Zobrazeno 1 - 6
of 6
pro vyhledávání: '"E. J. T. (Joanne) Verweij"'
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:
Angret de Boer, Pauline E. van Beek, Peter Andriessen, Floris Groenendaal, Marije Hogeveen, Julia S. Meijer, Sylvia A. Obermann-Borst, Wes Onland, Liesbeth (H. C. J.) Scheepers, Marijn J. Vermeulen, E. J. T. (Joanne) Verweij, Lien De Proost, Rosa Geurtzen
Publikováno v:
Children, Vol 10, Iss 10, p 1712 (2023)
Predicting the short- and long-term outcomes of extremely preterm infants remains a challenge. Multivariable prognostic models might be valuable tools for clinicians, parents, and policymakers for providing accurate outcome estimates. In this perspec
Externí odkaz:
https://doaj.org/article/c05535858893457c94099c3deb3967a8
Autor:
Maayke A. de Koning, Emilia K. Bijlsma, Esther A. R. Nibbeling, Phebe N. Adama‐Scheltema, E J T Joanne Verweij, Cacha M.P.C.D. Peeters-Scholte, Mariëtte J.V. Hoffer, Marieke B. Veenhof, Gijs W. E. Santen, Menno J. P. Toirkens
Publikováno v:
Clinical Genetics, 101(1), 65-77. WILEY
Prenatal exome sequencing (pES) is a promising tool for diagnosing genetic disorders when structural anomalies are detected on prenatal ultrasound. The aim of this study was to investigate the diagnostic yield and clinical impact of pES as an additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba07cbba6c9e2fac274ebaa0db86665
https://hdl.handle.net/1887/3249467
https://hdl.handle.net/1887/3249467
Autor:
null Maayke A. Koning, null Mariëtte J. V. Hoffer, null Esther A. R. Nibbeling, null Emilia K. Bijlsma, null Menno J. P. Toirkens, null Phebe N. Adama‐Scheltema, null E. J. T. (Joanne) Verweij, null Marieke B. Veenhof, null Gijs W. E. Santen, null Cacha M. P. C. D. Peeters‐Scholte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b96a50879a003d0e84cdd64f822fec4
https://doi.org/10.1111/cge.14070/v3/response1
https://doi.org/10.1111/cge.14070/v3/response1
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 155
A 5-year-old boy was seen for a second opinion as he had episodes of severe abdominal pain and a variably distended abdomen. Ultrasonography showed a suspected duplication cyst of the terminal ileum. A laparoscopically assisted resection was performe
Autor:
Anna L David, Mats Johansson, Magnus Westgren, Belinda Crowe, Dick Oepkes, Melissa Hill, Lyn S Chitty, Catherine DeVile, Peter Lindgren, Eva Åström, Cecilia Götherström, Nils-Eric Sahlin, Rachel L Sagar, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Caroline Lindemans, Wouter Nijhuis, Mirko Rehberg, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij
Publikováno v:
BMJ Open, Vol 14, Iss 6 (2024)
Introduction Severe osteogenesis imperfecta (OI) is a debilitating disease with no cure or sufficiently effective treatment. Mesenchymal stem cells (MSCs) have good safety profile, show promising effects and can form bone. The Boost Brittle Bones Bef
Externí odkaz:
https://doaj.org/article/582a3f441343419db9a89157809ffc1c