Pulmonary artery pseudoaneurysm after thoracic radiation therapy: A case report and review of the literature
Maessen, Gerdinique G C, Hoffman, Thijs T W, Graat-Verboom, Lidwien L, van Leersum, Marc M, Mager, Hans-Jurgen J J
Published in Respirology case reports (01.04.2024)
Published in Respirology case reports (01.04.2024)
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Journal Article
Thresholds of Endoglin Expression in Endothelial Cells Explains Vascular Etiology in Hereditary Hemorrhagic Telangiectasia Type 1
Galaris, Georgios, Montagne, Kévin, Thalgott, Jérémy H., Goujon, Geoffroy J. P. E., van den Driesche, Sander, Martin, Sabrina, Mager, Hans-Jurgen J., Mummery, Christine L., Rabelink, Ton J., Lebrin, Franck
Published in International journal of molecular sciences (19.08.2021)
Published in International journal of molecular sciences (19.08.2021)
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Journal Article
Prevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination
Shovlin, Claire, Bamford, Kathleen, Sabbà, Carlo, Mager, Hans-Jurgen, Kjeldsen, Anette, Droege, Freya, Buscarini, Elisabetta, Dupuis-Girod, Sophie
Published in Haematologica (Roma) (01.02.2019)
Published in Haematologica (Roma) (01.02.2019)
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Journal Article
BMP Receptor Inhibition Enhances Tissue Repair in Endoglin Heterozygous Mice
Bakker, Wineke, Dingenouts, Calinda K E, Lodder, Kirsten, Wiesmeijer, Karien C, de Jong, Alwin, Kurakula, Kondababu, Mager, Hans-Jurgen J, Smits, Anke M, de Vries, Margreet R, Quax, Paul H A, Goumans, Marie José T H
Published in International journal of molecular sciences (18.02.2021)
Published in International journal of molecular sciences (18.02.2021)
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Journal Article
The evolution of survival of pulmonary arterial hypertension over 15 years
Hendriks, Paul M., Staal, Diederik P., Groep, Liza D., Toorn, Leon M., Chandoesing, Prewesh P., Kauling, Robert M., Mager, Hans‐Jurgen, Bosch, Annemien E., Post, Marco C., Boomars, Karin A.
Published in Pulmonary circulation (01.10.2022)
Published in Pulmonary circulation (01.10.2022)
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Journal Article
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2
Bouma, Marga J., Orlova, Valeria, van den Hil, Francijna E., Mager, Hans-Jurgen, Baas, Frank, de Knijff, Peter, Mummery, Christine L., Mikkers, Harald, Freund, Christian
Published in Stem cell research (01.07.2020)
Published in Stem cell research (01.07.2020)
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Journal Article
Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia
Letteboer, Tom G.W., Mager, Hans-Jurgen, Snijder, Repke J., Lindhout, Dick, Ploos van Amstel, Hans-Kristian, Zanen, Pieter, Westermann, Kees J.J.
Published in American journal of medical genetics. Part A (01.11.2008)
Published in American journal of medical genetics. Part A (01.11.2008)
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Journal Article
European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)
Shovlin, Claire L, Buscarini, Elisabetta, Kjeldsen, Anette D, Mager, Hans Jurgen, Sabba, Carlo, Droege, Freya, Geisthoff, Urban, Ugolini, Sara, Dupuis-Girod, Sophie
Published in Orphanet journal of rare diseases (15.08.2018)
Published in Orphanet journal of rare diseases (15.08.2018)
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Journal Article
Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia
Buscarini, Elisabetta, Botella, Luisa Maria, Geisthoff, Urban, Kjeldsen, Anette D, Mager, Hans Jurgen, Pagella, Fabio, Suppressa, Patrizia, Zarrabeitia, Roberto, Dupuis-Girod, Sophie, Shovlin, Claire L
Published in Orphanet journal of rare diseases (04.02.2019)
Published in Orphanet journal of rare diseases (04.02.2019)
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Journal Article
Systematic screening in hereditary hemorrhagic telangiectasia: a review
Kroon, Steven, Snijder, Repke J, Faughnan, Marie E, Mager, Hans-Jurgen
Published in Current opinion in pulmonary medicine (01.05.2018)
Published in Current opinion in pulmonary medicine (01.05.2018)
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Journal Article
Vascular defects associated with hereditary hemorrhagic telangiectasia revealed in patient-derived isogenic iPSCs in 3D vessels on chip
Orlova, Valeria V., Nahon, Dennis M., Cochrane, Amy, Cao, Xu, Freund, Christian, van den Hil, Francijna, Westermann, Cornelius J.J., Snijder, Repke J., Ploos van Amstel, Johannes Kristian, ten Dijke, Peter, Lebrin, Franck, Mager, Hans-Jurgen, Mummery, Christine L.
