phenylalanine and Atrophy

phenylalanine has been researched along with Atrophy in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19902 (20.00)18.7374
1990's1 (10.00)18.2507
2000's4 (40.00)29.6817
2010's2 (20.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Berg, D; Brockmann, K; Deuschle, C; Freisinger, P; Gramer, G; Haas, D; Hauser, AK; Hoffmann, GF; Leks, E; Liepelt-Scarfone, I; Maetzler, W; Padovani, A; Pilotto, A; Schaeffer, E; Scheffler, K; Schulte, C; Trefz, F; van Spronsen, FJ; Zipser, CM1
Blakely, EL; Carter, JE; de Silva, RN; Kartsounis, LD; O'Donovan, DG; Swalwell, H; Taylor, RW; Turnbull, DM; Young, TM1
Burd, NA; Dendale, P; Dirks, ML; Hansen, D; Snijders, T; van Loon, LJ; Verdijk, LB; Vranckx, P; Wall, BT1
Filosto, M; Galli, R; Mancuso, M; Murri, L; Pizzanelli, C; Siciliano, G1
Hara, K; Nishizawa, M; Onodera, O; Shimohata, T; Takado, Y; Tokiguchi, S1
Berciano, J; Combarros, O; Domínguez-Perles, R; Gallardo, E; García, A; García-Barredo, R; Illa, I; Infante, J1
Antonozzi, I; Gualdi, GF; Leuzzi, V; Trasimeni, G1
Al Saffar, BY; Bydder, GM; Chaudhuri, KR; Curati, WL; Hajnal, JV; Horrobin, DF; Mitchell, L; Puri, BK; White, SJ1
Menge, H; Robinson, JW; Schroeder, P1
Buttè, C; Giovannini, M; Longhi, R; Paccanelli, S; Riva, E; Valsasina, R1

Trials

2 trial(s) available for phenylalanine and Atrophy

ArticleYear
Neuromuscular electrical stimulation increases muscle protein synthesis in elderly type 2 diabetic men.
    American journal of physiology. Endocrinology and metabolism, 2012, Sep-01, Volume: 303, Issue:5

    Topics: Aged; Atrophy; Bed Rest; Biopsy, Needle; Carbon Isotopes; Diabetes Mellitus, Type 2; Electric Stimulation Therapy; Gene Expression Regulation; Humans; Immobilization; Kinetics; Male; Muscle Proteins; Myostatin; Neuromuscular Junction; Phenylalanine; Quadriceps Muscle; RNA, Messenger; Sarcopenia

2012
MRI changes in multiple sclerosis following treatment with lofepramine and L-phenylalanine.
    Neuroreport, 2001, Jul-03, Volume: 12, Issue:9

    Topics: Adult; Antidepressive Agents, Tricyclic; Atrophy; Cerebral Cortex; Drug Therapy, Combination; Female; Humans; Lateral Ventricles; Lofepramine; Magnetic Resonance Imaging; Male; Middle Aged; Multiple Sclerosis; Nerve Fibers, Myelinated; Phenylalanine; Treatment Outcome

2001

Other Studies

8 other study(ies) available for phenylalanine and Atrophy

ArticleYear
Phenylalanine Effects on Brain Function in Adult Phenylketonuria.
    Neurology, 2021, 01-19, Volume: 96, Issue:3

    Topics: Adult; Atrophy; Cognition; Cross-Sectional Studies; Evoked Potentials, Motor; Female; Humans; Magnetic Resonance Imaging; Male; Neuropsychological Tests; Phenylalanine; Phenylketonurias; Prospective Studies; Putamen; Thalamus

2021
Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity.
    Archives of neurology, 2010, Volume: 67, Issue:11

    Topics: Atrophy; Brain; Dementia; Disease Progression; Female; Humans; Magnetic Resonance Imaging; Middle Aged; Mitochondrial Diseases; Muscle Rigidity; Mutation; Neurodegenerative Diseases; Neuropsychological Tests; Phenylalanine; RNA, Transfer

2010
Antimyoclonic effect of levetiracetam in MERRF syndrome.
    Journal of the neurological sciences, 2006, Apr-15, Volume: 243, Issue:1-2

    Topics: Activities of Daily Living; Anticonvulsants; Atrophy; Brain; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Humans; Levetiracetam; MERRF Syndrome; Middle Aged; Mitochondria; Muscle, Skeletal; Mutation; Myoclonus; Phenylalanine; Piracetam; Quality of Life; RNA, Transfer; Treatment Outcome; Ubiquinone; Valproic Acid

2006
New mutation in the non-gigantic exon of SACS in Japanese siblings.
    Movement disorders : official journal of the Movement Disorder Society, 2007, Apr-15, Volume: 22, Issue:5

    Topics: Adult; Amino Acid Substitution; Atrophy; Cerebellum; Chromosome Aberrations; Consanguinity; Exons; Female; Gait Ataxia; Genes, Recessive; Heat-Shock Proteins; Homozygote; Humans; Leucine; Male; Middle Aged; Mutation; Phenylalanine; Sequence Analysis, DNA; Siblings

2007
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
Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patients.
    Journal of inherited metabolic disease, 1995, Volume: 18, Issue:5

    Topics: Adolescent; Adult; Atrophy; Brain; Cerebral Cortex; Child; Child, Preschool; Female; Humans; Magnetic Resonance Imaging; Male; Phenylalanine; Phenylketonurias

1995
Functional and structural correlations in the atrophic mucosa of self-emptying blind loops of rat small intestine [proceedings].
    The Journal of physiology, 1978, Volume: 280

    Topics: Animals; Atrophy; Intestinal Mucosa; Intestine, Small; Kinetics; Methylglucosides; Phenylalanine; Rats

1978
Cranial computerized tomography in dihydropteridine reductase deficiency.
    Journal of inherited metabolic disease, 1985, Volume: 8, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Basal Ganglia Diseases; Brain Diseases; Calcinosis; Developmental Disabilities; Female; Humans; Infant; NADH, NADPH Oxidoreductases; Phenylalanine; Phenylketonurias; Tomography, X-Ray Computed

1985