Výsledky vyhledávání - F. Yesim Demirci

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  1. 1
    Genetic Aspects of Conjunctival Melanoma: A Review

    Genetic Aspects of Conjunctival Melanoma: A Review Autor Emily Chang, Hakan Demirci, F. Yesim Demirci

    Vydáno 2023
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  2. 2
    Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings

    Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings Autor Samantha L. Rosenthal, M. Michael Barmada, Xingbin Wang, F. Yesim Demirci, M. Ilyas Kamboh

    Vydáno 2014
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  3. 3
    Association of CLU and PICALM variants with Alzheimer's disease

    Association of CLU and PICALM variants with Alzheimer's disease Autor M. Ilyas Kamboh, Ryan L. Minster, F. Yesim Demirci, Mary Ganguli, Steven T. DeKosky, Oscar L. López, M. Michael Barmada

    Vydáno 2010
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  4. 4
    Genetic Determinants of Disease Progression in Alzheimer's Disease

    Genetic Determinants of Disease Progression in Alzheimer's Disease Autor Xingbin Wang, Oscar L. López, Robert A. Sweet, James T. Becker, Steven T. DeKosky, M. Michael Barmada, F. Yesim Demirci, M. Ilyas Kamboh

    Vydáno 2014
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  5. 5
    X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15

    X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15 Autor F. Yesim Demirci, Brian W. Rigatti, Gaiping Wen, Amy L. Radak, Tammy S. Mah, Corrine L. Baic, Elias I. Traboulsi, Tiina Alitalo, Juliane Ramser, Michael B. Gorin

    Vydáno 2002
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  6. 6
    More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk

    More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk Autor Samantha L. Rosenthal, Mikhil Bamne, Xingbin Wang, Sarah Berman, Beth E. Snitz, William E. Klunk, Robert A. Sweet, F. Yesim Demirci, Oscar L. López, M. Ilyas Kamboh

    Vydáno 2015
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  7. 7
    PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor

    PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor Autor Dharambir K. Sanghera, F. Yesim Demirci, Latonya Been, Lyda Ortega, Sarju Ralhan, Gurpreet Singh Wander, Narinder K. Mehra, Jairup Singh, Christopher E. Aston, John J. Mulvihill, M. Ilyas Kamboh

    Vydáno 2009
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  8. 8
    Genome-wide association analysis of age-at-onset in Alzheimer's disease

    Genome-wide association analysis of age-at-onset in Alzheimer's disease Autor M. Ilyas Kamboh, M. Michael Barmada, F. Yesim Demirci, Ryan L. Minster, Minerva M. Carrasquillo, V. Shane Pankratz, Samuel Younkin, Andrew J. Saykin, Robert A. Sweet, Eleanor Feingold, Steven T. DeKosky, Oscar L. López

    Vydáno 2011
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  9. 9
    Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging

    Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging Autor Qi Yan, Kwangsik Nho, Jorge L. Del-Águila, Xingbin Wang, Shannon L. Risacher, Kang-Hsien Fan, Beth E. Snitz, Howard Aizenstein, Chester A. Mathis, Oscar L. López, F. Yesim Demirci, Eleanor Feingold, William E. Klunk, Andrew J. Saykin, Carlos Cruchaga, M. Ilyas Kamboh

    Vydáno 2018
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  10. 10
    Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus

    Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus Autor Kimberly E. Taylor, Elaine F. Remmers, Annette T. Lee, Ward Ortmann, Robert M. Plenge, Chao Tian, Sharon A. Chung, Joanne Nititham, Geoffrey Hom, Amy Kao, F. Yesim Demirci, M. Ilyas Kamboh, Michelle Petri, Susan Manzi, Daniel L. Kastner, Michael F. Seldin, Peter K. Gregersen, Timothy W. Behrens, Lindsey A. Criswell

    Vydáno 2008
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  11. 11
    Differential Genetic Associations for Systemic Lupus Erythematosus Based on Anti–dsDNA Autoantibody Production

