Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Emilse, Bermejo"'
Autor:
Analía Sánchez-Luceros, Adriana I. Woods, Emilse Bermejo, Shilpa Shukla, Suchitra Acharya, Michelle Lavin, Natalia Rydz, Maha Othman
Publikováno v:
Platelets, Vol 28, Iss 5, Pp 484-490 (2017)
Despite the increased worldwide awareness, over the last decade, of the platelet-type von Willebrand Disease (PT-VWD), many uncertainties remain around this rare platelet bleeding disorder. This report aims to correctly identify and study the phenoty
Externí odkaz:
https://doaj.org/article/2ee8464533f5442cbbdcc252fe76142c
Autor:
Emilse Bermejo, Maria F. Alberto, David S. Paul, Aaron A. Cook, Paquita Nurden, Analia Sanchez Luceros, Alan T. Nurden, Wolfgang Bergmeier
Publikováno v:
Platelets, Vol 29, Iss 1, Pp 84-86 (2018)
Congenital platelet function disorders are often the result of defects in critical signal transduction pathways required for platelet adhesion and clot formation. Mutations affecting RASGRP2, the gene encoding the Rap GTPase activator, CalDAG-GEFI, g
Externí odkaz:
https://doaj.org/article/a7b7754dc5cb4cefa0780ee777b732fd
Autor:
Adriana I. Woods, Maria A. Lazzari, Maria Fabiana Alberto, Roberto Chuit, Analía Sánchez-Luceros, Ana Catalina Kempfer, Emilse Bermejo, Juvenal Paiva, Alicia N. Blanco
Publikováno v:
Seminars in Thrombosis and Hemostasis. 43:092-100
Von Willebrand disease type 2B (VWD2B) expresses gain-of-function mutations that enhance binding of an individual's von Willebrand factor (VWF) to its platelet ligand, glycoprotein Ib (GPIb), and which are usually identified by increased ristocetin-i
Autor:
Paquita Nurden, Analía Gabriela Sánchez Luceros, Wolfgang Bergmeier, Aaron A. Cook, David S. Paul, Emilse Bermejo, Alan T. Nurden, Maria Fabiana Alberto
Congenital platelet function disorders are often the result of defects in critical signal transduction pathways required for platelet adhesion and clot formation. Mutations affecting RASGRP2, the gene encoding the Rap GTPase activator, CalDAG-GEFI, g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f9c91cb148144b5d598f2ca78a49865
https://www.tandfonline.com/doi/full/10.1080/09537104.2017.1332759
https://www.tandfonline.com/doi/full/10.1080/09537104.2017.1332759
Autor:
Emilse Bermejo, Michele P. Lambert, Chris Van Geet, Samya Obaji, Marie-Christine Alessi, Sofia Papadia, Matthias Canault, Shoshana Revel-Vilk, Daniel Greene, Andrew D Mumford, Ernest Turro, Salih Tuna, Sarah K Westbury, Kate Downes, Willem H. Ouwehand, Carolyn M. Millar, Christopher Watt, Kathleen Freson, Katharine Hanlon, Paquita Nurden, Michael Laffan
Publikováno v:
Blood
Blood, American Society of Hematology, 2017, 130 (8), pp.1026-1030. ⟨10.1182/blood-2017-03-776773⟩
Blood, American Society of Hematology, 2017, 130 (8), pp.1026-1030. 〈10.1182/blood-2017-03-776773〉
Westbury, S K, Canault, M, Greene, D, Bermejo, E, Hanlon, K, Lambert, M P, Millar, C M, Nurden, P, Obaji, S G, Revel-Vilk, S, Van Geet, C, Downes, K, Papadia, S, Tuna, S, Watt, C, Consortium, N B-R D, Freson, K, Laffan, M A, Ouwehand, W H, Alessi, M-C, Turro, E & Mumford, A D 2017, ' Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding ', Blood, vol. 130, no. 8 . https://doi.org/10.1182/blood-2017-03-776773
Blood, 2017, 130 (8), pp.1026-1030. ⟨10.1182/blood-2017-03-776773⟩
Blood, American Society of Hematology, 2017, 130 (8), pp.1026-1030. ⟨10.1182/blood-2017-03-776773⟩
Blood, American Society of Hematology, 2017, 130 (8), pp.1026-1030. 〈10.1182/blood-2017-03-776773〉
Westbury, S K, Canault, M, Greene, D, Bermejo, E, Hanlon, K, Lambert, M P, Millar, C M, Nurden, P, Obaji, S G, Revel-Vilk, S, Van Geet, C, Downes, K, Papadia, S, Tuna, S, Watt, C, Consortium, N B-R D, Freson, K, Laffan, M A, Ouwehand, W H, Alessi, M-C, Turro, E & Mumford, A D 2017, ' Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding ', Blood, vol. 130, no. 8 . https://doi.org/10.1182/blood-2017-03-776773
