Bibliografia UJ CM



Zapytanie: ROSS OWEN A
Liczba odnalezionych rekordów: 22



Przejście do opcji zmiany formatu | Wyświetl/ukryj etykiety | Wersja do druku | | | Nowe wyszukiwanie
1/22
Lukasz M. Milanowski, Xu Hou, Jenny M. Bredenberg, Fabienne C. Fiesel, Liam T. Cocker, Alexandra I. Soto-Beasley, Ronald L. Walton, Audrey J. Strongosky, Ayman H. Faroqi, Maria Barcikowska, Magdalena Boczarska-Jedynak, Jaroslaw Dulski, Lyuda Fedoryshyn, Piotr Janik, Anna Potulska-Chromik, Katherine Karpinsky, Anna Krygowska-Wajs, Tim Lynch, Diana A. Olszewska, Grzegorz Opala, Aleksander Pulyk, Irena Rektorova, Yanosh Sanotsky, Joanna Siuda, Mariusz Widlak, Jaroslaw Slawek, Monika Rudzinska-Bar, Ryan Uitti, Monika Figura, Stanislaw Szlufik, Sylwia Rzonca-Niewczas, Elzbieta Podgorska, Pamela J. McLean, Dariusz Koziorowski, Owen A. Ross, Dorota Hoffman-Zacharska, Wolfdieter Springer, Zbigniew K. Wszolek.
Cathepsin B p.Gly284Val variant in Parkinson's disease pathogenesis.
International Journal of Molecular Sciences
2022 : Vol. 23, nr 13, il., bibliogr. 40 poz., abstr.
Autor korespondencyjny: Dorota Hoffman-Zacharska, Wolfdieter Springer.
Open Access Creative Commons Attribution License CC-BY 4.0
e-ISSN: 1422-0067
AZ
ORG
AIF
IF: 5.600
Adres url:
Streszczenie w PubMed:
Repozytorium UJ CM:
2/22
Thomas Jaworek, Huichun Xu, Brady J. Gaynor, John W. Cole, Kristiina Rannikmae, Tara M. Stanne, Liisa Tomppo, Vida Abedi, Philippe Amouyel, Nicole D. Armstrong, John Attia, Steven Bell, Oscar R. Benavente, Giorgio B. Boncoraglio, Adam Butterworth, Jara Carcel-Marquez, Zhengming Chen, Michael Chong, Carlos Cruchaga, Mary Cushman, John Danesh, Stephanie Debette, David J. Duggan, Jon Peter Durda, Gunnar Engstrom, Chris Enzinger, Jessica D. Faul, Natalie S. Fecteau, Israel Fernandez-Cadenas, Christian Gieger, Anne-Katrin Giese, Raji P. Grewal, Ulrike Grittner, Aki S. Havulinna, Laura Heitsch, Marc C. Hochberg, Elizabeth Holliday, Jie Hu, Andreea Ilinca, Marguerite R. Irvin, Rebecca D. Jackson, Mina A. Jacob, Raquel Rabionet, Jordi Jimenez-Conde, Julie A. Johnson, Yoichiro Kamatani, Sharon L.R. Kardia, Masaru Koido, Michiaki Kubo, Leslie Lange, Jin-Moo Lee, Robin Lemmens, Christopher R. Levi, Jiang Li, Liming Li, Kuang Lin, Haley Lopez, Sothear Luke, Jane Maguire, Patrick F. McArdle, Caitrin W. McDonough, James F. Meschia, Tiina Metso, Martina Muller-Nurasyid, Timothy D. O'Connor, Martin O'Donnell, Leema R. Peddareddygari, Joanna Pera, James A. Perry, Annette Peters, Jukka Putaala, Debashree Ray, Kathryn Rexrode, Marta Ribases, Jonathan Rosand, Peter M. Rothwell, Tatjana Rundek, Kathleen A. Ryan, Ralph L. Sacco, Veikko Salomaa, Cristina Sanchez-Mora, Reinhold Schmidt, Pankaj Sharma, Agnieszka Slowik, Jennifer A. Smith, Nicholas L. Smith, Sylvia Wassertheil-Smoller, Martin Soderholm, O. Colin Stine, Daniel Strbian, Cathie L.M. Sudlow, Turgut Tatlisumak, Chikashi Terao, Vincent Thijs, Nuria P. Torres-Aguila, David-Alexandre Tregouet, Anil M. Tuladhar, Jan H. Veldink, Robin G. Walters, David R. Weir, Daniel Woo, Bradford B. Worrall, Charles C. Hong, Owen A. Ross, Ramin Zand, Frank-Erik de Leeuw, Arne G. Lindgren, Guillaume Pare, Christopher D. Anderson, Hugh S. Markus, Christina Jern, Rainer Malik, Martin Dichgans, Braxton D. Mitchell, Steven J. Kittner.
