Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Ana G. Vigo"'
Autor:
Luigi Laghi, Jens U. Marquardt, Lude Franke, Harm-Jan Westra, Ralf Kiesslich, Cisca Wijmenga, Julio Perez de la Serna, Rosario Cuomo, Jan Tack, Peter R. Galle, Ines Gockel, Henning G. Schulz, Giovanni Sarnelli, Daniel Drescher, Jessica Becker, Stefan Niebisch, Elisabeth Mangold, Anna Latiano, Paul I.W. de Bakker, V. Annese, Uberto Fumagalli, Antonio Ruiz de León, Michael T. Heneka, Alexander J. Eckardt, Per Hoffmann, Mira M. Wouters, Hans Dieter Allescher, Julian Zimmermann, Timo Hess, Werner Kneist, Elena Urcelay, Ana G. Vigo, Hauke Lang, Markus M. Nöthen, Gosia Trynka, Henning R. Gockel, Burkhard H.A. von Rahden, Vinod Kumar, Karl-Peter Hopfner, David Ramonet, Stefan Herms, Stefanie Heilmann, Michael Knapp, Michaela Müller, Guy E. Boeckxstaens, Johannes Schumacher, Manuel Mattheisen
Publikováno v:
BASE-Bielefeld Academic Search Engine
Nature Genetics, 46(8), 901-904. Nature Publishing Group
Gockel, I, Becker, J, Wouters, M M, Niebisch, S, Gockel, H R, Hess, T, Ramonet, D, Zimmermann, J, Vigo, A G, Trynka, G, de León, A R, de la Serna, J P, Urcelay, E, Kumar, V, Franke, L, Westra, H-J, Drescher, D, Kneist, W, Marquardt, J U, Galle, P R, Mattheisen, M, Annese, V, Latiano, A, Fumagalli, U, Laghi, L, Cuomo, R, Sarnelli, G, Müller, M, Eckardt, A J, Tack, J, Hoffmann, P, Herms, S, Mangold, E, Heilmann, S, Kiesslich, R, von Rahden, B H A, Allescher, H-D, Schulz, H G, Wijmenga, C, Heneka, M T, Lang, H, Hopfner, K-P, Nöthen, M M, Boeckxstaens, G E, de Bakker, P I W, Knapp, M & Schumacher, J 2014, ' Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia ', Nature Genetics . https://doi.org/10.1038/ng.3029
Nature Genetics, 46(8), 901-904. Nature Publishing Group
Gockel, I, Becker, J, Wouters, M M, Niebisch, S, Gockel, H R, Hess, T, Ramonet, D, Zimmermann, J, Vigo, A G, Trynka, G, de León, A R, de la Serna, J P, Urcelay, E, Kumar, V, Franke, L, Westra, H-J, Drescher, D, Kneist, W, Marquardt, J U, Galle, P R, Mattheisen, M, Annese, V, Latiano, A, Fumagalli, U, Laghi, L, Cuomo, R, Sarnelli, G, Müller, M, Eckardt, A J, Tack, J, Hoffmann, P, Herms, S, Mangold, E, Heilmann, S, Kiesslich, R, von Rahden, B H A, Allescher, H-D, Schulz, H G, Wijmenga, C, Heneka, M T, Lang, H, Hopfner, K-P, Nöthen, M M, Boeckxstaens, G E, de Bakker, P I W, Knapp, M & Schumacher, J 2014, ' Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia ', Nature Genetics . https://doi.org/10.1038/ng.3029
Idiopathic achalasia is characterized by a failure of the lower esophageal sphincter to relax due to a loss of neurons in the myenteric plexus(1,2). This ultimately leads to massive dilatation and an irreversibly impaired megaesophagus. We performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b02350b253ac6a701faf5c4abdda99
https://doi.org/10.1038/ng.3029
https://doi.org/10.1038/ng.3029
Autor:
Severine Vermeire, Ana G. Vigo, Johannes Schumacher, Markus M. Nöthen, Mira M. Wouters, Elena Urcelay, Giovanni Zaninotto, Anna Latiano, Julio Perez de la Serna, Guy E. Boeckxstaens, Jessica Becker, Manuel Mattheisen, Luigi Laghi, Diether Lambrechts, Vito Annese, Michael Knapp, Rosario Cuomo, Hauke Lang, Wout O. Rohof, Uberto Fumagalli, Antonio Ruiz de León, Isabelle Cleynen, Giovanni Sarnelli, Michaela Mueller, Jan Tack, Ines Gockel, Orazio Palmieri
Publikováno v:
Wouters, M M, Lambrechts, D, Becker, J, Cleynen, I, Tack, J, Vigo, A G, Ruiz de León, A, Urcelay, E, Pérez de la Serna, J, Rohof, W, Annese, V, Latiano, A, Palmieri, O, Mattheisen, M, Mueller, M, Lang, H, Fumagalli, U, Laghi, L, Zaninotto, G, Cuomo, R, Sarnelli, G, Nöthen, M M, Vermeire, S, Knapp, K M, Gockel, I, Schumacher, J & Boeckxstaens, G E 2013, ' Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia ', Gut . https://doi.org/10.1136/gutjnl-2013-304848
Gut, 63(9), 1401-1409. BMJ Publishing Group
Gut, 63(9), 1401-1409. BMJ Publishing Group
BACKGROUND: Idiopathic achalasia is a rare motor disorder of the oesophagus characterised by neuronal loss at the lower oesophageal sphincter. Achalasia is generally accepted as a multifactorial disorder with various genetic and environmental factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0271730a428f8e6303e9faa2051a02e
https://doi.org/10.1136/gutjnl-2013-304848
https://doi.org/10.1136/gutjnl-2013-304848
Autor:
Antonio Ruiz de León, Ana G. Vigo, Julio Perez de la Serna, Elena Urcelay, Fermín Mearin, María Soledad Benito, Jose Luis Santiago, Maria Asuncion Garcia-Gonzalez, Concepción Núñez, Emilio G. de la Concha
Publikováno v:
Human Immunology. 72:749-752