    Differential Genetic Associations for Systemic Lupus Erythematosus Based on Anti–dsDNA Autoantibody Production Autor Sharon A. Chung, Robert P. Kimberly, Robert Graham, Joanne Nititham, Annette T. Lee, Ward Ortmann, Chaim O. Jacob, Marta E. Alarcón‐Riquelme, Betty P. Tsao, John B. Harley, Patrick M. Gaffney, Kathy L. Moser, Michelle Petri, F. Yesim Demirci, M. Ilyas Kamboh, Susan Manzi, Peter K. Gregersen, Carl D. Langefeld, Timothy W. Behrens, Lindsey A. Criswell

    Vydáno 2011
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  12. 12
    Genome-wide association study of Alzheimer's disease

    Genome-wide association study of Alzheimer's disease Autor M. Ilyas Kamboh, F. Yesim Demirci, X. Wang, Ryan L. Minster, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Andrew J. Saykin, Gyungah Jun, Clinton T. Baldwin, Mark W. Logue, Jacqueline L. Buros, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Jonathan L. Haines, Robert A. Sweet, Mary Ganguli, Eleanor Feingold, Steven T. DeKosky, Oscar L. López, M. Michael Barmada

    Vydáno 2012
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  13. 13
    Association of Systemic Lupus Erythematosus with<i>C8orf13–BLK</i>and<i>ITGAM–ITGAX</i>

    Association of Systemic Lupus Erythematosus with<i>C8orf13–BLK</i>and<i>ITGAM–ITGAX</i> Autor Geoffrey Hom, Robert Graham, Barmak Modrek, Robert P. Kimberly, Ward Ortmann, Sophie Garnier, Annette T. Lee, Sharon A. Chung, Ricardo C. Ferreira, P.V. Krishna Pant, Dennis G. Ballinger, Roman Kosoy, F. Yesim Demirci, M. Ilyas Kamboh, Amy Kao, Chao Tian, Iva Gunnarsson, Anders Bengtsson, Solbritt Rantapää‐Dahlqvist, Michelle Petri, Susan Manzi, Michael F. Seldin, Lars Rönnblom, Ann Christine Syvänen, Lindsey A. Criswell, Peter K. Gregersen, Timothy W. Behrens

    Vydáno 2008
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  14. 14
    Lupus Nephritis Susceptibility Loci in Women with Systemic Lupus Erythematosus

    Lupus Nephritis Susceptibility Loci in Women with Systemic Lupus Erythematosus Autor Sharon A. Chung, Elizabeth E. Brown, Adrienne H. Williams, Paula S. Ramos, Céline C. Berthier, Tushar Bhangale, Marta E. Alarcón‐Riquelme, Timothy W. Behrens, Lindsey A. Criswell, Deborah Cunninghame Graham, F. Yesim Demirci, Jeffrey C. Edberg, Patrick M. Gaffney, John B. Harley, Chaim O. Jacob, M. Ilyas Kamboh, Jennifer A. Kelly, Susan Manzi, Kathy L. Moser-Sivils, Laurie Russell, Michelle Petri, Betty P. Tsao, Tim J. Vyse, Raphael Zidovetzki, Matthias Kretzler, Robert P. Kimberly, Barry I. Freedman, Robert Graham, Carl D. Langefeld

    Vydáno 2014
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  15. 15
    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease Autor Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin, Bruno A. Benítez, Yefei Cai, Rita Guerreiro, Oscar Harari, Joanne Norton, John Budde, Sarah Bertelsen, Amanda T. Jeng, Breanna Cooper, Tara Skorupa, David Carrell, Denise Levitch, Simon Hsu, Jiyoon Choi, Mina Ryten, John Hardy, Mina Ryten, Daniah Trabzuni, Michael E. Weale, Adaikalavan Ramasamy, Colin Smith, Celeste Sassi, José Brás, J. Raphael Gibbs, Dena G. Hernandez, Michelle K. Lupton, John Powell, Paola Forabosco, Perry G. Ridge, Christopher Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ronald G. Munger, Cameron Schmutz, Maegan Leary, F. Yesim Demirci, Mikhil Bamne, Xingbin Wang, Oscar L. López, Mary Ganguli, Christopher Medway, James Turton, Jenny Lord, Anne Braae, Imelda Barber, Kristelle Brown, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, David Mann, Stuart Pickering‐Brown, Kristelle Brown, Noor Kalsheker, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes, Pau Pástor, Oswaldo Lorenzo‐Betancor, Zoran Brkanac, Erick R. Scott, Eric J. Topol, Kevin Morgan, Ekaterina Rogaeva, Andrew B. Singleton, John Hardy, M. Ilyas Kamboh, Peter St George‐Hyslop, Nigel J. Cairns, John C. Morris, John Kauwe, Alison Goate

