Hoppitt T, Pall H, Calvert M, Gill P, Yao L, Ramsay J, James G, Conduit J. A, Sackley C. Systematic review of the incidence and prevalence of long-term neurological conditions in the UK. Neuroepidemiology 2011; 36: 19-28. DOI: 10.1159/000321712
Cavanna AE, Eddy C, Mitchell R, Pall H, Mitchell I, Zrinzo L, Foltynie T, Jahanshahi M, Limousin P, Hariz M, Rickards H. An approach to deep brain stimulation for severe treatment-refractory Tourette syndrome: The UK perspective. Br J Neurosurg (E pub ahead of print) doi:10.3109/02688697.2010.534200
Hoppitt T, Calvert M, Pall H, Rickards H, Sackley C. Huntington’s disease. Lancet 2010; 376(9751): 1463-1464.
Shatunov A, Mok K, Newhouse S, Weale ME, Smith B, Vance C, Johnson L, Veldink JH, van Es MA, van den Berg LH, Robberecht W, van Damme P, Hardiman O, Farmer AE, Lewis CM, Butler AW, Abel O, Andersen PM, Fogh I, Silani V, Chio A, Traynor BJ, Melki J, Meininger V, Landers JE, McGuffin P, Glass JD, Pall H, Leigh PN, Hardy J, Brown RH Jr, Powell JF, Orrell RW, Morrison KE, Shaw PJ, Shaw CE, Al-Chalabi A. Chromosome 9p21in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Lancet Neurol 2010; 9(10): 986-994.
Heather Draper, Jonathan Ives, Hardev Pall, Stephen Smith, Sarah Damery, Sue Wilson, Reporting end of life practice: Can we trust doctors to be honest? Palliative Medicine 2009 Oct; 23(7): 673-674.
S Xiao, C Sato, T Kawarai, EF Goodall, HS Pall, LH Zinman, J Robertson, KE Morrison, K Rogaeva. 2006. Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis, Neurobiology of Aging 2008 Aug;29(8):1279-82.. ISSN: 0197-4580. Publication: 44635.
D Kasperaviciute, ME Weale, KV Shianna, GT Banks, CL Simpson, VK Hansen, MR Turner, C Shaw, A Al-Chalabi, HS Pall, EF Goodall, KE Morrison, R Orrell, M Beck, S Jablonka, M Sendtner, A Brockington, P Ince, J Hartley, H Nixon, P Shaw, G Schiavo, NW Wood, DB Goldstein, EM Fisher. Large-scale pathways based association study in amyotrophic lateral sclerosis. Brain. 2007 Sep;130(Pt 9):2292-301. Advance Access Published April 17, 2007.
Parkinson N, Ince PG, Smith MO, Highley R, Skibinski G, Andersen PM, Morrison KE, Pall HS, Hardiman O, Collinge J, Shaw PJ, Fisher EMC. ALS phenotypes with mutations in CHMP2B (Charged Multivesicular Body Protein 2B) Neurology 2006 Sep 26;67(6):1074-7. Epub 2006 Jun 28.