tryptophan and Melanosis

tryptophan has been researched along with Melanosis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM	1
Chirio, R; Foldès, C; Launay, JM; Wallach, D	1

Other Studies

2 other study(ies) available for tryptophan and Melanosis

Article	Year
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5 Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins	2010
Congenital dyschromia with erythrocyte, platelet, and tryptophan metabolism abnormalities. Journal of the American Academy of Dermatology, 1988, Volume: 19, Issue:4 Topics: Blood Platelets; Child, Preschool; Erythrocytes; Female; Humans; Infant; Melanocytes; Melanosis; Pigmentation Disorders; Skin; Syndrome; Tryptophan	1988

Article

Year

Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5

Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins

2010

Congenital dyschromia with erythrocyte, platelet, and tryptophan metabolism abnormalities.

Journal of the American Academy of Dermatology, 1988, Volume: 19, Issue:4

Topics: Blood Platelets; Child, Preschool; Erythrocytes; Female; Humans; Infant; Melanocytes; Melanosis; Pigmentation Disorders; Skin; Syndrome; Tryptophan

1988