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Acta neuropathologica communications, ISSN 2051-5960, 03/2019, Volume 7, Issue 1, pp. 47 - 47
First-degree family members refused genetic examination. [...]the case reported here differs from previously described cases because of the presence of a rapid... 
Prion diseases | R208H | Mutation | Neuropathology | Genetic Creutzfeldt-Jakob disease | Dementia | HAPLOTYPE | NEUROSCIENCES | Creutzfeldt-Jakob disease | Haplotypes | Proteins | Genotype & phenotype | Insomnia | BSE | Patients | Polymorphism
Journal Article
Headache, ISSN 0017-8748, 11/2004, Volume 44, Issue 10, pp. 961 - 968
ObjectiveTo investigate changes in the levels of calcitonin gene-related peptide and its intracellular messenger cyclic adenosine monophosphate in serial... 
Journal Article
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