Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Ester M M van Leeuwen"'
Autor:
Rosanne W Wieten, Emile F F Jonker, Ester M M van Leeuwen, Ester B M Remmerswaal, Ineke J M Ten Berge, Adriëtte W de Visser, Perry J J van Genderen, Abraham Goorhuis, Leo G Visser, Martin P Grobusch, Godelieve J de Bree
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0149871 (2016)
INTRODUCTION:Prompted by recent amendments of Yellow Fever (YF) vaccination guidelines from boost to single vaccination strategy and the paucity of clinical data to support this adjustment, we used the profile of the YF-specific CD8+ T-cell subset pr
Externí odkaz:
https://doaj.org/article/2202956733754a58ade553da704c1aaa
Autor:
Hanna K De Jong, Ahmed Achouiti, Gavin C K W Koh, Christopher M Parry, Stephen Baker, Mohammed Abul Faiz, Jaap T van Dissel, Albert M Vollaard, Ester M M van Leeuwen, Joris J T H Roelofs, Alex F de Vos, Johannes Roth, Tom van der Poll, Thomas Vogl, Willem Joost Wiersinga
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 9, Iss 4, p e0003663 (2015)
BACKGROUND:Typhoid fever, caused by the Gram-negative bacterium Salmonella enterica serovar Typhi, is a major cause of community-acquired bacteremia and death worldwide. S100A8 (MRP8) and S100A9 (MRP14) form bioactive antimicrobial heterodimers (calp
Externí odkaz:
https://doaj.org/article/17d137d5f0c64accbf9bc5fb2095daf4
Autor:
Pieter F. de Groot, Arjan J. Kwakernaak, Ester M. M. van Leeuwen, Rosalina M. L. van Spaendonk, Evert-Jan Kooi, Daphne de Jong, Taco W. Kuijpers, Josée M. Zijlstra, Godelieve J. de Bree
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Here we present the case of a 28-year-old man with X-linked immunodeficiency with magnesium defect, Epstein–Barr virus (EBV) infection and neoplasia (XMEN) disease. He presented with immune thrombocytopenia within 1 year after successful autologous
Externí odkaz:
https://doaj.org/article/597b8503eafe4290bec7cd6dc7af646d
Autor:
Samantha A. M. Tromp, Marijn A. Gillissen, Sophie J. Bernelot Moens, Ester M. M. van Leeuwen, Machiel H. Jansen, Lianne Koens, Caroline E. Rutten, Taco W. Kuijpers
Publikováno v:
Blood, 6(15), 4501-4505. American Society of Hematology
Tromp, S A M, Gillissen, M A, Bernelot Moens, S J, van Leeuwen, E M M, Jansen, M H, Koens, L, Rutten, C E & Kuijpers, T W 2022, ' Treatment of an HLH-mimic disease based on HAVCR2 variants with absent TIM-3 expression ', Blood, vol. 6, no. 15, pp. 4501-4505 . https://doi.org/10.1182/bloodadvances.2022007450
Blood advances, 6(15), 4501-4505. American Society of Hematology
Tromp, S A M, Gillissen, M A, Bernelot Moens, S J, van Leeuwen, E M M, Jansen, M H, Koens, L, Rutten, C E & Kuijpers, T W 2022, ' Treatment of an HLH-mimic disease based on HAVCR2 variants with absent TIM-3 expression ', Blood, vol. 6, no. 15, pp. 4501-4505 . https://doi.org/10.1182/bloodadvances.2022007450
Blood advances, 6(15), 4501-4505. American Society of Hematology
Autor:
