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New England Journal of Medicine, ISSN 0028-4793, 09/2018, Volume 379, Issue 13, pp. 1289 - 1290
Journal Article
NEW ENGLAND JOURNAL OF MEDICINE, ISSN 0028-4793, 09/2018, Volume 379, Issue 13, pp. 1289 - 1290
Journal Article
Medicina Clinica, ISSN 0025-7753, 04/2019, Volume 152, Issue 7, pp. 274 - 280
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant inherited Rare Disease that causes a systemic anomalous vascular overgrowth. The approach... 
Rare diseases | Vascular malformation | Haemorrhagic hereditary telangiectasia
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 09/2018, Volume 379, Issue 13, pp. 1289 - 1290
To the Editor: In their review article, Garcia and Erkan (May 24 issue) 1 describe current and future therapies in the prevention and treatment of thrombosis... 
MEDICINE, GENERAL & INTERNAL | Antiphospholipid Syndrome | Humans | Antibodies, Antiphospholipid | Anticoagulants | Immunoglobulins | Warfarin | Risk groups | Antibodies | Cardiolipin | Glycoprotein I | Thrombosis | Patients | Antiphospholipid syndrome
Journal Article
by Riera-Mestre, A and Mora-Lujan, JM and Trujillo-Santos, J and Del Toro, J and Nieto, JA and Pedrajas, JM and Lopez-Reyes, R and Soler, S and Ballaz, A and Cerda, P and Monreal, M and Prandoni, P and Brenner, B and Farge-Bancel, D and Barba, R and Di Micco, P and Bertoletti, L and Schellong, S and Tzoran, I and Reis, A and Bosevski, M and Bounameaux, H and Maly, R and Verhamme, P and Caprini, JA and Bui, HM and Adarraga, MD and Agud, M and Aibar, MA and Alcalde-Manero, M and Alfonso, J and Amado, C and Arcelus, JI and Barbagelata, C and Barron, M and Barron-Andres, B and Blanco-Molina, A and Camon, AM and Canas, I and Castro, J and de Miguel, J and del Toro, J and Demelo, P and Diaz-Pedroche, C and Diaz-Peromingo, JA and Dominguez, I and Escribano, JC and Falga, C and Fernandez-Capitan, C and Fernandez-Criado, MC and Fidalgo, MA and Flores, K and Font, C and Font, L and Furest, I and Garcia, MA and Garcia-Bragado, F and Garcia-Raso, A and Gavin-Bianco, O and Gavin-Sebastian, O and Gil-Diaz, A and Godoy-Diaz, D and Gomez, V and Gomez-Cuelvo, C and Gonzalez-Martinez, J and Grau, E and Guirado, L and Gutierrez, J and Hernandez-Blasco, LM and Jara-Palomares, L and Jaras, MJ and Jimenez, D and Joya, MD and Jou, I and Lalueza, A and Lecumberri, R and Lima, J and Llamas, P and Lobo, JL and Lopez-Jimenez, L and Lopez-Meseguer, M and Lopez-Miguel, P and Lopez-Nunez, JJ and Lopez-Saez, JB and Lorente, MA and Loring, M and Lumbierres, M and Madridano, O and Maestre, A and Marchena, PJ and Martin-Martos, F and Martinez-Baquerizo, C and Martinez-Garcia, MA and Mellado, M and Moises, J and Morales, MV and Munoz-Bianco, A and Nunez, MJ and Olivares, MC and Olivera, PE and ... and RIETE Investigators and the RIETE Investigators
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 08/2019, Volume 14, Issue 1, pp. 196 - 8
Journal Article
by López-Reyes, Raquel and Nauffal, Dolores and Ballester, Marta and Martín-Antorán, José Manuel and Saraiva De Sousa, Marta and Riera-Mestre, Antoni and Ruiz-Ruiz, Justo and Fernández-Capitán, Carmen and Uresandi, Fernando and Monreal, Manuel and Alcalde-Manero, M and Andútejar, V and Arcelus, J.I and Barba, R and Barrón, M and Barrón-Andrés, B and Bascuñana, J and Blanco-Molina, A and Casado, I and Conget, F and De Ancos, C and Del Molino, F and Del Toro, J and Díaz, J.A and Falgá, C and Farfán, A.I and Fernández-Capitán, C and Font, C and Font, L and Gallego, P and García-Bragado, F and Gómez, V and González, J and Gonźlez-Marcano, D and Grau, E and Guijarro, R and Gutiérrez, J and Hernández, L and Hernández-Huerta, S and Jara-Palomares, L and Jaras, M.J and Jiménez, D and Lobo, J.L and López-Jiménez, L and López-Montes, L and López-Reyes, Raquel and López-Sáez, J.B and Lorente, M.A and Lorenzo, A and Mací, M and Madridano, O and Marchena, P.J and Martín-Antorán, José Manuel and Martín-Martos, F and Mellado, M and Monreal, M and Morales, M.V and Nauffal, Dolores and Nieto, J.A and Núñez, M.J and Otero, R and Pagán, B and Pedrajas, J.M and Pérez-Rus, G and Peris, M.L and Pons, I and Porras, J.A and Riera-Mestre, A and Rivas, A and Rodríguez-Dávila, M.A and Román, P and Rosa, V and Ruiz-Giménez, N and Ruiz, J and Sampériz, A and Sánchez, R and Sanz, O and Soler, S and Suriñach, J.M and Tiberio, G and Tirado, R and Trujillo-Santos, J and Uresandi, F and Valero, B and Valle, R and Vela, J and Vilar, C and Villalobos, A and Villalta, J and Malfante, P and Verhamme, P and Vanassche, T and Gadelha, T and Wells, P and Malý, R and Hirmerova, J and Bertoletti, L and Bura-Riviere, A and Moustafa, F and Farge-Bancel, D and ... and RIETE Investigators and RIETE investigators
European Respiratory Journal, ISSN 0903-1936, 06/2015, Volume 45, Issue 6, pp. 1728 - 1731
Journal Article
Journal of clinical medicine, ISSN 2077-0383, 12/2019, Volume 9, Issue 1, p. 82
We aimed to describe risk factors for gastrointestinal (GI) bleeding and endoscopic findings in patients with hereditary hemorrhagic telangiectasia (HHT). This... 
