SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Andreas Lux, Ralf Müller, Mark Tulk, Carla Olivieri, Roberto Zarrabeita, Theresia Salonikios, Bernhard Wirnitzer, HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis, Orphanet Journal of Rare Diseases, 2013, 8, 1, 94

    CrossRef

  2. 2
    Alan E. Guttmacher, Douglas A. Marchuk, Scott O. Trerotola, Reed E. Pyeritz, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  3. 3
    Viet Q. Le, Kristi A. Wharton, Hyperactive BMP signaling induced by ALK2R206H requires type II receptor function in a Drosophila model for classic fibrodysplasia ossificans progressiva, Developmental Dynamics, 2012, 241, 1
  4. 4
    Behfar Eivazi, Jochen A. Werner, Marion Roessler, Hesham Negm, Afshin Teymoortash, Lack of significant estrogen and progesterone receptor expression in nasal telangiectasias in hereditary hemorrhagic telangiectasia: An immunohistochemical analysis, Acta Oto-laryngologica, 2012, 132, 1, 86

    CrossRef

  5. 5
    Vijayakumar Raju, Senthil Kumaran Sadhasivam, Chandrasekar Padmanabhan, Muralidharan Srinivasan, Pulmonary arteriovenous malformation with spontaneous haemothorax, Indian Journal of Thoracic and Cardiovascular Surgery, 2011, 27, 4, 176

    CrossRef

  6. 6
    K Brakensiek, H Frye-Boukhriss, M Mälzer, M Abramowicz, MJ Bahr, N Von Beckerath, C Bergmann, M Caselitz, E Holinski-Feder, P Muschke, K Oexle, G Strobl-Wildemann, G Wolff, EA El-Harith, M Stuhrmann, Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia, Clinical Genetics, 2008, 74, 2
  7. 7
    Marja Sankelo, Maija Halme, Tarja Laitinen, Petri S. Mattila, Hereditary hemorrhagic telangiectasia type 1 and 2 mutations in Finland, Acta Oto-laryngologica, 2008, 128, 11, 1238

    CrossRef

  8. 8
    Carla Olivieri, Fabio Pagella, Lucia Semino, Luca Lanzarini, Cristina Valacca, Andrea Pilotto, Sabrina Corno, Susi Scappaticci, Guido Manfredi, Elisabetta Buscarini, Cesare Danesino, Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies, Journal of Human Genetics, 2007, 52, 10, 820

    CrossRef

  9. 9
    C. SABBÀ, G. PASCULLI, G. M. LENATO, P. SUPPRESSA, P. LASTELLA, M. MEMEO, F. DICUONZO, G. GUANTI, Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers, Journal of Thrombosis and Haemostasis, 2007, 5, 6
  10. 10
    Aurore Curie, Gaëtan Lesca, Vincent Cottin, Patrick Edery, Gabriel Bellon, Marie E. Faughnan, Henri Plauchu, Long-Term Follow-Up in 12 Children with Pulmonary Arteriovenous Malformations: Confirmation of Hereditary Hemorrhagic Telangiectasia in all Cases, The Journal of Pediatrics, 2007, 151, 3, 299

    CrossRef

  11. 11
    Oscar Llorca, Arturo Trujillo, Francisco J. Blanco, Carmelo Bernabeu, Structural Model of Human Endoglin, a Transmembrane Receptor Responsible for Hereditary Hemorrhagic Telangiectasia, Journal of Molecular Biology, 2007, 365, 3, 694

    CrossRef

  12. 12
    Manda Sai Krishnaveni, Oliver Eickelberg, TGF-β receptors: Assembly, signalling, and disease relevance, Signal Transduction, 2006, 6, 5, 301

    CrossRef

  13. 13
    Manda Sai Krishnaveni, Oliver Eickelberg, TGF-β receptors: Assembly, signalling, and disease relevance, Signal Transduction, 2006, 6, 5