arginine and Myositis, Inclusion Body

arginine has been researched along with Myositis, Inclusion Body in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (66.67)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Auff, E; Djamshidian, A; Haubenberger, D; Schaefer, J; Stogmann, E; Zimprich, A; Zimprich, F	1
Cruts, M; De Deyn, PP; Engelborghs, S; Haubenberger, D; Hoffmann, M; Kumar-Singh, S; Martin, JJ; Mattheijssens, M; Peeters, K; Pirici, D; Pusswald, G; Van Broeckhoven, C; Van den Broeck, M; van der Zee, J; Van Langenhove, T; Vandenberghe, R; Zimprich, A	1
Ahn, BY; Chang, YH; Kim, DS; Kim, EJ; Kim, HJ; Kim, HS; Kim, S; Kim, SJ; Lee, HW; Park, YE; Seeley, WW	1

Trials

1 trial(s) available for arginine and Myositis, Inclusion Body

Article	Year
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. Neurology, 2009, Aug-25, Volume: 73, Issue:8 Topics: Adenosine Triphosphatases; Aged; Aged, 80 and over; Arginine; Cell Cycle Proteins; Dementia; Female; Follow-Up Studies; Genetic Heterogeneity; Genetic Linkage; Histidine; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Pedigree; Penetrance; Prospective Studies; Valosin Containing Protein	2009

Article

Year

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His.

Neurology, 2009, Aug-25, Volume: 73, Issue:8

Topics: Adenosine Triphosphatases; Aged; Aged, 80 and over; Arginine; Cell Cycle Proteins; Dementia; Female; Follow-Up Studies; Genetic Heterogeneity; Genetic Linkage; Histidine; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Pedigree; Penetrance; Prospective Studies; Valosin Containing Protein

2009

Other Studies

2 other study(ies) available for arginine and Myositis, Inclusion Body

Article	Year
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia. Muscle & nerve, 2009, Volume: 39, Issue:3 Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis; Family Health; Female; Germany; Glycine; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Valosin Containing Protein	2009
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family. Archives of neurology, 2011, Volume: 68, Issue:6 Topics: Adenosine Triphosphatases; Aged; Amino Acid Substitution; Arginine; Asian People; Cell Cycle Proteins; Cysteine; Female; Frontotemporal Dementia; Genetic Linkage; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Pedigree; Valosin Containing Protein	2011

Article

Year

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.

Muscle & nerve, 2009, Volume: 39, Issue:3

Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis; Family Health; Female; Germany; Glycine; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Valosin Containing Protein

2009

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family.

Archives of neurology, 2011, Volume: 68, Issue:6

Topics: Adenosine Triphosphatases; Aged; Amino Acid Substitution; Arginine; Asian People; Cell Cycle Proteins; Cysteine; Female; Frontotemporal Dementia; Genetic Linkage; Humans; Male; Middle Aged; Mutation, Missense; Myositis, Inclusion Body; Osteitis Deformans; Pedigree; Valosin Containing Protein

2011