Zobrazeno 1 - 10
of 11 231
pro vyhledávání: '"A Schols"'
Autor:
Wouter R. P. H. van deWorp, Jan Theys, Cecile J. A. Wolfs, Frank Verhaegen, Annemie M. W. J. Schols, Ardy vanHelvoort, Ramon C. J. Langen
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 5, Pp 1664-1676 (2024)
Abstract Background Cachexia, a syndrome with high prevalence in non‐small cell lung cancer patients, impairs quality of life and reduces tolerance and responsiveness to cancer therapy resulting in decreased survival. Optimal nutritional care is pi
Externí odkaz:
https://doaj.org/article/fc898882fc9b4a0daaa961b6d09c4238
Autor:
Esther van Santbrink, Antonius A. van den Hurk, Anneke Spekenbrink-Spooren, Juliette E. Hommes, Rutger M. Schols, Xavier H.A. Keuter
Publikováno v:
JPRAS Open, Vol 41, Iss , Pp 215-224 (2024)
SUMMARY: Finger arthroplasty is commonly used to treat pain in the finger joints due to osteoarthritis or rheumatoid arthritis. Despite the procedure having existed for a relatively long time, it is still unknown which characteristics influence impla
Externí odkaz:
https://doaj.org/article/4f1101439cb34fe5901d50593d770851
Autor:
Piyapan Suwattananuruk, Sukanya Yaset, Chanisa Chotipanich, Angel Moldes-Anaya, Rune Sundset, Rodrigo Berzaghi, Stine Figenschau, Sandra Claes, Dominique Schols, Pornchai Rojsitthisak, Mathias Kranz, Opa Vajragupta
Publikováno v:
EJNMMI Radiopharmacy and Chemistry, Vol 9, Iss 1, Pp 1-19 (2024)
Abstract Background This study aimed to develop a novel positron emission tomography (PET) tracer, [68Ga]Ga-TD-01, for CXCR4 imaging. To achieve this goal, the molecular scaffold of TIQ15 was tuned by conjugation with the DOTA chelator to make it sui
Externí odkaz:
https://doaj.org/article/c3db7fc51fd5432a9dad7507f7eb9509
Autor:
Klaudyna Borewicz, Bastian Hornung, Fangjie Gu, Pieter H. van der Zaal, Henk A. Schols, Peter J. Schaap, Hauke Smidt
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Isomalto/malto-polysaccharides (IMMPs) are a novel type of soluble dietary fibres with a prebiotic potential promoting growth of beneficial microbes in the gut. However, the mode of action of IMMPs remains unknown. Previous studies on IMMPs
Externí odkaz:
https://doaj.org/article/75aaa610ba83463785096f112b450a33
Autor:
Debbie Gach, Rosanne J. H. C. G. Beijers, Roel van Zeeland, Vivian van Kampen-van den Boogaart, Rein Posthuma, Annemie M. W. J. Schols, Joop P. van den Bergh, Frits H. M. van Osch
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract A significant proportion of COVID-19 survivors still experience a reduced diffusion capacity three and twelve months after discharge. We aimed to compare pulmonary function trajectories between hospitalized COVID-19 patients with pre-existin
Externí odkaz:
https://doaj.org/article/130006b27871431785aa666bcd3bb3a5
Autor:
Ilja Oomen, Amal Abdi, Ricardo M. Camelo, Fábia M.R.A. Callado, Luany E.M. Carvalho, Ilenia L. Calcaterra, Manuel Carcao, Giancarlo Castaman, Jeroen C.J. Eikenboom, Kathelijn Fischer, Vivian K.B. Franco, Martijn W. Heymans, Frank W.G. Leebeek, David Lillicrap, Cláudia S. Lorenzato, Maria Elisa Mancuso, Davide Matino, Matteo N.D. Di Minno, Alex B. Mohseny, Johannes Oldenburg, Suely Meireles Rezende, Georges-Etienne Rivard, Natalia Rydz, Saskia E.M. Schols, Jan Voorberg, Karin Fijnvandraat, Samantha C. Gouw
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 7, Pp 102580- (2024)
Background: Inhibitor eradication to restore factor (F)VIII efficacy is the treatment goal for persons with severe hemophilia A (HA) and inhibitors. Immune tolerance induction (ITI) is demanding and successful in about 70% of people. Until now, it ha
