Search Results - "van der Woerd, W."

Treatment of Chronic Hepatitis C Virus Infection in Children: A Position Paper by the Hepatology Committee of European Society of Paediatric Gastroenterology, Hepatology and Nutrition by Indolfi, Giuseppe, Hierro, Loreto, Dezsofi, Antal, Jahnel, Jörg, Debray, Dominique, Hadzic, Nedim, Czubowski, Piotr, Gupte, Girish, Mozer-Glassberg, Yael, van der Woerd, Wendy, Smets, Françoise, Verkade, Henkjan J, Fischler, Björn

“…OBJECTIVES:In 2017, the European Medicines Agency and the Food and Drug Administration approved the use of the fixed-dose combination of ledipasvir/sofosbuvir…”
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Management of Hepatitis B Virus Infection and Prevention of Hepatitis B Virus Reactivation in Children With Acquired Immunodeficiencies or Undergoing Immune Suppressive, Cytotoxic, or Biological Modifier Therapies by Indolfi, Giuseppe, Abdel‐Hady, Mona, Bansal, Sanjay, Debray, Dominique, Smets, Françoise, Czubkowski, Piotr, Woerd, Wendy, Samyn, Marianne, Jahnel, Jörg, Gupte, Girish, Zellos, Aglaia, Mozer‐Glassberg, Yael, Verkade, Henkjan J., Sokal, Etienne, Fischler, Björn

“…ABSTRACT Reactivation of hepatitis B virus (HBV) is a known complication of immune‐suppressive, cytotoxic, and biological modifier therapies in patients…”
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Defective Plasma Membrane Targeting of P.I661T-ATP8B1, Associated with Familial Intrahepatic Cholestasis, Can be Rescued in Vitro by CFTR Correctors by van der Woerd, W, Wichers, C, Vestergaard, A, Andersen, J.P, Paulusma, C, Houwen, R, Van De Graaf, S

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The natural course of FIC1 deficiency and BSEP deficiency: Initial results from the NAPPED-consortium (Natural course and Prognosis of PFIC and Effect of biliary Diversion) by van Wessel, D., Thompson, R., Grammatikopoulos, T., Kadaristiana, A., Jankowska, I., Lipiński, P., Czubkowski, P., Gonzales, E., Jacquemin, E., Spraul, A., Sokal, E., Shagrani, M.A., Broering, D.C., Algoufi, T., Mazhar, N., Nicastro, E., Kelly, D., Nebbia, G., Arnell, H., Fischler, B., Sankaranarayanan, S., Hulscher, J., Serranti, D., Arikan, C., Polat, E., Debray, D., Lacaille, F., Goncalves, C., Hierro, L., Bartolo, G.M., Mozer-Glassberg, Y., Azaz, A., Brecelj, J., Dezsőfi, A., Calvo, P.L., Pizzol, A., Schmitt, D., Sturm, E., van der Woerd, W., Hansen, B., Verkade, H.

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THU-452 - Defective Plasma Membrane Targeting of P.I661T-ATP8B1, Associated with Familial Intrahepatic Cholestasis, Can be Rescued in Vitro by CFTR Correctors by van der Woerd, W., Wichers, C., Vestergaard, A., Andersen, J.P., Paulusma, C., Houwen, R., Van De Graaf, S.