    Vydáno 2013
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  16. 16
    Analysis of shared heritability in common disorders of the brain

    Analysis of shared heritability in common disorders of the brain Autor Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Raymond K. Walters, José Brás, Laramie E. Duncan, Valentina Escott‐Price, Guido J. Falcone, Padhraig Gormley, Rainer Malik, Nikolaos A. Patsopoulos, Stephan Ripke, Zhi Wei, Dongmei Yu, Phil H. Lee, Patrick Turley, Benjamin Grenier‐Boley, Vincent Chouraki, Yoichiro Kamatani, Claudine Berr, Luc Letenneur, Didier Hannequin, Philippe Amouyel, Anne Boland, Jean‐François Deleuze, Emmanuelle Duron, Badri N. Vardarajan, Christiane Reitz, Alison Goate, Matthew J. Huentelman, M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Hákon Hákonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jonathan Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Antony Bayer, Magda Tsolaki, Petroula Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C. Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Markus J. Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte

    Vydáno 2018
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  17. 17
    Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

    Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals Autor Mahdi Ghani, Christiane Reitz, Rong Cheng, Badri N. Vardarajan, Gyungah Jun, Christine Sato, Adam C. Naj, Ruchita Rajbhandary, Li San Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Goldie S. Byrd, Walter A. Kukull, Tatiana M. Foroud, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Joseph H. Lee, Gerard D. Schellenberg, Peter St George‐Hyslop, Richard Mayeux, Ekaterina Rogaeva, Marilyn Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Robert C. Barber, M. Michael Barmada, Thomas G. Beach, Gary W. Beecham, Duane Beekly, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Guiqing Cai, Nigel J. Cairns, Chuanhai Cao, Chris Carlson, Regina M. Carney, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Charles DeCarli, Steven T. DeKosky, F. Yesim Demirci, Malcolm Dick, Kelley M. Faber, Kenneth B. Fallon, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Sid Gilman, Jonathan D. Glass, John H. Growdon, Hakon Hakonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Vahram Haroutunian, Lindy E. Harrell, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman

    Vydáno 2015
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  18. 18
    Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

    Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Autor Adam C. Naj, Gyungah Jun, Gary W. Beecham, Li‐San Wang, Badri N. Vardarajan, Jacqueline L. Buros, Paul J. Gallins, Joseph D. Buxbaum, Gail P. Jarvik, Paul K. Crane, Eric B. Larson, Thomas D. Bird, Bradley F. Boeve, Neill R. Graff‐Radford, Philip L. De Jager, Denis A. Evans, Julie A. Schneider, Minerva M. Carrasquillo, Nilüfer Ertekin‐Taner, Steven G. Younkin, Carlos Cruchaga, John Kauwe, Petra Nowotny, Patricia Kramer, John Hardy, Matthew J. Huentelman, Amanda Myers, M. Michael Barmada, F. Yesim Demirci, Clinton T. Baldwin, Robert C. Green, Ekaterina Rogaeva, Peter St George‐Hyslop, Steven E. Arnold, Robert C. Barber, Thomas G. Beach, Eileen H. Bigio, James D. Bowen, Adam Boxer, James R. Burke, Nigel J. Cairns, Chris Carlson, Regina M. Carney, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason J. Corneveaux, Carl W. Cotman, Jeffrey L. Cummings, Charles DeCarli, Steven T. DeKosky, Ramon Diaz‐Arrastia, Malcolm Dick, Dennis W. Dickson, William G. Ellis, Kelley M. Faber, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Sid Gilman, Bruno Giordani, Jonathan D. Glass, John H. Growdon, Ronald L. Hamilton, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin, Nancy Johnson, Jason Karlawish, Anna Karydas, Jeffrey Kaye, Ronald Kim, Edward H. Koo, Neil W. Kowall, James J. Lah, Allan I. Levey, Andrew P. Lieberman, Oscar L. López, Wendy J. Mack, Daniel Marson, Frank Martiniuk, Deborah C. Mash, Eliezer Masliah, Wayne C. McCormick, Susan M. McCurry, Andrew McDavid, Ann C. McKee, Marsel Mesulam, Bruce L. Miller

