tyrosine has been researched along with Keratoderma Blennorrhagicum in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 12 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (13.33) | 29.6817 |
| 2010's | 1 (6.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bau, AE; de Zwart-Storm, EA; Foelster-Holst, R; Frank, J; Graziadio, C; Kamps, MA; Martin, PE; Paskulin, GA; Rosa, RF; van Geel, M; van Steensel, MA; Zen, PR | 1 |
| Aydin, OF; Eken, A; Kunak, B; Tezic, T; Zorlu, P | 1 |
| Baden, HP; Hooker, PA | 1 |
| De Giacomoni, P; Larrègue, M; Odièvre, P; Prigent, F | 1 |
| Hinkle, D; Hummel, MB; Macsai, MS; Mulhern, MG; Rootman, D; Schwartz, TL | 1 |
| Bressieux, JM; de Giacomoni, P; Larrègue, M; Odièvre, M | 1 |
| D'Hermies, F; Dufier, JL; Foels, MO; Gounod, N; Pouliquen, Y; Renard, G | 1 |
| Beckenkamp, G; Sayar, RB; Schäfer, HJ; von Domarus, D | 1 |
| Irons, M; Levy, HL | 1 |
| Archard, HO; Tarpley, TM | 1 |
| Shklar, G | 1 |
| Dogliotti, M | 1 |
| Baden, HP; Bienfang, DC; Gerald, P; Goldsmith, LA; Jimbow, K; Kang, E | 1 |
| Hill, A; Kushniruk, W; Zaleski, WA | 1 |
| Gold, MB; Reynold, JM; Scriver, CR | 1 |
2 review(s) available for tyrosine and Keratoderma Blennorrhagicum
| Article | Year |
|---|---|
Advances in genetics in dermatology.
Topics: Acrodermatitis; Amino Acid Metabolism, Inborn Errors; Basal Cell Nevus Syndrome; Epidermolysis Bullosa; Hair Diseases; Humans; Ichthyosis; Keratins; Keratosis; Neurofibromatosis 1; Psoriasis; Refsum Disease; Skin; Skin Diseases; Skin Neoplasms; Tuberous Sclerosis; Tyrosine; Warts; Xeroderma Pigmentosum | 1982 |
Metabolic syndromes with dermatologic manifestations.
Topics: Albinism; Alkaptonuria; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biotinidase; Carbohydrate Metabolism; Eczema; Hartnup Disease; Homocystinuria; Humans; Keratosis; Menkes Kinky Hair Syndrome; Metabolic Diseases; Phenylketonurias; Porphyrias; Skin Diseases; Steryl-Sulfatase; Sulfatases; Tyrosine; Urea | 1986 |
13 other study(ies) available for tyrosine and Keratoderma Blennorrhagicum
| Article | Year |
|---|---|
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes.
Topics: Adult; Asparagine; Aspartic Acid; Cell Membrane; Child; Connexin 26; Connexins; Cytoplasm; Endoplasmic Reticulum; Female; Fluoresceins; Gap Junctions; Hearing Loss; HeLa Cells; Humans; Hypertrichosis; Keratoderma, Palmoplantar; Keratosis; Lysine; Male; Mutation, Missense; Nails, Malformed; Protein Transport; Skin; Skin Diseases; Syndrome; Transfection; Tyrosine | 2011 |
Two siblings with tyrosinaemia type 2.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Conjunctivitis; Diagnosis, Differential; Female; Foot Dermatoses; Humans; Keratosis; Male; Photophobia; Syndrome; Tyrosine | 2003 |
[Changes in the keratinocytes in oculo-cutaneous tyrosinosis: Richner-Hanhart syndrome (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Cornea; Epidermis; Female; Humans; Infant; Keratitis, Dendritic; Keratosis; Mitochondria; Rats; Tyrosine | 1980 |
Tyrosinemia type II: nine cases of ocular signs and symptoms.
Topics: Child; Child, Preschool; Cornea; Diet, Protein-Restricted; Female; Humans; Infant; Keratitis; Keratosis; Male; Mental Disorders; Tyrosine; Tyrosinemias; Visual Acuity | 2001 |
[Richner-Hanhart's syndrome or oculo-cutaneous tyrosinosis (about one case) (author's transl)].
Topics: Child, Preschool; Female; Humans; Infant; Intellectual Disability; Keratitis, Dendritic; Keratosis; Syndrome; Tongue Diseases; Transaminases; Tyrosine | 1979 |
[Type II oculo-cutaneous tyrosinosis or Richner-Hanhart syndrome--apropos of a case].
Topics: Amino Acid Metabolism, Inborn Errors; Corneal Ulcer; Diagnostic Errors; Female; Humans; Infant; Keratitis, Dendritic; Keratosis; Syndrome; Tyrosine; Tyrosine Transaminase | 1989 |
Clinical picture and problems of keratoplasty in Richner-Hanhart syndrome (tyrosinemia type II).
Topics: Amino Acid Metabolism, Inborn Errors; Cornea; Corneal Opacity; Corneal Transplantation; Cortisone; Female; Foot Dermatoses; Hand Dermatoses; Humans; Keratosis; Microscopy, Electron; Middle Aged; Tyrosine | 1988 |
Clinicopathologic and histochemical characterization of submucosal deposits in snuff dipper's keratosis.
Topics: Adult; Amyloid; Carbohydrates; Eosinophils; Histocytochemistry; Humans; Keratosis; Male; Middle Aged; Mouth Diseases; Mouth Mucosa; Nicotiana; Plants, Toxic; Staining and Labeling; Tryptophan; Tyrosine | 1972 |
Patterns of keratinization in oral leukoplakia.
Topics: Histocytochemistry; Humans; Keratosis; Leukoplakia; Mouth Diseases; Mouth Mucosa; Staining and Labeling; Sulfhydryl Compounds; Tyrosine | 1968 |
Actinic keratoses in Bantu albinos. Clinical experiences with the topical use of 5-fluoro-uracil.
Topics: Adult; Albinism; Carcinoma, Basal Cell; Carcinoma, Squamous Cell; Catechol Oxidase; Child; Female; Fluorouracil; Humans; Keratosis; Male; Middle Aged; Ointments; Skin Neoplasms; Sunlight; Tyrosine | 1973 |
Tyrosinemia with plantar and palmar keratosis and keratitis.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Consanguinity; Diet Therapy; Female; Foot Dermatoses; Growth Disorders; Hand Dermatoses; Humans; Intellectual Disability; Keratitis; Keratoderma, Palmoplantar; Keratosis; Male; Microscopy, Electron; Phenylacetates; Phenylpyruvic Acids; Renal Aminoacidurias; Tyrosine | 1973 |
Skin lesions in tyrosinosis: response to dietary treatment.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Biopsy; Cytoplasm; Diet Therapy; Edema; Eosinophils; Erythema; Female; Fingers; Foot; Humans; Intellectual Disability; Keratosis; Tyrosine | 1973 |
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
Topics: Ectodermal Dysplasia; Genes, Dominant; Hair; Humans; Keratosis; Nails, Malformed; Phenylalanine; Proline; Serine; Sulfur; Tyrosine; Urea; Water | 1971 |