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The phenotype of compound heterozygous BSEP deficiency patients is determined by the combined residual function of the two ABCB11 mutations: results from the NAPPED consortium by Felzen, Antonia, van Wessel, Daan, Thompson, Richard, Gonzales, Emmanuel, Jankowska, Irena, Sokal, Etienne, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jacquemin, Emmanuel, Spraul, Anne, Lipiński, Patryk, Czubkowski, Piotr, Rock, Nathalie, Shagrani, Mohammad Ali, Broering, Dieter Clemens, Algoufi, Talal, Mazhar, Nejat, Nicastro, Emanuele, Kelly, Deirdre, Nebbia, Gabriella, Arnell, Henrik, Fischler, Björn, Hulscher, JBF, Serranti, Daniele, Arıkan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Gonçalves, Cristina, Hierro, Loreto, Bartolo, Gema Muñoz, Glassberg, Yael Mozer, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, van der Woerd, Wendy, Kamath, Binita M., Wang, Jian-She, Liting, Li, Durmaz, Ozlem, Kerkar, Nanda, Jørgensen, Marianne Hørby, Fischer, Ryan, Jimenez-Rivera, Carolina, Alam, Seema, Cananzi, Mara, Ruiz, Mathias, Targa, Cristina, Ferrero, Felipe Ordoñez, Wang, Heng, Kim, Kyungmo, Chen, Huey-Ling, Carvalho, Elisa, Hansen, Bettina, Verkade, Henkjan

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SAT-048 - The natural course of FIC1 deficiency and BSEP deficiency: Initial results from the NAPPED-consortium (Natural course and Prognosis of PFIC and Effect of biliary Diversion) by van Wessel, D., Thompson, R., Grammatikopoulos, T., Kadaristiana, A., Jankowska, I., Lipiński, P., Czubkowski, P., Gonzales, E., Jacquemin, E., Spraul, A., Sokal, E., Shagrani, M.A., Broering, D.C., Algoufi, T., Mazhar, N., Nicastro, E., Kelly, D., Nebbia, G., Arnell, H., Fischler, B., Sankaranarayanan, S., Hulscher, J., Serranti, D., Arikan, C., Polat, E., Debray, D., Lacaille, F., Goncalves, C., Hierro, L., Bartolo, G.M., Mozer-Glassberg, Y., Azaz, A., Brecelj, J., Dezsőfi, A., Calvo, P.L., Pizzol, A., Schmitt, D., Sturm, E., van der Woerd, W., Hansen, B., Verkade, H.

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Genotype correlates with the natural history of severe bile salt export pump deficiency by van Wessel, Daan B.E., Thompson, Richard J., Gonzales, Emmanuel, Jankowska, Irena, Sokal, Etienne, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jacquemin, Emmanuel, Spraul, Anne, Lipiński, Patryk, Czubkowski, Piotr, Rock, Nathalie, Shagrani, Mohammad, Broering, Dieter, Algoufi, Talal, Mazhar, Nejat, Nicastro, Emanuele, Kelly, Deirdre A., Nebbia, Gabriella, Arnell, Henrik, Björn Fischler, Hulscher, Jan B.F., Serranti, Daniele, Arikan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Goncalves, Cristina, Hierro, Loreto, Muñoz Bartolo, Gema, Mozer-Glassberg, Yael, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, van der Woerd, Wendy J., Kamath, Binita M., Wang, Jian-She, Li, Liting, Durmaz, Özlem, Onal, Zerrin, Bunt, Ton M.G., Hansen, Bettina E., Verkade, Henkjan J.

“…Mutations in ABCB11 can cause deficiency of the bile salt export pump (BSEP), leading to cholestasis and end-stage liver disease. Owing to the rarity of the…”
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Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database by Hansen, Bettina, Valcheva, Velichka, Yu, Qifeng, van Wessel, Daan, Thompson, Richard, Gonzalès, Emmanuel, Jankowska, Irena, Sokal, Etienne, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jacquemin, Emmanuel, Spraul, Anne, Lipiński, Patryk, Czubkowski, Piotr, Rock, Nathalie, Shagrani, Mohammad, Kumar, Kishwer, Alkuraya, Fowzan, Sateesh, Meddirevula, Broering, Dieter Clemens, Nicastro, Emanuele, Kelly, Deirdre, Nebbia, Gabriella, Arnell, Henrik, Fischler, Björn, Serranti, Daniele, Arıkan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Gonçalves, Cristina, Llanillo, Loreto Hierro, Bartolo, Gema Muñoz, Mozer-Glassberg, Yael, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, van der Woerd, Wendy L., Kamath, Binita M., Wang, Jian-She, Liting, Li, Durmaz, Ozlem, Önal, Zerrin, Felzen, Antonia, Nomden, Mark, Sonajalg, Jaak, Stein, Philip, Ni, Quanhong, Clemson, Christine, Mattsson, Jan, Verkade, Henkjan J.