Blood, 2017, 130 (8), pp.1026-1030. ⟨10.1182/blood-2017-03-776773⟩
International audience; Heritable platelet function disorders (PFDs) are genetically heterogeneous and poorly characterised. Pathogenic variants in RASGRP2, which encodes calcium and diacylglycerol-regulated guanine exchange factor I (CalDAG-GEFI), h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8f07e9111c356adb245eb5eeef2346
https://hal-amu.archives-ouvertes.fr/hal-01753596
https://hal-amu.archives-ouvertes.fr/hal-01753596
Autor:
Sarah K, Westbury, Matthias, Canault, Daniel, Greene, Emilse, Bermejo, Katharine, Hanlon, Michele P, Lambert, Carolyn M, Millar, Paquita, Nurden, Samya G, Obaji, Shoshana, Revel-Vilk, Chris, Van Geet, Kate, Downes, Sofia, Papadia, Salih, Tuna, Christopher, Watt, Kathleen, Freson, Michael A, Laffan, Willem H, Ouwehand, Marie-Christine, Alessi, Ernest, Turro, Andrew D, Mumford
Publikováno v:
Blood. 130(8)
Eleven pedigrees were identified with biallelic pathogenic variants in RASGPR2, which encodes platelet CalDAG-GEFI.CalDAG-GEFI deficiency is a severe, recessive, nonsyndromic platelet function disorder with defective aggregation to multiple agonists.
Autor:
Adriana I. Woods, Ana C. Kempfer, Maria A. Lazzari, Emilse Bermejo, Analía Sánchez-Luceros, Maria Fabiana Alberto, S. H. Grosso, Juvenal Paiva
Publikováno v:
Seminars in Thrombosis and Hemostasis. 40:151-160
Platelet-type von Willebrand disease (PT-VWD) and type 2B von Willebrand disease (2B-VWD) are rare bleeding disorders characterized by increased ristocetin-induced platelet aggregation (RIPA) at low concentrations of ristocetin. Diagnosis of either c
Autor:
Emilse Bermejo, Adriana Ines Woods, Shilpa Shukla, Natalia Rydz, Maha Othman, Michelle Lavin, Suchitra Acharya, Analía Sánchez-Luceros
Despite the increased worldwide awareness, over the last decade, of the platelet-type von Willebrand Disease (PT-VWD), many uncertainties remain around this rare platelet bleeding disorder. This report aims to correctly identify and study the phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36807722f6f9b3dfab5b97bb3f226aa5
https://www.tandfonline.com/doi/abs/10.1080/09537104.2016.1237625?journalCode=iplt20
https://www.tandfonline.com/doi/abs/10.1080/09537104.2016.1237625?journalCode=iplt20
Autor:
Sol Schulman, Daniel J. Hampshire, Jennifer Jolley, Peter A. Smethurst, Willem H. Ouwehand, Alan T. Nurden, Ilenia Simeoni, William Stevenson, Paolo Gresele, Ri Liesner, Kathleen Freson, Christel Van Geet, Walter H. A. Kahr, Tadbir K. Bariana, Paquita Nurden, Minka J A Vries, David A. Wilcox, Mary Mathias, Fengyuan Hu, Maha Othman, Marguerite Neerman-Arbez, Pawan Poudel, Matthias Ballmaier, Pieter H. Reitsma, Peter William Collins, Jose A. Lopez, Artur J. Szkotak, Jose A. Guerrero, Marie-Christine Alessi, Manuela Germeshausen, Jonathan Stephens, Cedric Ghevaert, Michael Gattens, Carolyn M. Millar, Gareth Baynam, Marian Hill, Marco Cattaneo, Antony P. Attwood, Shoshana Revel-Vilk, Matthew T. Rondina, Anne M. Kelly, Sri V V Deevi, Sofia Papadia, Amit C. Nathwani, Paul F. Bray, Daniel B. Bellissimo, Michael Laffan, Deborah L. French, Daniel P. Hart, Shinji Kunishima, Bin Zhang, Rutendo Mapeta, Salih Tuna, Anne Goodeve, Keith Gomez, Nancy Hogg, Ernest Turro, Johan W. M. Heemskerk, Marta Bertoli, Karyn Megy, Ron Kerr, Christopher J. Penkett, David J. Perry, Claire Lentaigne, Deborah Whitehorn, Daniel Greene, Suthesh Sivapalaratnam, Myrto Kostadima, Andrew D Mumford, Bruce Furie, Emilse Bermejo, Rémi Favier, Michele P. Lambert, Louise C. Daugherty, Yvonne M. C. Henskens, Augusto Rendon, Loredana Bury, Kathelijne Peerlinck, Sarah K Westbury
Publikováno v:
Blood
