Bibliografia UJ CM

1/16
Sandro Marini, Katherine Crawford, Andrea Morotti, Myung J. Lee, Alessandro Pezzini, Charles J. Moomaw, Matthew L. Flaherty, Joan Montaner, Jaume Roquer, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano-Tarraga, Agnieszka Slowik, Jeremiasz M. Jagiella, Joanna Pera, Andrzej Urbanik, Alexander Pichler, Bjorn M. Hansen, Jacob L. McCauley, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Fernando D. Testai, Steven J. Kittner, Helena Schmidt, Christian Enzinger, Ian J. Deary, Kristiina Rannikmae, Neshika Samarasekera, Rustam Al-Shahi Salman, Catherine L. Sudlow, Catharina J. M. Klijn, Koen M. van Nieuwenhuizen, Israel Fernandez-Cadenas, Pilar Delgado, Bo Norrving, Arne Lindgren, Joshua N. Goldstein, Anand Viswanathan, Steven M. Greenberg, Guido J. Falcone, Alessandro Biffi, Carl D. Langefeld, Daniel Woo, Jonathan Rosand, Christopher D. Anderson.
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity.
JAMA Neurology
2019 : Vol. 76, nr 4, s. 480-491, il., bibliogr. 21 poz.
Formerly Archives of Neurology.
Autor korespondencyjny: Christopher D. Anderson.
Open Access Creative Commons Attribution License CC-BY.
p-ISSN: 2168-6149
AZ
ORG
AIF
IF: 13.608
Adres url:
Streszczenie w PubMed:
2/16
Jaeyoon Chung, Sandro Marini, Joanna Pera, Bo Norrving, Jordi Jimenez-Conde, Jaume Roquer, Israel Fernandez-Cadenas, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Stacie Demel, Steven M. Greenberg, Agnieszka Slowik, Arne Lindgren, Reinhold Schmidt, Matthew Traylor, Muralidharan Sargurupremraj, Steffen Tiedt, Rainer Malik, Stephanie Debette, Martin Dichgans, Carl D. Langefeld, Daniel Woo, Jonathan Rosand, Christopher D. Anderson.
Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Brain
2019 : Vol. 142, nr 10, s. 3176-3189, il., bibliogr.
Autor korespondencyjny: Christopher D. Anderson.
p-ISSN: 0006-8950
e-ISSN: 1460-2156
AZ
ORG
AIF
IF: 11.337
Adres url:
Streszczenie w PubMed:
3/16
John W. Cole, Huichun Xu, Kathleen Ryan, Thomas Jaworek, Nicole Dueker, Patrick McArdle, Brady Gaynor, Yu-Ching Cheng, Jeffrey O'Connell, Steve Bevan, Rainer Malik, Naveed Uddin Ahmed, Philippe Amouyel, Sheraz Anjum, Joshua C. Bis, David Crosslin, John Danesh, Stefan T. Engelter, Myriam Fornage, Philippe Frossard, Christian Gieger, Anne-Katrin Giese, Caspar Grond-Ginsbach, Weang Kee Ho, Elizabeth Holliday, Jemma Hopewell, M. Hussain, W. Iqbal, S. Jabeen, Jim Jannes, Ayeesha Kamal, Yoichiro Kamatani, Sandip Kanse, Manja Kloss, Mark Lathrop, Didier Leys, Arne Lindgren, W.T. Longstreth, Khalid Mahmood, Jr, Christa Meisinger, Tiina M. Metso, Thomas Mosley, Jr., Martina Muller-Nurasyid, Bo Norrving, Eugenio Parati, Annette Peters, Alessandro Pezzini, I. Quereshi, Asif Rasheed, A. Rauf, T. Salam, Jess Shen, Agnieszka Słowik, Tara Stanne, Konstantin Strauch, Turgut Tatlisumak, Vincent N. Thijs, Steffen Tiedt, Matthew Traylor, Melanie Waldenberger, Matthew Walters, Wei Zhao, Giorgio Boncoraglio, Stephanie Debette, Christina Jern, Christopher Levi, Hugh Markus, James Meschia, Arndt Rolfs, Peter Rothwell, Danish Saleheen, Sudha Seshadri, Pankaj Sharma, Cathie Sudlow, Bradford Worrall, O. Colin Stine, Steven J. Kittner, Braxton D. Mitchell.
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.
PLoS One
2018 : Vol. 13, nr 11 art. no. e0206554, s. 1-12, bibliogr. 26 poz., abstr.