    Vydáno 2011
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  19. 19
    Rarity of the Alzheimer Disease–Protective<i>APP</i>A673T Variant in the United States

    Rarity of the Alzheimer Disease–Protective<i>APP</i>A673T Variant in the United States Autor Li-San Wang, Adam C. Naj, Robert Graham, Paul K. Crane, Brian W. Kunkle, Carlos Cruchaga, Josue D. Gonzalez Murcia, Lisa Cannon‐Albright, Clinton T. Baldwin, Henrik Zetterberg, Kaj Blennow, Walter A. Kukull, Kelley M. Faber, Nicole Schupf, Maria C. Norton, JoAnn T. Tschanz, Ronald G. Munger, Christopher Corcoran, Ekaterina Rogaeva, Chiao‐Feng Lin, Beth A. Dombroski, Laura B. Cantwell, Amanda Partch, Otto Valladares, Hákon Hákonarson, Peter St George‐Hyslop, Robert C. Green, Alison Goate, Tatiana Foroud, Regina M. Carney, Eric B. Larson, Timothy W. Behrens, John Kauwe, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Richard Mayeux, Gerard D. Schellenberg, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Robert W. Barber, M. Michael Barmada, Lisa L. Barnes, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Joseph D. Buxbaum, Nigel J. Cairns, Chuanhai Cao, Chris Carlson, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Charles DeCarli, Steven T. DeKosky, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Nilüfer Ertekin‐Taner, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Jonathan D. Glass, Neill R. Graff‐Radford, John H. Growdon, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman, Gail P. Jarvik, Gregory A. Jicha, Lee‐Way Jin, Gyungah Jun, M. Ilyas Kamboh, Anna Karydas, Jeffrey Kaye

    Vydáno 2014
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  20. 20
    Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease

    Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease Autor Adam C. Naj, Gyungah Jun, Christiane Reitz, Brian W. Kunkle, William Perry, Yo Son Park, Gary W. Beecham, Ruchita Rajbhandary, Kara L. Hamilton‐Nelson, Li-San Wang, John Kauwe, Matthew J. Huentelman, Amanda Myers, Thomas D. Bird, Bradley F. Boeve, Clinton T. Baldwin, Gail P. Jarvik, Paul K. Crane, Ekaterina Rogaeva, M. Michael Barmada, F. Yesim Demirci, Carlos Cruchaga, Patricia L. Kramer, Nilüfer Ertekin‐Taner, John Hardy, Neill R. Graff‐Radford, Robert C. Green, Eric B. Larson, Peter St George‐Hyslop, Joseph D. Buxbaum, Denis A. Evans, Julie A. Schneider, Kathryn L. Lunetta, M. Ilyas Kamboh, Andrew J. Saykin, Eric M. Reiman, Philip L. De Jager, David Bennett, John C. Morris, Thomas J. Montine, Alison Goate, Deborah Blacker, Debby W. Tsuang, Hákon Hákonarson, Walter A. Kukull, Tatiana Foroud, Eden R. Martin, Jonathan L. Haines, Richard Mayeux, Lindsay A. Farrer, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Robert W. Barber, Lisa L. Barnes, Thomas G. Beach, James T. Becker, Duane Beekly, Eileen H. Bigio, James D. Bowen, Adam Boxer, James R. Burke, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Chris Carlson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason J. Corneveaux, David H. Cribbs, Elizabeth Crocco, Charles DeCarli, Steven T. DeKosky, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Kelley M. Faber, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Jonathan D. Glass, John H. Growdon, Ronald L. Hamilton, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette

    Vydáno 2014
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