Understanding terminal decline in cognition and risk of death - Methodological and theoretical implications of practice and dropout effects by Rabbitt, P, Lunn, M, Wong, D

Topiramate for neuropathic pain and fibromyalgia in adults. by Wiffen, P, Derry, S, Lunn, M, Moore, R

CIDP and nephrotic syndrome: A shared immune mechanism through anti-Contactin 1 antibodies? by Fehmi, J, Keddie, S, Lunn, M, Bennett, D, Carr, A, Rinaldi, S

Unhappiness, health and cognitive ability in old age. by Rabbitt, P, Lunn, M, Ibrahim, S, Cobain, M, McInnes, L

White matter lesions account for all age-related declines in speed but not in intelligence. by Rabbitt, P, Scott, M, Lunn, M, Thacker, N, Lowe, C, Pendleton, N, Horan, M, Jackson, A

Age-associated losses of brain volume predict longitudinal cognitive declines over 8 to 20 years. by Rabbitt, P, Ibrahim, S, Lunn, M, Scott, M, Thacker, N, Hutchinson, C, Horan, M, Pendleton, N, Jackson, A

Antiepileptic drugs for neuropathic pain and fibromyalgia - an overview of Cochrane reviews. by Wiffen, P, Derry, S, Moore, R, Aldington, D, Cole, P, Rice, A, Lunn, M, Hamunen, K, Haanpaa, M, Kalso, E

Variable phenotypes are associated with PMP22 missense mutations. by Russo, M, Laurá, M, Polke, J, Davis, M, Blake, J, Brandner, S, Hughes, R, Houlden, H, Bennett, D, Lunn, M, Reilly, M

Emergency neuromuscular admissions are avoidable: a regional audit of unplanned hospital admissions of neuromuscular patients 2009-2011: final results and recommendations. by Jaffer, F, Reilly, M, Quinlivan, R, Muntoni, F, Turner, C, Parton, M, Lunn, M, Hilton-Jones, D, Korkodilos, M, Hanna, MG

Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study. by Granerod, J, Ambrose, H, Davies, N, Clewley, J, Walsh, A, Morgan, D, Cunningham, R, Zuckerman, M, Mutton, K, Solomon, T, Ward, K, Lunn, M, Irani, SR, Vincent, A, Brown, D, Crowcroft, N

Novel Mutations Mapping to the Fourth Sodium Channel Domain of Nav1.7 Result in Variable Clinical Manifestations of Primary Erythromelalgia by Cregg, R, Laguda, B, Werdehausen, R, Cox, J, Linley, J, Ramirez, J, Bodi, I, Markiewicz, M, Howell, K, Chen, Y, Agnew, K, Houlden, H, Lunn, M, Bennett, D, Wood, J, Kinali, M

Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgia. by Cregg, R, Laguda, B, Werdehausen, R, Cox, J, Linley, J, Ramirez, J, Bodi, I, Markiewicz, M, Howell, K, Chen, Y, Agnew, K, Houlden, H, Lunn, M, Bennett, D, Wood, J, Kinali, M

Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes. by Carvajal-González, A, Leite, M, Waters, P, Woodhall, M, Coutinho, E, Balint, B, Lang, B, Pettingill, P, Carr, A, Sheerin, U, Press, R, Press, R, Lunn, M, Lim, M, Maddison, P, Meinck, H, Vandenberghe, W, Vincent, A

A multi-country analysis of COVID-19 hospitalizations by vaccination status by Gonçalves, BP, Jassat, W, Baruch, J, Hashmi, M, Rojek, A, Dasgupta, A, Martin-Loeches, I, Reyes, LF, Piubelli, C, Citarella, BW, Kartsonaki, C, Lefèvre, B, López Revilla, JW, Lunn, M, Harrison, EM, Kraemer, MUG, Shrapnel, S, Horby, P, Bisoffi, Z, Olliaro, PL, Merson, L

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease. by Pitceathly, R, Murphy, S, Cottenie, E, Chalasani, A, Sweeney, MG, Woodward, C, Mudanohwo, E, Hargreaves, I, Heales, S, Land, J, Holton, J, Houlden, H, Blake, J, Champion, M, Flinter, F, Robb, SA, Page, R, Rose, M, Palace, J, Crowe, C, Longman, C, Lunn, M, Rahman, S, Reilly, M, Hanna, MG