tecnazene has been researched along with Pregnancy in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Chaoui, R; Dittmayer, C; Englert, B; Goebel, HH; Korinth, D; Pelin, K; Rocha, ML; Rossi, R; Schlembach, D; Schmid, S; Schuelke, M; Stenzel, W; Suk, EK; Uruha, A | 1 |
Abdalla, E; Beecroft, SJ; Laing, NG; Ravenscroft, G; Zayed, L | 1 |
Chapmann, D; Chitayat, D; Chong, K; Feingold-Zadok, M; Injeyan, M; Maymon, R; Pillar, N; Reish, O; Shannon, P | 1 |
Achiron, R; Berkenstadt, M; Eisenberg-Barzilai, S; Frydman, M; Gilboa, Y; Lehtokari, VL; Mehta, L; Polak-Charcon, S; Pras, E; Reznik-Wolf, H; Wallgren-Pettersson, C; Winder, T; Yonath, H | 1 |
Fürst, DO; Osborn, M; Weber, K | 1 |
5 other study(ies) available for tecnazene and Pregnancy
Article | Year |
---|---|
A novel mutation in NEB causing foetal nemaline myopathy with arthrogryposis during early gestation.
Topics: Arthrogryposis; Female; Fetus; Gestational Age; Humans; Lebanon; Male; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Pregnancy; Ultrasonography, Prenatal | 2021 |
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin gene.
Topics: Abnormalities, Multiple; Aborted Fetus; Female; Gestational Age; Homozygote; Humans; Malignant Hyperthermia; Muscle Proteins; Mutation; Phenotype; Pregnancy; Pregnancy Complications; Skin Abnormalities | 2017 |
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita.
Topics: Abortion, Eugenic; Arthrogryposis; Fatal Outcome; Female; Genetic Testing; Humans; Infant, Newborn; Male; Muscle Proteins; Mutation; Pedigree; Pregnancy | 2017 |
Carrier state for the nebulin exon 55 deletion and abnormal prenatal ultrasound findings as potential signs of nemaline myopathy.
Topics: Adult; Codon, Nonsense; Exons; Female; Gene Deletion; Genetic Carrier Screening; Genetic Predisposition to Disease; Heterozygote; Humans; Infant, Newborn; Jews; Male; Muscle Proteins; Myopathies, Nemaline; Pedigree; Pregnancy; Ultrasonography, Prenatal | 2012 |
Myogenesis in the mouse embryo: differential onset of expression of myogenic proteins and the involvement of titin in myofibril assembly.
Topics: Actins; Animals; Cell Differentiation; Connectin; Desmin; Epitopes; Female; Fluorescent Antibody Technique; Gene Expression Regulation; Mice; Muscle Proteins; Muscles; Myosins; Pregnancy; Protein Kinases; Vimentin | 1989 |