histidine has been researched along with Muscle Weakness in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (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 |
| Adachi, Y; Kumada, H; Kusumi, M; Nakashima, K | 1 |
2 other study(ies) available for histidine and Muscle Weakness
| 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 |
Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis.
Topics: Adult; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Child; Codon; Female; Histidine; Humans; Hypokalemic Periodic Paralysis; Male; Muscle Weakness; Pedigree; Point Mutation | 2001 |