Výsledky vyhledávání - Peter Baxter
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Surgery for scoliosis in Duchenne muscular dystrophy Autor Daniel KL Cheuk, Virginia Wong, Elizabeth Wraige, Peter Baxter, Ashley Cole
Vydáno 2015Revisão -
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Hunter's Diseases of Occupations Autor Peter Baxter, Tar-Ching Aw, Anne Cockcroft, Paul N. Durrington, J Malcolm Harrington
Vydáno 2010Livro -
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Aquatic therapy for children with Duchenne muscular dystrophy: a pilot feasibility randomised controlled trial and mixed-methods process evaluation Autor Daniel Hind, James Parkin, Victoria Whitworth, Saleema Rex, Tracey Young, Lisa V. Hampson, Jennie Sheehan, Chin Maguire, Hannah Cantrill, Elaine Scott, Heather L. Van Epps, Marion Main, Michelle Geary, Heather McMurchie, Lindsey Pallant, Daniel Woods, Jennifer Freeman, Ellen Lee, Michelle Eagle, Tracey Willis, Francesco Muntoni, Peter Baxter
Vydáno 2017Artigo -
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Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency) Autor Philippa B. Mills, Emma Footitt, Kevin Mills, Karin Tuschl, Sarah Aylett, Sophia Varadkar, Cheryl Hemingway, Neil Marlow, Janet M. Rennie, Peter Baxter, Olivier Dulac, Rima Nabbout, William J. Craigen, Bernhard Schmitt, François Feillet, Ernst Christensen, Pascale de Lonlay, Mike Pike, M.I. Hughes, Eduard A. Struys, Cornelis Jakobs, Sameer M. Zuberi, Peter T. Clayton
Vydáno 2010Artigo -
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Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) Autor Tracy A. Briggs, Ghada M. H. Abdel‐Salam, Maryagnes R. Balicki, Peter Baxter, Enrico Bertini, Nick Bishop, B H Browne, David Chitayat, W.K. Chong, Maha M. Eid, William Halliday, Imelda Hughes, A. Klusmann‐Koy, Mary Kurian, Ken K. Nischal, Gillian Rice, John B.P. Stephenson, R. Surtees, J F Talbot, Nasrin Tehrani, John Tolmie, Carmel Toomes, Marjo S. van der Knaap, Yanick J. Crow
Vydáno 2007Artigo -
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Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations Autor Clara van Karnebeek, Sylvia Stöckler‐Ipsiroglu, Sravan Jaggumantri, Birgit Assmann, Peter Baxter, Daniela Buhaş, Levinus A. Bok, Barbara Cheng, Curtis R. Coughlin, Anibh M. Das, Alette Giezen, Walla Al‐Hertani, Gloria Y.F. Ho, Uta Meyer, Philippa B. Mills, Barbara Plecko, Eduard A. Struys, Keiko Ueda, Monique Albersen, Nanda M. Verhoeven, Sídney M. Gospe, Renata C. Gallagher, Johan K. L. Van Hove, Hans Hartmann
Vydáno 2014Artigo -
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A clinical diagnostic algorithm for early onset cerebellar ataxia Autor Rick Brandsma, Corien C. Verschuuren‐Bemelmans, Dina Amrom, Nina Barišić, Peter Baxter, Enrico Bertini, Lubov Blumkin, Vesna Branković-Srećković, Oebele F. Brouwer, Katrin Bürk, Coriene E. Catsman‐Berrevoets, Dana Craiu, I.F.M. de Coo, J. Gburek, C Kennedy, Tom J. de Koning, H.P.H. Kremer, Ram Kumar, Alfons Macaya, Alessia Micalizzi, Marisol Mirabelli-Badenier, Andrea H. Németh, Sara Nuovo, Bwee Tien Poll‐The, Tally Lerman‐Sagie, Maja Steinlin, Matthis Synofzik, Marina A.J. Tijssen, Gessica Vasco, Michèl A.A.P. Willemsen, Ginevra Zanni, Enza Maria Valente, Eugen Boltshauser, Deborah A. Sival
Vydáno 2019Revisão -
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Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 Autor A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud, Michael Gonzalez, Ahmad Alodaib, Alexander J. Abrams, Kumiko Sugano, Atsushi Yonezawa, Adnan Y. Manzur, Joshua Burns, Imelda Hughes, B.G. McCullagh, Heinz Jungbluth, Ming Lim, Jean‐Pierre Lin, André Mégarbané, J. Andoni Urtizberea, Ayaz Shah, Jayne Antony, Richard Webster, Alexander Broomfield, Joanne Ng, Ann Agnes Mathew, James J. O’Byrne, Eva Forman, Mariacristina Scoto, Manish Prasad, Katherine O’Brien, S. E. Olpin, Marcus Oppenheim, Iain P. Hargreaves, John M. Land, Min X. Wang, Kevin Carpenter, Rita Horváth, Volker Straub, Monkol Lek, Wendy Gold, Michael O. Farrell, Sebastian Brandner, Rahul Phadke, Kazuo Matsubara, Michael L. McGarvey, Steven S. Scherer, Peter Baxter, Mary D. King, Peter T. Clayton, Shamima Rahman, Mary M. Reilly, Robert Ouvrier, John Christodoulou, Stephan Züchner, Francesco Muntoni, Henry Houlden
