arginine has been researched along with Decreased Muscle Tone in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Groeneweg, S; Lima de Souza, EC; Meima, ME; Peeters, RP; Visser, TJ; Visser, WE | 1 |
| Birnbaum, R; Gur, H; Kidron, D; Lerman-Sagie, T; Lev, D; Malinger, G; Yanoov-Sharav, M; Yosha-Orpaz, N; Yosovich, K | 1 |
| Briand, G; Cheillan, D; Feillet, F; Montaut-Verient, B; Schmitt, E; Sorlin, A; Wiedemann, A | 1 |
| Clark, RD; Friez, MJ; Graham, JM; Jones, JR; Joseph, SM; May, M; Moeschler, JB; Opitz, JM; Peiffer, AP; Risheg, H; Rogers, RC; Schwartz, CE; Stevenson, RE | 1 |
4 other study(ies) available for arginine and Decreased Muscle Tone
| Article | Year |
|---|---|
Outward-Open Model of Thyroid Hormone Transporter Monocarboxylate Transporter 8 Provides Novel Structural and Functional Insights.
Topics: Animals; Arginine; Binding Sites; Biological Transport; Cell Line; Chlorocebus aethiops; COS Cells; Histidine; Humans; Mental Retardation, X-Linked; Models, Molecular; Molecular Structure; Monocarboxylic Acid Transporters; Muscle Hypotonia; Muscular Atrophy; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Symporters; Thyroid Hormones; Transfection; Triiodothyronine | 2017 |
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.
Topics: Arginine; Astrocytoma; Brachydactyly; Developmental Disabilities; Female; Fetal Growth Retardation; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Methylation; Muscle Hypotonia; Mutation; Orbital Neoplasms; Pregnancy; Protein-Arginine N-Methyltransferases | 2019 |
Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency.
Topics: Alanine Transaminase; Arginine; Aspartate Aminotransferases; Child; Child, Preschool; Deafness; Developmental Disabilities; Fatty Acids; Female; Humans; Infant; Membrane Proteins; Muscle Hypotonia; Peroxisomal Disorders; Phytanic Acid; Pipecolic Acids; Sialorrhea | 2016 |
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.
Topics: Amino Acid Substitution; Arginine; Family; Female; Genetic Diseases, X-Linked; Humans; Intellectual Disability; Male; Mediator Complex; Muscle Hypotonia; Mutation; Pedigree; Receptors, Thyroid Hormone; Syndrome; Tryptophan | 2007 |