Journal Article
ISSN 2073-4409, 08/2019
Hemorrhagic hereditary telangiectasia (HHT) type 2 patients have increased activation of the phosphatidylinositol 3-kinase (PI3K) signaling pathway in... 
Factors de creixement | Rare diseases | Malalties rares | Growth factors | Hemorrhage | Hemorràgia
Journal Article
ISSN 2073-4409, 08/2019
Hemorrhagic hereditary telangiectasia (HHT) type 2 patients have increased activation of the phosphatidylinositol 3-kinase (PI3K) signaling pathway in... 
Factors de creixement | Rare diseases | Malalties rares | Growth factors | Hemorrhage | Hemorràgia
Journal Article
Nature, ISSN 0028-0836, 02/2018, Volume 554, Issue 7693, pp. 538 - 543
Most patients with colorectal cancer die as a result of the disease spreading to other organs. However, no prevalent mutations have been associated with... 
STEM-CELLS | GENE | COLORECTAL-CANCER | MULTIDISCIPLINARY SCIENCES | MOUSE | LEADS | RECEPTOR | MICE | GROWTH-FACTOR | TUMORIGENESIS | EXPRESSION | Intestines - drug effects | Colonic Neoplasms - genetics | Intestinal Mucosa - metabolism | Colonic Neoplasms - drug therapy | Humans | Male | Programmed Cell Death 1 Receptor - antagonists & inhibitors | Stem Cells - metabolism | Th1 Cells - immunology | T-Lymphocytes, Cytotoxic - drug effects | Neoplasm Metastasis - drug therapy | Neoplasm Metastasis - immunology | Colonic Neoplasms - immunology | Immunotherapy | Transforming Growth Factor beta - antagonists & inhibitors | Female | Liver Neoplasms - secondary | Disease Models, Animal | T-Lymphocytes, Cytotoxic - immunology | Transforming Growth Factor beta - immunology | Tumor Microenvironment - drug effects | Th1 Cells - drug effects | Intestines - pathology | Liver Neoplasms - drug therapy | Liver Neoplasms - immunology | Drug Synergism | Tumor Microenvironment - immunology | Neoplasm Metastasis - genetics | Animals | Cell Differentiation - drug effects | Neoplasm Metastasis - pathology | Colonic Neoplasms - pathology | Alleles | Immune Evasion - drug effects | Stem Cells - drug effects | Stem Cells - pathology | Mice | Mutation | T-Lymphocytes, Cytotoxic - cytology | PD-1 protein | Liver | Colorectal carcinoma | Colorectal cancer | Stem cell transplantation | Cytotoxicity | Lymphocytes T | Metastasis | Metastases | Colon cancer | Intestine | Lymphocytes | Genetic analysis | Fibroblasts | Colon | Inhibition | Growth factors | Phenotypes | Data analysis | Liver diseases | Microsatellites | Organs | Gene expression | Patients | Signaling | Immune checkpoint | PD-L1 protein | Stem cells | Tumors | Cancer
Journal Article
Revista Espanola de Geriatria y Gerontologia, ISSN 0211-139X, 07/2015, Volume 50, Issue 4, pp. 159 - 160
Journal Article
ISSN 1465-993X, 07/2013
Background: Patients with chronic obstructive pulmonary disease (COPD) have a modified clinical presentation of venous thromboembolism (VTE) but also a worse... 
Pulmonary embolism | Prognosis | Embòlia pulmonar | Tromboembolisme | Pneumologia | Pronòstic mèdic | Thromboembolism | Pneumology
Journal Article
Journal Article
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