is an initial and essential step for the synthesis of the nucleotides of purines, pyrimidines, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aeca935c1a124180f10cfcc4ec01288
https://doi.org/10.5167/uzh-213638
https://doi.org/10.5167/uzh-213638