arginine has been researched along with Inferior Dislocation 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 | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ge, M; Ke, R; Lei, J; Mu, X; Tianyi, C; Yang, X | 1 |
| D'Antò, V; Esposito, L; Liguori, R; Michelotti, A; Sacchetti, L; Zagari, A | 1 |
| Hadzsiev, K; Kellermayer, R; Kestilä, M; Kosztolányi, G; Siitonen, HA | 1 |
3 other study(ies) available for arginine and Inferior Dislocation
| Article | Year |
|---|---|
The C342R mutation in FGFR2 causes Crouzon syndrome with elbow deformity.
Topics: Amino Acid Substitution; Arginine; Asian People; Child; Child, Preschool; China; Craniofacial Dysostosis; Cysteine; Elbow Joint; Female; Genetic Carrier Screening; Humans; Joint Dislocations; Male; Mutation; Olecranon Process; Phenotype; Receptor, Fibroblast Growth Factor, Type 2 | 2015 |
Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder.
Topics: Adenine; Adult; Arginine; Catechol O-Methyltransferase; Codon; Cytosine; Female; Humans; Joint Dislocations; Mutation; Neurotransmitter Agents; Pain Measurement; Range of Motion, Articular; Serine; Temporomandibular Joint Disc; Temporomandibular Joint Disorders; Temporomandibular Joint Dysfunction Syndrome | 2010 |
A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.
Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine | 2005 |