Sabine Haggenburg, Birgit I. Lissenberg-Witte, Rob S. van Binnendijk, Gerco den Hartog, Michel S. Bhoekhan, Nienke J. E. Haverkate, Dennis M. de Rooij, Johan van Meerloo, Jacqueline Cloos, Neeltje A. Kootstra, Dorine Wouters, Suzanne S. Weijers, Ester M. M. van Leeuwen, Hetty J. Bontkes, Saïda Tonouh-Aajoud, Mirjam H. M. Heemskerk, Rogier W. Sanders, Elianne Roelandse-Koop, Quincy Hofsink, Kazimierz Groen, Lucia Çetinel, Louis Schellekens, Yvonne M. den Hartog, Belle Toussaint, Iris M. J. Kant, Thecla Graas, Emma de Pater, Willem A. Dik, Marije D. Engel, Cheyenne R. N. Pierie, Suzanne R. Janssen, Edith van Dijkman, Meliawati Poniman, Judith A. Burger, Joey H. Bouhuijs, Gaby Smits, Nynke Y. Rots, Sonja Zweegman, Arnon P. Kater, Tom van Meerten, Pim G. N. J. Mutsaers, Jaap A. van Doesum, Annoek E. C. Broers, Marit J. van Gils, Abraham Goorhuis, Caroline E. Rutten, Mette D. Hazenberg, Inger S. Nijhof
Publikováno v:
Blood Advances, 6(5), 1537-1546. ELSEVIER
Blood Advances
Haggenburg, S, Lissenberg-Witte, B I, van Binnendijk, R S, den Hartog, G, Bhoekhan, M S, Haverkate, N J E, de Rooij, D M, van Meerloo, J, Cloos, J, Kootstra, N A, Wouters, D, Weijers, S S, van Leeuwen, E M M, Bontkes, H J, Tonouh-Aajoud, S, Heemskerk, M H M, Sanders, R W, Roelandse-Koop, E, Hofsink, Q, Groen, K, Çetinel, L, Schellekens, L, den Hartog, Y M, Toussaint, B, Kant, I M J, Graas, T, de Pater, E, Dik, W A, Engel, M D, Pierie, C R N, Janssen, S R, van Dijkman, E, Poniman, M, Burger, J A, Bouhuijs, J H, Smits, G, Rots, N Y, Zweegman, S, Kater, A P, van Meerten, T, Mutsaers, P G N J, van Doesum, J A, Broers, A E C, van Gils, M J, Goorhuis, A, Rutten, C E, Hazenberg, M D & Nijhof, I S 2022, ' Quantitative analysis of mRNA-1273 COVID-19 vaccination response in immunocompromised adult hematology patients ', BLOOD ADVANCES, vol. 6, no. 5, pp. 1537-1546 . https://doi.org/10.1182/bloodadvances.2021006917
BLOOD ADVANCES, 6(5), 1537-1546. American Society of Hematology
Blood advances, 6(5), 1537-1546. American Society of Hematology
Blood Advances, 6(5), 1537-1546. AMER SOC HEMATOLOGY
Blood Advances
Haggenburg, S, Lissenberg-Witte, B I, van Binnendijk, R S, den Hartog, G, Bhoekhan, M S, Haverkate, N J E, de Rooij, D M, van Meerloo, J, Cloos, J, Kootstra, N A, Wouters, D, Weijers, S S, van Leeuwen, E M M, Bontkes, H J, Tonouh-Aajoud, S, Heemskerk, M H M, Sanders, R W, Roelandse-Koop, E, Hofsink, Q, Groen, K, Çetinel, L, Schellekens, L, den Hartog, Y M, Toussaint, B, Kant, I M J, Graas, T, de Pater, E, Dik, W A, Engel, M D, Pierie, C R N, Janssen, S R, van Dijkman, E, Poniman, M, Burger, J A, Bouhuijs, J H, Smits, G, Rots, N Y, Zweegman, S, Kater, A P, van Meerten, T, Mutsaers, P G N J, van Doesum, J A, Broers, A E C, van Gils, M J, Goorhuis, A, Rutten, C E, Hazenberg, M D & Nijhof, I S 2022, ' Quantitative analysis of mRNA-1273 COVID-19 vaccination response in immunocompromised adult hematology patients ', BLOOD ADVANCES, vol. 6, no. 5, pp. 1537-1546 . https://doi.org/10.1182/bloodadvances.2021006917
BLOOD ADVANCES, 6(5), 1537-1546. American Society of Hematology
Blood advances, 6(5), 1537-1546. American Society of Hematology
Blood Advances, 6(5), 1537-1546. AMER SOC HEMATOLOGY
Vaccination guidelines for patients treated for hematological diseases are typically conservative. Given their high risk for severe COVID-19, it is important to identify those patients that benefit from vaccination. We prospectively quantified serum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910d395eeba8d201206c2b0c53c0f7f9
https://hdl.handle.net/1887/3566457
