Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Marjolein Bos"'
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Accuracy of postvoid residual volumes after vaginal delivery: a prospective equivalence study to compare an automatic scanning device with transurethral catheterization
Autor: Jules H. Schagen van Leeuwen, Marjolein Bos, R. A. Hakvoort, Femke E. M. Mulder, Sytske van der Velde, Jan-Paul W. R. Roovers, Viviane Dietz, Fraukje Pol
Publikováno v: International urogynecology journal and pelvic floor dysfunction, 30(5), 773-778. Springer London
International Urogynecology Journal
Introduction and hypothesis: Abnormal postvoid residual volumes (PVRV) after delivery are common in daily clinical practice. By using an automatic scanning device, unnecessary catheterizations can be prevented. The aim of this study was to determine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07839b079c488deb6e7e3957b53801fd
https://pure.amc.nl/en/publications/accuracy-of-postvoid-residual-volumes-after-vaginal-delivery-a-prospective-equivalence-study-to-compare-an-automatic-scanning-device-with-transurethral-catheterization(828d1652-485d-45fe-9d06-8ee423078ade).html
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2
Akademický článek
The malate-aspartate shuttle is important for de novo serine biosynthesis
Autor: Melissa H. Broeks, Nils W.F. Meijer, Denise Westland, Marjolein Bosma, Johan Gerrits, Hannah M. German, Jolita Ciapaite, Clara D.M. van Karnebeek, Ronald J.A. Wanders, Fried J.T. Zwartkruis, Nanda M. Verhoeven-Duif, Judith J.M. Jans
Publikováno v: Cell Reports, Vol 42, Iss 9, Pp 113043- (2023)
Summary: The malate-aspartate shuttle (MAS) is a redox shuttle that transports reducing equivalents across the inner mitochondrial membrane while recycling cytosolic NADH to NAD+. We genetically disrupted each MAS component to generate a panel of MAS
Externí odkaz: https://doaj.org/article/ac08eb6204fc47578f078cc37db1f420
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3
Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Autor: Dwight Odland, William van’t Hoff, Brian L. Rayner, David C. Wheeler, Christoph Wanner, Kyongtae T. Bae, Daniel Renault, Oliver Gross, Rémi Salomon, Lisa M. Guay-Woodford, Marie C. Hogan, Ronald D. Perrone, Julia Höfele, Martin Konrad, Peter C. Harris, Marjolein Storm, Carsten Bergmann, Annet Nieuwenhoven, Yves Pirson, Jane de la Fosse, Wolfgang C. Winkelmayer, Etienne Cosyns, Vicente E. Torres, Craig B. Langman, Aude Servais, Bénédicte Stengel, Jie Ding, Giuseppe Remuzzi, Franz Schaefer, Martina Cornel, Anthony J. Bleyer, Tess Harris, Paul Goodyer, Elizabeth Vroom, Roser Torra, Nine V A M Knoers, Robert Kleta, Julie R. Ingelfinger, York Pei, Avital Cnaan, Richard J.H. Smith, Alberto Ortiz, Klemens Budde, S. Mariz, Susie Gear, Katherine R. Bull, Nicole Harr, Detlef Bockenhauer, Hui-Kim Yap, Marjolein Bos, Gayle McKerracher, Julia Roberts, Shigeo Horie, Michael Cheung, Ewout J. Hoorn, Olivier Devuyst, Timothy H.J. Goodship, Simon Day, Dominique Chauveau, Corinne Antignac, Eric Olinger, Aris Angelis, Clifford E. Kashtan, Rosa Vargas-Poussou, Larissa Kerecuk, Jon B. Klein, Ségolène Aymé, Neveen A. Soliman
Publikováno v: Kidney International, 92(4), 796. Nature Publishing Group
Kidney International, 92(4), 796-808. Elsevier Inc.
