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Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation by Jaffer, F, Fawcett, K, Sims, D, Heger, A, Houlden, H, Hanna, MG, Kingston, H, Sisodiya, SM
Published 2017Journal article -
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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
Published 2013Journal article -
3
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype by Matthews, E, Neuwirth, C, Jaffer, F, Scalco, RS, Fialho, D, Parton, M, Rayan, D, Suetterlin, K, Sud, R, Spiegel, R, Mein, R, Houlden, H, Schaefer, A, Healy, E, Palace, J, Quinlivan, R, Treves, S, Holton, JL, Jungbluth, H, Hanna, MG
Published 2018Journal article