tetraethyleneglycol dimethacrylate has been researched along with Dermatitis Exfoliativa in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 6 (85.71) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Malchin, N; Malovitski, K; McGrath, J; Mohamad, J; Nanda, A; Pavlovsky, M; Peled, A; Pramanik, R; Sarig, O; Shomron, N; Sprecher, E; Weissglas-Volkov, D | 1 |
| Baty, D; Browne, F; Greenblatt, DT; Has, C; Kowalewski, C; Liu, L; McGrath, JA; Mellerio, JE; Morton, J; Moss, C; Nesteruk, D; Ozoemena, L; Szczecinska, W; Terron-Kwiatkowski, A; Wertheim-Tysarowska, K; Woźniak, K | 1 |
| Azzouzi, S; Benchat, L; Mernissi, FZ; Mikou, O; Soughi, M | 1 |
| Bruckner-Tuderman, L; Has, C; Kiritsi, D; Mileounis, K; Valari, M | 1 |
| Bowden, PE | 1 |
| Hamm, H; Jonkman, MF; McLean, WH; Steijlen, PM; van der Velden, JJ; van Geel, M; van Steensel, MA | 1 |
| Aho, H; Bruckner-Tuderman, L; Cobzaru, C; Faletra, F; Has, C; Kern, JS; Kiritsi, D; Mäkelä, L; Pigors, M; Schwieger-Briel, A; Suárez, J | 1 |
1 review(s) available for tetraethyleneglycol dimethacrylate and Dermatitis Exfoliativa
| Article | Year |
|---|---|
'Double trouble': diagnostic challenges in genetic skin disorders.
Topics: Anodontia; Breast; Child; Dermatitis, Exfoliative; Ectodermal Dysplasia; Female; Heterozygote; Humans; Lacrimal Duct Obstruction; Limb Deformities, Congenital; Male; Mutation; Nails, Malformed; Pigmentation Disorders; Skin Diseases; Transcription Factors; Transglutaminases; Tumor Suppressor Proteins | 2015 |
6 other study(ies) available for tetraethyleneglycol dimethacrylate and Dermatitis Exfoliativa
| Article | Year |
|---|---|
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.
Topics: Cell Adhesion; Cells, Cultured; Child; Dermatitis, Exfoliative; DNA Mutational Analysis; Epidermal Cells; Exome Sequencing; Female; Foot Dermatoses; Hand Dermatoses; Heterozygote; Homozygote; Humans; Ichthyosis, Lamellar; Lipoxygenase; Male; Pedigree; Phenotype; Primary Cell Culture; Skin Diseases, Genetic; Transglutaminases | 2020 |
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations.
Topics: Child; Dermatitis, Exfoliative; Diagnosis, Differential; Epidermolysis Bullosa Simplex; Founder Effect; Genetic Testing; Germany; Heterozygote; Homozygote; Humans; Keratin-14; Keratin-5; Mutation; Pigmentation Disorders; Poland; Skin Diseases; Transglutaminases; United Kingdom | 2014 |
[Acral peeling skin syndrome].
Topics: Administration, Cutaneous; Biomarkers; Child; Child, Preschool; Dermatitis, Exfoliative; Education, Medical, Continuing; Emollients; Female; Foot; Hand; Humans; Hyperhidrosis; Male; Mutation; Pigmentation Disorders; Siblings; Skin Diseases; Transglutaminases | 2014 |
Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis.
Topics: Dermatitis, Exfoliative; Diagnosis, Differential; Glycoproteins; Humans; Intercellular Signaling Peptides and Proteins; Mutation, Missense; Pigmentation Disorders; Skin Diseases; Transglutaminases | 2011 |
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome.
Topics: Dermatitis, Exfoliative; DNA Mutational Analysis; Europe; Family Health; Haplotypes; Homozygote; Humans; Models, Genetic; Mutation; Pigmentation Disorders; Skin Diseases; Skin Diseases, Vesiculobullous; Transglutaminases | 2012 |
TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome.
Topics: Adult; Biopsy; Case-Control Studies; Cell Differentiation; Cells, Cultured; Child; Child, Preschool; Dermatitis, Exfoliative; Epidermis; Glycoproteins; Humans; Infant; Intercellular Signaling Peptides and Proteins; Keratin-1; Keratin-10; Keratinocytes; Mutation; Pigmentation Disorders; Protein Precursors; Skin Diseases; Transglutaminases | 2012 |