Contribution of common genetic variants to risk of early-onset ischemic stroke.
Neurology
2022 : Vol. 99, nr 16, s. e1738-e1754, il., bibliogr. 41 poz., abstr.
Autor korespondencyjny: Braxton D. Mitchell.
Online First 2022-08-31
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 0028-3878
e-ISSN: 1526-632X
AZ
ORG
AIF
IF: 9.900
Adres url:
Streszczenie w PubMed:
3/22
Łukasz M. Milanowski, Jennifer A. Lindemann, Dorota Hoffman-Zacharska, Alexandra I. Soto-Beasley, Maria Barcikowska, Magdalena Boczarska-Jedynak, Angela Deutschlander, Gabriela Kłodowska, Jarosław Dulski, Lyuda Fedoryshyn, Andrzej Friedman, Zygmunt Jamrozik, Piotr Janik, Katherine Karpinsky, Dariusz Koziorowski, Anna Krygowska-Wajs, Barbara Jasińska-Myga, Grzegorz Opala, Anna Potulska-Chromik, Aleksander Pulyk, Irena Rektorova, Yanosh Sanotsky, Joanna Siuda, Jarosław Sławek, Katarzyna Śmiłowska, Lech Szczechowski, Monika Rudzińska-Bar, Ronald L. Walton, Owen A. Ross, Zbigniew K. Wszolek.
Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe.
Parkinsonism & Related Disorders
2021 : Vol. 86, s. 48-51, bibliogr. 11 poz., abstr.
Autor korespondencyjny: Zbigniew K. Wszolek.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 4.402
Adres url:
Streszczenie w PubMed:
4/22
Catherine Labbe, Kotaro Ogaki, Oswaldo Lorenzo-Betancor, Minerva M. Carrasquillo, Michael G. Heckman, Allan McCarthy, Alexandra I. Soto-Ortolaza, Ronald L. Walton, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Dennis W. Dickson, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus.
PLoS One
2015 : Vol. 10, nr 6 art. no. e0128586, s. 1-10, il., bibliogr. 23 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 1932-6203
AZ
ORG
AIF
IF: 3.057
Adres url:
Streszczenie w PubMed:
5/22
Kotaro Ogaki, Shunsuke Koga, Michael G. Heckman, Fabienne C. Fiesel, Maya Ando, Catherine Labbe, Oswaldo Lorenzo- Betancor,, Elisabeth L. Moussaud- Lamodiere, Alexandra I. Soto- Ortolaza, Ronald L. Walton, Audrey J. Strongosky, Ryan J. Uitti, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzinska, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Andreas Puschmann, Kenya Nishioka, Manabu Funayama, Nobutaka Hattori, Joseph E. Parisi, Ronald C. Petersen, Neill R. Graff-Radford, Bradley F. Boeve, Wolfdieter Springer, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross.
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
Neurology
2015 : Vol. 85, nr 23, s. 2016-2025, il., bibliogr., abstr.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
6/22
Catherine Labbe, Kotaro Ogaki, Lorenzo Lorenzo-Betancor,, Alexandra Soto-Ortolaza, Antony S. Walton, Sruti Rayaprolu, Shinsuke Fujioka, Melissa E. Murray, Michael G. Heckman, Andreas Puschmann, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzinska, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Yanosh Sanotsky, Irena Rektorova, Pamela J. McLean, Rosa Rademakers, Nilufer Ertekin-Taner, Anhar Hassan, J.Eric Ahlskog, Bradley F. Boeve, Ronald C. Petersen, Demetrius M. Maraganore, Charles H. Adler, Tanis J. Ferman, Joseph E. Parisi, Neill R. Graff-Radford, Ryan J. Uitti, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross.
Role for the microtubule-associated protein tau variant p.A152T in risk of Α-synucleinopathies.
Neurology
2015 : Vol. 85, nr 19, s. 1680-1686
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
7/22
Barbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, Heather D. Cannon, Catherine Labbe, Bruno A. Benitez, Jiyoon Choi, Timothy Lynch, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Jay A. Van Gerpen, Ryan J. Uitti, Wolfdieter Springer, Carlos Cruchaga, Zbigniew K. Wszolek, Owen A. Ross.
