phenylalanine has been researched along with Muscle Disorders in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (66.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Antozzi, C; Brancati, F; D Apice, MR; Federici, L; Maggi, L; Marshall, CR; Massa, R; Minassian, BA; Mora, M; Morandi, L; Novelli, G; Pasanisi, MB; Ruggieri, A; Sangiuolo, F; Saredi, S; Scherer, SW; Terracciano, C; Zanotti, S | 1 |
| Arima, M; Chui, DH; Kotorii, S; Santa, Y; Tabira, T; Takahashi, K; Uyama, E | 1 |
| Bönnemann, CG; Brune, T; Denecke, J; Feuer, A; Ketelsen, UP; Kirschner, J; Korinthenberg, R; Marquardt, T; Wasner, C; Wehnert, M; Wieacker, P | 1 |
| Chinkes, DL; Gore, DC; Wolfe, RR | 1 |
| Berciano, J; Combarros, O; Domínguez-Perles, R; Gallardo, E; García, A; García-Barredo, R; Illa, I; Infante, J | 1 |
| Kar, NC; Pearson, CM | 1 |
6 other study(ies) available for phenylalanine and Muscle Disorders
| Article | Year |
|---|---|
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy.
Topics: Adult; Aged; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; HSP40 Heat-Shock Proteins; HSP70 Heat-Shock Proteins; Humans; Italy; Male; Middle Aged; Models, Molecular; Molecular Chaperones; Muscular Diseases; Mutation, Missense; Nerve Tissue Proteins; Phenylalanine; Tomography Scanners, X-Ray Computed; Valine; Young Adult | 2015 |
Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
Topics: Age of Onset; Arginine; Arteries; Brain; Cerebral Arterial Diseases; Cerebral Infarction; Cysteine; DNA Mutational Analysis; Family Health; Female; Humans; Immunohistochemistry; Japan; Lysine; Magnetic Resonance Imaging; Male; Microscopy, Electron; Muscular Diseases; Mutation; Phenylalanine; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2003 |
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria.
Topics: Blotting, Western; Child; DNA Mutational Analysis; Female; Humans; Lamin Type A; Muscles; Muscular Diseases; Mutation, Missense; Phenylalanine; Progeria; Serine; Staining and Labeling | 2005 |
Quantification of amino acid transport through interstitial fluid: assessment of four-compartment modeling for muscle protein kinetics.
Topics: Adult; Amino Acids; Biological Transport; Cell Compartmentation; Critical Illness; Extracellular Fluid; Humans; Leg; Metabolism; Middle Aged; Models, Biological; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Phenylalanine; Regional Blood Flow; Sepsis | 2007 |
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
Topics: Adipose Tissue; Adult; Aged; Amino Acid Substitution; Atrophy; Biopsy; Chromosome Aberrations; Codon; Connectin; Creatine Kinase; Cytoskeletal Proteins; DNA Mutational Analysis; Electromyography; Exons; Female; Genes, Dominant; Genetic Carrier Screening; Humans; Leg; Magnetic Resonance Imaging; Male; Microfilament Proteins; Middle Aged; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Muscular Atrophy; Muscular Diseases; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Neurologic Examination; Pedigree; Phenotype; Phenylalanine; Serine | 2008 |
Acetyl-DL-phenylalanine beta-naphthyl esterase activity in human muscle disease.
Topics: Adolescent; Adult; Aged; Carboxylic Ester Hydrolases; Child; Child, Preschool; Esterases; Humans; Hydrogen-Ion Concentration; Hydrolysis; Middle Aged; Muscles; Muscular Diseases; Neuromuscular Diseases; Phenylalanine; Substrate Specificity | 1978 |