Page last updated: 2024-08-18

tecnazene and Disease Exacerbation

tecnazene has been researched along with Disease Exacerbation 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's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Acker, M; Amburgey, K; Amin, R; Beggs, AH; Bönnemann, CG; Brudno, M; Constantinescu, A; Dastgir, J; Diallo, M; Dowling, JJ; Genetti, CA; Glueck, M; Hewson, S; Hum, C; Jain, MS; Lawlor, MW; Meyer, OH; Nelson, L; Saeed, S; Sultanum, N; Syed, F; Tran, T; Wang, CH1
Abe, K; Hishikawa, N; Motokura, E; Nishikawa, A; Nishino, I; Ohta, Y; Sato, K; Takahashi, Y; Takemoto, M; Tsunoda, K; Yamashita, T1
Allsop, J; Bydder, G; Chattopadhyay, A; Counsell, S; Jungbluth, H; Laing, N; Mercuri, E; Muntoni, F; North, K; Pelin, K; Sewry, CA; Wallgren-Pettersson, C1

Other Studies

3 other study(ies) available for tecnazene and Disease Exacerbation

ArticleYear
A Cross-Sectional Study of Nemaline Myopathy.
    Neurology, 2021, 03-09, Volume: 96, Issue:10

    Topics: Actins; Adolescent; Adult; Child; Child, Preschool; Cohort Studies; Cross-Sectional Studies; Disability Evaluation; Disease Progression; Enteral Nutrition; Female; Genotype; Humans; Infant; Longitudinal Studies; Male; Middle Aged; Muscle Proteins; Myopathies, Nemaline; Pilot Projects; Psychomotor Performance; Respiratory Function Tests; Sialorrhea; Tracheostomy; Treatment Outcome; Wheelchairs; Young Adult

2021
A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.
    Journal of the neurological sciences, 2017, Feb-15, Volume: 373

    Topics: Diagnosis, Differential; Disease Progression; Heterozygote; Humans; Male; Middle Aged; Muscle Proteins; Muscle Weakness; Mutation; Myopathies, Nemaline; Respiratory Insufficiency

2017
Magnetic resonance imaging of muscle in nemaline myopathy.
    Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:12

    Topics: Actins; Adolescent; Adult; Child; Child, Preschool; Diagnosis, Differential; Disease Progression; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Leg; Magnetic Resonance Imaging; Male; Muscle Proteins; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Phenotype; Predictive Value of Tests

2004