Compounds > lysine
Page last updated: 2024-08-17

lysine and Decreased Muscle Tone

lysine has been researched along with Decreased Muscle Tone in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ajeawung, NF; Almannai, M; Baskin, B; Bi, W; Campeau, PM; Camurri, MV; Canham, N; Cho, MT; Fu, H; Gardham, A; Kiss, C; Lehman, A; Li, L; Littlejohn, RO; MacKenzie, JJ; McKinnon, M; Nguyen, TTM; Panis, B; Parker, MJ; Potjer, TP; Potocki, L; Robak, L; Roeder, ER; Rosenfeld, JA; Rousseau, J; Ruivenkamp, C; Sacoto, MJG; Santen, GWE; Scaglia, F; Stegmann, APA; Stumpel, CTR; Xia, F; Yan, K; Yang, XJ1
Deschauer, M; Gellerich, FN; Gizatullina, Z; Knape, M; Knöppel, C; Pritsch, M; Schulze, A; Zierz, S1
Arneson, DW; Tipton, RE; Ward, JC1

Other Studies

3 other study(ies) available for lysine and Decreased Muscle Tone

ArticleYear
Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation.
    American journal of human genetics, 2017, Jan-05, Volume: 100, Issue:1

    Topics: Acetylation; Adaptor Proteins, Signal Transducing; Adolescent; Alleles; Animals; Carrier Proteins; Child; Chromatin; Developmental Disabilities; DNA-Binding Proteins; Face; Female; Histone Acetyltransferases; Histones; Humans; Intellectual Disability; Lysine; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Muscle Hypotonia; Mutation; Nuclear Proteins; Syndrome

2017
Molecular and biochemical investigations in fumarase deficiency.
    Molecular genetics and metabolism, 2006, Volume: 88, Issue:2

    Topics: Amino Acid Substitution; Cell Respiration; Child, Preschool; Fatal Outcome; Fumarate Hydratase; Fumarates; Heterozygote; Humans; Infant; Infant, Newborn; Lysine; Male; Metabolism, Inborn Errors; Mitochondria; Models, Molecular; Muscle Hypotonia; Muscle, Skeletal; Mutation; Psychomotor Disorders

2006
Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome.
    Archives of neurology, 1982, Volume: 39, Issue:11

    Topics: 2-Aminoadipic Acid; Abnormalities, Multiple; Bone and Bones; Bone Diseases; Facial Asymmetry; Female; Humans; Hypoprothrombinemias; Infant; Jaundice; Kidney Diseases; Kidney Diseases, Cystic; Liver Diseases; Lysine; Muscle Hypotonia; Pipecolic Acids; Skull; Syndrome

1982