Autor korespondencyjny: John W. Cole.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 1932-6203
AZ
ORG
AIF
IF: 2.776
Adres url:
Streszczenie w PubMed:
4/16
Chia-Ling Phuah, Tushar Dave, Rainer Malik, Miriam R. Raffeld, Alison M. Ayres, Joshua N. Goldstein, Anand Viswanathan, Steven M. Greenberg, Jeremiasz M. Jagiella, Bjorn M. Hansen, Bo Norrving, Jordi Jimenez-Conde, Jaume Roquer, Alexander Pichler, Christian Enzinger, Joan Montaner, Israel Fernandez- Cadenas, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Alessandro Biffi, Natalia Rost, Carl D. Langefeld, Hugh S. Markus, Braxton D. Mitchell, Brad B. Worrall, Steven J. Kittner, Daniel Woo, Martin Dichgans, Jonathan Rosand, Christopher D. Anderson.
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.
Brain
2017 : Vol. 140, nr 10, s. 2663-2672, il., bibliogr.
Autor korespondencyjny: Christopher D. Anderson.
p-ISSN: 0006-8950
AZ
ORG
AIF
IF: 10.840
Adres url:
Streszczenie w PubMed:
5/16
Christopher D. Anderson, Guido J. Falcone, Chia-Ling Phuah, Farid Radmanesh, H. Bart Brouwers, Thomas W. K. Battey, Alessandro Biffi, Gina M. Peloso, Dajiang J. Liu, Alison M. Ayres, Joshua N. Goldstein, Anand Viswanathan, Steven M. Greenberg, Magdy Selim, James F. Meschia, Devin L. Brown, Bradford B. Worrall, Scott L. Silliman, David L. Tirschwell, Matthew L. Flaherty, Peter Kraft, Jeremiasz M. Jagiella, Helena Schmidt, Bjorn M. Hansen, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano, Koen M. van Nieuwenhuizen, Catharina J. M. Klijn, Kristiina Rannikmae, Neshika Samarasekera, Rustam Al-Shahi Salman, Catherine L. Sudlow, Ian J. Deary, Andrea Morotti, Alessandro Pezzini, Joana Pera, Andrzej Urbanik, Alexander Pichler, Christian Enzinger, Bo Norrving, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Chelsea S. Kidwell, Steven J. Kittner, Salina P. Waddy, Carl D. Langefeld, Goncalo Abecasis, Cristen J. Willer, Sekar Kathiresan, Daniel Woo, Jonathan Rosand.
Genetic variants in CETP increase risk of intracerebral hemorrhage.
Annals of Neurology
2016 : Vol. 80, nr 5, s. 730-740, il., bibliogr. 47 poz.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 0364-5134
AZ
ORG
AIF
IF: 9.890
BB: PubMed ; Scopus ; Web of Science Core Collection
PubMed; Scopus; Web of Science Core Collection
Adres url:
Streszczenie w PubMed:
6/16
Yu-Ching Cheng, Tara M. Stanne, Anne-Katrin Giese, Weang Kee Ho, Matthew Traylor, Philippe Amouyel, Elizabeth G. Holliday, Rainer Malik, Huichun Xu, Steven J. Kittner, John W. Cole, Jeffrey R. O'Connell, John Danesh, Asif Rasheed, Wei Zhao, Stefan Engelter, Caspar Grond-Ginsbach, Yoichiro Kamatani, Mark Lathrop, Didier Leys, Vincent Thijs, Tiina M. Metso, Turgut Tatlisumak, Alessandro Pezzini, Eugenio A. Parati, Bo Norrving, Steve Bevan, Peter M. Rothwell, Cathie Sudlow, Agnieszka Slowik, Arne Lindgren, Matthew R. Walters, Jum Jannes, Jess Shen, David Crosslin, Kimberly Doheny, Cathy C. Laurie, Sandip M. Kanse, Joshua C. Bis, Myriam Fornage, Thomas H. Mosley, Jemma C. Hopewell, Konstantin Strauch, Martina Muller-Nurasyid, Christian Gieger, Melanie Waldenberger, Annette Peters, Christine Meisinger, M. Arfan Ikram, W.T. Longstreth Jr, James F. Meschia, Sudha Seshadri, Pankaj Sharma, Bradford Worrall, Christina Jern, Christopher Levi, Martin Dichgans, Giorgio B. Boncoraglio, Hugh S. Markus, Stephanie Debette, Arndt Rolfs, Danish Saleheen, Braxton D. Mitchell.
