tyrosine and Myopathies, Nemaline

tyrosine has been researched along with Myopathies, Nemaline in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's3 (42.86)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bendahan, D; Bryson-Richardson, RJ; Gineste, C; Gondin, J; Hahne, D; Laing, NG; McNamara, EL; Messineo, AM; Nowak, KJ; Ogier, AC; Sztal, TE; Vilmen, C1
Bidev, D; Oguz, SS; Okur, N; Oncel, MY; Sahin, S; Talim, B1
Domazetovska, A; Gunning, PW; Hardeman, EC; Hook, JW; Joya, JE; Kee, AJ; Kettle, E; Lemckert, FA; Mitchell, CA; Nguyen, MA; North, KN; Robinson, PJ; Valova, VA; Yang, N1
Laing, NG; Wallgren-Pettersson, C1
Appleton, RE; Barois, A; Childs, AM; Clement, S; Dobbie, JA; Jayawant, SS; Laing, NG; Mountford, RC; Muntoni, F; Navarro, C; Nowak, KJ; Reina, C; Ricoy, JR; Romero, NB; Sewry, CA; Squier, W; Walker, KR1
Ellaway, C; Iannaccone, ST; Ketteridge, D; Kornberg, AJ; North, KN; Roddick, LG; Rudge, S; Ryan, MM; Sy, C1
Healy, JM; Keating, KE; Krivosic, I; Krivosic-Horber, R; Lunardi, J; Manning, BM; McCarthy, TV; Monnier, N; Quane, KA1

Reviews

1 review(s) available for tyrosine and Myopathies, Nemaline

ArticleYear
109th ENMC International Workshop: 5th workshop on nemaline myopathy, 11th-13th October 2002, Naarden, The Netherlands.
    Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:6

    Topics: Animals; Clinical Trials as Topic; Humans; Myopathies, Nemaline; Tyrosine

2003

Other Studies

6 other study(ies) available for tyrosine and Myopathies, Nemaline

ArticleYear
L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy.
    Scientific reports, 2018, 07-31, Volume: 8, Issue:1

    Topics: Actins; Animals; Dietary Supplements; Disease Models, Animal; Energy Metabolism; Female; Male; Mice; Mice, Inbred C57BL; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Tyrosine; Zebrafish

2018
[Nemaline rod myopathy treated with L-tyrosine to relieve symptoms in a neonate].
    Archivos argentinos de pediatria, 2019, 08-01, Volume: 117, Issue:4

    Topics: Female; Humans; Infant, Newborn; Muscle Hypotonia; Myopathies, Nemaline; Sialorrhea; Treatment Outcome; Tyrosine

2019
Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy.
    Brain : a journal of neurology, 2011, Volume: 134, Issue:Pt 12

    Topics: Animals; Disease Models, Animal; Hand Strength; Hypertrophy; Mice; Mice, Transgenic; Muscle Contraction; Muscle Weakness; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Phenotype; Tyrosine

2011
Nemaline myopathy caused by absence of alpha-skeletal muscle actin.
    Annals of neurology, 2007, Volume: 61, Issue:2

    Topics: Actins; Arginine; Aspartic Acid; Blotting, Western; Child, Preschool; Homozygote; Humans; Immunohistochemistry; Infant; Male; Microscopy, Electron; Muscle, Skeletal; Mutation; Myocardium; Myopathies, Nemaline; Tyrosine

2007
Dietary L-tyrosine supplementation in nemaline myopathy.
    Journal of child neurology, 2008, Volume: 23, Issue:6

    Topics: Adolescent; Appetite; Biopsy; Child, Preschool; Chromosomes, Human, Pair 1; Dietary Supplements; Dose-Response Relationship, Drug; Female; Follow-Up Studies; Humans; Infant; Infant, Newborn; Male; Microscopy, Electron; Muscle Strength; Muscle, Skeletal; Mutation, Missense; Myopathies, Nemaline; Phenotype; Sialorrhea; Treatment Outcome; Tropomyosin; Tyrosine; Weight Gain

2008
Mutation screening of the RYR1 gene in malignant hyperthermia: detection of a novel Tyr to Ser mutation in a pedigree with associated central cores.
    Genomics, 1994, Sep-01, Volume: 23, Issue:1

    Topics: Amino Acid Sequence; Base Sequence; Calcium Channels; Cardiomyopathy, Hypertrophic; Chromosomes, Human, Pair 19; DNA Mutational Analysis; Female; Genes; Genetic Linkage; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Malignant Hyperthermia; Molecular Sequence Data; Muscle Proteins; Myopathies, Nemaline; Pedigree; Point Mutation; Polymorphism, Single-Stranded Conformational; Ryanodine Receptor Calcium Release Channel; Serine; Tyrosine

1994