https://hdl.handle.net/1887/3566457
Autor:
Paul Tuijnenburg, Ester M. M. van Leeuwen, Cor Lieftink, Roderick L. Beijersbergen, Machiel H. Jansen, Taco W. Kuijpers, Daan J. aan de Kerk, Ben Morris
Publikováno v:
European journal of immunology, 50(1), 73-85. Wiley-VCH Verlag
European Journal of Immunology
European Journal of Immunology
Antibody production by the B cell compartment is a crucial part of the adaptive immune response. Dysregulated antibody production in the form of autoantibodies can cause autoimmune disease. To date, B‐cell depletion with anti‐CD20 antibodies is c
Autor:
Hannah A W Walter, Renske G Kamperman, Joost Raaphorst, Camiel Verhamme, Johannes H T M Koelman, Wouter V Potters, Robert Hemke, Frank F Smithuis, Eleonora Aronica, Ester M M van Leeuwen, Paul A Baars, Marianne de Visser, Ivo N van Schaik, Patrick M M Bossuyt, Anneke J van der Kooi
Publikováno v:
BMJ Open, 11(12):e053594. BMJ Publishing Group
Walter, H A W, Kamperman, R G, Raaphorst, J, Verhamme, C, Koelman, J H T M, Potters, W V, Hemke, R, Smithuis, F F, Aronica, E, van Leeuwen, E M M, Baars, P A, de Visser, M, van Schaik, I N, Bossuyt, P M M & van der Kooi, A J 2021, ' OptimisAtion of Diagnostic Accuracy in idioPathic inflammaTory myopathies (ADAPT study) : A protocol for a prospective diagnostic accuracy study of multimodality testing in patients suspected of a treatable idiopathic inflammatory myopathy ', BMJ Open, vol. 11, no. 12, e053594 . https://doi.org/10.1136/bmjopen-2021-053594
BMJ Open
BMJ open, 11(12):e053594. BMJ Publishing Group
Walter, H A W, Kamperman, R G, Raaphorst, J, Verhamme, C, Koelman, J H T M, Potters, W V, Hemke, R, Smithuis, F F, Aronica, E, van Leeuwen, E M M, Baars, P A, de Visser, M, van Schaik, I N, Bossuyt, P M M & van der Kooi, A J 2021, ' OptimisAtion of Diagnostic Accuracy in idioPathic inflammaTory myopathies (ADAPT study) : A protocol for a prospective diagnostic accuracy study of multimodality testing in patients suspected of a treatable idiopathic inflammatory myopathy ', BMJ Open, vol. 11, no. 12, e053594 . https://doi.org/10.1136/bmjopen-2021-053594
BMJ Open
BMJ open, 11(12):e053594. BMJ Publishing Group
IntroductionIdiopathic inflammatory myopathies (IIMs) excluding inclusion body myositis (IBM) are a group of heterogeneous autoimmune disorders characterised by subacute-onset and progressive proximal muscle weakness, which are frequently part of a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c657bc1901354988e59f8360639e26
https://research.vumc.nl/en/publications/a1a57bb8-52e3-43ec-bd69-346734a0a12e
https://research.vumc.nl/en/publications/a1a57bb8-52e3-43ec-bd69-346734a0a12e
Autor:
Jacqueline C.P. Langeslag, Ester M. M. van Leeuwen, Katja H. de Jong, Saskia Kuipers, Sander C. Kuijpers, Frans A. G. Reubsaet, Godelieve J. de Bree, Michelle J. Klouwens, Joppe W. Hovius, Martin P. Grobusch
Publikováno v:
Travel medicine and infectious disease, 42:102080. Elsevier USA
Travel Medicine and Infectious Disease, 42
Travel Medicine and Infectious Disease, 42
Contains fulltext : 238274.pdf (Publisher’s version ) (Open Access) A 27 years-old Dutch male returning from Nepal presented with a painful abscess on the left forearm without fever or other systemic complications. Signs and symptoms consisted of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fa8678471cf658dcc13be3db83cb96
