Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period von Sframeli, Maria, Sarkozy, Anna, Bertoli, Marta, Astrea, Guja, Hudson, Judith, Scoto, Mariacristina, Mein, Rachael, Yau, Michael, Phadke, Rahul, Feng, Lucy, Sewry, Caroline, Fen, Adeline Ngoh Seow, Longman, Cheryl, McCullagh, Gary, Straub, Volker, Robb, Stephanie, Manzur, Adnan, Bushby, Kate, Muntoni, Francesco

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Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 von FOLEY, A. Reghan, MENEZES, Manoj P, HUGHES, Imelda, MCCULLAGH, B. Gary, JUNGBLUTH, Heinz, LIM, Ming J, LIN, Jean-Pierre, MEGARBANE, Andre, ANDONI URTIZBEREA, J, SHAH, Ayaz H, ANTONY, Jayne, WEBSTER, Richard, PANDRAUD, Amelie, BROOMFIELD, Alexander, NG, Joanne, MATHEW, Ann A, O'BYRNE, James J, FORMAN, Eva, SCOTO, Mariacristina, PRASAD, Manish, O'BRIEN, Katherine, OLPIN, Simon, OPPENHEIM, Marcus, GONZALEZ, Michael A, HARGREAVES, Iain, LAND, John M, WANG, Min X, CARPENTER, Kevin, HORVATH, Rita, STRAUB, Volker, LEK, Monkol, GOLD, Wendy, FARRELL, Michael O, BRANDNER, Sebastian, AL-ODAIB, Ahmad, PHADKE, Rahul, MATSUBARA, Kazuo, McCGARVEY, Michael L, SCHERER, Steven S, BAXTER, Peter S, KING, Mary D, CLAYTON, Peter, RAHMAN, Shamima, REILLY, Mary M, OUVRIER, Robert A, ABRAMS, Alexander J, CHRISTODOULOU, John, ZÜCHNER, Stephan, MUNTONI, Francesco, HOULDEN, Henry, SUGANO, Kumiko, YONEZAWA, Atsushi, MANZUR, Adnan Y, BURNS, Joshua

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T2-highlighted U-fibres and rapid parenchymal volume loss in AESD: An under-recognised subtype of paediatric acute encephalopathy syndromes von Ramji, Saipriya, McCullagh, Gary, Ram, Dipak, Vassallo, Grace, Pavaine, Julija

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Spinal cord infarction: Not to be mistaken for acute transverse myelitis von Hassan, Eusra, Ram, Dipak, West, Siobhan, McCullagh, Gary

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, GI, Kitabayashi, N, Barth, M, Briggs, TA, Burton, ACE, Carpanelli, ML, Cerisola, AM, Colson, C, Dale, RC, Danti, FR, Darin, N, De Azua, B, De Giorgis, V, De Goede, CGL, Desguerre, I, De Laet, C, Eslahi, A, Fahey, MC, Fallon, P, Fay, A, Fazzi, E, Gorman, MP, Gowrinathan, NR, Hully, M, Kurian, MA, Leboucq, N, Lin, JPSM, Lines, MA, Mar, SS, Maroofian, R, Marti-Sanchez, L, McCullagh, G, Mojarrad, M, Narayanan, V, Orcesi, S, Ortigoza-Escobar, JD, Perez-Duenas, B, Petit, F, Ramsey, KM, Rasmussen, M, Rivier, F, Rodriguez-Pombo, P, Roubertie, A, Stodberg, TI, Toosi, MB, Toutain, A, Uettwiller, F, Ulrick, N, Vanderver, A, Waldman, A, Livingston, JH, Crow, YJ