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Stroke
2016 : Vol. 47, nr 2, s. 307-316, il., bibliogr. 17 poz.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 6.032
Adres url:
Streszczenie w PubMed:
7/16
Laura L. Kilarski, Sefanja Achterberg, William J. Devan, Matthew Traylor, Rainer Malik, Arne Lindgren, Guillaume Pare, Pankaj Sharma, Agnieszka Slowik, Vincent Thijs, Matthew Walters, Bradford B. Worrall, Michele Sale, Ale Algra, L. Jaap Kappelle, Cisca Wijmenga, Bo Norrving, Johanna K. Sandling, Lars Ronnblom, An Goris, Andre Franke, Cathie Sudlow, Peter M. Rothwell, Christopher Levi, Elizabeth G. Holliday, Myriam Fornage, Bruce Psaty, Solveig Gretarsdottir, Unnar Thorsteinsdottir, Sudha Seshadri, Braxton D. Mitchell, Steven Kittner, Robert Clarke, Jemma C. Hopewell, Joshua C. Bis, Giorgio B. Boncoraglio, James Meschia, M. Arfan Ikram, Bjorn M. Hansen, Joan Montaner, Gudmar Thorleifsson, Kari Stefanson, Jonathan Rosand, Paul I.W. de Bakker, Martin Farrall, Martin Dichgans, Hugh S. Markus.
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.
Neurology
2014 : Vol. 83, nr 8, s. 678-685, il., bibliogr. 21 poz., abstr.
Open Access Creative Commons Attribution License CC-BY.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.286
Adres url:
Streszczenie w PubMed:
8/16
Daniel Woo, Guido J. Falcone, William J. Devan, W. Mark Brown, Alessandro Biffi, Timothy D. Howard, Christopher D. Anderson, H. Bart Brouwers, Valerie Valant, Thomas W.K. Battey, Farid Radmanesh, Miriam R. Raffeld, Sylvia Baedorf-Kassis, Ranjan Deka, Jessica G. Woo, Lisa J. Martin, Mary Haverbusch, Charles J. Moomaw, Guangyun Sun, Joseph P. Broderick, Matthew L. Flaherty, Sharyl L. Martini, Dawn O. Kleindorfer, Brett Kissela, Mary E. Comeau, Jeremiasz M. Jagiella, Helena Schmidt, Paul Freudenberger, Alexander Pichler, Christian Enzinger, Bjorn M. Hansen, Bo Norrving, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano, Jaime Roquer, Peter Kraft, Alison M. Ayres, Kristian Schwab, Jacob L. McCauley, Joanna Pera, Andrzej Urbanik, Natalia S. Rost, Joshua N. Goldstein, Anand Viswanathan, Eva-Maria Stogerer, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Rainer Malik, Martin Dichgans, Steven M. Greenberg, Peter M. Rothwell, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Carl D. Langefeld, Jonathan Rosand.
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
American Journal of Human Genetics
2014 : Vol. 94, nr 4, s. 511-521
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.931
Adres url:
DOI:
9/16
Hakan Ay, Ethem Murat Arsava, Gunnar Andsberg, Thomas Benner, Robert D. Brown Jr, Sherita N. Chapman, John W. Cole, Hossein Delavaran, Martin Dichgans, Gunnar Engstrom, Eva Giralt-Steinhauer, Raji P. Grewal, Katrina Gwinn, Christina Jern, Jordi Jimenez-Conde, Katarina Jood, Michael Katsnelson, Brett Kissela, Steven J. Kittner, Dawn O. Kleindorfer, Daniel L. Labovitz, Silvia Lanfranconi, Jin-Moo Lee, Manuel Lehm, Robin Lemmens, Chris Levi, Linxin Li, Arne Lindgren, Hugh S. Markus, Patrick F. McArdle, Olle Melander, Bo Norrving, Leema Reddy Peddareddygari, Annie Pedersen, Joanna Pera, Kristiina Rannikmae, Kathryn M. Rexrode, David Rhodes, Stephen S. Rich, Jaume Roquer, Jonathan Rosand, Peter M. Rothwell, Tatjana Rundek, Ralph L. Sacco, Reinhold Schmidt, Markus Schurks, Stephan Seiler, Pankaj Sharma, Agnieszka Slowik, Cathie Sudlow, Vincent Thijs, Rebecca Woodfield, Bradford B. Worrall, James F. Meschia.
Pathogenic ischemic stroke phenotypes in the NINDS-Stroke Genetics Network.
