전남대학교 중앙도서관

Impact of postoperative non-steroidal anti-inflammatory drugs on adverse events after gastrointestinal surgery

학술저널

issue: British Journal of Surgery. Oct 01, 2014 101(11):1413-1423
Author: Chapman, S. J.
Glasbey, J.
Kelly, M.
Khatri, C.
Nepogodiev, D.
Fitzgerald, J. E. F.
Bhangu, A.
Harrison, E. M.
Adams, R.
Patel, K.
Retchless, A. R.
Elsaddig, M.
Curtis, A. E.
McMahon, R.
Mittapalli, D.
Ferguson, L. A.
Gentry, S. V.
Kong, C. Y. N.
Naqvi, Z.
Amin, H.
Chaudhry, B.
Burke, J.
Henderson, I.
Trecarten, S.
Clements, J. M.
Drake, T. M.
Wild, J. R. L.
Venkatesh, H.
Butters, N.
Ahmeidat, H.
Goergen, N.
Black, D.
Robertson, K.
Jama, G. M.
McGuire, S. A.
Ahl, R.
Suri, T. S.
Kuo, R.
Fadhlillah, M.
Mills, H.
Mitchell, R.
Goodship, J.
Tan, M.
Barker, T.
Wright, T.
Mohamad, W.
Hanna, N.
Laing, G.
Warnock, M. W. C.
Baird-Fraser, P. R.
Logan, T.
Young, F. M.
Fane De Salis, A. C.
McHugh, R.
Hickson, C.
Paszkiewicz, J.
Anderson, L. B.
Neeson, D.
Mohan, M.
Narang, Y.
Brophy, T.
Punj, R.
Majumdar, S.
Kauser, S.
Jong, G.
Palkhi, E.
Finch, D.
Mitchell, H.
Carter, N.
Viyasar, T.
Sammut, T.
Cook, N.
Powell, M. M.
Horne, S.
Allen, J. L. Y.
Marshall, D.
McIntyre, C.
S Koh, D. T.
Shi, J.
Reid, T.
Armugam, N. P.
Luck, J.
Fozard, T.
OʼCallaghan, J.
Copley, P. C.
Tilliriou, V.
Aiyer, R.
Yazdi, A.
Wiltshire, A.
Blower, E.
Jewitt, C.
Cheung, L. K.
Fourali, S.
Rahimi, Y.
Velho, R.
Taylor, C.
Satterthwaite, L.
Eze, N. V.
Johnston, J. P. M.
McCain, R. S.
Hess, E. C. F.
Thumbadoo, R. P.
Turner, E. J. H.
Wookey, R.
Morris, R.
Gasteratos, K.
Heywood, E.
Simpson, S. J.
Rai, Z.
Kazzazi, D.
Ducey, J.
Livesey, M. J.
Finan, C.
Staunton, E.
Haddad, S. D.
Karanjia, R.
Bokobza, I.
Ahmed, M.
Howell, J.
Grainger, C.
Woo, A.
McDowall, M.
Bulley, F.
Keating, R.
Tan, B.
Sng, S.
Brown, C.
Aidoo-Micah, G.
Champsi, A.
Ellis, R.
Darwazeh, S.
Polson, R.
Chan, J. Z.
Chong, B. F. H. K.
Park, J. H.
Kong, C. Y.
Mogan, Y. P.
Stevens, S.
Sekhon, H. K.
McIntosh, R.
Ochiltree, D. W.
Jamieson, P. D.
Naumann, D. N.
Bowley, D. M.
Howell, G.
Clark, T.
Dear, K.
James, L.
Upchurch, E.
Wilson, H.
Hughes, M.
Modayur, S. M.
Datta, U.
Chen, J. H. C.
Williams, L. J. L.
Selby, J.
Prabhudesai, A.
Mahomed, K.
Shah, H. A.
Kong, K.
Chandramoorthy, S.
Marshall, L.
De Kauwe, C.
Rana, R.
Patel, J.
Pezas, T.
Ma, J.
Stohlner, V.
Kinsella, M. S.
Gardiner, S. N.
Smith, R. A.
Glover, M.
Akinfala, M.
Lee, J. Z. C.
Aggarwal, V.
Waters, S.
Atif, M.
Hill, M.
Ramasubramoni, A.
Jaffry, Z.
Sagoo, H.
Jeyakumar, J.
Kosasih, S.
Davis, J.
Stanley, G. H. M.
Nijran, J.
Tang, I.
Mehta, K.
Fillery, A.
Watson, N. F.
Shah, D.
Naidu, S.
Grewal, T. K.
Singh, P.
Reissis, D.
Marusza, C.
Pettit, W.
Timbrell, S.
Woods, R.
Phillips, J.
Vaughan, R.
Dean, S.
Gibby, R.
Jones, T. F.
Rao, R.
Torrance, H. D. T.
Thirumal, V.
McMahon, R. K.
Yap, D.
Shaw, A.
Claireaux, H. A.
Pang, Y. L.
Narramore, R.
Holmes, C.
Caldwell, A.
Daoub, A.
Bibby, L.
Hague, A. G.
Sykes, M. C.
