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nad and Limb-Girdle Muscular Dystrophies

nad has been researched along with Limb-Girdle Muscular Dystrophies in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antonini, G; Bertini, ES; Bortolotti, CA; Brochier, G; Di Rocco, G; Fattori, F; Garibaldi, M; Gibellini, L; Labasse, C; Paradas, C; Pennisi, EM; Pinti, M; Raffa, S; Romero, NB; Servian-Morilla, E; Verardo, M1
Abramov, AY; Bartolome, F; Burchell, VS; Calvo, A; Canosa, A; Chiò, A; Fox, NC; Hardy, J; Houlden, H; Mahoney, CJ; Mandrioli, J; Moglia, C; Orrell, RW; Plun-Favreau, H; Preza, E; Wray, S; Wu, HC1
Hayashi, YK; Matsuda, C; Minami, N; Mitsuhashi, H; Nishino, I; Noguchi, S; Nonaka, I; Shalaby, S1
Chrobáková, T; Fajkusová, L; Hermanová, M; Kroupová, I; Letocha, O; Maríková, T; Mazanec, R; Sedlácková, J; Vohánka, S; Vondrácek, P; Zámecník, J; Zapletalová, E1

Other Studies

4 other study(ies) available for nad and Limb-Girdle Muscular Dystrophies

ArticleYear
Core-rod myopathy due to a novel mutation in BTB/POZ domain of KBTBD13 manifesting as late onset LGMD.
    Acta neuropathologica communications, 2018, 09-13, Volume: 6, Issue:1

    Topics: Aged; BTB-POZ Domain; Creatine Kinase; Green Fluorescent Proteins; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Models, Molecular; Muscle Proteins; Muscle, Skeletal; Muscular Dystrophies, Limb-Girdle; Mutation; NAD; Tomography Scanners, X-Ray Computed

2018
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels.
    Neuron, 2013, Apr-10, Volume: 78, Issue:1

    Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Adult; Aged; Analysis of Variance; Animals; Animals, Newborn; Case-Control Studies; Cell Cycle Proteins; Cells, Cultured; Cerebral Cortex; Family Health; Female; Fibroblasts; Frontotemporal Dementia; Humans; Lipid Peroxidation; Luminescent Proteins; Magnesium; Male; Membrane Potential, Mitochondrial; Mice; Mice, Inbred C57BL; Middle Aged; Mitochondria; Muscular Dystrophies, Limb-Girdle; Mutation; Myositis, Inclusion Body; NAD; Neuroblastoma; Neurons; Osteitis Deformans; Oxygen Consumption; RNA, Small Interfering; Transfection; Valosin Containing Protein

2013
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient.
    Journal of neuropathology and experimental neurology, 2009, Volume: 68, Issue:6

    Topics: Actinin; Animals; Arginine; Chlorocebus aethiops; Connectin; COS Cells; Cytoskeletal Proteins; DNA Mutational Analysis; Exons; Female; Humans; Immunoprecipitation; Japan; Lysine; Male; Microfilament Proteins; Middle Aged; Molecular Sequence Data; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; NAD; Protein Structure, Tertiary; Serine; Transfection; Two-Hybrid System Techniques

2009
Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients.
    Muscle & nerve, 2006, Volume: 33, Issue:3

    Topics: Adolescent; Adult; Alleles; Calpain; Child; Child, Preschool; Chromatography, High Pressure Liquid; Czech Republic; DNA Mutational Analysis; Dysferlin; Female; Fluorescent Antibody Technique; Genotype; Humans; Immunohistochemistry; Isoenzymes; Male; Membrane Proteins; Middle Aged; Muscle Proteins; Muscle, Skeletal; Muscular Dystrophies, Limb-Girdle; NAD; Nerve Tissue Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

2006