Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Wendy L van der Woerd"'
Autor:
Wendy L van der Woerd, Désirée Y van Haaften-Visser, Stan F J van de Graaf, Claude Férec, Emmanuelle Masson, Janneke M Stapelbroek, Peter Bugert, Heiko Witt, Roderick H J Houwen
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80553 (2013)
BackgroundMutations in genes encoding cationic trypsinogen (PRSS1), pancreatic secretory trypsin inhibitor (SPINK1) and chymotrypsinogen C (CTRC) are associated with chronic pancreatitis. However, in many patients with a familial chronic pancreatitis
Externí odkaz:
https://doaj.org/article/b90d8d07498a443c93be36298c0f66c2
Autor:
Richard J. Thompson, Reha Artan, Ulrich Baumann, Pier Luigi Calvo, Piotr Czubkowski, Buket Dalgic, Lorenzo D’Antiga, Angelo Di Giorgio, Özlem Durmaz, Emmanuel Gonzalès, Tassos Grammatikopoulos, Girish Gupte, Winita Hardikar, Roderick H.J. Houwen, Binita M. Kamath, Saul J. Karpen, Florence Lacaille, Alain Lachaux, Elke Lainka, Kathleen M. Loomes, Cara L. Mack, Jan P. Mattsson, Patrick McKiernan, Quanhong Ni, Hasan Özen, Sanjay R. Rajwal, Bertrand Roquelaure, Eyal Shteyer, Etienne Sokal, Ronald J. Sokol, Nisreen Soufi, Ekkehard Sturm, Mary Elizabeth Tessier, Wendy L. van der Woerd, Henkjan J. Verkade, Jennifer M. Vittorio, Terese Wallefors, Natalie Warholic, Qifeng Yu, Patrick Horn, Lise Kjems
Publikováno v:
JHEP Reports, Vol 5, Iss 8, Pp 100782- (2023)
Background & Aims: PEDFIC 2, an ongoing, open-label, 72-week study, evaluates odevixibat, an ileal bile acid transporter inhibitor, in patients with progressive familial intrahepatic cholestasis. Methods: PEDFIC 2 enrolled and dosed 69 patients acros
Externí odkaz:
https://doaj.org/article/943aa785601b46a586443dc2851475ff
Autor:
Henkjan J. Verkade, Dominique Debray, Giuseppe Indolfi, Yael Mozer-Glassberg, Joerg Jahnel, Mona Abdel-Hady, Aglaia Zellos, Etienne Sokal, Piotr Czubkowski, Björn Fischler, Françoise Smets, Sanjay Bansal, Wendy L. van der Woerd, Girish Gupte, M. Samyn
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition, Vol. 70, no. 4, p. 527-538 (2020)
Journal of Pediatric Gastroenterology and Nutrition, Vol. 70, no.4, p. 527-538 (2020)
Journal of Pediatric Gastroenterology and Nutrition, 70(4), 527-538. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, Vol. 70, no.4, p. 527-538 (2020)
Journal of Pediatric Gastroenterology and Nutrition, 70(4), 527-538. Lippincott Williams and Wilkins
Reactivation of hepatitis B virus (HBV) is a known complication of immune-suppressive, cytotoxic, and biological modifier therapies in patients currently infected with HBV or who have had past exposure to HBV. Nowadays, newer and emerging forms of ta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaaace3d6abab098c2eb43963573d083
https://doi.org/10.1097/mpg.0000000000002628
https://doi.org/10.1097/mpg.0000000000002628
Autor:
