Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Yvonne, Hendriks"'
Autor:
Veronica Weterings, Wouter van den Bijllaardt, Martin Bootsma, Yvonne Hendriks, Linda Kilsdonk, Ans Mulders, Jan Kluytmans
Publikováno v:
Antimicrobial Resistance and Infection Control, Vol 11, Iss 1, Pp 1-9 (2022)
Abstract Background In 2016, a study in a Dutch nursing home showed prolonged colonization duration of extended-spectrum β-lactamase-producing (ESBL)-ST131 compared to ESBL-non-ST131. In this study, we assessed the duration of rectal ESBL-producing
Externí odkaz:
https://doaj.org/article/76def97580f546a6ac940e39bd66199d
Autor:
Julian Delanne, Magali Lecat, Patrick Blackburn, Eric Klee, Constance Stumpel, Sander Stegmann, Servi Stevens, Caroline Nava, Delphine Heron, Boris Keren, Sonal Mahida, Sakkubai Naidu, Dusica Babovic-Vuksanovic, Johanna Herkert, Pernille Toerring, Maria Kibæk, Isabelle De Bie, Rolph Pfundt, Yvonne Hendriks, Lilian Bomme Ousager, Renee Bend, Hannah Warren, Steve Skinner, Michael Lyons, Charlotte Poe, Martin Chevarin, Thibaud Jouan, Aurore Garde, Quentin Thomas, Paul Kuentz, Emilie Tisserant, Yannis Duffourd, Christophe Philippe, Laurence Faivre, Christel Thauvin
Publikováno v:
SSRN Electronic Journal.
Autor:
Veronica Mericq, Isabel Huang-Doran, Dhekra Al-Naqeb, Javiera Basaure, Claudia Castiglioni, Christiaan de Bruin, Yvonne Hendriks, Enrico Bertini, Fowzan S Alkuraya, Monique Losekoot, Khalid Al-Rubeaan, Robert K Semple, Jan M Wit
Publikováno v:
Mericq, V, Huang-Doran, I, Al-naqeb, D, Basaure, J, Castiglioni, C, De Bruin, C, Hendriks, Y, Bertini, E, Alkuraya, F S, Losekoot, M, Al-rubeaan, K, Semple, R K & Wit, J M 2022, ' Biallelic POC1A variants cause syndromic severe insulin resistance with muscle cramps ', European Journal of Endocrinology . https://doi.org/10.1530/EJE-21-0609
European journal of endocrinology, 186(5), 543-552. BIOSCIENTIFICA LTD
European journal of endocrinology, 186(5), 543-552. BIOSCIENTIFICA LTD
Objective To describe clinical, laboratory, and genetic characteristics of three unrelated cases from Chile, Portugal, and Saudi Arabia with severe insulin resistance, SOFT syndrome, and biallelic pathogenic POC1A variants. Design Observational study
Autor:
Jasper van der Slegt, Lijckle van der Laan, Eelco J Veen, Yvonne Hendriks, Jannie Romme, Jan Kluytmans
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e71566 (2013)
BACKGROUND: Surgical site infections (SSI's) are associated with severe morbidity, mortality and increased health care costs in vascular surgery. OBJECTIVE: To implement a bundle of care in vascular surgery and measure the effects on the overall and
Externí odkaz:
https://doaj.org/article/20fc4a07f44c49aea5b4be570b6c7f5c
Autor:
Yvonne Hendriks, Veronica Weterings, Bregje van de Wier, Linda Kilsdonk, Jan Kluytmans, Ans Mulders, Tineke de Goede
Background Escherichia coli sequence type ST131 is a recently emerged worldwide pandemic clonal group. Antibiotic resistance, virulence factors or colonisation fitness are mentioned among other as possible factors contributing to the worldwide succes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9b3406c49c880197373c094528bd91f
https://doi.org/10.21203/rs.3.rs-136458/v1
https://doi.org/10.21203/rs.3.rs-136458/v1
Autor:
Rogier M P H Crolla, Lijckle van der Laan, Eelco J Veen, Yvonne Hendriks, Caroline van Schendel, Jan Kluytmans
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e44599 (2012)
BACKGROUND: Surgical Site Infections (SSI) are relatively frequent complications after colorectal surgery and are associated with substantial morbidity and mortality. OBJECTIVE: Implementing a bundle of care and measuring the effects on the SSI rate.
