histidine has been researched along with Myopathies, Nemaline in 3 studies
| 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 | Studies |
|---|---|
| Durling, HJ; Gunning, P; Laing, NG; Lochmüller, H; Mendel, B; Müller-Höcker, J; Pongratz, D; Reilich, P; Wallgren-Pettersson, C | 1 |
| Dubas, F; Laing, N; Monnier, N; Pénisson-Besnier, I; Toutain, A | 1 |
| Ilkovski, B; Koy, A; Laing, N; Mayatepek, E; Neuen-Jacob, E; North, K; Voit, T; Weis, J | 1 |
3 other study(ies) available for histidine and Myopathies, Nemaline
| Article | Year |
|---|---|
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy.
Topics: Adenosine Triphosphatases; Adolescent; Arginine; DNA Mutational Analysis; Drosophila Proteins; Exons; Female; Genetic Carrier Screening; Histidine; Humans; Muscle Fibers, Skeletal; Muscle Weakness; Mutation, Missense; Myopathies, Nemaline; Tropomyosin | 2002 |
A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
Topics: Adolescent; Adult; Arginine; Family Health; Female; Histidine; Humans; Male; Microscopy, Electron, Transmission; Middle Aged; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Pedigree; Tropomyosin | 2007 |
Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H).
Topics: Actins; DNA Mutational Analysis; Female; Glutamine; Histidine; Humans; Infant; Intranuclear Inclusion Bodies; Microscopy, Electron, Transmission; Models, Molecular; Muscle, Skeletal; Mutation; Myopathies, Nemaline | 2007 |