tyrosine has been researched along with Hyperkeratosis Palmaris et Plantaris in 38 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 26 (68.42) | 18.7374 |
1990's | 8 (21.05) | 18.2507 |
2000's | 1 (2.63) | 29.6817 |
2010's | 3 (7.89) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Arnoux, JB; Aubin, F; Blanc, D; Locatelli, F; Puzenat, E | 1 |
Abbott, J; Mohite, AA | 1 |
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 |
Audebert, S; Bouadjar, B; Cure, S; Fischer, J; Has, C; Hohl, D; Jobard, F; Lefèvre, C; Marrakchi, S; Morlot, S; Munro, C; Prud'homme, JF; Turki, H; Zahaf, A | 1 |
Anton-Lamprecht, I; Bohnert, A | 1 |
de Prost, Y; Dufier, JL; Gounod, N; Larrègue, M; Ogier, H; Saudubray, JM | 1 |
Kawatsu, T; Kida, K; Machino, H; Matsuda, H; Miki, Y | 1 |
Bay, C; Kelts, D; Ney, D; Nyhan, WL; Schneider, JA | 1 |
Balato, N; de Crecchio, G; Federico, A; Lembo, G; Pallini, R; Sammartino, A | 1 |
Hunziker, N | 1 |
Rehák, A; Selim, MM; Yadav, G | 1 |
Binder, PS; Charlton, KH; Digby, DJ; Wozniak, L | 1 |
al-Hazzaa, SA; al-Hemidan, AI | 1 |
Anderson, CE; Kaplan, P; Mazur, A; Rabinowitz, LG; Williams, LR | 1 |
Jimenez-Acosta, F | 1 |
Bergoend, H; Delaporte, E; le Flohic, X; Piette, F; Podglajen-Wecxsteen, O | 1 |
el-Badramany, MH; Farag, TI; Fawzy, AR | 1 |
Bardelli, AM; Borgogni, P; Farnetani, MA; Fois, A; Frezzotti, R; Mattei, R; Molinelli, M; Sargentini, I | 1 |
Goddé-Jolly, D; Larregue, M; Roussat, B; Van Effenterre, G | 1 |
Goldsmith, LA; Roe, CR; Thorpe, J | 1 |
Goldsmith, LA; Reed, J | 1 |
Callan, NJ | 1 |
Goldsmith, LA | 1 |
Gallasch, G; Jaeger, W; Lutz, P; Schmidt, H; Schnyder, UW | 2 |
Antener, I; Faggioni, R; Gautier, E; Pelet, B; Spahr, A | 1 |
Bienfang, DC; Kuwabara, T; Pueschel, SM | 1 |
Bowron, A; Clayton, P; Harper, JI; Paige, DG | 1 |
Horii, I; Kudoh, K; Kuramoto, Y; Saijo, S; Tagami, H | 1 |
Ito, K; Ito, M; Maruyama, T; Nakamura, A; Sato, Y; Shimizu, N | 1 |
Charpentier, C; De Prost, Y; Duffier, JL; Frézal, J; Hervé, F; Lemonnier, F; Moreno, JL; Ogier, H; Saudubray, JM | 1 |
Charpentier, C; Dufier, JL; Frezal, J; Hervé, F; Lemonnier, F; Moreno, JL; Ogier, H; Saudubray, JM | 1 |
Balato, N; Cusano, F; Lembo, G; Santoianni, P | 1 |
Basić, V; Cerkez, A; Hrnjica, M; Lazović, O; Popović, N; Salamon, T; Schnyder, UW; Softić, M; Stolić, V; Topić, B | 1 |
Fraser, NG; Griffiths, WA; MacDonald, J; McPhie, JL | 1 |
Callan, NJ; Danks, DM | 1 |
Babbini, N; Crovato, F; Desirello, G; Gatti, R; Rebora, A | 1 |
Baden, HP; Bienfang, DC; Gerald, P; Goldsmith, LA; Jimbow, K; Kang, E | 1 |
3 review(s) available for tyrosine and Hyperkeratosis Palmaris et Plantaris
Article | Year |
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Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Consanguinity; Cornea; Corneal Opacity; Diagnosis, Differential; Female; Humans; Intellectual Disability; Keratitis; Keratitis, Herpetic; Keratoderma, Palmoplantar; Liver; Syndrome; Tyrosine; Tyrosine Transaminase; Visual Acuity | 1995 |
Painful keratoderma and photophobia: hallmarks of tyrosinemia type II.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Humans; Keratoderma, Palmoplantar; Light; Male; Tyrosine | 1995 |
Tyrosine-induced skin disease.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Corneal Ulcer; Diagnosis, Differential; Disease Models, Animal; Female; Humans; Infant; Keratoderma, Palmoplantar; Male; Rats; Syndrome; Tyrosine | 1978 |
35 other study(ies) available for tyrosine and Hyperkeratosis Palmaris et Plantaris
Article | Year |
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Richner-Hanhart syndrome (tyrosinemia type II).
