arginine has been researched along with Collodion Baby Syndrome in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akiyama, M; Suga, Y; Sugiura, K | 1 |
| Akiyama, M; Arita, K; Chaplin, T; Happle, R; Jacyk, WK; McGrath, JA; Mein, CA; Shimizu, H; van Rensburg, EJ; Wessagowit, V | 1 |
2 other study(ies) available for arginine and Collodion Baby Syndrome
| Article | Year |
|---|---|
Very mild lamellar ichthyosis with compound heterozygous TGM1 mutations including the novel missense mutation p.Leu693Phe.
Topics: Amino Acid Sequence; Arginine; Base Sequence; DNA Mutational Analysis; Heterozygote; Humans; Ichthyosis, Lamellar; Infant; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Male; Molecular Sequence Data; Mutation; Mutation, Missense; Phenylalanine; Prognosis; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Transglutaminases | 2013 |
The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1.
Topics: Adolescent; Adult; Arginine; Child; Female; Homozygote; Humans; Ichthyosis, Lamellar; Leucine; Male; Mutation, Missense; South Africa; Transglutaminases | 2007 |