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Efficacy and safety of onasemnogene abeparvovec in children with spinal muscular atrophy type 1: real-world evidence from 6 infusion centres in the United Kingdom von Gowda, Vasantha, Atherton, Mark, Murugan, Archana, Servais, Laurent, Sheehan, Jennie, Standing, Emma, Manzur, Adnan, Scoto, Mariacristina, Baranello, Giovanni, Munot, Pinki, McCullagh, Gary, Willis, Tracey, Tirupathi, Sandya, Horrocks, Iain, Dhawan, Anil, Eyre, Michael, Vanegas, Maria, Fernandez-Garcia, Miguel A., Wolfe, Amy, Pinches, Laura, Illingworth, Marjorie, Main, Marion, Abbott, Lianne, Smith, Hayley, Milton, Emily, D’Urso, Sarah, Vijayakumar, Kayal, Marco, Silvia Sanchez, Warner, Sinead, Reading, Emily, Douglas, Isobel, Muntoni, Francesco, Ong, Min, Majumdar, Anirban, Hughes, Imelda, Jungbluth, Heinz, Wraige, Elizabeth

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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia von Gorman, Kathleen M, Meyer, Esther, Grozeva, Detelina, Spinelli, Egidio, McTague, Amy, Sanchis-Juan, Alba, Carss, Keren J, Bryant, Emily, Reich, Adi, Schneider, Amy L, Pressler, Ronit M, Simpson, Michael A, Debelle, Geoff D, Wassmer, Evangeline, Morton, Jenny, Sieciechowicz, Diana, Jan-Kamsteeg, Eric, Paciorkowski, Alex R, King, Mary D, Cross, J. Helen, Poduri, Annapurna, Mefford, Heather C, Scheffer, Ingrid E, Haack, Tobias B, McCullagh, Gary, Millichap, John J, Carvill, Gemma L, Clayton-Smith, Jill, Maher, Eamonn R, Raymond, F. Lucy, Kurian, Manju A

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Congenital muscular dystrophies in the UK population: clinical and molecular spectrum of a large cohort diagnosed over a 12-years period von Sframeli, Maria, Sarkozy, Anna, Bertoli, Marta, Astrea, Guja, Hudson, Judith, Scoto, Mariacristina, Mein, Rachael, Yau, Michael, Phadke, Rahul, Feng, Lucy, Sewry, Caroline, Fen, Adeline Ngoh Seow, Longman, Cheryl, McCullagh, Gary, Straub, Volker, Robb, Stephanie, Manzur, Adnan, Bushby, Kate, Muntoni, Francesco

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A valuable non‐invasive diagnostic investigation for paediatric idiopathic brachial neuritis von VASSALLO, GRACE, MARTLAND, TIM, FORBES, WELLESLEY, MCCULLAGH, GARY

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A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial von Finkel, Richard S., McDonald, Craig M., Lee Sweeney, H., Finanger, Erika, Neil Knierbein, Erin, Wagner, Kathryn R., Mathews, Katherine D., Marks, Warren, Statland, Jeffrey, Nance, Jessica, McMillan, Hugh J., McCullagh, Gary, Tian, Cuixia, Ryan, Monique M., O’Rourke, Declan, Müller-Felber, Wolfgang, Tulinius, Mar, Burnette, W. Bryan, Nguyen, Cam-Tu, Vijayakumar, Kayal, Johannsen, Jessika, Phan, Han C., Eagle, Michelle, MacDougall, James, Mancini, Maria, Donovan, Joanne M.

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How to become a paediatric neurologist von Montague, Emily, Ram, Dipak, Parker, Alasdair, McCullagh, Gary

