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Variant CJD in an individual heterozygous for PRNP codon 129.
Kaski D, Mead S, Hyare H, Cooper S, Jampana R, Overell J, Knight R, Collinge J, Rudge P. Kaski D, et al. Among authors: hyare h. Lancet. 2009 Dec 19;374(9707):2128. doi: 10.1016/S0140-6736(09)61568-3. Lancet. 2009. PMID: 20109837 No abstract available.
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation.
Alner K, Hyare H, Mead S, Rudge P, Wroe S, Rohrer JD, Ridgway GR, Ourselin S, Clarkson M, Hunt H, Fox NC, Webb T, Collinge J, Cipolotti L. Alner K, et al. Among authors: hyare h. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):109-14. doi: 10.1136/jnnp-2011-300167. Epub 2011 Aug 17. J Neurol Neurosurg Psychiatry. 2012. PMID: 21849340
A novel prion disease associated with diarrhea and autonomic neuropathy.
Mead S, Gandhi S, Beck J, Caine D, Gallujipali D, Carswell C, Hyare H, Joiner S, Ayling H, Lashley T, Linehan JM, Al-Doujaily H, Sharps B, Revesz T, Sandberg MK, Reilly MM, Koltzenburg M, Forbes A, Rudge P, Brandner S, Warren JD, Wadsworth JDF, Wood NW, Holton JL, Collinge J. Mead S, et al. Among authors: hyare h. N Engl J Med. 2013 Nov 14;369(20):1904-14. doi: 10.1056/NEJMoa1214747. N Engl J Med. 2013. PMID: 24224623 Free PMC article.
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