Externí odkaz:
https://doaj.org/article/e4ad23e69c714542b827b9252634e7b4
Autor:
Charlotte A. Haaxma, Daan M. Panneman, Nicole I. Wolf, Els M.A. van de Westerlo, Sjenet E. van Emst-de Vries, Werner J.H. Koopman, Maaike de Vries, Saskia B. Wortmann, Dirk Lefeber, Frans van den Brandt, Yvonne Hendriks, Richard J. Rodenburg, Jan A.M. Smeitink, Peter M. van Hasselt, Benno Küsters, Liesbeth T. Wintjes
Publikováno v:
Clinical Genetics, 97, 4, pp. 556-566
Clinical Genetics, 97, 556-566
Panneman, D M, Wortmann, S B, Haaxma, C A, van Hasselt, P M, Wolf, N I, Hendriks, Y, Küsters, B, van Emst-de Vries, S, van de Westerlo, E, Koopman, W J H, Wintjes, L, van den Brandt, F, de Vries, M, Lefeber, D J, Smeitink, J A M & Rodenburg, R J 2020, ' Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction ', Clinical Genetics, vol. 97, no. 4, pp. 556-566 . https://doi.org/10.1111/cge.13706
Clinical Genetics, 97(4), 556-566. Wiley-Blackwell
Clinical Genetics
Clin. Genet. 97, 556-566 (2020)
Clinical Genetics, 97, 556-566
Panneman, D M, Wortmann, S B, Haaxma, C A, van Hasselt, P M, Wolf, N I, Hendriks, Y, Küsters, B, van Emst-de Vries, S, van de Westerlo, E, Koopman, W J H, Wintjes, L, van den Brandt, F, de Vries, M, Lefeber, D J, Smeitink, J A M & Rodenburg, R J 2020, ' Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction ', Clinical Genetics, vol. 97, no. 4, pp. 556-566 . https://doi.org/10.1111/cge.13706
Clinical Genetics, 97(4), 556-566. Wiley-Blackwell
Clinical Genetics
Clin. Genet. 97, 556-566 (2020)
Contains fulltext : 218925.pdf (Publisher’s version ) (Open Access) NGLY1 encodes the enzyme N-glycanase that is involved in the degradation of glycoproteins as part of the endoplasmatic reticulum-associated degradation pathway. Variants in this ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8963f6324659dbd47f99639baf9be848
https://doi.org/10.1111/cge.13706
https://doi.org/10.1111/cge.13706
Autor:
Liesbeth T. Wintjes, Maaike de Vries, Charlotte A. Haaxma, Richard R. J. Rodenburg, Saskia B Wortmann, Els M.A. van de Westerlo, Frans van den Brandt, Yvonne Hendriks, Nicole I. Wolf, Sjenet E. van Emst-de Vries, Dirk J. Lefeber, Jan A.M. Smeitink, Benno Kusters, W.J.H. Koopman, Peter M. Hasselt, Daan M. Panneman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a817167d064bd3e7a011dab8a47c2a79
https://doi.org/10.1111/cge.13706/v2/response1
https://doi.org/10.1111/cge.13706/v2/response1
Autor:
Ans Mulders, Jan Kluytmans, Robert Roosendaal, Carlo Verhulst, Kim van der Zwaluw, Jolande Nelson, Paul G.H. Mulder, Marjolein F. Q. Kluytmans-van den Bergh, Sandrien Verhoeff, Ina Willemsen, Yvonne Hendriks
Publikováno v:
Infection Control and Hospital Epidemiology, 36, 4, pp. 394-400
