Zobrazeno 1 - 10
of 514
pro vyhledávání: '"M Vossen"'
Autor:
Anne Russcher, Michiel van Boven, Elisa Benincà, E. J. T. (Joanne) Verweij, Marijke W. A. Molenaar-de Backer, Hans L. Zaaijer, Ann C. T. M. Vossen, Aloys C. M. Kroes
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Parvovirus B19V (B19V) infection during pregnancy can be complicated by potentially life-threatening fetal hydrops, which can be managed by intrauterine transfusion (IUT). This study investigates the long-term temporal patterns in the epidem
Externí odkaz:
https://doaj.org/article/a54246fd285f44f2acfea8e1b4debaf9
Autor:
Carel G. M. Meskers, Sabina van der Veen, Jenia Kim, Caroline J. W. Meskers, Quirine T. S. Smit, Stella Verkijk, Edwin Geleijn, Guy A. M. Widdershoven, Piek T. J. M. Vossen, Marike van der Leeden
Publikováno v:
Annals of Medicine, Vol 54, Iss 1, Pp 235-243 (2022)
Purpose To address the feasibility, reliability and internal validity of natural language processing (NLP) for automated functional assessment of hospitalised COVID-19 patients in key International Classification of Functioning, Disability and Health
Externí odkaz:
https://doaj.org/article/f63bd2e6745749869696d06b220c8d41
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Duchenne and Becker muscular dystrophy are X-linked recessive inherited disorders characterized by progressive weakness due to skeletal muscle degeneration. Different mutations in the DMD gene, which encodes for dystrophin protein, are responsible fo
Externí odkaz:
https://doaj.org/article/ea1ac177079d4302b599fa054f790739
Autor:
A. A. Kampfraath, L. Klasson, S. Y. Anvar, R. H. A. M. Vossen, D. Roelofs, K. Kraaijeveld, J. Ellers
Publikováno v:
BMC Genomics, Vol 20, Iss 1, Pp 1-14 (2019)
Abstract Background Theory predicts that dependency within host-endosymbiont interactions results in endosymbiont genome size reduction. Unexpectedly, the largest Wolbachia genome was found in the obligate, parthenogenesis-associated wFol. In this st
Externí odkaz:
https://doaj.org/article/0a17562cab594af6bd8805f16cb57b23
Autor:
F. Khalaveh, N. Fazel, M. Mischkulnig, M. Vossen, A. Reinprecht, C. Dorfer, K. Rössler, J. Herta
Publikováno v:
Brain and Spine, Vol 1, Iss , Pp 100739- (2021)
Externí odkaz:
https://doaj.org/article/d0ea312d3634470ca6ac791a66c0959b
Autor:
Lexie Prokopuk, Jessica M. Stringer, Craig R. White, Rolf H. A. M. Vossen, Stefan J. White, Ana S. A. Cohen, William T. Gibson, Patrick S. Western
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-14 (2018)
Abstract Background Investigating how epigenetic information is transmitted through the mammalian germline is the key to understanding how this information impacts on health and disease susceptibility in offspring. EED is essential for regulating the
Externí odkaz:
https://doaj.org/article/62884fb084604d299cae3ecb012060ec
Publikováno v:
Nutrients, Vol 12, Iss 1, p 100 (2019)
Vascular calcification is an independent predictor of cardiovascular disease, and therefore, inhibition or regression of this processes is of clinical importance. The standard care regarding prevention and treatment of cardiovascular disease at this
Externí odkaz:
https://doaj.org/article/5405c4aad3a04f9793a7171ff78721eb
Congenital Cytomegalovirus Infection: Maternal–Child HLA-C, HLA-E, and HLA-G Affect Clinical Outcome
Autor:
Roberta Rovito, Frans H. J. Claas, Geert W. Haasnoot, Dave L. Roelen, Aloys C. M. Kroes, Michael Eikmans, Ann C. T. M. Vossen
Publikováno v:
Frontiers in Immunology, Vol 8 (2018)
Congenital CMV infection (cCMV) is the most common congenital infection causing permanent long-term impairments (LTI). cCMV immunopathogenesis is largely unknown due to the complex interplay between viral, maternal, placental, and child factors. In t
Externí odkaz:
https://doaj.org/article/aadb88b92e3342fa94e3e9af29775dd9
Autor:
David M Vossen, Caroline V M Verhagen, Reidar Grénman, Roelof J C Kluin, Marcel Verheij, Michiel W M van den Brekel, Lodewyk F A Wessels, Conchita Vens
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206632 (2018)
BACKGROUND:Large cancer genome studies continue to reveal new players in treatment response and tumorigenesis. The discrimination of functional alterations from the abundance of passenger genetic alterations still poses challenges and determines DNA
Externí odkaz:
https://doaj.org/article/1ece493379cf446194cdc3f9516511b8
Autor:
Roberta Rovito, Hans-Jörg Warnatz, Szymon M Kiełbasa, Hailiang Mei, Vyacheslav Amstislavskiy, Ramon Arens, Marie-Laure Yaspo, Hans Lehrach, Aloys C M Kroes, Jelle J Goeman, Ann C T M Vossen
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200652 (2018)
Congenital Cytomegalovirus infection (cCMV) is the leading infection in determining permanent long-term impairments (LTI), and its pathogenesis is largely unknown due to the complex interplay between viral, maternal, placental, and child factors. The
Externí odkaz:
https://doaj.org/article/d0aec4e74df94aa6afe02fab2c3e2ce1