Liting Li, Jian-She Wang, Ozlem Durmaz, Felipe Ordonez, Wikrom Karnsakul, Seema Alam, Cristina Targa Ferreira, Natural Course, Bettina E. Hansen, Kyung Mo Kim, Etienne Sokal, Ryan T. Fischer, Valerie Sency, Estella M. Alonso, Simon Horslen, Elisa de Carvalho, Piotr Czubkowski, Emanuele Nicastro, Nanda Kerkar, Dieter C. Broering, Björn Fischler, Dorothee Krebs-Schmitt, Kathleen M. Loomes, Dominique Debray, Marianne Hørby Jørgensen, Benjamin L. Shneider, Emmanuel Gonzales, Cigdem Arikan, Nathalie Rock, Antal Dezsőfi, Tassos Grammatikopoulos, Steffen Hartleif, Mara Cananzi, Talal Algoufi, Ronald J. Sokol, Jan B F Hulscher, Carolina Jimenez-Rivera, Emmanuel Jacquemin, Anne Spraul, Henkjan J. Verkade, Patryk Lipiński, Daan B E van Wessel, Nejat Mazhar, Maria Rogalidou, Deirdre Kelly, Alexandre Fabre, Daniele Serranti, Pier Luigi Calvo, Yael Mozer-Glassberg, Richard J. Thompson, Cristina Goncalves, Yumirle P. Turmelle, Jesus Quintero Bernabeu, Agustina Kadaristiana, Florence Lacaille, Loreto Hierro, Mohammad Shagrani, Patrick J. McKiernan, Girish S. Rao, Gema Muñoz Bartolo, Huey-Ling Chen, Wendy L. van der Woerd, Irena Jankowska, Amer Azaz, Philip J. Rosenthal, Frederick J. Suchy, Jernej Brecelj, Gabriella Nebbia, Noemie Laverdure, Henrik Arnell, Binita M. Kamath, Heng Wang
Publikováno v:
Hepatology
Hepatology, Wiley-Blackwell, 2021, 74 (2), pp.892-906. ⟨10.1002/hep.31787⟩
Hepatology, 74(2), 892-906. Wiley
Hepatology, Vol. 74, no. 2, p. 892-906 (2021)
Hepatology (Baltimore, Md.)
Hepatology, Wiley-Blackwell, 2021, 74 (2), pp.892-906. ⟨10.1002/hep.31787⟩
Hepatology, 74(2), 892-906. Wiley
Hepatology, Vol. 74, no. 2, p. 892-906 (2021)
Hepatology (Baltimore, Md.)
Mutations in ATP8B1 can lead to familial intrahepatic cholestasis type 1 (FIC1) deficiency, or progressive familial intrahepatic cholestasis type 1 (PFIC1). The rarity of FIC1 deficiency has largely prevented a detailed analysis of its natural histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecc4ae32d84b425ddef55c91928639e
https://hal-amu.archives-ouvertes.fr/hal-03663238
https://hal-amu.archives-ouvertes.fr/hal-03663238
Autor:
Wendy L. van der Woerd, Stan F.J. van de Graaf, Catharina G.K. Wichers, Coen C. Paulusma, Anna L. Vestergaard, Roderick H.J. Houwen, Jens Peter Andersen
Publikováno v:
Journal of hepatology, 64(6), 1339-1347. Elsevier
van der Woerd, W L, Wichers, C G K, Vestergaard, A L, Andersen, J P, Paulusma, C C, Houwen, R H J & van de Graaf, S F J 2016, ' Rescue of defective ATP8B1 trafficking by CFTR correctors as a therapeutic strategy for familial intrahepatic cholestasis ', Journal of Hepatology, vol. 64, no. 6, pp. 1339-47 . https://doi.org/10.1016/j.jhep.2016.02.001
Journal of Hepatology, 64(6), 1339. Elsevier
van der Woerd, W L, Wichers, C G K, Vestergaard, A L, Andersen, J P, Paulusma, C C, Houwen, R H J & van de Graaf, S F J 2016, ' Rescue of defective ATP8B1 trafficking by CFTR correctors as a therapeutic strategy for familial intrahepatic cholestasis ', Journal of Hepatology, vol. 64, no. 6, pp. 1339-47 . https://doi.org/10.1016/j.jhep.2016.02.001
Journal of Hepatology, 64(6), 1339. Elsevier
BACKGROUND & AIMS: ATP8B1 deficiency is an autosomal recessive liver disease characterized by intrahepatic cholestasis. ATP8B1 mutation p.I661T, the most frequent mutation in European patients, results in protein misfolding and impaired targeting to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd8056678305169a7e1eaae9bcb5bb2b
https://doi.org/10.1016/j.jhep.2016.02.001
https://doi.org/10.1016/j.jhep.2016.02.001
Autor:
Piotr Czubowski, Girish Gupte, Giuseppe Indolfi, Françoise Smets, Antal Dezsofi, Dominique Debray, Jörg Jahnel, Henkjan J. Verkade, Wendy L. van der Woerd, Nedim Hadzic, Björn Fischler, Yael Mozer-Glassberg, Loreto Hierro
