International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia von Faughnan, M E, Palda, V A, Garcia-Tsao, G, Geisthoff, U W, McDonald, J, Proctor, D D, Spears, J, Brown, D H, Buscarini, E, Chesnutt, M S, Cottin, V, Ganguly, A, Gossage, J R, Guttmacher, A E, Hyland, R H, Kennedy, S J, Korzenik, J, Mager, J J, Ozanne, A P, Piccirillo, J F, Picus, D, Plauchu, H, Porteous, M E M, Pyeritz, R E, Ross, D A, Sabba, C, Swanson, K, Terry, P, Wallace, M C, Westermann, C J J, White, R I, Young, L H, Zarrabeitia, R

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ConoServer, a database for conopeptide sequences and structures von Kaas, Quentin, Westermann, Jan-C., Halai, Reena, Wang, Conan K. L., Craik, David J.

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Framework for personalized prediction of treatment response in relapsing remitting multiple sclerosis von Stuehler, E., Brauner, S., Lionetto, F., Heer, Y., Jules, E., Westermann, C., Bergmann, A., van Hoevell, P.

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SMAD4 mutations found in unselected HHT patients von Gallione, C J, Richards, J A, Letteboer, T G W, Rushlow, D, Prigoda, N L, Leedom, T P, Ganguly, A, Castells, A, Ploos van Amstel, J K, Westermann, C J J, Pyeritz, R E, Marchuk, D A

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SMAD4 gene mutation increases the risk of aortic dilation in patients with hereditary haemorrhagic telangiectasia von Vorselaars, V.M.M., Diederik, A., Prabhudesai, V., Velthuis, S., Vos, J.-A., Snijder, R.J., Westermann, C.J.J., Mulder, B.J., Ploos van Amstel, J.K., Mager, J.J., Faughnan, M.E., Post, M.C.

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Hypoglycin A Concentrations in Maple Tree Species in the Netherlands and the Occurrence of Atypical Myopathy in Horses von Westermann, C.M., Leeuwen, R., Raamsdonk, L.W.D., Mol, H.G.J.

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Life expextancy of parents with Hereditary Haemorrhagic Telangiectasia von de Gussem, E M, Edwards, C P, Hosman, A E, Westermann, C J J, Snijder, R J, Faughnan, M E, Mager, J J

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Screening for pulmonary arteriovenous malformations using transthoracic contrast echocardiography: a prospective study von van Gent, M. W. F, Post, M. C, Luermans, J. G. L. M, Snijder, R. J, Westermann, C. J. J, Plokker, H. W. M, Overtoom, T. T, Mager, J. J

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QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation von Gödiker, J, Grüneberg, M, DuChesne, I, Reunert, J, Rust, S, Westermann, C, Wada, Y, Classen, G, Langhans, C D, Schlingmann, K P, Rodenburg, R J, Pohlmann, R, Marquardt, T

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Field Anesthesia of the Maned Wolf (Chrysocyon brachyurus) in Bolivia von Bronson, Ellen, Deem, Sharon L., Westermann, Lena C. Patino, Alpire, Sixto Angulo, Emmons, Louise H.

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Follow-up of Thalidomide treatment in patients with Hereditary Haemorrhagic Telangiectasia von Hosman, A, Westermann, C J J, Snijder, R, Disch, F, Mummery, C L, Mager, J J

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Evidence‐based therapy for atypical myopathy in horses von Fabius, L. S., Westermann, C. M.

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Reproducibility of right-to-left shunt quantification using transthoracic contrast echocardiography in hereditary haemorrhagic telangiectasia von Vorselaars, V. M. M., Velthuis, S., Huitema, M. P., Hosman, A. E., Westermann, C. J. J., Snijder, R. J., Mager, J. J., Post, M. C.

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Pulmonary arteriovenous malformations associated with migraine with aura von Post, M. C, van Gent, M. W. F, Plokker, H. W. M, Westermann, C. J. J, Kelder, J. C, Mager, J. J, Overtoom, T. T, Schonewille, W. J, Thijs, V, Snijder, R. J

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Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine von POST, M. C, THIJS, V, SCHONEWILLE, W. J, BUDTS, W, SNIJDER, R. J, PLOKKER, H. W. M, WESTERMANN, C. J. J

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European outbreaks of atypical myopathy in grazing equids (2006-2009): Spatiotemporal distribution, history and clinical features von van GALEN, G., MARCILLAUD PITEL, C., SAEGERMAN, C., PATARIN, F., AMORY, H., BAILY, J. D., CASSART, D., GERBER, V., HAHN, C., HARRIS, P., KEEN, J. A., KIRSCHVINK, N., LEFERE, L., McGORUM, B., MULLER, J. M. V., PICAVET, M. T. J. E., PIERCY, R. J., ROSCHER, K., SERTEYN, D., UNGER, L., van der KOLK, J. H., van LOON, G., VERWILGHEN, D., WESTERMANN, C. M., VOTION, D. M.

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Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients von LETTEBOER, T. G. W, ZEWALD, R. A, KAMPING, E. J, DE HAAS, G, MAGER, J. J, SNIJDER, R. J, LINDHOUT, D, HENNEKAM, F. A. M, WESTERMANN, C. J. J, PLOOS VAN AMSTEL, J. K

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Effect of exercise on apparent total tract digestibility of nutrients and faecal recovery of ADL and TiO2 in ponies von Schaafstra, F. J. W. C., van Doorn, D. A., Schonewille, J. T., Roelfsema, E., Westermann, C. M., Dansen, O., Jacobs, M., Lee, J.-Y., Spronck, E. A., Blok, M. C., Hendriks, W. H.

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Follow-up of Thalidomide treatment in patients with Hereditary Haemorrhagic Telangiectasia von Hosman, A., Westermann, C.J.J., Snijder, R., Disch, F., Mummery, C.L., Mager, J.J.

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The effect of N-acetylcysteine on epistaxis and quality of life in patients with HHT : a pilot study von DE GUSSEM, E. M, SNIJDER, R. J, DISCH, F. J, ZANEN, P, WESTERMANN, C. J. J, MAGER, J. J

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