Morar, P.
Downes, G.
Shah, S.
Walimohamed, S.
Alsulaimi, A.
Biswas, V.
Gnaneswaran, B.
Davies, N.
Narwani, V.
Hernon, J.
Jumbu, A.
Ilyas, M.
Johal, G.
Atia, F.
Williams, A.
Chan, C.
McAnelly, S.
Evans, A.
Chan, K. Y.
Flegg, K.
Carter, S.
Coley, J.
Khaw, R.
Jayakody, N.
Jones, B.
Fawcett, N.
Ghali, C.
Jalundhwala, K.
Ariyaratnam, P.
Colville, H.
Walls, M.
Lindsay, J.
Keane, M.
Ban, V. S.
Kambasha, C.
Sait, S.
Tahir, M.
Tharakan, R.
Voll, J.
Shiwani, H.
Al-Omran, Y.
Hawash, A.
McCaughan, V.
Shatkar, V.
Gohil, K.
Greenhalgh, A.
Higgins, E.
Moody, T.
Booth, M. B.
Chan, W. H.
Shanthakumaran, S.
Maple, N.
McNish, D.
Shahin, B.
Nicholas, J.
McDermid, R.
Narayan, P.
Brodie, C.
Hurrey, S.
Panayi, V.
Turner, B.
Kopala, K.
Winfield, Clayton S. A.
Mohamud, A.
Venkatesh, A.
Hosein, S.
Olimpio, C.
Gkiousias, V.
Kilgour, J. M.
Cogbill, E.
Ramcham, M.
Carr, G.
Bannerman, A.
Grundy, L.
White, S.
Beamish, A.
Neo, Y. N.
Cragg, A. R.
Perkins, A.
Wynn-Hebden, A.
Khan, T.
Ali, M.
Battersby, C. L. F.
Pinto, R. S.
Poon, S. S.
Patel, M.
Patel, P.
Shafi, A. M. A.
Vedage, D.
Ghorbhanian, S.
Klimach, S.
Bradley, J.
de Sausmarez, E.
Hayward, P.
Naqib, S.
Flanigan, C.
Shuttleworth, R. H. A.
McElvanna, K.
Shelton, B.
Westbrook, N.
Weir, A.
Webb, P.
Alam, M.
Bhanderi, S.
Roberts, C.
Al-Shakarchi, J.
Lu, M.
Harvey, J.
Chowdhury, M. U.
McGow, C.
Antoniou, I.
Good, D. F.
Gerasimova, N.
Eragat, M.
Pressler, N.
Santos, C. R. D.
Arshad, W.
Patel, H. R.
Kassim, Y.
Jayaratne, N.
Perera, A.
Chandramoorthy, L.
Quan, V.
Ponweera, A.
Tadjkarimi, J.
Moyes, L.
Metcalfe, C.
Napier-Hemy, T
Bull, A.
Jaffer, Y.
Mushtaq, J.
Warren, M.
Jarrar, Z.
Wickenden, R.
Kang, M.
Holohan, G.
Isbister, T.
Strachan, E.
Varma, R.
Simpson, R.
Rajasekar, N.
Panayiotou, H.
Walsh, E.
Thacoor, A.
Willson, J. M. H.
Mustafa, A.
Barai, I.
Menon, A.
Soon, W. C.
Thakrar, C.
McCurdie, S.
Carr, E. C. F.
Westwood, K. J.
Wardell, H.
Weinberg, D.
Craig, A. R. J.
Khan, F. A. S.
Mulla, A.
Dann, P.
Saleh, M.
Pignatelli, I. C.
Igbagiri, K. V.
Panagoulas, E. V.
Tilston, T. W.
Thayaparan, A. J.
Navaratnam, J.
Aryasomayajula, S.
Joji, N.
Screen, R.
Quinn, C.
Harrison, R.
Arnaout, A.
McCartan, N.
Allen, W.
Gabriel, R.
Hartelius, C. F.
Makinde, M. L.
Sivasubramaniam, S.
Spreadborough, P.
Lobo, R.
Surendran, H.
Couch, L.
Butters, T.
Beale, K.
Markiewicz, O.
Kennedy, E. D.
Neely, D. M.
Martin, A.
Al-Moasseb, Z. H.
Ong, K. K.
Letchumanan, S.
Lam, W. L.
Yapp, L.
Skelly, B. L.
Stallard, S.
Westhuizen, P. V. D.
Rafferty, A. R.
Lambert, A.
Tay, Y. Z.
Koshnow, Z.
Elamin, O.
Shah, A.
Kim, E.
English, W.
Farrell, A.
Sharma, J.
Rowan, Chudek. D. K.
Mullan, B.
Brown, R. J.
McCarter, J. A.
Johnston, D.
Symonds, C.
Gatfield, W.
Messenger, D.
Knox, J. D.
Jani, P.
Trinquet, J.
Naqvi, Z. B.
Hussain, K.
Jaffer, A.
McAleer, E.
Joshi, H.
Cecil, E.
Lochrane, A.
Woolley, T.
Marriott, P.
Bolton, W.
Balian, V.
Scott, A. J.
Tan, Y. H.
DB Label: Database : Journals@OVID

