Compounds > threonine

threonine and Muscular Dystrophy

threonine has been researched along with Muscular Dystrophy in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19905 (62.50)18.7374
1990's1 (12.50)18.2507
2000's1 (12.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Deschauer, M; Kraya, T; Kress, W; Stoevesant, D; Zierz, S1
Aksmanovic, VM; Bagshaw, J; Coomber, E; Ellis, JA; Kendrick-Jones, J; McMahon, R; Morrison, PJ; Whittaker, JL; Yates, JR1
Bartoloni, L; Carpen, O; Dancel, R; Gaskell, PC; Gilbert, JR; Gilchrist, JM; Hauser, MA; Horrigan, SK; Pericak-Vance, MA; Salmikangas, P; Speer, MC; Stajich, JM; Taivainen, A; Tim, RW; Torian, UM; Vance, JM; Viles, KD; Westbrook, CA1
Hurwitz, LJ; McCormick, D2
Gusev, EI1
Nakahara, M; Yamada, S1
Gross, S; Maskaleris, ML; Milhorat, AT1

Other Studies

8 other study(ies) available for threonine and Muscular Dystrophy

ArticleYear
[Myofibrillary myopathy due to the ZASP mutation Ala147Thr : two cases with exclusively distal leg involvement].
    Der Nervenarzt, 2013, Volume: 84, Issue:2

    Topics: Adaptor Proteins, Signal Transducing; Aged; Alanine; Biopsy; Distal Myopathies; DNA Mutational Analysis; Female; Genetic Carrier Screening; Humans; LIM Domain Proteins; Magnetic Resonance Imaging; Muscle Weakness; Muscle, Skeletal; Muscular Dystrophies; Neurologic Examination; Phenotype; Threonine

2013
Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype.
    Neuromuscular disorders : NMD, 1999, Volume: 9, Issue:3

    Topics: Amino Acid Substitution; DNA; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; Genotype; Humans; Male; Membrane Proteins; Muscular Dystrophies; Muscular Dystrophy, Emery-Dreifuss; Mutation, Missense; Nuclear Proteins; Pedigree; Phenotype; Proline; Threonine; Thymopoietins; X Chromosome

1999
Myotilin is mutated in limb girdle muscular dystrophy 1A.
    Human molecular genetics, 2000, Sep-01, Volume: 9, Issue:14

    Topics: Actinin; Adult; Alleles; Amino Acid Sequence; Animals; Blotting, Western; Cell Nucleus; Chromatography, High Pressure Liquid; Chromosomes, Human, Pair 5; Connectin; Conserved Sequence; Cytoskeletal Proteins; Expressed Sequence Tags; Female; Genes, Dominant; Humans; Immunohistochemistry; Isoleucine; Male; Mice; Microfilament Proteins; Microscopy, Electron; Molecular Sequence Data; Muscle Proteins; Muscular Dystrophies; Mutation; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Protein Binding; Sequence Analysis, DNA; Threonine; Transcription, Genetic; Two-Hybrid System Techniques

2000
Muscular dystrophy in Northern Ireland. Paper chromatographic survey of urinary aminoacids.
    Irish journal of medical science, 1971, Volume: 140, Issue:12

    Topics: Amino Acids; Chromatography, Paper; Female; Humans; Male; Muscular Dystrophies; Northern Ireland; Threonine

1971
Paper chromatographic survey of urinary amino-acids in muscular dystrophy.
    British medical journal, 1970, Jul-04, Volume: 3, Issue:5713

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Chromatography, Paper; Female; Histidine; Humans; Lysine; Male; Middle Aged; Muscular Dystrophies; Threonine

1970
[Hyperaminoaciduria in children suffering from progressive muscular dystrophy].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1967, Volume: 67, Issue:7

    Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Child; Child, Preschool; Creatine; Creatinine; Female; Glutamates; Histidine; Humans; Leucine; Lysine; Male; Methionine; Muscular Dystrophies; Nitrogen; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine; Valine

1967
Studies on progressive muscular dystrophy. IV. Effects of original amino acids mixture on progressive muscular dystrophy.
    Arzneimittel-Forschung, 1967, Volume: 17, Issue:6

    Topics: Adenosine Triphosphate; Adolescent; Adult; Amino Acids; Arginine; Asparagine; Aspartic Acid; Blood Proteins; Child; Deficiency Diseases; Glutamates; Glycine; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Methionine; Muscles; Muscular Dystrophies; Phenylalanine; Threonine; Tryptophan; Tyrosine; Valine

1967
Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer.
    Clinical chemistry, 1969, Volume: 15, Issue:7

    Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Autoanalysis; Child; Child, Preschool; Glutamates; Glycine; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Muscular Dystrophies; Peptides; Phenylalanine; Serine; Threonine; Tyrosine; Valine

1969