Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Arend Bokenkamp"'
Autor:
Esmée Botman, Bernard J. Smilde, Max Hoebink, Sanne Treurniet, Pieter Raijmakers, Otto Kamp, Bernd P. Teunissen, Arend Bökenkamp, Patrick Jak, Adriaan A. Lammertsma, Joost G. van den Aardweg, Anco Boonstra, Elisabeth M.W. Eekhoff
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100758- (2021)
Fibrodysplasia Ossificans Progressiva (FOP) is a genetic disease characterized by the formation of heterotopic ossification (HO) in connective tissues. HO first develops in the thoracic region, before more peripheral sites are affected. Due to HO alo
Externí odkaz:
https://doaj.org/article/498e6fc3e344424dabc6e9417f3d57fc
Autor:
Ariadne Bosman, Natasha Appelman-Dijkstra, Joop van den Bergh, Arend Bökenkamp, Annemieke Boot, Martin de Borst, Bram van der Eerden, M. Carola Zillikens
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 101003- (2021)
Externí odkaz:
https://doaj.org/article/c954f250efc54771ada0178822d60670
Autor:
Esmée Botman, Bernd P Teunissen, Pieter Raijmakers, Pim deGraaf, Maqsood Yaqub, Sanne Treurniet, Ton Schoenmaker, Nathalie Bravenboer, Dimitra Micha, Gerard Pals, Arend Bökenkamp, J Coen Netelenbos, Adriaan A Lammertsma, Elisabeth MW Eekhoff
Publikováno v:
JBMR Plus, Vol 4, Iss 6, Pp n/a-n/a (2020)
ABSTRACT Using [18F] Sodium Fuoride (NaF) Positron Emission Tomography (PET) it is not only possible to identify the ossifying potency of a flare‐up, but also to identify an asymptomatic chronic stage of fibrodysplasia ossificans progressiva (FOP).
Externí odkaz:
https://doaj.org/article/f07bb8c400fe410dbe941852b1467ed2
Autor:
Marie Morimoto, Clara Myung, Kimberly Beirnes, Kunho Choi, Yumi Asakura, Arend Bokenkamp, Dominique Bonneau, Milena Brugnara, Joel Charrow, Estelle Colin, Amira Davis, Georges Deschenes, Mattia Gentile, Mario Giordano, Andrew K. Gormley, Rajeshree Govender, Mark Joseph, Kory Keller, Evelyne Lerut, Elena Levtchenko, Laura Massella, Christy Mayfield, Behzad Najafian, David Parham, Jurgen Spranger, Peter Stenzel, Uluc Yis, Zhongxin Yu, Jonathan Zonana, Glenda Hendson, Cornelius F. Boerkoel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-12 (2016)
Abstract Background Schimke immuno-osseous dysplasia (SIOD) is a multisystemic disorder caused by biallelic mutations in the SWI/SNF-related matrix-associated actin-dependent regulator of chromatin, subfamily A-like 1 (SMARCAL1) gene. Changes in gene
Externí odkaz:
https://doaj.org/article/3b7ef2c5e2c44cff8f2914c3b624b808
Autor:
Pierre Delanaye, Jonas Bjork, Emmanuelle Vidal-Petiot, Natalie Ebert, Bjørn Odvar Eriksen, Laurence Dubourg, Anders Grubb, Magnus Hansson, Edmund Lamb, Karin Littman, Christophe Mariat, Toralf Melsom, Elke Schaeffner, Per-Ola Sundin, Arend Bokenkamp, Ulla Berg, Kasja Asling-Monemi, Anna Åkesson, Anders Larsson, Etienne Cavalier, Neil Dalton, Marie Courbebaisse, Lionel Couzi, François Gaillard, Cyril Garrouste, Lola Jacquemont, Nassim Kamar, Christophe Legendre, Lionel Rostaing, Thomas Stehlé, Jean-Philippe Haymann, Luciano Selistre, Jorge Strogoff-de-Matos, Justine Bukabau, Ernest Sumaili, Eric Yayo, Dagui Monnet, Ulf Nyman, Hans Pottel, Martin Flamant
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS Current Glomerular filtration rate (GFR) estimating equations based on serum creatinine are facing increased criticism due to the inclusion of a race correction in black Americans with the CKD-EPI equation (CKD-EPIASR, A = Age, S
Publikováno v:
Endocrinology&Metabolism International Journal. 2
Background: Adolescents with gender dysphoria are treated with gonadotropin releasing hormone analogues (GnRHa) as part of the gender reassignment procedure. The mid- and long-term health effects of this treatment are not known. Cases: Three cases of