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Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1and MSH2missense variants

정기출판물

issue: Genetics in Medicine; 20220101, Issue: Preprints
Author: Loong, Lucy
Cubuk, Cankut
Choi, Subin
Allen, Sophie
Torr, Beth
Garrett, Alice
Loveday, Chey
Durkie, Miranda
Callaway, Alison
Burghel, George J.
Drummond, James
Robinson, Rachel
Berry, Ian R.
Wallace, Andrew
Eccles, Diana M.
Tischkowitz, Marc
Ellard, Sian
Ware, James S.
Hanson, Helen
Turnbull, Clare
Samant, S.
Lucassen, A.
Znaczko, A.
Shaw, A.
Ansari, A.
Kumar, A.
Donaldson, A.
Murray, A.
Ross, A.
Taylor-Beadling, A.
Taylor, A.
Innes, A.
Brady, A.
Kulkarni, A.
Hogg, A.-C.
Bowden, A. Ramsay
Hadonou, A.
Coad, B.
McIldowie, B.
Speight, B.
DeSouza, B.
Mullaney, B.
McKenna, C.
Brewer, C.
Olimpio, C.
Clabby, C.
Crosby, C.
Jenkins, C.
Armstrong, C.
Bowles, C.
Brooks, C.
Byrne, C.
Maurer, C.
Baralle, D.
Chubb, D.
Stobo, D.
Moore, D.
O'Sullivan, D.
Donnelly, D.
Randhawa, D.
Halliday, D.
Atkinson, E.
Baple, E.
Rauter, E.
Johnston, E.
Woodward, E.
Maher, E.
Sofianopoulou, E.
Petrides, E.
Lalloo, F.
McRonald, F.
Pelz, F.
Frayling, I.
Evans, G.
Corbett, G.
Rea, G.
Clouston, H.
Powell, H.
Williamson, H.
Carley, H.
Thomas, H.J.W.
Tomlinson, I.
Cook, J.
Hoyle, J.
Tellez, J.
Whitworth, J.
Williams, J.
Murray, J.
Campbell, J.
Tolmie, J.
Field, J.
Mason, J.
Burn, J.
Bruty, J.
Callaway, J.
Grant, J.
Del Rey Jimenez, J.
Pagan, J.
VanCampen, J.
Barwell, J.
Monahan, K.
Tatton-Brown, K.
Ong, K.-R.
Murphy, K.
Andrews, K.
Mokretar, K.
Cadoo, K.
Smith, K.
Baker, K.
Brown, K.
Reay, K.
McKay Bounford, K.
Bradshaw, K.
Russell, K.
Stone, K.
Snape, K.
Crookes, L.
Reed, L.
Taggart, L.
Yarram, L.
Cobbold, L.
Walker, L.
Walker, L.
Hawkes, L.
Busby, L.
Izatt, L.
Kiely, L.
Hughes, L.
Side, L.
Sarkies, L.
Greenhalgh, K.-L.
Shanmugasundaram, M.
Duff, M.
Bartlett, M.
Watson, M.
Owens, M.
Bradford, M.
Huxley, M.
Slean, M.
Ryten, M.
Smith, M.
Ahmed, M.
Roberts, N.
O'Brien, C.
Middleton, O.
Tarpey, P.
Logan, P.
Dean, P.
May, P.
Brace, P.
Tredwell, R.
Harrison, R.
Hart, R.
Kirk, R.
Martin, R.
Nyanhete, R.
Wright, R.
Martin, R.
Davidson, R.
Cleaver, R.
Talukdar, S.
Butler, S.
Sampson, J.
Ribeiro, S.
Dell, S.
Mackenzie, S.
Hegarty, S.
Albaba, S.
McKee, S.
Palmer-Smith, S.
Heggarty, S.
MacParland, S.
Greville-Heygate, S.
Daniels, S.
Prapa, S.
Abbs, S.
Tennant, S.
Hardy, S.
MacMahon, S.
McVeigh, T.
Foo, T.
Bedenham, T.
Cranston, T.
McDevitt, T.
Clowes, V.
Tripathi, V.
McConnell, V.
Woodwaer, N.
Wallis, Y.
Kemp, Z.
Mullan, G.
Pierson, L.
Rainey, L.
Joyce, C.
Timbs, A.
Reuther, A.-M.
Frugtniet, B.
DeSouza, B.
Husher, C.
Lawn, C.
Corbett, C.
Nocera-Jijon, D.
Reay, D.
Cross, E.
Ryan, F.
Lindsay, H.
Oliver, J.
Dring, J.
Spiers, J.
Harper, J.
Ciucias, K.
Connolly, L.
Tsang, M.
Brown, R.
Shepherd, S.
Begum, S.
Daniels, S.
Tadiso, T.
Linton-Willoughby, T.
Heppell, H.
Sahan, K.
Worrillow, L.
Allen, Z.
Barlett, M.
Watt, C.
Hegarty, M.
DB Label: Database : Supplemental Index

