Page last updated: 2024-08-17

histidine and Inclusion Body Myopathy, Sporadic

histidine has been researched along with Inclusion Body Myopathy, Sporadic 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	3 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I	1
Asaka, T; Hirohata, M; Komai, K; Motozaki, Y; Ono, K; Yamada, M	1

Trials

1 trial(s) available for histidine and Inclusion Body Myopathy, Sporadic

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 histidine and Inclusion Body Myopathy, Sporadic

Article	Year
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5 Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia	2005
Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy. European journal of neurology, 2007, Volume: 14, Issue:9 Topics: Adult; Creatine Kinase; Genetic Predisposition to Disease; Histidine; Humans; Leg; Male; Multienzyme Complexes; Mutation; Myelitis, Transverse; Myositis, Inclusion Body; Proline	2007

Article

Year

Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.

Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5

Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia

2005

Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy.

European journal of neurology, 2007, Volume: 14, Issue:9

Topics: Adult; Creatine Kinase; Genetic Predisposition to Disease; Histidine; Humans; Leg; Male; Multienzyme Complexes; Mutation; Myelitis, Transverse; Myositis, Inclusion Body; Proline

2007