arginine has been researched along with Congenital Poikiloderma in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hadzsiev, K; Kellermayer, R; Kestilä, M; Kosztolányi, G; Siitonen, HA | 1 |
Culler, FL; Jones, KL; Jones, M; Kaufmann, S | 1 |
2 other study(ies) available for arginine and Congenital Poikiloderma
Article | Year |
---|---|
A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.
Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine | 2005 |
Growth hormone deficiency in the Rothmund-Thomson syndrome.
Topics: Arginine; Child; Dwarfism; Female; Growth Hormone; Growth Hormone-Releasing Hormone; Humans; Insulin-Like Growth Factor I; Levodopa; Rothmund-Thomson Syndrome; Skin Diseases | 1986 |