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Increased Diagnostic Yield by Reanalysis of Whole Exome Sequencing Data in Mitochondrial Disease.

학술저널

issue: Journal of neuromuscular diseases [J Neuromuscul Dis] 2024 May 13. Date of Electronic Publication: 2024 May 13.
Author: Olimpio C; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, CB2 0PY Cambridge, UK.; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB2 0QQ Cambridge United Kingdom.
Paramonov I; Centro Nacional de Análisis Genómico, C/Baldiri Reixac 4, 08028 Barcelona, Spain.
Matalonga L; Centro Nacional de Análisis Genómico, C/Baldiri Reixac 4, 08028 Barcelona, Spain.
Laurie S; Centro Nacional de Análisis Genómico, C/Baldiri Reixac 4, 08028 Barcelona, Spain.
Schon K; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, CB2 0PY Cambridge, UK.; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB2 0QQ Cambridge United Kingdom.
Polavarapu K; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON K1H 8M5, Canada.
Kirschner J; Department of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center-University of Freiburg, Freiburg 79110, Germany.
Schara-Schmidt U; Department of Pediatric Neurology, Center for Neuromuscular Disorders, Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Hospital Essen, Hufelandstr. 55, Essen 45147, Germany.
Lochmüller H; Centro Nacional de Análisis Genómico, C/Baldiri Reixac 4, 08028 Barcelona, Spain.; Department of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center-University of Freiburg, Freiburg 79110, Germany.; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.; Brain and Mind Research Institute, University of Ottawa, Ottawa, ON K1H 8M5, Canada.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON K1H 8M5, Canada.
Chinnery PF; MRC Mitochondrial Biology Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Horvath R; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, CB2 0PY Cambridge, UK.
DB Label: Database : MEDLINE

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Variants in mitochondrial disease genes are common causes of inherited peripheral neuropathies.

학술저널

issue: Journal of neurology [J Neurol] 2024 Mar 28. Date of Electronic Publication: 2024 Mar 28.
Author: Ferreira T; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, School of Clinical Medicine, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK.
Polavarapu K; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada.
Olimpio C; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, School of Clinical Medicine, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK.; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Paramonov I; Centro Nacional de Análisis Genómico, Barcelona, Spain.
Lochmüller H; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada.; Centro Nacional de Análisis Genómico, Barcelona, Spain.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Canada.; Brain and Mind Research Institute, University of Ottawa, Ottawa, Canada.; Department of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center - University of Freiburg, Freiburg, Germany.
Horvath R; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, School of Clinical Medicine, University of Cambridge, Robinson Way, Cambridge, CB2 0PY, UK. rh732@medschl.cam.ac.uk.
DB Label: Database : MEDLINE

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Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals.

