Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Ataxia and PRNP[original query] |
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Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders. Human genetics 2001 Sep 109 (3): 319-25. Schröder B, Franz B, Hempfling P, Selbert M, Jürgens T, Kretzschmar H A, Bodemer M, Poser S, Zerr |
Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain : a journal of neurology 2003 Jul 126 (Pt 7): 1599-603. Stevanin Giovanni, Fujigasaki Hiroto, Lebre Anne-Sophie, Camuzat Agnes, Jeannequin Cecile, Dode Catherine, Takahashi Junko, San Chankranira, Bellance Robert, Brice Alexis, Durr Alexand |
Clinical and genetic features of human prion diseases in Catalonia: 1993-2002. European journal of neurology : the official journal of the European Federation of Neurological Societies 2004 Oct 11 (10): 649-55. Sanchez-Valle R, Nos C, Yagüe J, Graus F, Domínguez A, Saiz A, |
Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders. Journal of the neurological sciences 2023 6 451 120707. Martin Paucar, José Laffita-Mesa, Valter Niemelä, Helena Malmgren, Inger Nennesmo, Kristina Lagerstedt-Robinson, Magnus Nordenskjöld, Per Svenningss |
Accumulation Area of a Japanese PRNP P102L Variant: The Ariake PRNP P102L Variant. Journal of clinical neurology (Seoul, Korea) 2024 1 . Kohei Suzuyama, Makoto Eriguchi, Hiromu Minagawa, Hiroyuki Honda, Keita Kai, Tetsuyuki Kitamoto, Hideo Ha |
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