Search Results - Holleboom, Adriaan G.

Tuberculous meningitis: treat upon suspicion by Sonneveld, Myrthe Elisabeth, Zinkstok, SM, Nellen, FJB, Holleboom, Adriaan G

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Dietary Interventions in Patients With Non-alcoholic Fatty Liver Disease: A Systematic Review and Meta-Analysis by Houttu, Veera, Csader, Susanne, Nieuwdorp, Max, Holleboom, Adriaan G., Schwab, Ursula

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The HDL hypothesis: does high-density lipoprotein protect from atherosclerosis? by Vergeer, Menno, Holleboom, Adriaan G., Kastelein, John J. P., Kuivenhoven, Jan Albert

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Referral care paths for non‐alcoholic fatty liver disease—Gearing up for an ever more prevalent and severe liver disease by van Dijk, Anne‐Marieke, Schattenberg, Jörn M., Holleboom, Adriaan G., Tushuizen, Maarten E.

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The Role of Lipophagy in the Development and Treatment of Non-Alcoholic Fatty Liver Disease by Grefhorst, Aldo, van de Peppel, Ivo P., Larsen, Lars E., Jonker, Johan W., Holleboom, Adriaan G.

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The role of the gut microbiome and exercise in non-alcoholic fatty liver disease by Houttu, Veera, Boulund, Ulrika, Grefhorst, Aldo, Soeters, Maarten R., Pinto-Sietsma, Sara-Joan, Nieuwdorp, Max, Holleboom, Adriaan G.

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Clinicians’ Perspectives on Barriers and Facilitators for the Adoption of Non-Invasive Liver Tests for NAFLD: A Mixed-Method Study by Vali, Yasaman, Eijk, Roel, Hicks, Timothy, Jones, William S., Suklan, Jana, Holleboom, Adriaan G., Ratziu, Vlad, Langendam, Miranda W., Anstee, Quentin M., Bossuyt, Patrick M. M.

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Adrenal Function in Females with Low Plasma HDL-C Due to Mutations in ABCA1 and LCAT by Bochem, Andrea E., Holleboom, Adriaan G., Romijn, Johannes A., Hoekstra, Menno, Dallinga, Geesje M., Motazacker, Mahdi M., Hovingh, G. Kees, Kuivenhoven, Jan A., Stroes, Erik S. G.

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High density lipoprotein as a source of cholesterol for adrenal steroidogenesis: a study in individuals with low plasma HDL-C by Bochem, Andrea E., Holleboom, Adriaan G., Romijn, Johannes A., Hoekstra, Menno, Dallinga-Thie, Geesje M., Motazacker, Mahdi M., Hovingh, G. Kees, Kuivenhoven, Jan A., Stroes, Erik S. G.

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Esterification of 4β-hydroxycholesterol and other oxysterols in human plasma occurs independently of LCAT by Yamamuro, Daisuke, Yamazaki, Hisataka, Osuga, Jun-ichi, Okada, Kenta, Wakabayashi, Tetsuji, Takei, Akihito, Takei, Shoko, Takahashi, Manabu, Nagashima, Shuichi, Holleboom, Adriaan G., Kuroda, Masayuki, Bujo, Hideaki, Ishibashi, Shun

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Systematic Review with Meta-Analyses: Diagnostic Accuracy of FibroMeter Tests in Patients with Non-Alcoholic Fatty Liver Disease by Van Dijk, Anne-Marieke, Vali, Yasaman, Mak, Anne Linde, Lee, Jenny, Tushuizen, Maarten E., Zafarmand, Mohammad Hadi, Anstee, Quentin M., Brosnan, M. Julia, Nieuwdorp, Max, Bossuyt, Patrick M., Holleboom, Adriaan G.

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Lipid Oxidation in Carriers of Lecithin:Cholesterol Acyltransferase Gene Mutations by Holleboom, Adriaan G., Daniil, Georgios, Fu, Xiaoming, Zhang, Renliang, Hovingh, G. Kees, Schimmel, Alinda W., Kastelein, John J.P., Stroes, Erik S.G., Witztum, Joseph L., Hutten, Barbara A., Tsimikas, Sotirios, Hazen, Stanley L., Chroni, Angeliki, Kuivenhoven, Jan Albert

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In vivo tissue cholesterol efflux is reduced in carriers of a mutation in APOA1 by Holleboom, Adriaan G., Jakulj, Lily, Franssen, Remco, Decaris, Julie, Vergeer, Menno, Koetsveld, Joris, Luchoomun, Jayraz, Glass, Alexander, Hellerstein, Marc K., Kastelein, John J. P., Hovingh, G. Kees, Kuivenhoven, Jan Albert, Groen, Albert K., Turner, Scott M., Stroes, Erik S. G.

