Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Neurodegenerative Diseases and PRNP[original query] |
|---|
| Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies? Clinical neuropathology 0 20 (1): 19-25. Masullo C, Macchi |
| Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia. Annals of neurology 2005 Dec 58 (6): 858-64. Li Xiaohong, Rowland Lewis P, Mitsumoto Hiroshi, Przedborski Serge, Bird Thomas D, Schellenberg Gerard D, Peskind Elaine, Johnson Nancy, Siddique Teepu, Mesulam M-Marsel, Weintraub Sandra, Mastrianni James |
| Polymorphism distribution of prion protein codon 117, 129 and 171 in Taiwan. European journal of epidemiology 2007 22 (4): 257-61. Wang Kaw-Chen, Wang Vinchi, Sun Ming-Chieh, Chiueh Ti-I, Soong Bing-Wen, Shan Din |
| Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors. Brain : a journal of neurology 2011 Jun 134 (Pt 6): 1829-38. Kaski Diego N, Pennington Catherine, Beck Jon, Poulter Mark, Uphill James, Bishop Matthew T, Linehan Jaqueline M, O'Malley Catherine, Wadsworth Jonathan D F, Joiner Susan, Knight Richard S G, Ironside James W, Brandner Sebastian, Collinge John, Mead Sim |
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Human molecular genetics 2012 Apr 21 (8): 1897-906. Mead Simon, Uphill James, Beck John, Poulter Mark, Campbell Tracy, Lowe Jessica, Adamson Gary, Hummerich Holger, Klopp Norman, Rückert Ina-Maria, Wichmann H-Erich, Azazi Dhoyazan, Plagnol Vincent, Pako Wandagi H, Whitfield Jerome, Alpers Michael P, Whittaker John, Balding David J, Zerr Inga, Kretzschmar Hans, Collinge Jo |
| Analysis of the prion protein gene in multiple system atrophy. Neurobiology of aging 2017 Jan 49 216.e15-216.e18. Chelban Viorica, Manole Andreea, Pihlstrøm Lasse, Schottlaender Lucia, Efthymiou Stephanie, OConnor Emer, Meissner Wassilios G, Holton Janice L, Houlden Hen |
| Early-onset Alzheimer's disease patient with prion (PRNP) p.Val180Ile mutation. Neuropsychiatric disease and treatment 2019 8 15 2003-2013. Bagyinszky Eva, Kang Min Ju, Pyun Jungmin, Giau Vo Van, An Seong Soo A, Kim SangY |
| Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases. Neuropathology and applied neurobiology 2019 Jun . Llorens F, Villar-Piqué A, Schmitz M, Diaz-Lucena D, Wohlhage M, Hermann P, Goebel S, Schmidt I, Glatzel M, Hauw J-J, Sikorska B, Liberski P P, Riggert J, Ferrer I, Zerr |
| Genetic analyses of early-onset Alzheimer's disease using next generation sequencing. Scientific reports 2019 6 9 (1): 8368. Giau Vo Van, Bagyinszky Eva, Yang Young Soon, Youn Young Chul, An Seong Soo A, Kim Sang Y |
| Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity. Frontiers in neurology 2020 12 11 596108. Parobkova Eva, van der Zee Julie, Dillen Lubina, Van Broeckhoven Christine, Rusina Robert, Matej Radosl |
| The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (PRNP) with Sporadic Creutzfeldt-Jakob Disease. Cells 2021 11 10 (11): . Kim Yong-Chan, Jeong Byung-Ho |
| Genetic landscape of early-onset dementia in Hungary. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jun . Csaban Dora, Illes Anett, Renata Toth-Bencsik, Balicza Peter, Pentelenyi Klara, Molnar Viktor, Gezsi Andras, Grosz Zoltan, Gal Aniko, Kovacs Tibor, Klivenyi Peter, Molnar Maria Jud |
| Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia. Movement disorders : official journal of the Movement Disorder Society 2024 8 . Adeline Su Lyn Ng, Ai Huey Tan, Yi Jayne Tan, Jia Lun Lim, Michelle Mulan Lian, Alfand Marl Dy Closas, Azlina Ahmad-Annuar, Shanthi Viswanathan, Yuen Kang Chia, Jia Nee Foo, Weng Khong Lim, Eng-King Tan, Shen-Yang L |
- Page last reviewed:Feb 1, 2024
- Content source: