檢索結果 - Nicola Roberts
- Showing 1 - 16 results of 16
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Health literacy in COPD 由 Nicola Roberts, Ramesh Ghiassi, Martyn R Partridge
出版 2008Revisão -
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Effects of Regular Physical Activity on the Immune System, Vaccination and Risk of Community-Acquired Infectious Disease in the General Population: Systematic Review and Meta-Analy... 由 Sébastien Chastin, Ukachukwu Okoroafor Abaraogu, Jan Bourgois, Philippa Dall, J. Darnborough, Elaine Duncan, Jasmien Dumortier, David Jiménez Pavón, Joanna McParland, Nicola Roberts, Mark Hamer
出版 2021Revisão -
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Melatonin and health: an umbrella review of health outcomes and biological mechanisms of action 由 Paul Posadzki, Ram Bajpai, Bhone Myint Kyaw, Nicola Roberts, Amnon Brzezinski, George I. Christopoulos, Ushashree Divakar, Shweta Bajpai, Michael Soljak, Gerard Dunleavy, Krister Järbrink, Nang Ei Ei Khaing, Chee Kiong Soh, Josip Car
出版 2018Revisão -
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Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling 由 Kate Baker, Sarah L. Gordon, Detelina Grozeva, Margriet van Kogelenberg, Nicola Roberts, Michael Pike, Edward Blair, Matthew E. Hurles, W.K. Chong, Torsten Baldeweg, Manju A. Kurian, Stewart Boyd, Michael A. Cousin, F. Lucy Raymond
出版 2015Artigo -
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Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia 由 Periklis Makrythanasis, Mitsuhiro Kato, Maha S. Zaki, Hirotomo Saitsu, Kazuyuki Nakamura, Federico Santoni, Satoko Miyatake, Mitsuko Nakashima, Mahmoud Y. Issa, Michel Guipponi, Audrey Letourneau, Clare V. Logan, Nicola Roberts, David Parry, Colin A. Johnson, Naomichi Matsumoto, Hanan Hamamy, Eamonn Sheridan, Taroh Kinoshita, Stylianos E. Antonarakis, Yoshiko Murakami
出版 2016Artigo -
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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 由 Ghayda Mirzaa, David Parry, Andrew E. Fry, Kristin A. Giamanco, Jeremy Schwartzentruber, Megan R. Vanstone, Clare V. Logan, Nicola Roberts, Colin A. Johnson, Shawn Singh, Stanislav S. Kholmanskikh, Carissa Adams, Rebecca D. Hodge, Robert F. Hevner, David T. Bonthron, Kees P. J. Braun, Laurence Faivre, Jean‐Baptiste Rivière, Judith St‐Onge, Karen W. Gripp, Grazia M.S. Mancini, Ki Pang, Elizabeth Sweeney, Hilde Van Esch, Nienke E. Verbeek, Dagmar Wieczorek, Michelle Steinraths, Jacek Majewski, Kym M. Boycott, Daniela T. Pilz, M. Elizabeth Ross, William B. Dobyns, Eamonn Sheridan
出版 2014Artigo -
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Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling 由 Clare V. Logan, György Szabadkai, Jenny A. Sharpe, David Parry, Silvia Torelli, Anne‐Marie Childs, Marjolein Kriek, Rahul Phadke, Colin A. Johnson, Nicola Roberts, David T. Bonthron, Karen Pysden, Tamieka Whyte, Iulia Munteanu, A. Reghan Foley, Gabrielle Wheway, Katarzyna Szymańska, Subaashini Natarajan, Zakia A. Abdelhamed, Joanne Morgan, H. Roper, Gijs W.E. Santen, Erik H. Niks, W. Ludo van der Pol, Dick Lindhout, Anna Raffaello, Diego De Stefani, Johan T. den Dunnen, Yu Sun, Ieke B. Ginjaar, Caroline A. Sewry, Matthew E. Hurles, Rosario Rizzuto, Michael R. Duchen, Francesco Muntoni, Eamonn Sheridan
出版 2013Artigo
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