https://pure.amc.nl/en/publications/primary-cutaneous-melioidosis-acquired-in-nepal--case-report-and-literature-review(3e0e7e38-6e4a-42b2-bafc-481c7f1b47e6).html
https://pure.amc.nl/en/publications/primary-cutaneous-melioidosis-acquired-in-nepal--case-report-and-literature-review(3e0e7e38-6e4a-42b2-bafc-481c7f1b47e6).html
Autor:
Jovanka R King, Cristina Bottino, Patrick Quinn, Alexander Blank, Asbjørg Stray-Pedersen, Michael Gold, Ulrich Pannicke, Emily M. Mace, Lisa R. Forbes, Marwan Abu-Halaweh, Eva-Maria Jacobsen, Anton T.J. Tool, Sabrina Chiesa, Roberta Caorsi, Marco Gattorno, Silvia Giliani, Stefano Volpi, Jordan S. Orange, Ivan K. Chinn, Taco W. Kuijpers, Immacolata Brigida, Hamid Ahanchian, Paul Tuijnenburg, Federica Barzaghi, Bertrand Boisson, Zeynep Coban Akdemir, Gregor Dückers, Chris Pearson, Machiel H. Jansen, Alexander B. Meijer, Maria Pia Cicalese, Ansgar Schulz, Filiz O. Seeborg, Eloy Cuadrado, Hasan Tawamie, Ehsan Ghayoor Karimiani, Jean-Laurent Casanova, Raed Alzyoud, Tomasz Gambin, Stefania Marcenaro, Luigi D. Notarangelo, Anselm Enders, Rae S. M. Yeung, Klaus Schwarz, Reza Maroofian, Hans Christian Erichsen, Paolo Picco, Ester M. M. van Leeuwen, Tim Niehues, Ronald M. Laxer, James R. Lupski, Alessandro Aiuti
Publikováno v:
Journal of Allergy and Clinical Immunology, 143(6), 2296-2299. Mosby Inc.
Journal of allergy and clinical immunology, 143(6), 2296-2299. Mosby Inc.
Journal of Allergy and Clinical Immunology, 143(6), 2296. Mosby Inc.
Journal of allergy and clinical immunology, 143(6), 2296-2299. Mosby Inc.
Journal of Allergy and Clinical Immunology, 143(6), 2296. Mosby Inc.
We report the natural history, clinical manifestations, genetics, and immunohematological findings in 14 patients from 11 families with ARPC1B deficiency, delineating the spectrum of the disease that appears progressive and challenging to manage clin
Autor:
Sandrine Florquin, Ester M. M. van Leeuwen, Jonas Johannes Papendorf, Frédéric Ebstein, Silvana van Koningsbruggen, Machiel H. Jansen, Dorit Verhoeven, Taco W. Kuijpers, Saskia M. Maas, J. Merlijn van den Berg, Mirjam van der Burg, Elke Krüger, Dieneke Schonenberg-Meinema, Paul A. Baars, Arjan C. Lankester
Publikováno v:
Journal of allergy and clinical immunology. Mosby Inc.
Journal of Allergy and Clinical Immunology, 149(3), 1120-1127.e8. MOSBY-ELSEVIER
Journal of Allergy and Clinical Immunology, 149(3), 1120-1127.e8. MOSBY-ELSEVIER
Background: Proteasome-associated autoinflammatory syndromes (PRAASs) form a family of recently described rare autosomal recessive disorders of disturbed proteasome assembly and proteolytic activity caused by mutations in genes coding for proteasome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b00577084f02766dc8a5c6d117fbaf
https://pure.amc.nl/en/publications/hematopoietic-stem-cell-transplantation-in-a-patient-with-proteasomeassociated-autoinflammatory-syndrome-praas(31630366-3491-4564-b3de-9f6e593d1a38).html
https://pure.amc.nl/en/publications/hematopoietic-stem-cell-transplantation-in-a-patient-with-proteasomeassociated-autoinflammatory-syndrome-praas(31630366-3491-4564-b3de-9f6e593d1a38).html