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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 5, 2024. (Total: 232220Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Seizures and PRNP[original query]
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant.
Neurology 2003 Nov 61 (9): 1204-10.
Walz R, Castro R M R P S, Velasco T R, Alexandre V, Lopes M H, Leite J P, Santos A C, Assirati J A, Wichert-Ana L, Terra-Bustamante V C, Bianchin M M, Maciag P C, Ribeiro K B, Guarnieri R, Araújo D, Cabalero O, Moura R, Salim A C M, Kindlmann K, Landemberger M C, Marques W, Fernandes R M F, Serafini L N, Machado H R, Carlotti C G, Brentani R R, Sakamoto A C, Martins V
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,
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series.
Neurobiology of aging 2012 Feb 33 (2): 426.e13-21.
McNaughton Daniel, Knight William, Guerreiro Rita, Ryan Natalie, Lowe Jessica, Poulter Mark, Nicholl David J, Hardy John, Revesz Tamas, Lowe James, Rossor Martin, Collinge John, Mead Sim
Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge.
Alzheimer's research & therapy 2022 6 14 (1): 90.
Chen Zhongyun, Chu Min, Liu Li, Zhang Jing, Kong Yu, Xie Kexin, Cui Yue, Ye Hong, Li Junjie, Wang Lin, Wu Liyo
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