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease.
Neurobiol. Aging
2014 : Vol. 35, nr 8, s. 1958.e1-1958.e2, bibliogr., abstr.
p-ISSN: 0197-4580
AZ
ORG
AIF
IF: 5.013
Adres url:
8/22
Jessie Theuns, Aline Verstraeten, Kristel Sleegers, Eline Wauters, Ilse Gijselinck, Stefanie Smolders, David Crosiers, Ellen Corsmit, Ellen Elinck, Manu Sharma, Rejko Kruger, Suzanne Lesage, Alexis Brice, Sun Ju Chung, Mi-Jung Kim, Young Jin Kim, Owen A. Ross, Zbigniew K. Wszolek, Ekaterina Rogaeva, Zhengrui Xi, Anthony E. Lang, Christine Klein, Anne Weissbach, George D. Mellick, Peter A. Silburn, Georgios M. Hadjigeorgiou, Efthimios Dardiotis, Nobutaka Hattori, Ogaki Kotaro, Eng-King Tan, Yi Zhao, Jan Aasly, Enza Maria Valente, Simona Petrucci, Grazia Annesi, Aldo Quattrone, Carlo Ferrarese, Laura Brighina, Angela Deutschlnder, Andreas Puschmann, Christer Nilsson, Gaetan Garraux, Mark S. LeDoux, Ronald F. Pfeiffer, Magdalena Boczarska-Jedynak, Grzegorz Opala, Demetrius M. Maraganore, Sebastiaan Engelborghs, Peter Paul De Deyn, Patrick Cras, Marc Cruts, Christine Van Broeckhoven, GEO-PD Consortium.
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Neurology
2014 : Vol. 83, nr 21, s. 1906-1913, il., bibliogr. 30 poz., abstr.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.286
9/22
Michael G. Heckman, Alexis Elbaz, Alexandra I. Soto-Ortolaza, Daniel J. Serie, Jan O. Aasly, Grazia Annesi, Georg Auburger, Justin A. Bacon, Magdalena Boczarska-Jedynak, Maria Bozi, Laura Brighina, Marie-Christine Chartier-Harlin, Efthimios Dardiotis, Alain Destee, Carlo Ferrarese, Alessandro Ferraris, Brian Fiske, Suzana Gispert, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P.A. Ioannidis, Barbara Jasinska-Myga, Beom S Jeon, Yun Joong Kim, Christine Klein, Rejko Kruger, Elli Kyratzi, Chin-Hsien Lin, Katja Lohmann, Marie-Anne Loriot, Timothy Lynch, George D. Mellick, Eugenie Mutez, Grzegorz Opala, Sung Sup Park, Simona Petrucci, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Young Ho Sohn, Leonidas Stefanis, Vera Tadic, Hiroyuki Tomiyama, Ryan J. Uitti, Enza Maria Valente, Demetrios K. Vassilatis, Carles Vilarino-Guell, Linda R. White, Karin Wirdefeldt, Zbigniew Wszolek, Ruey-Meei Wu, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer, Owen A. Ross, Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium.
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Neurobiol. Aging
2014 : Vol. 35, nr 1, s. 266.e5-266.e14, il., bibliogr., abstr.
p-ISSN: 0197-4580
AZ
ORG
AIF
IF: 5.013
10/22
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:
11/22
Alexandra I. Soto-Ortolaza, Michael G. Heckman, Catherine Labbe, Daniel J. Serie, Andreas Puschmann, Sruti Rayaprolu, Audrey Strongosky, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Timothy Lynch, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.
American Journal of Neurodegenerative Disease
2013 : Vol. 2, nr 4, s. 287-299, bibliogr. 23 poz., abstr.
p-ISSN: 2165-591X
AZ
ORG
APZ
Adres url:
12/22
Dorota Hoffman-Zacharska, Dariusz Koziorowski, Owen A. Ross, Michał Milewski, Jarosław Poznański, Marta Jurek, Zbigniew K. Wszolek, Alexandra Soto-Ortolaza, Jarosław Sławek, Piotr Janik, Zygmunt Jamrozik, Anna Potulska-Chromik, Barbara Jasińska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Krzysztof Czyżewski, Dennis W. Dickson, Jerzy Bal, Andrzej Friedman.
Novel A18T and pA29S substitutions in Α-synuclein may be associated with sporadic Parkinson's disease.