Stroke
2014 : Vol. 45, nr 12, s. 3589-3596, il., bibliogr. 16 poz.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 5.723
10/16
Christopher D. Anderson, Alessandro Biffi, Michael A. Nalls, William J. Devan, Kristin Schwab, Alison M. Ayres, Valerie Valant, Owen A. Ross, Natalia S. Rost, Richa Saxena, Anand Viswanathan, Bradford B. Worrall, Thomas G. Grott, Joshua N. Goldstein, Devin Brown, Joseph P. Broderick, Bo Norrving, Steven M. Greenberg, Scott L. Silliman, Bjorn M. Hansen, David L. Tirschwell, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Magdy Selim, Jaume Roquer, Joan Montaner, Andrew B. Singleton, Chelsea S. Kidwell, Daniel Woo, Karen L. Furie, James F. Meschia, Jonathan Rosand.
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage.
Stroke
2013 : Vol. 44, nr 3, s. 612-619, il., bibliogr. 30 poz., abstr.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 6.018
Adres url:
11/16
William J. Devan, Guido J. Falcone, Christopher D. Anderson, Jeremiasz M. Jagiella, Helena Schmidt, Bjorn M. Hansen, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Elisa Cuadrado-Godia, Carolina Soriano, Alison M. Ayres, Kristin Schwab, Sylwia Baedorf Kassis, Valerie Valant, Joanna Pera, Andrzej Urbanik, Anand Viswanathan, Natalia S. Rost, Joshua N. Goldstein, Paul Freudenberger, Eva-Maria Stogerer, Bo Norrving, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Steven M. Greenberg, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Daniel Woo, Jonathan Rosand, Alessandro Biffi.
Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage.
Stroke
2013 : Vol. 44, nr 6, s. 1578-1583, il., bibliogr. 30 poz.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 6.018
Adres url:
Streszczenie w PubMed:
12/16
Alessandro Biffi, Christopher D. Anderson, Guido J. Falcone, Brett Kissela, Bo Norrving, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joseph P. Broderick, Steven M. Greenberg, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Daniel Woo, Jonathan Rosand.
Novel insights into the genetics of intracerebral hemorrhage.
Stroke
2013 : Vol. 44, nr 6 suppl. 1, s. S137
Princeton Conference XXVIII-Cincinnati, Ohio, 17-19 May 2012.
p-ISSN: 0039-2499
SZZ
SIF
13/16
Guido J. Falcone, Alessandro Biffi, William J. Devan, Jeremiasz M. Jagiella, Helena Schmidt, Brett Kissela, Bjorn M. Hansen, Jordi Jimenez-Conde, Eva Giralt-Steinhauer, Roberto Elosua, Elisa Cuadrado-Godia, Carolina Soriano, Alison M. Ayres, Kristin Schwab, Joanna Pera, Andrzej Urbanik, Natalia S. Rost, Joshua N. Goldstein, Anand Viswanathan, Alexander Pichler, Christian Enzinger, Bo Norrving, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joan Montaner, Israel Fernandez-Cadenas, Pilar Delgado, Joseph P. Broderick, Steven M. Greenberg, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Matthew L. Flaherty, Dawn O. Kleindorfer, Carl D. Langefeld, Daniel Woo, Jonathan Rosand.
Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage.
Stroke
2012 : Vol. 43, nr 11, s. 2877-2883, il., bibliogr. 31 poz.
p-ISSN: 0039-2499
AZ
ORG
AIF
IF: 6.158
14/16
Matthew Traylor, Martin Farrall, Elizabeth G. Holliday, Cathie Sudlow, Jemma C. Hopewell, Yu-Ching Cheng, Myriam Fornage, M. Arfan Ikram, Rainer Malik, Steve Bevan, Unnur Thorsteinsdottir, Mike A. Nalls, W.T. Longstreth, Kerri L. Wiggins, Sunaina Yadav, Eugenio A. Parati, Anita L. DeStefano, Bradford B. Worrall, Steven J. Kittner, Muhammad Saleem Khan, Alex P. Reiner, Anna Helgadottir, Sefanja Achterberg, Israel Fernandez-Cadenas, Sherine Abboud, Reinhold Schmidt, Matthew Walters, Wei-Min Chen, E. Bernd Ringelstein, Martin O'Donnell, Weang Kee Ho, Joanna Pera, Robin Lemmens, Bo Norrving, Peter Higgins, Marianne Benn, Michele Sale, Gregor Kuhlenbaumer, Alexander S. F. Doney, Astrid M. Vicente, Hossein Delavaran, Ale Algra, Gail Davies, Sofia A. Oliveira, Colin N. A. Palmer, Ian Deary, Helena Schmidt, Massimo Pandolfo, Joan Montaner, Cara Carty, Paul I.W. de Bakker, Konstantinos Kostulas, Jose M. Ferro, Natalie R. van Zuydam, Einar Valdimarsson, Borge G. Nordestgaard, Arne Lindgren, Vincent Thijs, Agnieszka Slowik, Danish Saleheen, Guillaume Pare, Klaus Berger, Gudmar Thorleifsson, Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2), Albert Hofman, Thomas H. Mosley, Braxton D. Mitchell, Karen Furie, Robert Clarke, Christopher Levi, Sudha Seshadri, Andreas Gschwendtner, Giorgio B. Boncoraglio, Pankaj Sharma, Joshua C. Bis, Solveig Gretarsdottir, Bruce M. Psaty, Peter M. Rothwell, Jonathan Rosand, James F. Meschia, Kari Stefansson, Martin Dichgans, Hugh S. Markus.
