phenylalanine and Muscle Weakness

phenylalanine has been researched along with Muscle Weakness in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Berciano, J; Combarros, O; Domínguez-Perles, R; Gallardo, E; García, A; García-Barredo, R; Illa, I; Infante, J	1

Other Studies

1 other study(ies) available for phenylalanine and Muscle Weakness

Article	Year
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype. Journal of neurology, neurosurgery, and psychiatry, 2008, Volume: 79, Issue:2 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

Article

Year

Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.

Journal of neurology, neurosurgery, and psychiatry, 2008, Volume: 79, Issue:2

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