Topics: Child Development; Diet Therapy; Female; Humans; Infant; Keratitis, Dendritic; Keratoderma, Palmoplantar; Mutation; Patient Care Management; Treatment Outcome; Tyrosine; Tyrosine Transaminase; Tyrosinemias | 2017 |
Photophobia accompanied by painful plantar punctate hyperkeratotic patches: Tyrosinemia type 2.
Topics: Diet, Protein-Restricted; Female; Humans; Infant; Keratoderma, Palmoplantar; Pain; Photophobia; Tyrosine; Tyrosinemias | 2018 |
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 |
Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.
Topics: Aged; Antigens, Ly; Base Sequence; Conserved Sequence; Cysteine; Female; Founder Effect; Haplotypes; Heterozygote; Homozygote; Humans; Infant; Infant, Newborn; Keratoderma, Palmoplantar; Male; Molecular Sequence Data; Mutation; Pedigree; Protein Sorting Signals; Tyrosine; Urokinase-Type Plasminogen Activator | 2003 |
Richner-Hanhart's syndrome: ultrastructural abnormalities of epidermal keratinization indicating a causal relationship to high intracellular tyrosine levels.
Topics: Adult; Child; Corneal Dystrophies, Hereditary; Female; Humans; Intellectual Disability; Keratoderma, Palmoplantar; Male; Middle Aged; Pedigree; Skin; Skin Abnormalities; Syndrome; Tyrosine; Tyrosine Transaminase | 1982 |
[Type II oculo-cutaneous tyrosinosis].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Eye Diseases; Female; Humans; Keratoderma, Palmoplantar; Tyrosine; Tyrosine Transaminase | 1984 |
Successful dietary control of tyrosinemia II.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corneal Opacity; Female; Humans; Keratins; Keratoderma, Palmoplantar; Phenylacetates; Phenylalanine; Phenylpropionates; Phenylpyruvic Acids; Syndrome; Tyrosine; Tyrosine Transaminase | 1983 |
Dietary management of oculocutaneous tyrosinemia in an 11-year-old child.
Topics: Adolescent; Adult; Ambulatory Care; Child; Child, Preschool; Female; Humans; Infant; Intellectual Disability; Keratitis; Keratoderma, Palmoplantar; Male; Phenylalanine; Seasons; Syndrome; Tyrosine | 1983 |
Familial Richner-Hanhart syndrome: genetic, clinical, and metabolic studies.
Topics: Adolescent; Adult; Child; Corneal Opacity; Eye Diseases; Female; Humans; Keratitis, Dendritic; Keratoderma, Palmoplantar; Male; Pedigree; Syndrome; Tyrosine | 1984 |
Richner-Hanhart syndrome and tyrosinemia type II.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Female; Humans; Keratitis; Keratoderma, Palmoplantar; Male; Pedigree; Syndrome; Tyrosine | 1980 |
Richner-Hanhart syndrome (tyrosinaemia-II) (report of four cases without ocular involvement).
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Female; Humans; Keratoderma, Palmoplantar; Male; Pedigree; Syndrome; Tyrosine | 1981 |
Pseudodendritic keratitis and systemic tyrosinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant; Keratitis, Dendritic; Keratoderma, Palmoplantar; Male; Syndrome; Tyrosine | 1981 |
Painful plantar callouses and mental retardation. Tyrosinemia type II.
Topics: Bony Callus; Corneal Ulcer; Humans; Intellectual Disability; Keratoderma, Palmoplantar; Male; Middle Aged; Pain; Syndrome; Tyrosine; Tyrosine Transaminase | 1994 |
[Oculocutaneous type II tyrosinosis].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Humans; Intellectual Disability; Keratitis; Keratoderma, Palmoplantar; Male; Syndrome; Tyrosine | 1993 |
Familial richner-Hanhart syndrome in Kuwait: twelve-year clinical reassessment by a multidisciplinary approach.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Female; Humans; Intellectual Disability; Keratoderma, Palmoplantar; Kuwait; Male; Pedigree; Point Mutation; Syndrome; Tyrosine; Tyrosine Transaminase | 1995 |
Familial tyrosinaemia with eye and skin lesions. Presentation of two cases.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corneal Diseases; Female; Humans; Infant; Keratoderma, Palmoplantar; Male; Syndrome; Tyrosine; Tyrosine Transaminase | 1977 |
[A case of Richner-Hanhart syndrome (tyrosinosis with ocular, cutaneous and mental manifestations].
