tetraethyleneglycol dimethacrylate has been researched along with Syndrome in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ammar, D; El Fekih, N; Fazaa, B; Fischer, J; Jaafoura, H; Kamoun, MR; Kharfi, M; Schwonbeck, S; van Steensel, MA | 1 |
| Bruckner-Tuderman, L; Cosgarea, I; Franzke, CW; Has, C; Kiritsi, D; Kohlhase, J; Oji, V; Schumann, H | 1 |
| Ammar, D; El Fekih, N; Ezzine, N; Fazaa, B; Jaafoura, H; Kamoun, MR; Khaled, A; Kharfi, M | 1 |
| Garg, K; Mishra, D; Singh, D | 1 |
| Candi, E; Cassidy, AJ; McLean, WH; Melino, G; Morley, SM; Steijlen, PM; Terrinoni, A; van der Velden, J; van Geel, M; van Steensel, MA | 1 |
1 review(s) available for tetraethyleneglycol dimethacrylate and Syndrome
| Article | Year |
|---|---|
Generalized peeling skin syndrome: Case report and review of the literature.
Topics: Adult; Consanguinity; Female; Humans; Ichthyosis; Syndrome; Transglutaminases | 2010 |
4 other study(ies) available for tetraethyleneglycol dimethacrylate and Syndrome
| Article | Year |
|---|---|
A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family.
Topics: Child, Preschool; Genetic Predisposition to Disease; Humans; Male; Mutation, Missense; Skin Diseases; Syndrome; Transglutaminases; Tunisia | 2009 |
Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.
Topics: Adolescent; Adult; Blister; Case-Control Studies; Child; Child, Preschool; Diagnosis, Differential; Epidermolysis Bullosa; Erythema; Humans; Infant; Infant, Newborn; Mutation, Missense; Skin; Skin Aging; Skin Diseases; Syndrome; Transglutaminases; Young Adult | 2010 |
Peeling skin syndrome: Current status.
Topics: Child; Female; Homozygote; Humans; Hyperkeratosis, Epidermolytic; Hypoproteinemia; Immunoglobulin E; Mutation, Missense; Syndrome; Transglutaminases | 2010 |
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
Topics: Binding Sites; Catalytic Domain; Cell Line; Chromosome Mapping; Consanguinity; Cross Reactions; DNA Mutational Analysis; Epidermis; Female; Genes, Recessive; Genetic Linkage; Genetic Markers; Genetic Vectors; Haplotypes; Homozygote; Humans; Male; Microsatellite Repeats; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Pedigree; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Analysis, DNA; Skin Diseases; Syndrome; Transglutaminases | 2005 |