arginine has been researched along with Hyperkeratosis Palmaris et Plantaris in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baserer, N; Baykal, C; Emiroglu, M; Eris, H; Ghanbari, A; Hafiz, G; Tukel, T; Uyguner, O; Wollnik, B; Yuksel-Apak, M | 1 |
| Eckl, KM; Frossard, PM; Hennies, HC; Hinz, B; Leigh, IM; Lestringant, GG; Nürnberg, P; Reis, A; Stadler, R; Stevens, HP; Traupe, H; Westenberger-Treumann, M | 1 |
| Itagaki, K; Kon, A; Takagaki, K; Yoneda, K | 1 |
| Bergman, R; Kashi, Y; Keren, H; Mizrachi, M; Sprecher, E | 1 |
| Kang, HJ; Lee, ES; Lee, JH; Lee, S; Park, KB; Son, IY; Steinert, PM; Yang, JM; Yeo, UC | 1 |
5 other study(ies) available for arginine and Hyperkeratosis Palmaris et Plantaris
| Article | Year |
|---|---|
The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family.
Topics: Amino Acid Substitution; Arginine; Connexin 26; Connexins; Deafness; Female; Genes, Dominant; Glutamic Acid; Heterozygote; Humans; Keratoderma, Palmoplantar; Male; Pedigree; Point Mutation; Turkey | 2002 |
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.
Topics: Adult; Amino Acid Substitution; Antigens, Ly; Arginine; Chromosomes, Human, Pair 8; Consanguinity; Female; Genes, Recessive; Genetic Heterogeneity; Germany; Haplotypes; Homozygote; Humans; Infant; Keratoderma, Palmoplantar; Male; Mutation; Mutation, Missense; Pedigree; Point Mutation; Turkey; United Arab Emirates; Urokinase-Type Plasminogen Activator | 2003 |
A novel mutation of keratin 9 gene (R162P) in a Japanese family with epidermolytic palmoplantar keratoderma.
Topics: Arginine; Asian People; Base Sequence; Female; Heterozygote; Humans; Keratins; Keratoderma, Palmoplantar; Middle Aged; Mutation; Pedigree; Proline | 2005 |
Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1.
Topics: Arginine; Cadherins; Chromosomes, Human, Pair 18; Codon, Nonsense; Codon, Terminator; Cytosine; Desmoglein 1; Genes, Dominant; Genetic Linkage; Genotype; Haplotypes; Heterozygote; Humans; Keratoderma, Palmoplantar; Male; Microsatellite Repeats; Middle Aged; Thymine | 2005 |
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.
Topics: Arginine; Base Sequence; Child, Preschool; Conserved Sequence; Cysteine; Epidermolysis Bullosa Simplex; Female; Genes, Dominant; Genes, Recessive; Glutamic Acid; Humans; Keratins; Keratoderma, Palmoplantar; Korea; Male; Microscopy, Electron; Pedigree; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA; Tryptophan | 1998 |