Parkinsonism & Related Disorders
2013 : Vol. 19, nr 11, s. 1057-1060, il., bibliogr. 12 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 4.126
Adres url:
13/22
Sruti Rayaprolu, Bianca Mullen, Matt Baker, Timothy Lynch, Elizabeth Finger, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen-Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol Lippa, Keith A. Josephs, Davis S. Knopman, Charles L. White III, Richard Caselli, Ian R. Mackenzie, Bruce L. Miller, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Steven G. Younkin, Ronald C. Petersen, Nilufer Ertekin-Taner, Ryan J. Uitti, James F. Meschia, Kevin B. Boylan, Bradley F. Boeve, Neill R. Graff-Radford, Zbigniew K. Wszolek, Dennis W. Dickson, Rosa Rademakers, Owen A. Ross.
TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.
Molecular Neurodegeneration
2013 : Vol. 8, nr 1 art. no. 19, s. 1-5, bibliogr. 19 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 2.0.
p-ISSN: 1750-1326
AZ
ORG
AIF
IF: 5.286
Adres url:
Streszczenie w PubMed:
14/22
Manu Sharma, John P.A. Ioannidis, Jan O. Aasly, Grazia Annesi, Alexis Brice, Lars Bertram, Maria Bozi, Maria Barcikowska, David Crosiers, Carl E. Clarke, Maurizio F. Facheris, Matthew Farrer, Gaetan Garraux, Suzana Gispert, Georg Auburger, Carles Vilarino-Guell, Georgios M. Hadjigeorgiou, Andrew A. Hicks, Nobutaka Hattori, Beom S Jeon, Zygmunt Jamrozik, Anna Krygowska-Wajs, Suzanne Lesage, Christina M. Lill, Juei-Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E. Lang, Cecile Libioulle, Miho Murata, Vincent Mok, Barbara Jasinska-Myga, George D. Mellick, Karen E. Morrison, Thomas Meitnger, Alexander Zimprich, Grzegorz Opala, Peter P. Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne D. Stockton, Wataru Satake, Peter A. Silburn, Tim M. Strom, Jessie Theuns, Eng-King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J. Uitti, Christine Van Broeckhoven, Karin Wirdefeldt, Zbigniew Wszolek, Georgia Xiromerisiou, Harumi S. Yomono, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius Maraganore, Rejko Krüger.
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.
Journal of Medical Genetics
2012 : Vol. 49, nr 11, s. 721-726, il., bibliogr. 20 poz., abstr.
Open Access
p-ISSN: 0022-2593
AZ
ORG
AIF
IF: 5.703
15/22
Katarzyna Gaweda-Walerych, Krzysztof Safranow, Barbara Jasinska-Myga, Monika Bialecka, Gabriela Klodowska-Duda, Monika Rudzinska, Krzysztof Czyzewski, Stephanie A. Cobb, Jaroslaw Slawek, Maria Styczynska, Grzegorz Opala, Marek Drozdzik, Kenya Nishioka, Matthew J. Farrer, Owen A. Ross, Zbigniew K. Wszolek, M. Barcikowska, Cezary Zekanowski.
PARK2 variability in Polish Parkinson's disease patients - interaction with mitochondrial haplogroups.
Parkinsonism & Related Disorders
2012 : Vol. 15, nr 5, s. 520-524, bibliogr. 30 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 3.274
16/22
Christopher D. Anderson, Alessandro Biffi, Rosanna Rahman, Owen A. Ross, Jeremiasz M. Jagiella, Brett Kissela, John W. Cole, Lynelle Cortellini, Natalia S. Rost, Yu-Ching Cheng, Steven M. Greenberg, Paul I.W. Bakker, de, Robert D. Brown, Jr., Thomas G. Brott, Braxton D. Mitchell, Joseph P. Broderick, Bradford B. Worrall, Karen L. Furie, Steven J. Kittner, Daniel Woo, Agnieszka Slowik, James F. Meschia, Richa Saxena, Jonathan Rosand.
Common mitochondrial sequence variants in ischemic stroke.
Annals of Neurology
2011 : Vol. 69, nr 3, 471-480, il., bibliogr. 33 poz.
p-ISSN: 0364-5134
AZ
ORG
AIF
IF: 11.089
17/22
Andreas Puschmann, Christophe Verbeeck, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Timothy Lynch, Barbara Jasinska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
Human leukocyte antigen variation and Parkinson's disease.
