Ngā hua rapu - Holleboom, Adriaan G.

Tuberculous meningitis: treat upon suspicion mā 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 mā 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? mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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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