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, Gillian, Kitabayashi, Naoki, Barth, Magalie, Briggs, Tracy, Burton, Annabel C.E, Luisa Carpanelli, Maria, Cerisola, Alfredo M, Colson, Cindy, Dale, Russell C, Danti, Federica Rachele, Darin, Niklas, De Azua, Begoña, De Giorgis, Valentina, De Goede, Christian G E L, Desguerre, Isabelle, De Laet, Corinne, Eslahi, Atieh, Fahey, Michael C, Fallon, Penny, Fay, Alexander J, Fazzi, Elisa, Gorman, Mark P, Gowrinathan, Nirmala Rani, Hully, Marie, Kurian, Manju A, Leboucq, Nicolas, Lin, Jean-Pierre S-M, Lines, Matthew A, Mar, Soe S, Maroofian, Reza, Martí-Sanchez, Laura, McCullagh, Gary, Mojarrad, Majid, Narayanan, Vinodh, Orcesi, Simona, Ortigoza-Escobar, Juan Dario, Pérez-Dueñas, Belén, Petit, Florence, Ramsey, Keri M, Rasmussen, Magnhild, Rivier, François, Rodríguez-Pombo, Pilar, Roubertie, Agathe, Stödberg, Tommy I, Beiraghi Toosi, Mehran, Toutain, Annick, Uettwiller, Florence, Ulrick, Nicole, Vanderver, Adeline, Waldman, Amy, Livingston, John H, Crow, Yanick

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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia von Gorman, Kathleen M, Meyer, Esther, Grozeva, Detelina, Spinelli, Egidio, McTague, Amy, Sanchis-Juan, Alba, Carss, Keren J, Bryant, Emily, Reich, Adi, Schneider, Amy L, Pressler, Ronit M, Simpson, Michael A, Debelle, Geoff D, Wassmer, Evangeline, Morton, Jenny, Sieciechowicz, Diana, Jan-Kamsteeg, Eric, Paciorkowski, Alex R, King, Mary D, Cross, J Helen, Poduri, Annapurna, Mefford, Heather C, Scheffer, Ingrid E, Haack, Tobias B, McCullagh, Gary, Deciphering Developmental Disorders Study, UK10K Consortium, NIHR BioResource, Millichap, John J, Carvill, Gemma L, Clayton-Smith, Jill, Maher, Eamonn R, Raymond, F Lucy, Kurian, Manju A

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Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 von Foley, A Reghan, Menezes, Manoj P, Pandraud, Amelie, Gonzalez, Michael A, Al-Odaib, Ahmad, Abrams, Alexander J, Sugano, Kumiko, Yonezawa, Atsushi, Manzur, Adnan Y, Burns, Joshua, Hughes, Imelda, McCullagh, B Gary, Jungbluth, Heinz, Lim, Ming J, Lin, Jean-Pierre, Megarbane, Andre, Urtizberea, J Andoni, Shah, Ayaz H, Antony, Jayne, Webster, Richard, Broomfield, Alexander, Ng, Joanne, Mathew, Ann A, O'Byrne, James J, Forman, Eva, Scoto, Mariacristina, Prasad, Manish, O'Brien, Katherine, Olpin, Simon, Oppenheim, Marcus, Hargreaves, Iain, Land, John M, Wang, Min X, Carpenter, Kevin, Horvath, Rita, Straub, Volker, Lek, Monkol, Gold, Wendy, Farrell, Michael O, Brandner, Sebastian, Phadke, Rahul, Matsubara, Kazuo, McGarvey, Michael L, Scherer, Steven S, Baxter, Peter S, King, Mary D, Clayton, Peter, Rahman, Shamima, Reilly, Mary M, Ouvrier, Robert A, Christodoulou, John, Züchner, Stephan, Muntoni, Francesco, Houlden, Henry

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Collagen characterisation and cell transformation in human atherosclerosis von MCCULLAGH, KEITH A, BALIAN, GARY

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Apparatus for supplying air to an air-source heat pump von GARY BENNETT, PAUL FRANCIS MCCULLAGH, RICHARD EDWARD BELL

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Air-source heat pump air supply arrangement von GARY BENNETT, PAUL FRANCIS MCCULLAGH, RICHARD EDWARD BELL

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Iowa Journal of School Social Work, 1994-1998 von McCullagh, Cheryl, Ed, Froyen, Gary, Ed

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Iowa Journal of School Social Work, 1993-1995 von Andreasen, Sara A., Ed, Froyen, Gary, Ed, McCullagh, Cheryl, Ed, Harrington, Danette, Ed

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