Willemsen, I, Nelson, J, Hendriks, Y, Mulders, A, Verhoeff, S, Mulder, P, Roosendaal, R, van der Zwaluw, K, Verhulst, C, Kluytmans-van d Bergh, M & Kluytmans, J 2015, ' Extensive Dissemination of Extended Spectrum beta-Lactamase-Producing Enterobacteriaceae in a Dutch Nursing Home ', Infection Control and Hospital Epidemiology, vol. 36, no. 4, pp. 394-400 . https://doi.org/10.1017/ice.2014.76
Infection Control and Hospital Epidemiology, 36, 394-400
Infection control and hospital epidemiology, 36(4), 394. University of Chicago Press
Infection Control and Hospital Epidemiology, 36(4), 394-400. Cambridge University Press
Willemsen, I, Nelson, J, Hendriks, Y, Mulders, A, Verhoeff, S, Mulder, P, Roosendaal, R, van der Zwaluw, K, Verhulst, C, Kluytmans-van d Bergh, M & Kluytmans, J 2015, ' Extensive Dissemination of Extended Spectrum beta-Lactamase-Producing Enterobacteriaceae in a Dutch Nursing Home ', Infection Control and Hospital Epidemiology, vol. 36, no. 4, pp. 394-400 . https://doi.org/10.1017/ice.2014.76
Infection Control and Hospital Epidemiology, 36, 394-400
Infection control and hospital epidemiology, 36(4), 394. University of Chicago Press
Infection Control and Hospital Epidemiology, 36(4), 394-400. Cambridge University Press
OBJECTIVERisk factors for rectal carriage of ESBL-E and transmission were investigated in an outbreak of extended-spectrum β-lactamase–producing Enterobacteriaceae (ESBL-E).DESIGNRectal carriage of ESBL-E was determined in a cross-sectional survey
Autor:
Yu Sun, Martijn H. Breuning, Gijs W. E. Santen, Arie van Haeringen, Cacha M.P.C.D. Peeters-Scholte, Rowida Almomani, Yvonne Hendriks, Johan T. den Dunnen, Yvonne Hilhorst-Hofstee, Emmelien Aten, Marjolein Kriek
Publikováno v:
American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, 161(5), 973-976. Wiley-Liss Inc.
American Journal of Medical Genetics Part A, 161A(5), 973-976
Almomani, R, Sun, Y, Aten, E, Hilhorst-Hofstee, Y, Peeters-Scholte, C M P C, van Haeringen, A, Hendriks, Y M C, den Dunnen, J T, Breuning, M H, Kriek, M & Santen, G W E 2013, ' GPSM2 and Chudley-McCullough Syndrome: A Dutch Founder Variant Brought to North America ', American Journal of Medical Genetics Part A, vol. 161, no. 5, pp. 973-976 . https://doi.org/10.1002/ajmg.a.35808
American Journal of Medical Genetics Part A, 161(5), 973-976. Wiley-Liss Inc.
American Journal of Medical Genetics Part A, 161A(5), 973-976
Almomani, R, Sun, Y, Aten, E, Hilhorst-Hofstee, Y, Peeters-Scholte, C M P C, van Haeringen, A, Hendriks, Y M C, den Dunnen, J T, Breuning, M H, Kriek, M & Santen, G W E 2013, ' GPSM2 and Chudley-McCullough Syndrome: A Dutch Founder Variant Brought to North America ', American Journal of Medical Genetics Part A, vol. 161, no. 5, pp. 973-976 . https://doi.org/10.1002/ajmg.a.35808
Chudley-McCullough syndrome (CMS) is characterized by profound sensorineural hearing loss and brain anomalies. Variants in GPSM2 have recently been reported as a cause of CMS by Doherty et al. In this study we have performed exome sequencing of three