Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bart G. Koot"'
Autor:
Mary E. Rinella, Jeffrey V. Lazarus, Vlad Ratziu, Sven M. Francque, Arun J. Sanyal, Fasiha Kanwal, Diana Romero, Manal F. Abdelmalek, Quentin M. Anstee, Juan Pablo Arab, Marco Arrese, Ramon Bataller, Ulrich Beuers, Jerome Boursier, Elisabetta Bugianesi, Christopher D. Byrne, Graciela E. Castro Narro, Abhijit Chowdhury, Helena Cortez-Pinto, Donna R. Cryer, Kenneth Cusi, Mohamed El-Kassas, Samuel Klein, Wayne Eskridge, Jiangao Fan, Samer Gawrieh, Cynthia D. Guy, Stephen A. Harrison, Seung Up Kim, Bart G. Koot, Marko Korenjak, Kris V. Kowdley, Florence Lacaille, Rohit Loomba, Robert Mitchell-Thain, Timothy R. Morgan, Elisabeth E. Powell, Michael Roden, Manuel Romero-Gómez, Marcelo Silva, Shivaram Prasad Singh, Silvia C. Sookoian, C. Wendy Spearman, Dina Tiniakos, Luca Valenti, Miriam B. Vos, Vincent Wai-Sun Wong, Stavra Xanthakos, Yusuf Yilmaz, Zobair Younossi, Ansley Hobbs, Marcela Villota-Rivas, Philip N. Newsome
Publikováno v:
Annals of Hepatology, Vol 29, Iss 1, Pp 101133- (2024)
The principal limitations of the terms NAFLD and NASH are the reliance on exclusionary confounder terms and the use of potentially stigmatising language. This study set out to determine if content experts and patient advocates were in favor of a chan
Externí odkaz:
https://doaj.org/article/f02c612b79da4aaa8837228f72393227
Autor:
Christian A. Hudert, Leon A. Adams, Anna Alisi, Quentin M. Anstee, Annalisa Crudele, Laura G. Draijer, EU‐PNAFLD investigators, Samuel Furse, Jan G. Hengstler, Benjamin Jenkins, Kylie Karnebeek, Deirdre A. Kelly, Bart G. Koot, Albert Koulman, David Meierhofer, Phillip E. Melton, Trevor A. Mori, Stuart G. Snowden, Indra vanMourik, Anita Vreugdenhil, Susanna Wiegand, Jake P. Mann
Publikováno v:
Hepatology Communications, Vol 6, Iss 8, Pp 1934-1948 (2022)
Abstract Genome‐wide association studies in adults have identified variants in hydroxysteroid 17‐beta dehydrogenase 13 (HSD17B13) and mitochondrial amidoxime reducing component 1 (MTARC1) as protective against nonalcoholic fatty liver disease (NA
Externí odkaz:
https://doaj.org/article/3bb2c6a027504d0481422e3c44348ecb
Autor:
Glen R. Monroe, Albertien M. van Eerde, Federico Tessadori, Karen J. Duran, Sanne M. C. Savelberg, Johanna C. van Alfen, Paulien A. Terhal, Saskia N. van der Crabben, Klaske D. Lichtenbelt, Sabine A. Fuchs, Johan Gerrits, Markus J. van Roosmalen, Koen L. van Gassen, Mirjam van Aalderen, Bart G. Koot, Marlies Oostendorp, Marinus Duran, Gepke Visser, Tom J. de Koning, Francesco Calì, Paolo Bosco, Karin Geleijns, Monique G. M. de Sain-van der Velden, Nine V. Knoers, Jeroen Bakkers, Nanda M. Verhoeven-Duif, Gijs van Haaften, Judith J. Jans
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
D-lactic acidosis typically occurs in the context of short bowel syndrome; excess D-lactate is produced by intestinal bacteria. Here, the authors identify two point mutations in the human lactate dehydrogenase D (LDHD) gene that cause enzymatic loss
Externí odkaz:
https://doaj.org/article/0dc2cc8f517f49eaa57ea85a84853e50
Autor:
Jake P. Mann, Benjamin Jenkins, Samuel Furse, Stuart G. Snowden, Anna Alisi, Laura G. Draijer, Kylie Karnebeek, Deirdre A. Kelly, Bart G. Koot, Antonella Mosca, Camilla Salvestrini, Indra van Mourik, Anita Vreugdenhil, Matthias Zilbauer, Albert Koulman
Publikováno v:
