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Assessing initial MRI reports for suspected CJD patients.
Jesuthasan A, Sequeira D, Hyare H, Odd H, Rudge P, Mok TH, Nihat A, Collinge J, Mead S. Jesuthasan A, et al. Among authors: hyare h. J Neurol. 2022 Aug;269(8):4452-4458. doi: 10.1007/s00415-022-11087-x. Epub 2022 Apr 1. J Neurol. 2022. PMID: 35362733 Free PMC article. Review.
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
Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease.
De Vita E, Ridgway GR, Scahill RI, Caine D, Rudge P, Yousry TA, Mead S, Collinge J, Jäger HR, Thornton JS, Hyare H. De Vita E, et al. Among authors: hyare h. AJNR Am J Neuroradiol. 2013 Sep;34(9):1723-30. doi: 10.3174/ajnr.A3504. Epub 2013 Mar 28. AJNR Am J Neuroradiol. 2013. PMID: 23538406 Free PMC article.
69 results