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Child, Preschool; Corneal Opacity; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Keratoconjunctivitis; Keratoderma, Palmoplantar; Rats; Syndrome; Tyrosine; Tyrosine Transaminase; Vision Disorders | 1979 |
Hepatic enzymes of tyrosine metabolism in tyrosinemia II.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartate Aminotransferases; Foot Dermatoses; Humans; Keratoderma, Palmoplantar; Liver; Male; Middle Aged; Syndrome; Tyrosine; Tyrosine Transaminase | 1979 |
Tyrosine-induced eye and skin lesions. A treatable genetic disease.
Topics: Female; Growth Disorders; Humans; Infant; Intellectual Disability; Keratoderma, Palmoplantar; Syndrome; Tyrosine | 1976 |
Tyrosinaemia in circumscribed palmo-plantar keratoderma-follow-up of a previously reported case.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Female; Humans; Keratoderma, Palmoplantar; Tyrosine | 1976 |
[Herpetiform bilateral epithelial corneal dystrophy caused by Tyrosinemia (Richner-Hanhart-Syndrome) (author's transl)].
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Animals; Corneal Dystrophies, Hereditary; Humans; Infant; Intellectual Disability; Keratoderma, Palmoplantar; Male; Rats; Syndrome; Tyrosine | 1978 |
[Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency)].
Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromosome Aberrations; Chromosome Disorders; Genes, Recessive; Humans; Intellectual Disability; Keratitis, Dendritic; Keratoderma, Palmoplantar; Syndrome; Tyrosine | 1978 |
Tyrosinemia without liver or renal damage with plantar and palmar keratosis and keratitis (hypertyrosinemia type II).
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child, Preschool; Humans; Hydroxy Acids; Infant; Intellectual Disability; Keratitis; Keratoderma, Palmoplantar; Male; Syndrome; Tyrosine | 1979 |
The Richner-Hanhart syndrome: report of a case with associated tyrosinemia.
Topics: Adolescent; Conjunctiva; Cornea; Corneal Opacity; Endothelium; Epithelium; Humans; Inclusion Bodies; Intellectual Disability; Keratoderma, Palmoplantar; Male; Parakeratosis; Phenylalanine; Syndrome; Tyrosine | 1976 |
Richner-Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II)
Topics: Amino Acid Metabolism, Inborn Errors; Dietary Proteins; Female; Humans; Infant; Keratoderma, Palmoplantar; Tyrosine; Tyrosine Transaminase | 1992 |
Tyrosinemia II: report of an incomplete case and studies on the hyperkeratotic stratum corneum.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Heel; Humans; Keratoderma, Palmoplantar; Male; Patient Compliance; Recurrence; Tyrosine | 1991 |
Richner-Hanhart's syndrome. Electron microscopic study of the skin lesion.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Humans; Keratoderma, Palmoplantar; Male; Skin; Syndrome; Tyrosine | 1990 |
[Incurable keratitis and chronic palmoplantar hyperkeratosis with hypertyrosinemia. Cure using a tyrosine-restricted diet. Type II tyrosinemia].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant; Keratitis; Keratoderma, Palmoplantar; Time Factors; Tyrosine | 1986 |
[Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Humans; Keratitis; Keratoderma, Palmoplantar; Time Factors; Tyrosine | 1986 |
Tyrosinemia type II in two cases previously reported as Richner-Hanhart syndrome.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Female; Humans; Keratitis, Dendritic; Keratoderma, Palmoplantar; Male; Tyrosine | 1986 |
[4 cases of Richner-Hanhart syndrome (tyrosinemia type II) with neurological symptomatology in a Yugoslav family].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Diseases in Twins; Female; Humans; Keratoderma, Palmoplantar; Male; Middle Aged; Nervous System Diseases; Neurologic Examination; Skin Transplantation; Syndrome; Tyrosine; Yugoslavia | 1988 |
Tyrosinaemia type II (Richner-Hanhart syndrome)--report of two cases treated with etretinate.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Etretinate; Humans; Keratoderma, Palmoplantar; Male; Tyrosine | 1987 |
Palmoplantar keratoderma with normal intelligence in tyrosinaemia II.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Humans; Keratitis; Keratoderma, Palmoplantar; Tyrosine | 1988 |
Richner-Hanhart syndrome spares a plantar autograft.
Topics: Adult; Eye Diseases; Female; Graft Survival; Heel; Humans; Intellectual Disability; Keratoderma, Palmoplantar; Skin; Skin Transplantation; Syndrome; Tyrosine | 1985 |
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 |