EU-PNAFLD investigators^ 2022, ' Comparison of the Lipidomic Signature of Fatty Liver in Children and Adults : A Cross-Sectional Study ', Journal of Pediatric Gastroenterology and Nutrition, vol. 74, no. 6, pp. 734-741 . https://doi.org/10.1097/MPG.0000000000003418
Journal of pediatric gastroenterology and nutrition, 74(6), 734-741. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 74(6), 734-741. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 74(6), 734-741. LIPPINCOTT WILLIAMS & WILKINS
Journal of pediatric gastroenterology and nutrition, 74(6), 734-741. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 74(6), 734-741. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 74(6), 734-741. LIPPINCOTT WILLIAMS & WILKINS
OBJECTIVE: Non-alcoholic fatty liver disease (NAFLD) is an increasingly common condition in children characterized by insulin resistance and altered lipid metabolism. Affected patients are at increased risk of cardiovascular disease (CVD) and childre
Autor:
Karen Duran, Johanna C. van Alfen, Paolo Bosco, Judith J.M. Jans, Paulien A Terhal, Saskia N. van der Crabben, Gepke Visser, Koen L.I. van Gassen, Markus J. van Roosmalen, Karin Geleijns, Tom J. de Koning, Nanda M. Verhoeven-Duif, Marinus Duran, Francesco Calì, Monique G.M. de Sain-van der Velden, Glen R. Monroe, Klaske D. Lichtenbelt, Bart G. Koot, Sabine A. Fuchs, Marlies Oostendorp, Johan Gerrits, Nine V A M Knoers, Albertien M. van Eerde, Mirjam van Aalderen, Sanne M C Savelberg, Federico Tessadori, Jeroen Bakkers, Gijs van Haaften
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
Nature Communications, 10(1):1477. Nature Publishing Group
Nature Communications, 10(1). Nature Publishing Group
Monroe, G R, van Eerde, A M, Tessadori, F, Duran, K J, Savelberg, S M C, van Alfen, J C, Terhal, P A, van der Crabben, S N, Lichtenbelt, K D, Fuchs, S A, Gerrits, J, van Roosmalen, M J, van Gassen, K L, van Aalderen, M, Koot, B G, Oostendorp, M, Duran, M, Visser, G, de Koning, T J, Calì, F, Bosco, P, Geleijns, K, de Sain-van der Velden, M G M, Knoers, N V, Bakkers, J, Verhoeven-Duif, N M, van Haaften, G & Jans, J J 2019, ' Identification of human D lactate dehydrogenase deficiency ', Nature Communications, vol. 10, no. 1, 1477 . https://doi.org/10.1038/s41467-019-09458-6
Nature communications, 10(1):1477. Nature Publishing Group
Nature Communications, 10:1477. Nature Publishing Group
Nature Communications
Nature Communications, 10(1):1477. Nature Publishing Group
Nature Communications, 10(1). Nature Publishing Group
Monroe, G R, van Eerde, A M, Tessadori, F, Duran, K J, Savelberg, S M C, van Alfen, J C, Terhal, P A, van der Crabben, S N, Lichtenbelt, K D, Fuchs, S A, Gerrits, J, van Roosmalen, M J, van Gassen, K L, van Aalderen, M, Koot, B G, Oostendorp, M, Duran, M, Visser, G, de Koning, T J, Calì, F, Bosco, P, Geleijns, K, de Sain-van der Velden, M G M, Knoers, N V, Bakkers, J, Verhoeven-Duif, N M, van Haaften, G & Jans, J J 2019, ' Identification of human D lactate dehydrogenase deficiency ', Nature Communications, vol. 10, no. 1, 1477 . https://doi.org/10.1038/s41467-019-09458-6
Nature communications, 10(1):1477. Nature Publishing Group
Nature Communications, 10:1477. Nature Publishing Group
Nature Communications
Phenotypic and biochemical categorization of humans with detrimental variants can provide valuable information on gene function. We illustrate this with the identification of two different homozygous variants resulting in enzymatic loss-of-function i