Kidney International, 92(4), 796-808. ELSEVIER SCIENCE INC
Aymé, S, Bockenhauer, D, Day, S, Devuyst, O, Guay-Woodford, L M, Ingelfinger, J R, Klein, J B, Knoers, N V A M, Perrone, R D, Roberts, J, Schaefer, F, Torres, V E, Cheung, M, Wheeler, D C, Winkelmayer, W C & Conference Participants 2017, ' Common Elements in Rare Kidney Diseases : Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference ', Kidney International, vol. 92, no. 4, pp. 796-808 . https://doi.org/10.1016/j.kint.2017.06.018
Kidney International, 92(4), 796-808. Nature Publishing Group
Rare kidney diseases encompass at least 150 different conditions, most of which are inherited. Although individual rare kidney diseases raise specific issues, as a group these rare diseases can have overlapping challenges in diagnosis and treatment.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b89e6248c1619aa4c645627016c4646
https://pubmed.ncbi.nlm.nih.gov/29153144
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4
Controversies and research agenda in nephropathic cystinosis: conclusions from a 'Kidney Disease: Improving Global Outcomes' (KDIGO) Controversies Conference
Autor: Rezan Topaloglu, Monte Del Monte, Lambertus P. van den Heuvel, Thomas D. Brown, Victor Gomez, Marcella Greco, Galina Nesterova, Aude Servais, Mirian C. H. Janssen, Julian P. Midgley, Marjolein Bos, Patrick Niaudet, Jerry A. Schneider, William van’t Hoff, Paul Goodyer, Francesco Emma, Leticia Belmont-Martínez, Larry A. Greenbaum, Aurélia Bertholet-Thomas, Georges Deschênes, Maria Helena Vaisbich, Philip Newsholme, Doris A. Trauner, Jess G. Thoene, Patrice Rioux, Paul C. Grimm, Frederick J. Kaskel, Bruce A. Barshop, Graham Lipkin, Valerie Hotz, Oliver Amon, Christy Greeley, Neveen A. Soliman, Elena Levtchenko, Chris Ottolenghi, Maya Doyle, Jie Ding, Stephanie Cherqui, William A. Gahl, Minnie M. Sarwal, Maryan Basurto, Gema Ariceta, Katharina Hohenfellner, Elisabeth A.M. Cornelissen, Ranjan Dohil, Ewa Elenberg, Craig B. Langman, Teresa Holm, Rita Magriço
Publikováno v: Kidney International. Supplement, 89, 6, pp. 1192-203
Kidney International. Supplement, 89, 1192-203
Item does not contain fulltext Nephropathic cystinosis is an autosomal recessive metabolic, lifelong disease characterized by lysosomal cystine accumulation throughout the body that commonly presents in infancy with a renal Fanconi syndrome and, if u
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635546248ea09931552c6117da8853cf
https://hdl.handle.net/2066/172214
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6
Akademický článek
NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome.
Autor: Wout J Weuring, Sakshi Singh, Linda Volkers, Martin B Rook, Ruben H van 't Slot, Marjolein Bosma, Marco Inserra, Irina Vetter, Nanda M Verhoeven-Duif, Kees P J Braun, Mirko Rivara, Bobby P C Koeleman
Publikováno v: PLoS ONE, Vol 15, Iss 3, p e0219106 (2020)
Dravet syndrome is caused by dominant loss-of-function mutations in SCN1A which cause reduced activity of Nav1.1 leading to lack of neuronal inhibition. On the other hand, gain-of-function mutations in SCN8A can lead to a severe epileptic encephalopa
Externí odkaz: https://doaj.org/article/6bee8c3f2c6649e9a69da93d49666e56
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7
Akademický článek
Vitamin B6 in plasma and cerebrospinal fluid of children.
Autor: Monique Albersen, Marjolein Bosma, Judith J M Jans, Floris C Hofstede, Peter M van Hasselt, Monique G M de Sain-van der Velden, Gepke Visser, Nanda M Verhoeven-Duif
Publikováno v: PLoS ONE, Vol 10, Iss 3, p e0120972 (2015)
Over the past years, the essential role of vitamin B6 in brain development and functioning has been recognized and genetic metabolic disorders resulting in functional vitamin B6 deficiency have been identified. However, data on B6 vitamers in childre
Externí odkaz: https://doaj.org/article/00831343381649e5981fad5b4cb0d96a
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8
Akademický článek
The intestine plays a substantial role in human vitamin B6 metabolism: a Caco-2 cell model.
Autor: Monique Albersen, Marjolein Bosma, Nine V V A M Knoers, Berna H B de Ruiter, Eugène F Diekman, Jessica de Ruijter, Wouter F Visser, Tom J de Koning, Nanda M Verhoeven-Duif
Publikováno v: PLoS ONE, Vol 8, Iss 1, p e54113 (2013)
BACKGROUND: Vitamin B6 is present in various forms (vitamers) in the diet that need to be metabolized to pyridoxal phosphate (PLP), the active cofactor form of vitamin B6. In literature, the liver has been reported to be the major site for this conve
Externí odkaz: https://doaj.org/article/ecb17a6321e44639acc700d73b65319e
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