Autor:
Johanna Magdalena Rieke, Rong Zhang, Doreen Braun, Öznur Yilmaz, Anna S. Japp, Filipa M. Lopes, Michael Pleschka, Alina C. Hilger, Sophia Schneider, William G. Newman, Glenda M. Beaman, Agneta Nordenskjöld, Anne-Karoline Ebert, Martin Promm, Wolfgang H. Rösch, Raimund Stein, Karin Hirsch, Frank-Mattias Schäfer, Eberhard Schmiedeke, Thomas M. Boemers, Martin Lacher, Dietrich Kluth, Jan-Hendrik Gosemann, Magnus Anderberg, Gillian Barker, Gundela Holmdahl, Göran Läckgren, David Keene, Raimondo M. Cervellione, Elisa Giorgio, Massimo Di Grazia, Wouter F. J. Feitz, Carlo L. M. Marcelis, Iris A. L. M. Van Rooij, Arend Bökenkamp, Goedele M. A. Beckers, Catherine E. Keegan, Amit Sharma, Tikam Chand Dakal, Lars Wittler, Phillip Grote, Nadine Zwink, Ekkehart Jenetzky, Alfredo Brusco, Holger Thiele, Michael Ludwig, Ulrich Schweizer, Adrian S. Woolf, Benjamin Odermatt, Heiko Reutter
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Previous studies in developing Xenopus and zebrafish reported that the phosphate transporter slc20a1a is expressed in pronephric kidneys. The recent identification of SLC20A1 as a monoallelic candidate gene for cloacal exstrophy further suggests its
Externí odkaz:
https://doaj.org/article/9c651c06182b43e58e089d5b84ebbebc
Autor:
Elisabeth M. W. Eekhoff, Dimitra Micha, Tymour Forouzanfar, Teun J. de Vries, J. Coen Netelenbos, Jenneke Klein-Nulend, Jack J. W. A. van Loon, Wouter D. Lubbers, Lothar Schwarte, Patrick Schober, Pieter G. H. M. Raijmakers, Bernd P. Teunissen, Pim de Graaf, Adriaan A. Lammertsma, Maqsood M. Yaqub, Esmée Botman, Sanne Treurniet, Bernard J. Smilde, Arend Bökenkamp, Anco Boonstra, Otto Kamp, Jakko A. Nieuwenhuijzen, Marieke C. Visser, Hans J. C. Baayen, Max Dahele, Guus A. M. Eeckhout, Thadé P. M. Goderie, Cas Smits, Marjolijn Gilijamse, K. Hakki Karagozoglu, Paul van de Valk, Chris Dickhoff, Annette C. Moll, Frank F. D. Verbraak, Katie K. R. Curro-Tafili, Ebba A. E. Ghyczy, Thomas Rustemeyer, Peeroz Saeed, Alessandra Maugeri, Gerard Pals, Angela Ridwan-Pramana, Esther Pekel, Ton Schoenmaker, Willem Lems, Henri A. H. Winters, Matthijs Botman, Georgios F. Giannakópoulos, Peter Koolwijk, Jeroen J. W. M. Janssen, Peter Kloen, Nathalie Bravenboer, Jan Maerten Smit, Marco N. Helder
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
In the field of rare bone diseases in particular, a broad care team of specialists embedded in multidisciplinary clinical and research environment is essential to generate new therapeutic solutions and approaches to care. Collaboration among clinical
Externí odkaz:
https://doaj.org/article/146d6a3fe51a42159fb5580d3b4cb88a
Autor:
Eva H. Visser, Daan J. C. Berkhout, Jiwanjot Singh, Annemieke Vermeulen, Niloufar Ashtiani, Nanne K. de Boer, Joanna A. E. van Wijk, Tim G. de Meij, Arend Bökenkamp
Publikováno v:
Biosensors, Vol 10, Iss 5, p 48 (2020)
Background: Urinary tract infections (UTI) are among the most common infections in children. The primary tool to detect UTI is dipstick urinalysis; however, this has limited sensitivity and specificity. Therefore, urine culture has to be performed to
Externí odkaz:
https://doaj.org/article/fa37df3ce3c6453390ef670041d40742
Autor:
Sarah Kuipers MD, Eric H. J. R. van der Horst MD, Jonathan I. M. L. Verbeke MD, Arend Bökenkamp MD, PhD
Publikováno v:
Global Pediatric Health, Vol 3 (2016)
The endoscopic STING procedure using Deflux is a common and minimal invasive treatment for vesicoureteral reflux. Herein we present the case of an 11-year-old girl with loin pain and de novo hydronephrosis and megaureter on the left. Ultrasound and p
Externí odkaz:
https://doaj.org/article/3239e863a7c04720bcb5f203f9d04992