Vydáno 2013Artigo -
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Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial Autor Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber, Mario Cortina‐Borja, Eleanor Hancock, Anthony L. Johnson, Colin Kennedy, Marcus Likeman, Andrew Lux, Mark T. Mackay, Andrew A. Mallick, Richard Newton, Melinda Nolan, Ronit Pressler, D. Rating, Bernhard Schmitt, Christopher Verity, John Osborne, Maysara Abdel Aziz, Triloknath Acharya, Carolyn Adcock, Robert Jones, Rachel Howells, Ben Marsh, Kemi Adejare, Rashmi Adiga, Mary Wheater, Mansoor Ahmed, Mohammad Sawal, Chhavi Goel, Mas Ahmed, Michael Alber, Markus Wolff, Susanne Ruf, Asya M Al-Kharusi, Hassan Al-Moasseb, Ruchi Arora, R.C. Beach, Patricia Atkinson, Kunle Ayonrinde, Pronab Bala, Nicola Bamford, Nagi Barakat, Nigel Basheer, Peter Baxter, Santosh Mordekar, Chris Rittey, Ingo Borggraefe, Peter Borusiak, Sabine Cagnoli, Richard Brown, Sophie Calvert, Sophie Calvert, Duncan Cameron, Ramesh Chaniyil, Ravi Chinthapalli, Gabriel Chow, William Whitehouse, V. Clarke, Chris Cooper, Alexane Datta, Selwyn D'Costa, Christian de Goede, Helen Basu, David Deekollu, Adela Della Marina, Penelope Dison, Colin Dunkley, Megan M. Eaton, Julie Ellison, R. C. B. Pugh, Penny Fallon, Hani Faza, Imti Choonara, Richard E. Morton, Mal Ratnayaka, Colin D. Ferrie, Amanda Freeman, Stephen Warriner, María del Carmen García, Malihe Ghazavi, Frances Gibbon, J. M. Gibbs, Des Ginbey, Iolanda Guarino, Rajesh Gupta, Mary Hanlon, Siân Harris, Paul Munyard, Cheryl Hemingway, Christin Eltze, Marios Kaliakatsos, V. Murugan, Robert Robinson, Jeen Tan, Daniel Hindley, Adrian Hughes, Akmal Hussain, Greg Boden, Munir A. Hussain
Vydáno 2018Artigo -
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Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome Autor Gillian Rice, Teresa Patrick, Rekha Parmar, Claire Taylor, Alec Aeby, Jean Aicardi, Rafael Artuch, Simon Attard Montalto, Carlos A. Bacino, Bruno Barroso, Peter Baxter, Willam S. Benko, Carsten Bergmann, Enrico Bertini, Roberta Biancheri, Edward Blair, Nenad Blau, David T. Bonthron, Tracy A. Briggs, Louise Brueton, Han G. Brunner, Christopher J. Burke, Ian Carr, Daniel R. Carvalho, Kate Chandler, H.‐J. Christen, Peter Corry, Frances M. Cowan, Helen Cox, Stefano D’Arrigo, John Dean, Corinne De Laet, Claudine De Praeter, Catherine Déry, Colin D. Ferrie, Kim Flintoff, Suzanna G.M. Frints, Àngels García‐Cazorla, Blanca Gener, Cyril Goizet, Françoise Goutières, Andrew Green, Agnès Guët, Ben C.J. Hamel, Bruce E. Hayward, Arvid Heiberg, Raoul C. M. Hennekam, Marie Husson, Andrew P. Jackson, Rasieka Jayatunga, Yong‐hui Jiang, Sarina G. Kant, Amy Kao, Mary D. King, Helen Kingston, Joerg Klepper, Marjo S. van der Knaap, Andrew J. Kornberg, Dieter Kotzot, W Kratzer, Didier Lacombe, Lieven Lagae, P. Landrieu, Giovanni Lanzi, Andrea Leitch, Ming Lim, John H. Livingston, Charles Marques Lourenço, E G Hermione Lyall, Sally Ann Lynch, Michael J. Lyons, Daphna Marom, John P. McClure, Robert McWilliam, Serge B. Melançon, Leena Mewasingh, Marie‐Laure Moutard, Ken K. Nischal, John R. Østergaard, Julie Prendiville, Magnhild Rasmussen, R. Curtis Rogers, Dominique Roland, Elisabeth Rosser, Kevin Rostásy, Agathe Roubertie, Amparo Sanchís, Raphael Schiffmann, Sabine Scholl‐Bürgi, Sunita Seal, Stavit A. Shalev, Concepción Sierra Córcoles, Gyan P. Sinha, Doriette Soler, Ronen Spiegel, John B.P. Stephenson, Uta Tacke, Tiong Yang Tan, Marianne Till, John Tolmie
Vydáno 2007Artigo
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Pediatrics
Psychiatry
Epilepsy
Biology
Gene
Genetics
Pathology
Pyridoxine
Randomized controlled trial
Surgery
Ataxia
Clinical trial
Disease
Duchenne muscular dystrophy
Genotype
Mutation
Neuroscience
Ophthalmology
Phenotype
Physical therapy
Psychological intervention
Adverse effect
Algorithm
Allele
Ambulatory
Anticonvulsant
Asphyxia
Atrophy