Externí odkaz:
https://doaj.org/article/81986c3b0b0948108260f0f7bf03d9f4
Autor:
I Oomen, RM Camelo, M Carcao, G Castaman, JCJ Eikenboom, K Fischer, WG Frank Leebeek, D Lillicrap, ME Mancuso, D Matino, DMN Di Minno, AB Mohseny, J Oldenburg, SM Rezende, GE Rivard, N Rydz, S Schols, Voorberg Jan, FMRA Callado, LEM Carvalho, VKB Franco, CS Lorenzato, K Fijnvandraat, S Gouw
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S562-S563 (2024)
Background: Eradicating inhibitors to restore the effectiveness of Factor VIII (FVIII) is a desirable treatment goal for People with Severe Hemophilia A (PwSHA) and inhibitors, as this enables treatment of bleeding episodes with FVIII concentrates. H
Externí odkaz:
https://doaj.org/article/9a14647d2e784f2e9ac3886aafab9e62
Autor:
RM Camelo, C Smit, J Eikenboom, F Rosendaal, LFD van Vulpen, EAM Beckers, L Hooimeijer, M Coppens, SEM Schols, FWG Leebeek, MH Driessens, JGVD Bom, SM Rezende, SC Gouw
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S561-S562 (2024)
Clinical data on people with mild hemophilia (mPwH) is important to guide their treatment but remains scarce worldwide. In addition, since modern hemophilia therapies can turn severe phenotypes into mild or normal ones, knowing the clinical, therapeu
Externí odkaz:
https://doaj.org/article/f01b98d651fe4bb3a898374288d1abcc
Autor:
Aspire Mudavanhu, Ruben Schols, Emilie Goossens, Tamuka Nhiwatiwa, Tawanda Manyangadze, Luc Brendonck, Tine Huyse
Publikováno v:
Parasites & Vectors, Vol 17, Iss 1, Pp 1-17 (2024)
Abstract Background Snail-borne trematodes afflict humans, livestock, and wildlife. Recognizing their zoonotic potential and possible hybridization, a One Health approach is essential for effective control. Given the dearth of knowledge on African tr
Externí odkaz:
https://doaj.org/article/f685e9bd78ca409694bd558432b1b005
Autor:
Sarah L. Stenton, Melanie C. O’Leary, Gabrielle Lemire, Grace E. VanNoy, Stephanie DiTroia, Vijay S. Ganesh, Emily Groopman, Emily O’Heir, Brian Mangilog, Ikeoluwa Osei-Owusu, Lynn S. Pais, Jillian Serrano, Moriel Singer-Berk, Ben Weisburd, Michael W. Wilson, Christina Austin-Tse, Marwa Abdelhakim, Azza Althagafi, Giulia Babbi, Riccardo Bellazzi, Samuele Bovo, Maria Giulia Carta, Rita Casadio, Pieter-Jan Coenen, Federica De Paoli, Matteo Floris, Manavalan Gajapathy, Robert Hoehndorf, Julius O. B. Jacobsen, Thomas Joseph, Akash Kamandula, Panagiotis Katsonis, Cyrielle Kint, Olivier Lichtarge, Ivan Limongelli, Yulan Lu, Paolo Magni, Tarun Karthik Kumar Mamidi, Pier Luigi Martelli, Marta Mulargia, Giovanna Nicora, Keith Nykamp, Vikas Pejaver, Yisu Peng, Thi Hong Cam Pham, Maurizio S. Podda, Aditya Rao, Ettore Rizzo, Vangala G. Saipradeep, Castrense Savojardo, Peter Schols, Yang Shen, Naveen Sivadasan, Damian Smedley, Dorian Soru, Rajgopal Srinivasan, Yuanfei Sun, Uma Sunderam, Wuwei Tan, Naina Tiwari, Xiao Wang, Yaqiong Wang, Amanda Williams, Elizabeth A. Worthey, Rujie Yin, Yuning You, Daniel Zeiberg, Susanna Zucca, Constantina Bakolitsa, Steven E. Brenner, Stephanie M. Fullerton, Predrag Radivojac, Heidi L. Rehm, Anne O’Donnell-Luria
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-25 (2024)
Abstract Background A major obstacle faced by families with rare diseases is obtaining a genetic diagnosis. The average "diagnostic odyssey" lasts over five years and causal variants are identified in under 50%, even when capturing variants genome-wi
Externí odkaz:
https://doaj.org/article/29fbe7d26d88463789f004c8908aa4a7