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Neo-aortic root dilation and valve regurgitation up to 21 years after staged reconstruction for hypoplastic left heart syndrome by Cohen, Meryl S, Marino, Bradley S, McElhinney, Doff B, Robbers-Visser, Daniëlle, van der Woerd, Wendy, Gaynor, J.William, Spray, Thomas L, Wernovsky, Gil

“…We sought to assess the prevalence and progression of neo-aortic root dilation and valvar regurgitation after staged reconstruction for hypoplastic left heart…”
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Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium by van Wessel, D, Thompson, R, Grammatikopoulos, T, Kadaristiana, A, Jankowska, I, Lipineski, P, Czubkowski, P, Gonzales, E, Jacquemin, E, Spraul, A, Sokal, E, Shagrani, MA, Broering, DC, Algoufi, T, Mazhar, N, Nicastro, E, Kelly, D, Nebbia, G, Arnell, H, Fischler, B, Hulscher, JBF, Serranti, D, Arikan, C, Polat, E, Debray, D, Lacaille, F, Gonccalves, C, Hierro, L, Bartolo, GM, Mozer-Glassberg, Y, Azaz, A, Brecelj, J, Dezsofi, A, Calvo, PL, Grabhorn, E, Sturm, E, van der Woerd, W, Kamath, BM, Wang, JS, Li, LT, Durmaz, O, Hansen, B, Verkade, H

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GENOTYPE-PHENOTYPE RELATIONSHIPS IN PATIENTS WITH RELATIVELY MILD MUTATIONS IN ABCB11 : RESULTS FROM THE NAPPED CONSORTIUM by van Wessel, D, Thompson, RJ, Gonzales, EM, Jankowska, I, Sokal, EM, Grammatikopoulos, T, Kadaristiana, A, Lipinski, P, Czubkowski, P, Jacquemin, E, Spraul, A, Rock, N, Shagrani, M, Broering, D, Algoufi, T, Mazhar, N, Nicastro, E, Kelly, DA, Nebbia, G, Arnell, H, Fischler, B, Hulscher, J, Serranti, D, Arikan, C, Polat, E, Debray, D, Lacaille, F, Goncalves, C, Hierro, L, Bartolo, GM, Mozer-Glassberg, Y, Azaz, A, Brecelj, J, Dezsofi, A, Calvo, PL, Grabhorn, E, Sturm, E, Van der Woerd, W, Kamath, BM, Wang, JS, Li, LT, Durmaz, O, Hansen, BE, Verkade, HJ

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THE PRESENCE OF A TRUNCATING MUTATION IN ABCB11 ABROGATES THE BENEFICIAL EFFECT OF A RESIDUAL FUNCTION MUTATION ON THE COURSE OF SEVERE BILE SALT EXPORT PUMP DEFICIENCY by Felzen, A, van Wessel, D, Thompson, RJ, Gonzales, EM, Jankowska, I, Shneider, BL, Sokal, E, Grammatikopoulos, T, Kadaristiana, A, Jacquemin, E, Spraul, A, Lipinski, P, Czubkowski, P, Rock, N, Shagrani, M, Broering, D, Algoufi, T, Mazhar, N, Nicastro, E, Kelly, D, Nebbia, G, Arnell, H, Fischler, B, Hulscher, J, Serranti, D, Arikan, C, Polat, E, Debray, D, Lacaille, F, Goncalves, C, Hierro, L, Bartolo, GM, Mozer-Glassberg, Y, Azaz, A, Brecelj, J, Dezsofi, A, Calvo, PL, Grabhorn, E, Hartleif, S, Van der Woerd, W, Kamath, BM, Wang, JS, Li, LT, Durmaz, O, Kerkar, N, Jorgensen, MH, Fischer, RT, Jimenez-Rivera, C, Alam, S, Cananzi, M, Ruiz, M, Ferreira, CT, Ferrero, FO, Wang, H, Sency, V, Kim, KM, Chen, HL, Carvalho, E, Fabre, A, Bernabeu, JQ, Alonso, EM, Sokol, RJ, Suchy, FJ, Loomes, KM, McKiernan, PJ, Rosenthal, P, Turmelle, Y, Horslen, SP, Schwarz, KB, Bezerra, JA, Wang, KS, Hansen, BE, Verkade, HJ