Published in Stem cell reports (12.07.2022)
Published in Stem cell reports (12.07.2022)
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Journal Article
European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)
Eker, Omer F., Boccardi, Edoardo, Sure, Ulrich, Patel, Maneesh C., Alicante, Saverio, Alsafi, Ali, Coote, Nicola, Droege, Freya, Dupuis, Olivier, Fialla, Annette Dam, Jones, Bryony, Kariholu, Ujwal, Kjeldsen, Anette D., Lefroy, David, Lenato, Gennaro M., Mager, Hans Jurgen, Manfredi, Guido, Nielsen, Troels H., Pagella, Fabio, Post, Marco C., Rennie, Catherine, Sabbà, Carlo, Suppressa, Patrizia, Toerring, Pernille M., Ugolini, Sara, Buscarini, Elisabetta, Dupuis-Girod, Sophie, Shovlin, Claire L.
Published in Orphanet journal of rare diseases (29.06.2020)
Published in Orphanet journal of rare diseases (29.06.2020)
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Journal Article
European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod, Sophie, Shovlin, Claire L., Kjeldsen, Anette D., Mager, Hans-Jurgen, Sabba, Carlo, Droege, Freya, Fargeton, Anne-Emmanuelle, Fialla, Annette D., Gandolfi, Silvia, Hermann, Ruben, Lenato, Gennaro M., Manfredi, Guido, Post, Marco C., Rennie, Catherine, Suppressa, Patrizia, Sure, Ulrich, Crocione, Claudia, Blom, Ria, Botella, Luisa Maria, Brocca, Fernando, Coxall, Caroline, Druckman, Karen T., Erasme, Didier, Federici, Paolo, Grabowski, Christina, Lundgren, Mildred, Søderman, Tone, Woods, Dara, Buscarini, Elisabetta
Published in European journal of medical genetics (01.10.2022)
Published in European journal of medical genetics (01.10.2022)
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Journal Article
Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia
Thompson, K P, Nelson, J, Kim, H, Weinsheimer, S M, Marchuk, D A, Lawton, M T, Krings, T, Faughnan, M E
Published in Orphanet journal of rare diseases (19.09.2021)
Published in Orphanet journal of rare diseases (19.09.2021)
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Journal Article
Hereditary Hemorrhagic Telangiectasia: Recent Advances and Future Challenges
Year of Publication 2021
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Circulation of avian Chlamydia abortus in the Netherlands and community-acquired pneumonia: an outbreak investigation and retrospective cohort study
Raven, Stijn, Heijne, Marloes, Koomen, Jeroen, Doornenbal, Gert, Maas, Miriam, Jacobs, Pieter, Keur, Ingrid, Dijkstra, Frederika, Reukers, Daphne, Platenburg, Mark, Verweij, Stephan P, Mager, Hans-Jurgen, Totté, Joan, Vainio, Saara, Bongaerts, Maarten, Heddema, Edou
Published in The Lancet infectious diseases (16.10.2024)
Published in The Lancet infectious diseases (16.10.2024)
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Neurovascular Complications and Pulmonary Arteriovenous Malformation Feeding Artery Size
Ananiadis, Theodora, Faughnan, Marie E, Clark, Dewi, Prabhudesai, Vikram, Kim, Helen, Lawton, Michael T, Vozoris, Nicholas T
Published in Annals of the American Thoracic Society (01.08.2022)
Published in Annals of the American Thoracic Society (01.08.2022)
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Journal Article
Predictors of mortality in patients with hereditary hemorrhagic telangiectasia
Thompson, K P, Nelson, J, Kim, H, Pawlikowska, L, Marchuk, D A, Lawton, M T, Faughnan, Marie E
Published in Orphanet journal of rare diseases (06.01.2021)
Published in Orphanet journal of rare diseases (06.01.2021)
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