Compounds > arginine

arginine and CJD (Creutzfeldt-Jakob Disease)

arginine has been researched along with CJD (Creutzfeldt-Jakob Disease) in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	5 (38.46)	29.6817
2010's	7 (53.85)	24.3611
2020's	1 (7.69)	2.80

Authors

Authors	Studies
Aiba, I; Akagi, A; Hashimoto, R; Inukai, A; Iwasaki, Y; Kitamoto, T; Mimuro, M; Miyahara, H; Riku, Y; Yoshida, M	1
Alboini, PE; Bizzarro, A; Capellari, S; Di Giuda, D; Gangemi, E; Gaudino, S; Masullo, C; Parchi, P; Sauchelli, D; Scaricamazza, E; Vita, MG	1
Abdi, Z; Adamson, G; Barnes, J; Beck, JA; Blair, M; Campbell, T; Clegg, SL; Collinge, J; Crutch, SJ; Druyeh, R; Fox, NC; Gambetti, P; Guerreiro, RJ; Harper, L; Kenny, J; Kretzschmar, H; Leung, KK; Lowe, J; Mahoney, CJ; Mead, S; Nicholas, JM; Ponto, C; Rohrer, JD; Rossor, MN; Rowe, JB; Schott, JM; Slattery, CF; Uphill, J; Warren, JD; Zerr, I	1
Kim, YS; Lee, A; Lim, JG; Oh, E; Park, S	1
de Bot, ST; Dooijes, D; Kremer, HP; Verbeek, MM	1
Cali, I; DeArmond, SJ; Geschwind, MD; Harbaugh, R; Kuo, A; Raudabaugh, B; Sanchez, H; Sattavat, M; See, T; Tartaglia, MC; Thai, JN	1
Ito, D; Kitamoto, T; Nishimoto, Y; Shimizu, T; Suzuki, N; Suzuki, S	1
Johanidesová, S; Keller, J; Keller, O; Kovacs, GG; Matěj, R; Matějčková, M; Nováková, J; Rusina, R; Sigut, V	1
Klein, C; Kumar, KR	1
Stockdale, T	1
Grasbon-Frodl, EM; Krebs, B; Kretzschmar, HA; Neumann, M; Roeber, S; Windl, O; Zerr, I	1
Andreoletti, O; Basset-Leobon, C; Delisle, MB; Haik, S; Hauw, JJ; Peoc'h, K; Rigal, M; Sazdovitch, V; Uro-Coste, E	1
Doh-ura, K; Fujihara, K; Hidaka, M; Itoyama, Y; Kanno, S; Kim, K; Kitamoto, T; Konishi, T; Konno, H; Kuroda, S; Matsuda, Y; Mizusawa, H; Nagasato, K; Nakamura, Y; Nakashima, I; Nobukuni, K; Sano, Y; Sasaki, K; Sato, S; Sato, T; Satoh, A; Satoh, K; Shiga, Y; Takahashi, H; Takano, H; Takata, H; Umeda, Y; Yamada, M	1

Other Studies

13 other study(ies) available for arginine and CJD (Creutzfeldt-Jakob Disease)

Article	Year
A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies. Journal of the neurological sciences, 2020, 02-15, Volume: 409 Topics: Aged; Arginine; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Fatal Outcome; Humans; Lewy Body Disease; Male; Methionine; Prion Proteins	2020
R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease. Journal of neurology, 2013, Volume: 260, Issue:10 Topics: Arginine; Brain; Creutzfeldt-Jakob Syndrome; Female; Haplotypes; Histidine; Humans; Middle Aged; Neuroimaging; Phenotype; Prions; Radiography; Radionuclide Imaging	2013
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association, 2014, Volume: 10, Issue:6 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; Brain; Cohort Studies; Creutzfeldt-Jakob Syndrome; Exons; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Histidine; Humans; Male; Membrane Glycoproteins; Middle Aged; Phenotype; Receptors, Immunologic; Risk Factors	2014
Familial Creutzfeldt-Jakob disease with M232R mutation presented with corticobasal syndrome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2015, Volume: 36, Issue:7 Topics: 14-3-3 Proteins; Aged; Arginine; Basal Ganglia; Brain Diseases; Cerebral Cortex; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Humans; Methionine; Mutation; Prions	2015
CSF studies facilitate DNA diagnosis in familial Alzheimer's disease due to a presenilin-1 mutation. Journal of Alzheimer's disease : JAD, 2009, Volume: 17, Issue:1 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alzheimer Disease; Amyloid beta-Peptides; Arginine; Creutzfeldt-Jakob Syndrome; Dementia; Female; Humans; Leucine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Peptide Fragments; Presenilin-1; Reference Values; tau Proteins; Young Adult	2009
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease. Journal of neuropathology and experimental neurology, 2010, Volume: 69, Issue:12 Topics: Arginine; Creutzfeldt-Jakob Syndrome; Dementia; Fatal Outcome; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Prion Diseases; Prion Proteins; Prions; Threonine	2010
Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP). Clinical neurology and neurosurgery, 2011, Volume: 113, Issue:8 Topics: Arginine; Cerebellar Ataxia; Cerebral Angiography; Creutzfeldt-Jakob Syndrome; Electroencephalography; Female; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Methionine; Middle Aged; Point Mutation; Prion Proteins; Prions; Tomography, Emission-Computed, Single-Photon; Vision Disorders	2011
Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy. Movement disorders : official journal of the Movement Disorder Society, 2012, Volume: 27, Issue:4 Topics: Arginine; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Histidine; Humans; Magnetic Resonance Imaging; Middle Aged; Mutation; Prion Proteins; Prions; Supranuclear Palsy, Progressive	2012
Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy". Movement disorders : official journal of the Movement Disorder Society, 2014, Volume: 29, Issue:7 Topics: Arginine; Creutzfeldt-Jakob Syndrome; Female; Humans; Mutation; Prions; Supranuclear Palsy, Progressive	2014
Malnutrition as the cause of variant Creutzfeldt-Jacob disease. Medical hypotheses, 2002, Volume: 59, Issue:6 Topics: Animals; Arginine; Cattle; Creutzfeldt-Jakob Syndrome; Humans; Meat; Nutrition Disorders; Prions	2002
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment. Acta neuropathologica, 2005, Volume: 109, Issue:4 Topics: Aged; Arginine; Blotting, Western; Brain; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Histidine; Histological Techniques; Humans; Immunohistochemistry; Molecular Weight; Mutation; Prions	2005
Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques. Archives of neurology, 2006, Volume: 63, Issue:3 Topics: Amyloid; Arginine; Blotting, Western; Brain; Creutzfeldt-Jakob Syndrome; Haplotypes; Histidine; Humans; Immunohistochemistry; Male; Middle Aged; Mutation; Plaque, Amyloid; Prion Proteins; Prions; Protein Precursors; Valine	2006
Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution. Journal of neurology, 2007, Volume: 254, Issue:11 Topics: 14-3-3 Proteins; Aged; Arginine; Creutzfeldt-Jakob Syndrome; Electroencephalography; Female; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Mutation; Phenotype; Prions	2007