Zobrazeno 1 - 10
of 1 306
pro vyhledávání: '"A. Zwaveling"'
Autor:
Grit, Geeske F, van Geffen, Esmée, Malmberg, Ruben, van Leeuwen, Roelof, Böhringer, Stefan, JM Smit, Hans, Brocken, Pepijn, FH Eijsink, Job, Dronkers, Esther, Gal, Pim, Jaarsma, Eva, JHM van Drie-Pierik, Regine, MP Eldering-Heldens, Anne, Machteld Wymenga, AN, GM Mol, Peter, Zwaveling, Juliëtte, Hilarius, Doranne
Publikováno v:
In Lung Cancer October 2024 196
Autor:
van Braak, Hendrik, de Beer, Sjoerd A., al Ghouch, Youssef, Zwaveling, Sander, Oomen, Matthijs W.N., van Heurn, L.W. Ernest, de Jong, Justin R.
Publikováno v:
In Journal of Pediatric Surgery February 2025 60(2)
Autor:
van Braak, Hendrik, de Beer, Sjoerd A., Twisk, Jos W.R., Zwaveling, Sander, Oomen, Matthijs W.N., de Jong, Justin R., Ernest van Heurn, L.W.
Publikováno v:
In Journal of Pediatric Surgery January 2025 60(1)
Autor:
Mark R. Garrelfs, Tuula Rinne, Jacquelien J. Hillebrand, Peter Lauffer, Merijn W. Bijlsma, Hedi L. Claahsen-van der Grinten, Nicole de Leeuw, Martijn J.J. Finken, Joost Rotteveel, Nitash Zwaveling-Soonawala, Max Nieuwdorp, A.S. Paul van Trotsenburg, Christiaan F. Mooij
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 95-101 (2024)
Isolated aldosterone synthase deficiency is a rare autosomal recessive disorder caused by pathogenic variants in CYP11B2, resulting in impaired aldosterone synthesis. We report on a neonate with isolated aldosterone synthase deficiency caused by a no
Externí odkaz:
https://doaj.org/article/6da2ce501da6495ab743ea29f1a57ab9
Autor:
Carvello, Michele, Van Dieren, Susan, Frontali, Alice, Govaert, Johannes, Hompes, Roel, Koot, Bart, Lameris, Wytze, Van der Marel, Sander, Sileri, Pierpaolo, Vlug, Malaika, Wildenberg, Manon, Wiggers, Jimme, Zwaveling, Sander, van der Does de Willebois, Eline M L, Bellato, Vittoria, Duijvestein, Marjolijn, van der Bilt, Jarmila D W, van Dongen, Koen, Spinelli, Antonino, D'Haens, Geert R, Mundt, Marco W, Furfaro, Federica, Danese, Silvio, Vignali, Andrea, Bemelman, Willem A, Buskens, Christianne J *
Publikováno v:
In The Lancet Gastroenterology & Hepatology September 2024 9(9):793-801
Autor:
Heleen I Jansen, Marije van Haeringen, Marelle J Bouva, Wendy P J den Elzen, Eveline Bruinstroop, Catharina P B van der Ploeg, A S Paul van Trotsenburg, Nitash Zwaveling-Soonawala, Annemieke C Heijboer, Annet M Bosch, Robert de Jonge, Mark Hoogendoorn, Anita Boelen
Publikováno v:
European Thyroid Journal, Vol 12, Iss 6, Pp 1-10 (2023)
Objective: Congenital hypothyroidism (CH) is an inborn thyroid hormone (TH) deficiency mostly caused by thyroidal (primary CH) or hypothalamic/pituitary (central CH) disturbances. Most CH newborn screening (NBS) programs are thyroid-stimulating-hormo
Externí odkaz:
https://doaj.org/article/f3136411e702473c8b935f5fc33c8927
Autor:
van Braak, Hendrik, de Beer, Sjoerd A., Zwaveling, Sander, Oomen, Matthijs W.N., de Jong, Justin R.
Publikováno v:
In The Annals of Thoracic Surgery January 2024 117(1):144-150
Autor:
McLin, Valérie Anne, Franchi-Abella, Stéphanie, Brütsch, Timothée, Bahadori, Atessa, Casotti, Valeria, de Ville de Goyet, Jean, Dumery, Grégoire, Gonzales, Emmanuel, Guérin, Florent, Hascoet, Sebastien, Heaton, Nigel, Kuhlmann, Béatrice, Lador, Frédéric, Lambert, Virginie, Marra, Paolo, Plessier, Aurélie, Quaglia, Alberto, Rougemont, Anne-Laure, Savale, Laurent, Sarma, Moinak Sen, Sitbon, Olivier, Superina, Riccardo Antonio, Uchida, Hajime, van Albada, Mirjam, van der Doef, Hubert Petrus Johannes, Vilgrain, Valérie, Wacker, Julie, Zwaveling, Nitash, Debray, Dominique, Wildhaber, Barbara Elisabeth
Publikováno v:
In JHEP Reports January 2024 6(1)
Publikováno v:
European Thyroid Journal, Vol 12, Iss 4, Pp 1-9 (2023)
Thyroid hormone (TH) is indispensable for brain development in utero and during the first 2–3 years of life, and the negative effects of TH deficiency on brain development are irreversible. Detection of TH deficiency early in life by neonat al scre
Externí odkaz:
https://doaj.org/article/b94d963e152146bebeb1a2d2349c47d9
Autor:
Valérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, Atessa Bahadori, Valeria Casotti, Jean de Ville de Goyet, Grégoire Dumery, Emmanuel Gonzales, Florent Guérin, Sebastien Hascoet, Nigel Heaton, Béatrice Kuhlmann, Frédéric Lador, Virginie Lambert, Paolo Marra, Aurélie Plessier, Alberto Quaglia, Anne-Laure Rougemont, Laurent Savale, Moinak Sen Sarma, Olivier Sitbon, Riccardo Antonio Superina, Hajime Uchida, Mirjam van Albada, Hubert Petrus Johannes van der Doef, Valérie Vilgrain, Julie Wacker, Nitash Zwaveling, Dominique Debray, Barbara Elisabeth Wildhaber
Publikováno v:
JHEP Reports, Vol 6, Iss 1, Pp 100933- (2024)
Summary: Congenital portosystemic shunts are often associated with systemic complications, the most challenging of which are liver nodules, pulmonary hypertension, endocrine abnormalities, and neurocognitive dysfunction. In the present paper, we offe
Externí odkaz:
https://doaj.org/article/78b59ccf97fc4fb1b0c1890877aad9c0