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition, 66(3), 505-515. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 66(3), 505. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 66(3), 505. Lippincott Williams and Wilkins
Objectives: In 2017, the European Medicines Agency and the Food and Drug Administration approved the use of the fixed-dose combination of ledipasvir/sofosbuvir and of the combination of sofosbuvir and ribavirin for treatment of adolescents (12-17 yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f67da43eb7061d1d882765be512c9b2
https://research.rug.nl/en/publications/cb92a39c-edc2-43fc-b2ed-71b93c1d9e42
https://research.rug.nl/en/publications/cb92a39c-edc2-43fc-b2ed-71b93c1d9e42
Autor:
Roderick H. J. Houwen, Franco Pagani, Stan F.J. van de Graaf, Ulrich Beuers, Wendy L. van der Woerd, Johanna Mulder
Publikováno v:
Hepatology (Baltimore, Md.), 61(4), 1382-1391. John Wiley and Sons Ltd
Hepatology, 61(4), 1382. John Wiley and Sons Ltd
Hepatology, 61(4), 1382. John Wiley and Sons Ltd
ATP8B1 deficiency is a severe autosomal recessive liver disease resulting from mutations in the ATP8B1 gene characterized by a continuous phenotypical spectrum from intermittent (benign recurrent intrahepatic cholestasis; BRIC) to progressive familia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f877e4ba764b83fed37eb8f121cfe0a5
https://doi.org/10.1002/hep.27620
https://doi.org/10.1002/hep.27620
Autor:
Danielle Robbers-Visser, Doff B. McElhinney, Wendy L. van der Woerd, Meryl S. Cohen, Thomas L. Spray, Gil Wernovsky, J. William Gaynor, Bradley S. Marino
Publikováno v:
Journal of the American College of Cardiology. 42:533-540
OBJECTIVES We sought to assess the prevalence and progression of neo-aortic root dilation and valvar regurgitation after staged reconstruction for hypoplastic left heart syndrome (HLHS). BACKGROUND In HLHS, the pulmonary valve functions as the neo-ao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56cd1ab803b829c6b1b24ddd48a55b4e
https://doi.org/10.1016/s0735-1097(03)00715-0
https://doi.org/10.1016/s0735-1097(03)00715-0
Publikováno v:
Current Opinion in Pulmonary Medicine, 23(6), 551. Lippincott Williams and Wilkins
Purpose of review Several new therapeutic modalities have recently become available to be used in patients with cystic fibrosis such as potentiators, modulators, and probiotics. Although the effects on pulmonary function have been well documented, ga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4dec1531b804023e4710214cf641a2c
https://hdl.handle.net/1874/356672
https://hdl.handle.net/1874/356672
Publikováno v:
World Journal of Gastroenterology
World Journal of Gastroenterology, 23(5), 763. WJG Press
World Journal of Gastroenterology, 23(5), 763. WJG Press
Familial intrahepatic cholestasis (FIC) comprises a group of rare cholestatic liver diseases associated with canalicular transport defects resulting predominantly from mutations in ATP8B1, ABCB11 and ABCB4 . Phenotypes range from benign recurrent int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc29559f060af6678f156b7e353dcf5b
https://doi.org/10.3748/wjg.v23.i5.763
https://doi.org/10.3748/wjg.v23.i5.763