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Systematic Review with Meta-Analysis: Diagnostic Accuracy of Pro-C3 for Hepatic Fibrosis in Patients with Non-Alcoholic Fatty Liver Disease by Mak, Anne Linde, Lee, Jenny, van Dijk, Anne-Marieke, Vali, Yasaman, Aithal, Guruprasad P., Schattenberg, Jörn M., Anstee, Quentin M., Brosnan, M. Julia, Zafarmand, Mohammad Hadi, Ramsoekh, Dewkoemar, Harrison, Stephen A., Nieuwdorp, Max, Bossuyt, Patrick M., Holleboom, Adriaan G.

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Reduced CETP glycosylation and activity in patients with homozygous B4GALT1 mutations by van den Boogert, Marjolein A.W., Crunelle, Cleo L., Ali, Lubna, Larsen, Lars E., Kuil, Sacha D., Levels, Johannes H.M., Schimmel, Alinda W.M., Konstantopoulou, Vassiliki, Guerin, Maryse, Kuivenhoven, Jan Albert, Dallinga‐Thie, Geesje M., Stroes, Erik S.G., Lefeber, Dirk J., Holleboom, Adriaan G.

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Assessment of Imaging Modalities Against Liver Biopsy in Nonalcoholic Fatty Liver Disease: The Amsterdam NAFLD‐NASH Cohort by Troelstra, Marian A., Witjes, Julia J., van Dijk, Anne‐Marieke, Mak, Anne L., Gurney‐Champion, Oliver, Runge, Jurgen H., Zwirs, Diona, Stols‐Gonçalves, Daniela, Zwinderman, Aelko H., ten Wolde, Marije, Monajemi, Houshang, Ramsoekh, Sandjai, Sinkus, Ralph, van Delden, Otto M., Beuers, Ulrich H., Verheij, Joanne, Nieuwdorp, Max, Nederveen, Aart J., Holleboom, Adriaan G.

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Defective Lipid Droplet–Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutations in TMEM199 and CCDC115 by Larsen, Lars E., van den Boogert, Marjolein A.W., Rios-Ocampo, Wilson A., Jansen, Jos C., Conlon, Donna, Chong, Patrick L.E., Levels, J. Han M., Eilers, Roos E., Sachdev, Vinay V., Zelcer, Noam, Raabe, Tobias, He, Miao, Hand, Nicholas J., Drenth, Joost P.H., Rader, David J., Stroes, Eric S.G., Lefeber, Dirk J., Jonker, Johan W., Holleboom, Adriaan G.

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Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis by Witjes, Julia J., Smits, Loek P., Pekmez, Ceyda T., Prodan, Andrei, Meijnikman, Abraham S., Troelstra, Marian A., Bouter, Kristien E.C., Herrema, Hilde, Levin, Evgeni, Holleboom, Adriaan G., Winkelmeijer, Maaike, Beuers, Ulrich H., van Lienden, Krijn, Aron‐Wisnewky, Judith, Mannisto, Ville, Bergman, Jacques J., Runge, Jurgen H., Nederveen, Aart J., Dragsted, Lars O., Konstanti, Prokopis, Zoetendal, Erwin G., de Vos, Willem, Verheij, Joanne, Groen, Albert K., Nieuwdorp, Max

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Heterozygosity for a Loss-of-Function Mutation in GALNT2 Improves Plasma Triglyceride Clearance in Man by Holleboom, Adriaan G., Karlsson, Helen, Lin, Ruei-Shiuan, Beres, Thomas M., Sierts, Jeroen A., Herman, Daniel S., Stroes, Erik S.G., Aerts, Johannes M., Kastelein, John J.P., Motazacker, Mohammad M., Dallinga-Thie, Geesje M., Levels, Johannes H.M., Zwinderman, Aeilko H., Seidman, Jonathan G., Seidman, Christine E., Ljunggren, Stefan, Lefeber, Dirk J., Morava, Eva, Wevers, Ron A., Fritz, Timothy A., Tabak, Lawrence A., Lindahl, Mats, Hovingh, G. Kees, Kuivenhoven, Jan Albert

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Mutations in the V‐ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease by Cannata Serio, Magda, Graham, Laurie A., Ashikov, Angel, Larsen, Lars Elmann, Raymond, Kimiyo, Timal, Sharita, Le Meur, Gwenn, Ryan, Margret, Czarnowska, Elzbieta, Jansen, Jos C., He, Miao, Ficicioglu, Can, Pichurin, Pavel, Hasadsri, Linda, Minassian, Berge, Rugierri, Alessandra, Kalimo, Hannu, Ríos‐Ocampo, W. Alfredo, Gilissen, Christian, Rodenburg, Richard, Jonker, Johan W., Holleboom, Adriaan G., Morava, Eva, Veltman, Joris A., Socha, Piotr, Stevens, Tom H., Simons, Matias, Lefeber, Dirk J.

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