보고서

issue: Frontiers in neurology [Front Neurol] 2023 Dec 01; Vol. 14, pp. 1292320. Date of Electronic Publication: 2023 Dec 01 (Print Publication: 2023).
Author: Major TC; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Arany ES; School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Schon K; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.; Department of Clinical Genetics, East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge, United Kingdom.
Simo M; University Clinic of Neurology, Semmelweis University, Budapest, Hungary.
Karcagi V; Istenhegyi Genetic Diagnostic Center, Budapest, Hungary.
van den Ameele J; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Yu Wai Man P; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.; NIHR Biomedical Research Centre, Moorfields Eye Hospital & UCL Institute of Ophthalmology, London, United Kingdom.; Cambridge Eye Unit, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, United Kingdom.
Chinnery PF; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Olimpio C; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.; Department of Clinical Genetics, East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge, United Kingdom.
Horvath R; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
DB Label: Database : MEDLINE

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TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

학술저널

issue: Nature communications [Nat Commun] 2023 Feb 23; Vol. 14 (1), pp. 1009. Date of Electronic Publication: 2023 Feb 23.
Author: Van Haute L; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.
O'Connor E; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
Díaz-Maldonado H; Department of Biochemistry and Cell Biology, University of Gothenburg, SE-405 30, Gothenburg, Sweden.
Munro B; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Polavarapu K; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Hock DH; Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, 30 Flemington Road, Parkville, VIC, 3052, Australia.
Arunachal G; Department of Human genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Athanasiou-Fragkouli A; UCL London, Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, UK.
Bardhan M; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Barth M; Department of Genetics, Mitovasc INSERM 1083, CNRS 6015, University Hospital of Angers, Angers, France.
Bonneau D; Department of Genetics, Mitovasc INSERM 1083, CNRS 6015, University Hospital of Angers, Angers, France.
Brunetti-Pierri N; Department of Translational Medicine, University of Naples Federico II, Via s. Pansini, 5, 80131, Naples, Italy.
Cappuccio G; Department of Translational Medicine, University of Naples Federico II, Via s. Pansini, 5, 80131, Naples, Italy.
Caruana NJ; Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, 30 Flemington Road, Parkville, VIC, 3052, Australia.; Institute for Health and Sport (IHES), Victoria University, Melbourne, VIC, 3011, Australia.
Dominik N; UCL London, Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, UK.
Goel H; Hunter Genetics, Waratah, University of Newcastle, Callaghan, NSW, 2298, Australia.
Helman G; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.
Houlden H; UCL London, Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, UK.
Lenaers G; Department of Genetics, Mitovasc INSERM 1083, CNRS 6015, University Hospital of Angers, Angers, France.
Mention K; Pediatric Inherited Metabolic Disorders, Hôpital Jeanne de Flandre, Lille, France.
Murphy D; UCL London, Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, UK.
Nandeesh B; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Olimpio C; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Powell CA; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.
Preethish-Kumar V; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Procaccio V; Department of Genetics, Mitovasc INSERM 1083, CNRS 6015, University Hospital of Angers, Angers, France.
Rius R; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3010, Australia.
Rebelo-Guiomar P; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.
Simons C; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.
Vengalil S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, 12311, Egypt.
Ziegler A; Department of Genetics, Mitovasc INSERM 1083, CNRS 6015, University Hospital of Angers, Angers, France.
Thorburn DR; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3010, Australia.
Stroud DA; Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, 30 Flemington Road, Parkville, VIC, 3052, Australia.; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.
Maroofian R; UCL London, Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, UK.
Christodoulou J; Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia.; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3010, Australia.
Gustafsson C; Department of Biochemistry and Cell Biology, University of Gothenburg, SE-405 30, Gothenburg, Sweden.
Nalini A; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Lochmüller H; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
Minczuk M; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK. michal.minczuk@mrc-mbu.cam.ac.uk.
Horvath R; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK. rh732@medschl.cam.ac.uk.
DB Label: Database : MEDLINE

원문보기: Open Access (PubMed Central) OA (Nature) OA (Springer) 조회 - Impact Factor (JCR) 등재 - Web of Science (SCIE) 등재 - SCOPUS

Primary mitochondrial myopathies in childhood.

학술저널

issue: Neuromuscular disorders : NMD [Neuromuscul Disord] 2021 Oct; Vol. 31 (10), pp. 978-987.
Author: Olimpio C; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
Tiet MY; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
Horvath R; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom. Electronic address: rh732@medschl.cam.ac.uk.
DB Label: Database : MEDLINE

원문보기: Full Text (ScienceDirect) Full Text (Clinical Key) 조회 - Impact Factor (JCR) 등재 - Web of Science (SCIE)

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