Blood, American Society of Hematology, 2016, 127 (23), pp.2791-803. ⟨10.1182/blood-2015-12-688267⟩
Simeoni, I, Stephens, J C, Hu, F, Deevi, S V V, Megy, K, Bariana, T K, Lentaigne, C, Schulman, S, Sivapalaratnam, S, Vries, M J A, Westbury, S K, Greene, D, Papadia, S, Alessi, M-C, Attwood, A P, Ballmaier, M, Baynam, G, Bermejo, E, Bertoli, M, Bray, P F, Bury, L, Cattaneo, M, Collins, P, Daugherty, L C, Favier, R, French, D L, Furie, B, Gattens, M, Germeshausen, M, Ghevaert, C, Goodeve, A, Guerrero, J, Hampshire, D J, Hart, D P, Heemskerk, J W M, Henskens, Y M C, Hill, M, Hogg, N, Jolley, J D, Kahr, W H, Kelly, A M, Kerr, R, Kostadima, M, Kunishima, S, Lambert, M P, Liesner, R, Lopez, J, Mapeta, R P, Mathias, M, Millar, C M, Nathwani, A, Neerman-Arbez, M, Nurden, A T, Nurden, P, Othman, M, Peerlinck, K, Perry, D J, Poudel, P, Reitsma, P, Rondina, M, Smethurst, P A, Stevenson, W, Szkotak, A, Tuna, S, van Geet, C, Whitehorn, D, Wilcox, D A, Zhang, B, Revel-Vilk, S, Gresele, P, Bellissimo, D, Penkett, C J, Laffan, M A, Mumford, A D, Rendon, A, Gomez, K, Freson, K, Ouwehand, W H & Turro, E 2016, ' A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorderdisorders ', Blood, vol. 127, no. 23, pp. 2791-2803 . https://doi.org/10.1182/blood-2015-12-688267
Blood, 127(23), 2791-2803
Blood, 127(23), 2791-2803. The American Society of Hematology
Blood, American Society of Hematology, 2016, 127 (23), pp.2791-803. ⟨10.1182/blood-2015-12-688267⟩
Simeoni, I, Stephens, J C, Hu, F, Deevi, S V V, Megy, K, Bariana, T K, Lentaigne, C, Schulman, S, Sivapalaratnam, S, Vries, M J A, Westbury, S K, Greene, D, Papadia, S, Alessi, M-C, Attwood, A P, Ballmaier, M, Baynam, G, Bermejo, E, Bertoli, M, Bray, P F, Bury, L, Cattaneo, M, Collins, P, Daugherty, L C, Favier, R, French, D L, Furie, B, Gattens, M, Germeshausen, M, Ghevaert, C, Goodeve, A, Guerrero, J, Hampshire, D J, Hart, D P, Heemskerk, J W M, Henskens, Y M C, Hill, M, Hogg, N, Jolley, J D, Kahr, W H, Kelly, A M, Kerr, R, Kostadima, M, Kunishima, S, Lambert, M P, Liesner, R, Lopez, J, Mapeta, R P, Mathias, M, Millar, C M, Nathwani, A, Neerman-Arbez, M, Nurden, A T, Nurden, P, Othman, M, Peerlinck, K, Perry, D J, Poudel, P, Reitsma, P, Rondina, M, Smethurst, P A, Stevenson, W, Szkotak, A, Tuna, S, van Geet, C, Whitehorn, D, Wilcox, D A, Zhang, B, Revel-Vilk, S, Gresele, P, Bellissimo, D, Penkett, C J, Laffan, M A, Mumford, A D, Rendon, A, Gomez, K, Freson, K, Ouwehand, W H & Turro, E 2016, ' A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorderdisorders ', Blood, vol. 127, no. 23, pp. 2791-2803 . https://doi.org/10.1182/blood-2015-12-688267
Blood, 127(23), 2791-2803
Blood, 127(23), 2791-2803. The American Society of Hematology
Inherited bleeding, thrombotic and platelet disorders (BPDs) are diseases affecting approximately 300 individuals per million births. With the exception of haemophilia and von Willebrand disease patients, a molecular analysis for patients with a BPD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa352cd1eafdc5697d70b553f05b0503
http://hdl.handle.net/11391/1386441
http://hdl.handle.net/11391/1386441
Autor:
Juan Gagliardi, Emilse Bermejo, José L. Castellano, Osvaldo Masoli, Maria A. Lazzari, Neiva Maciel, Verónica Miksztowicz, Gabriela Berg, Ricardo J. Gelpi
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Background: The aim of our study was to evaluate the effect of programmed physical activity and a single exercise test on the number of CD309+ circulating endothelial progenitor cell (EPC) and their relation to the variation in plasma levels of VEGF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4288ae0334977edfcdf05f72b5a63f34
https://www.sciencedirect.com/science/article/pii/S0049384815301882
https://www.sciencedirect.com/science/article/pii/S0049384815301882