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NATIVE LIVER SURVIVAL IN PATIENTS WITH FIC1 DEFICIENCY: IMPACT OF GENOTYPE, SERUM BILE ACID CONCENTRATIONS AND SURGICAL BILIARY DIVERSION by van Wessel, D, Thompson, RJ, Gonzales, EM, Jankowska, I, Shneider, BL, Sokal, E, Grammatikopoulos, T, Kadaristiana, A, Jacquemin, E, Spraul, A, Lipinski, P, Czubkowski, P, Rock, N, Shagrani, M, Broering, D, Algoufi, T, Mazhar, N, Nicastro, E, Kelly, D, Nebbia, G, Arnell, H, Fischler, B, Hulscher, J, Serranti, D, Arikan, C, Polat, E, Debray, D, Lacaille, F, Goncalves, C, Hierro, L, Bartolo, GM, Mozer-Glassberg, Y, Azaz, A, Brecelj, J, Dezsofi, A, Calvo, PL, Grabhorn, E, Hartleif, S, Van der Woerd, W, Wang, JS, Li, LT, Durmaz, O, Kerkar, N, Jorgensen, MH, Fischer, RT, Jimenez-Rivera, C, Alam, S, Cananzi, M, Laverdure, N, Ferreira, CT, Ferrero, FO, Wang, H, Sency, V, Kim, KM, Chen, HL, Carvalho, E, Fabre, A, Bernabeu, JQ, Alonso, EM, Sokol, RJ, Suchy, FJ, Loomes, KM, McKiernan, PJ, Rosenthal, P, Turmelle, YP, Rao, GS, Horslen, SP, Kamath, BM, Rogalidou, M, Karnsakul, W, Hansen, BE, Verkade, HJ

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Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11 by van Mil, Saskia W C, van der Woerd, Wendy L, van der Brugge, Gerda, Sturm, Ekkehard, Jansen, Peter L M, Bull, Laura N, van den Berg, Inge E T, Berger, Ruud, Houwen, Roderick H J, Klomp, Leo W J

“…Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are hereditary liver disorders; PFIC is characterized…”
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The Natural Course of Bsep Deficiency: Results from the Global Napped-Consortium by van Wessel, D, Thompson, RJ, Grammatikopoulos, T, Kadaristiana, A, Jankowska, I, Lipinski, P, Czubkowski, P, Gonzales, EM, Jacquemin, E, Spraul, A, Sokal, EM, Shagrani, M, Broering, D, Algoufi, T, Mazhar, N, Nicastro, E, Kelly, DA, Nebbia, G, Arnell, H, Fischler, B, Hulscher, J, Serranti, D, Arikan, C, Polat, E, Debray, D, Lacaille, F, Goncalves, C, Hierro, L, Bartolo, GM, Mozer-Glassberg, Y, Azaz, A, Brecelj, J, Dezsofi, A, Calvo, PL, Grabhorn, E, Sturm, E, Van der Woerd, W, Hansen, BE, Verkade, HJ

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Cyclic vomiting in children by van der Woerd, W L, Fontijn, J R, Rövekamp, M H, van Diemen-Steenvoorde, J A A M

“…Two girls aged 13 and 10 suffered from recurrent episodes of severe vomiting. After excluding underlying pathological conditions the diagnosis of…”
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