Idiopathic achalasia is an esophageal motor disorder of unknown etiology. A wealth of evidence supports the concept that achalasia is an immune-mediated disease. According to this evidence, achalasia has been significantly associated with specific al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343cdbcbab8e438db35cc773265e73df
https://doi.org/10.1016/j.humimm.2011.05.017
https://doi.org/10.1016/j.humimm.2011.05.017
Autor:
Benjamín Fernández-Gutiérrez, Dora Pascual-Salcedo, José Ramón Lamas, Ana G. Vigo, Emilio G. de la Concha, Alfonso Martínez, Nieves Perdigones, Elena Urcelay, Alejandro Balsa
Publikováno v:
Arthritis & Rheumatism. 62:705-710
Objective Genetic variants located close to 2 genes codifying for members of the tumor necrosis factor receptor superfamily (TNFRSF), TNFRSF14 and TNFRSF6B, have recently been associated with rheumatoid arthritis (RA) and with inflammatory bowel dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd9c91e46f89dd1c42ab2feded97a324
https://doi.org/10.1002/art.27292
https://doi.org/10.1002/art.27292
Autor:
Elena Urcelay, Emilio G. de la Concha, Nieves Perdigones, Alfonso Martínez, Ana G. Vigo, Benjamín-Fernández Gutiérrez, José Ramón Lamas, Juan Angel Jover
Publikováno v:
Rheumatology (Oxford, England). 48(6)
OBJECTIVE The aim of this work is to replicate the role of two recently described RA genetic markers (rs10499194 and rs6920220) situated at 6q23 in the autoantibody-positive phenotype. METHODS A case-control study (630 RA patients and 664 healthy blo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fcce6b606640cddf21febaf73081227
https://pubmed.ncbi.nlm.nih.gov/19321514
https://pubmed.ncbi.nlm.nih.gov/19321514
Publikováno v:
The American Journal of Gastroenterology. 104:1326-1327
Suggested Association of NOS2A Polymorphism in Idiopathic Achalasia: No Evidence in a Large Case–Control Study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c287a37dfb72111c28b0be69ce0b4b8
https://doi.org/10.1038/ajg.2009.72
https://doi.org/10.1038/ajg.2009.72
Autor:
Vinod Kumar, Stefan Niebisch, Hauke Lang, Jessica Becker, Giovanni Zaninotto, Jan Tack, Ralf Kiesslich, Cisca Wijmenga, Ana G. Vigo, Guy E. Boeckxstaens, Gosia Trynka, Michael Knapp, Burkhard H.A. von Rahden, Paul I.W. de Bakker, Harm-Jan Westra, Michaela Mueller, Alexander J. Eckardt, Mira M. Wouters, Markus M. Noethen, Henning G. Schulz, Daniel Drescher, Lude Franke, Henning R. Gockel, Paola Brun, Johannes Schumacher, Ines Gockel
Publikováno v:
Gastroenterology. 144:S-142
G A A b st ra ct s secretion volume despite significant decrease in intragastric acidity. Gastric secretion accumulates on the top of the liquid meal forming a "floating" layer. We assume that this layer is the correlate for the so called "acid pocke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d01b7764adae2ce1809df9c81c3be99
https://doi.org/10.1016/s0016-5085(13)60510-7
https://doi.org/10.1016/s0016-5085(13)60510-7
Autor:
Ana G. Vigo, Nora Butta, Francisco Javier López-Longo, Víctor Jiménez-Yuste, Isabel Rivas, Miguel Canales, Mayte Álvarez Román, Elena G. Arias Salgado, Ihosvany Fernández Bello, Mónica Martín Salces
Publikováno v:
Blood. 118:3313-3313
Abstract 3313 Objectives: Behçet's disease (BD) is a chronic inflammatory disease of unknown etiology associated with an increased risk of venous and arterial thrombosis. To date, no studies for haemostasis have been conducted in this population by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fad06686e7194949e72ae143a552186
https://doi.org/10.1182/blood.v118.21.3313.3313
https://doi.org/10.1182/blood.v118.21.3313.3313
Autor:
E G de la Concha, J. P. De La Serna, Elena Urcelay, Concepcion Sevilla, Miguel Fernández-Arquero, Ana G. Vigo, Jose Luis Santiago, A. R. De León, Concepción Núñez
Publikováno v:
Neurogastroenterology & Motility. 22:734-e218
Background Idiopathic achalasia is a primary esophageal motor disorder of unknown etiology. Different evidences have been reported in support of achalasia as the result of an autoimmune and inflammatory process leading to neuronal cell loss. Accordin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e281b7b8ebb91f3bfadf97158eb34ffc
https://doi.org/10.1111/j.1365-2982.2010.01497.x
https://doi.org/10.1111/j.1365-2982.2010.01497.x
Autor:
Wouters, Mira M., Lambrechts, Diether, Becker, Jessica, Cleynen, Isabelle, Tack, Jan, Vigo, Ana G., de León, Antonio Ruiz, Urcelay, Elena, de la Serna, Julio Pérez, Rohof, Wout, Annese, Vito, Latiano, Anna, Palmieri, Orazio, Mattheisen, Manuel, Mueller, Michaela, Lang, Hauke, Fumagalli, Uberto, Laghi, Luigi, Zaninotto, Giovanni, Cuomo, Rosario
Publikováno v:
Gut; Sep2014, Vol. 63 Issue 9, p1401-1409, 9p, 2 Diagrams, 3 Charts