Parkinsonism & Related Disorders
2011 : Vol. 17, nr 5, s. 376-378, bibliogr. 12 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 3.795
18/22
Marie-Christine Chartier-Harlin, Justus C. Dachsel, Carles Vilarino-Guell, Sarah J. Lincoln, Frederic Lepretre, Mary M. Hulihan, Jennifer Kachergus, Austen J. Milnerwood, Lucia Tapia, Mee-Sook Song, Emilie Le Rhun, Eugenie Mutez, Lydie Larvor, Aurelie Duflot, Christel Vanbesien-Mailliot, Alexandre Kreisler, Owen A. Ross, Kenya Nishioka, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Heather A. Melrose, Bahareh Behrouz, Brett H. Keeling, Justin A. Bacon, Emna Hentati, Lindsey Williams, Akiko Yanagiya, Nahum Sonenberg, Paul J. Lockhart, Abba C. Zubair, Ryan J. Uitti, Jan O. Aasly, Anna Krygowska-Wajs, Grzegorz Opala, Zbigniew K. Wszolek, Roberta Frigerio, Demetrius M. Maraganore, David Gosal, Tim Lynch, Michael Hutchinson, Anna Rita Bentivoglio, Enza Maria Valente, William C. Nichols, Nathan Pankratz, Tatiana Foroud, Rachel A. Gibson, Faycal Hentati, Dennis W. Dickson, Alain Destee, Matthew J. Farrer.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 3, s. 398-406, bibliogr. 25 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
19/22
Carles Vilarino-Guell, C. Wider, Owen A. Ross, Justus C. Dachsel, Jennifer M. Kachergus, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon, Bahareh Behrouz, Heather A. Melrose, Emna Hentati, Andreas Puschmann, Daniel M. Evans, Elizabeth Conibear, Wyeth W. Wasserman, Jan O. Aasly, Pierre R. Burkhard, Ruth Djaldetti, Joseph Ghika, Faycal Hentati, Anna Krygowska-Wajs, Tim Lynch, Eldad Melamed, Alex Rajput, Ali H. Rajput, Alessandra Solida, Ruey-Meei Wu, Ryan J. Uitti, Zbigniew K. Wszolek, Francois Vingerhoets, Matthew J. Farrer.
VPS35 mutations in Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 1, s. 162-167, bibliogr. 24 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
20/22
Carles Vilarino-Guell, Christian Wider, Jan O. Aasly, Linda R. White, Alex Rajput, Ali H. Rajput, Timothy Lynch, Anna Krygowska-Wajs, Barbara Jasinska-Myga, Grzegorz Opala, Maria Barcikowska, Krzysztof Czyzewski, Ruey-Meei Wu, Ryan J. Uitti, Zbigniew K. Wszolek, Matthew J. Farrer, Owen A. Ross.
Association of pyridoxal kinase and Parkinson disease.
Annals of Neurology
2010 : Vol. 67, nr 3, s. 409-411, bibliogr. 4 poz.
p-ISSN: 0364-5134
LR
AIF
IF: 10.746
21/22
Owen A. Ross, Michael G. Heckman, Alexandra I. Soto, Nancy N. Diehl, Kristoffer Haugarvoll, Carles Vilarino-Guell, Jan O. Aasly, Sigrid Sando, J. Mark Gibson, Timothy Lynch, Anna Krygowska-Wajs, Grzegorz Opala, Maria Barcikowska, Krzysztof Czyzewski, Ryan J. Uitti, Zbigniew K. Wszolek, Matthew J. Farrer.
Dopamine β-hydroxylase -1021C>T association and Parkinson's disease.
Parkinsonism & Related Disorders
2008 : Vol. 14, nr 7, s. 544-547, bibliogr. 11 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 1.907
Adres url:
22/22
Owen A. Ross, Alexandra I. Soto, Carles Vilarino-Guell, Michael G. Heckman, Nancy N. Diehl, Mary M. Hulihan, Jan O. Aasly, Sigrid Sando, J. Mark Gibson, Timothy Lynch, Anna Krygowska-Wajs, Grzegorz Opala, Maria Barcikowska, Krzysztof Czyzewski, Ryan J. Uitti, Zbigniew K. Wszolek, Matthew J. Farrer.
Genetic variation of Omi/HtrA2 and Parkinson's disease.
Parkinsonism & Related Disorders
2008 : Vol. 14, nr 7, s. 539-543, il., bibliogr. 11 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 1.907
Adres url:
  Wyświetl ponownie stosując format:
Wyświetl/ukryj etykiety | Wyświetlenie wyników w wersji do druku | Pobranie pliku do edytora | Nowe wyszukiwanie | Biblioteka Medyczna UJ