Page last updated: 2024-08-23

heme and Muscular Weakness

heme has been researched along with Muscular Weakness in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bisceglie, L; Braren, R; Gehrig, P; Hopp, AK; Hottiger, MO; Koch-Nolte, F; Leutert, M; Li, H; Menzel, S; Nowak, K; Rissiek, B; Zolkiewska, A1
Baiges, JJ; Bassez, G; Battistuzzi, G; Bellei, M; Benseny-Cases, N; Borsari, M; Bortolotti, CA; Cabrera-Serrano, M; Cladera, J; Claeys, KG; Clemente, P; Di Rocco, G; Edström, L; Engvall, M; Ferrer, I; Forrest, ARR; Freyer, C; Goris, A; Hofbauer, S; Hool, LC; Jiang, H; Jiao, H; Kere, J; Lagerstedt-Robinson, K; Laing, NG; Lambrughi, M; Lammens, M; Malfatti, E; Miralles, F; Obinger, C; Olivé, M; Pignataro, M; Ravenscroft, G; Romero, NB; Sejersen, T; Straathof, CSM; Streichenberger, N; Udd, B; Vial, C; Vidal, N; Viola, HM; Wedell, A; Wredenberg, A; Xiang, F1
Kasap, B; Kavukcu, S; Soylu, A; Türkmen, M1

Other Studies

3 other study(ies) available for heme and Muscular Weakness

ArticleYear
Proteomic Characterization of the Heart and Skeletal Muscle Reveals Widespread Arginine ADP-Ribosylation by the ARTC1 Ectoenzyme.
    Cell reports, 2018, 08-14, Volume: 24, Issue:7

    Topics: ADP Ribose Transferases; ADP-Ribosylation; Animals; Arginine; Carrier Proteins; Cell Line; Gene Ontology; Heme; Hemopexin; Isoenzymes; Male; Membrane Proteins; Mice; Mice, Knockout; Molecular Sequence Annotation; Muscle Fibers, Skeletal; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Myocardium; Protein Binding; Protein Processing, Post-Translational; Proteome; Proteomics; Signal Transduction

2018
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.
    Nature communications, 2019, 03-27, Volume: 10, Issue:1

    Topics: Adult; Female; Heart Failure; Heme; Humans; Inclusion Bodies; Male; Middle Aged; Muscle Fibers, Skeletal; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Mutation; Myocytes, Cardiac; Myoglobin; Oxygen; Pedigree; Respiratory Insufficiency; Superoxides; Tomography, X-Ray Computed; White People

2019
An adolescent girl with Meyer-Betz syndrome.
    Clinical rheumatology, 2006, Volume: 25, Issue:6

    Topics: Adolescent; Female; Follow-Up Studies; Heme; Humans; Leg; Muscle Weakness; Muscular Diseases; Myoglobinuria; Pain; Physical Exertion; Rhabdomyolysis; Syndrome

2006