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.
Lancet. Neurology
2012 : Vol. 11, nr 11, s. 951-962, il., bibliogr. 31 poz., sum.
p-ISSN: 1474-4422
AZ
ORG
AIF
IF: 23.917
15/16
Celine Bellenguez, Steve Bevan, Andreas Gschwendtner, Chris C.A. Spencer, Annette I. Burgess, Matti Pirinen, Caroline A. Jackson, Matthew Traylor, Amy Strange, Zhan Su, Gavin Band, Paul D. Syme, Rainer Malik, Joanna Pera, Bo Norrving, Robin Lemmens, Colin Freeman, Renata Schanz, Tom James, Deborah Poole, Lee Murphy, Helen Segal, Lynelle Cortellini, Yu-Ching Cheng, Daniel Woo, Michael A. Nalls, Bertram Muller-Myhsok, Christa Meisinger, Udo Seedorf, Helen Ross-Adams, Steven Boonen, Dorota Wloch-Kopec, Valerie Valant, Julia Slark, Karen Furie, Hossein Delavaran, Cordelia Langford, Panos Deloukas, Sarah Edkins, Sarah Hunt, Emma Gray, Serge Dronov, Leena Peltonen, Solveig Gretarsdottir, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Kari Stefansson, Giorgio B. Boncoraglio, Eugenio A. Parati, John Attia, Elizabeth Holliday, Chris Levi, Maria-Grazia Franzosi, Anuj Goel, Anna Helgadottir, Jenefer M. Blackwell, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Audrey Duncanson, Janusz Jankowski, Christopher G. Mathew, Colin N. A. Palmer, Robert Plomin, Anna Rautanen, Stephen J. Sawcer, Richard C. Trembath, Ananth C. Viswanathan, Nicholas W. Wood, Bradford B. Worrall, Steven J. Kittner, Braxton D. Mitchell, Brett Kissela, James F. Meschia, Vincent Thijs, Arne Lindgren, Mary Joan Macleod, Agnieszka Slowik, Matthew Walters, Jonathan Rosand, Pankaj Sharma, Martin Farrall, Cathie L.M. Sudlow, Peter M. Rothwell, Martin Dichgans, Peter Donnelly, Hugh S. Markus.
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.
Nature Genetics
2012 : Vol. 44, nr 3, s. 326-333, il., bibliogr. 23 poz.
p-ISSN: 1061-4036
LR
AIF
IF: 35.209
16/16
Alessandro Biffi, Christopher D. Anderson, Jeremiasz M. Jagiella, Helena Schmidt, Brett Kissela, Bjorn M. Hansen, Jordi Jimenez-Conde, Caroline R. Pires, Alison M. Ayres, Kristin Schwab, Lynelle Cortellini, Joanna Pera, Andrzej Urbanik, Javier M. Romero, Natalia S. Rost, Joshua N. Goldstein, Anand Viswanathan, Alexander Pichler, Christian Enzinger, Raquel Rabionet, Bo Norrving, David L. Tirschwell, Magdy Selim, Devin L. Brown, Scott L. Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joseph P. Broderick, Steven M. Greenberg, Jaume Roquer, Arne Lindgren, Agnieszka Slowik, Reinhold Schmidt, Daniel Woo, Jonathan Rosand.
APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage : a genetic association study.
Lancet. Neurology
2011 : Vol. 10, nr 8, s. 702-709, il., bilbiogr. 29 poz., summ.
p-ISSN: 1474-4422
AZ
ORG
AIF
IF: 23.462
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