Compounds > tyrosine

tyrosine and Diseases in Twins

tyrosine has been researched along with Diseases in Twins in 8 studies

Research

Studies (8)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (62.50)	18.7374
1990's	2 (25.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (12.50)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kankariya, VP; Kontadakis, GA; Kymionis, GD; Ziakas, NG	1
ANDERSON, JA; ERTEL, R; FISCH, R; GRAVEM, H; McCARTHY, J	1
Gray, RG; Patrick, AD; Preston, FE; Whitfield, MF	1
Berger, R; Jansen, RP; Ploos van Amstel, JK; van den Berg, IE; Verjaal, M	1
Chalmers, RA; Purkiss, P; Watts, RW	1
Clayton, PT; Hyland, K	1
Basić, V; Cerkez, A; Hrnjica, M; Lazović, O; Popović, N; Salamon, T; Schnyder, UW; Softić, M; Stolić, V; Topić, B	1
Heyne, K	1

Other Studies

8 other study(ies) available for tyrosine and Diseases in Twins

Article	Year
Isolated corneal pseudodendrites as the initial manifestation of tyrosinemia type II in monozygotic twins. Journal of pediatric ophthalmology and strabismus, 2012, May-08, Volume: 49 Online Topics: Blepharospasm; Corneal Diseases; Dendrites; Diet, Protein-Restricted; Diseases in Twins; Humans; Infant; Male; Photophobia; Twins, Monozygotic; Tyrosine; Tyrosinemias	2012
Two-dose phenylalanine tolerance test for detection of phenylketonuric heterozygotes. Value of tyrosine responses. The Journal-lancet, 1961, Volume: 81 Topics: Disease; Diseases in Twins; Drug Tolerance; Heterozygote; Humans; Immune Tolerance; Phenylalanine; Phenylketonurias; Twins; Tyrosine	1961
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twins. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:1 Topics: Acetoacetates; Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Diseases in Twins; Erythrocytes; Fibroblasts; Fumarates; Humans; Hydrolases; Infant, Newborn; Infant, Newborn, Diseases; Male; Platelet Aggregation; Porphobilinogen Synthase; Tyrosine; Urine	1981
Prenatal diagnosis of type I hereditary tyrosinaemia. Lancet (London, England), 1994, Jul-30, Volume: 344, Issue:8918 Topics: Amino Acid Metabolism, Inborn Errors; Diseases in Twins; DNA Mutational Analysis; Female; Fetal Diseases; Humans; Pregnancy; Pregnancy, Multiple; Prenatal Diagnosis; Tyrosine	1994
A new variant form of phenylketonuria. The Quarterly journal of medicine, 1979, Volume: 48, Issue:191 Topics: Adult; Child; Diseases in Twins; Drug Combinations; Drug Tolerance; Female; Humans; Intelligence; Male; Middle Aged; Pedigree; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Sulfamethoxazole; Trimethoprim; Trimethoprim, Sulfamethoxazole Drug Combination; Tyrosine	1979
Aromatic amino acid decarboxylase deficiency in twins. Journal of inherited metabolic disease, 1990, Volume: 13, Issue:3 Topics: Aromatic-L-Amino-Acid Decarboxylases; Bromocriptine; Diseases in Twins; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; Male; Norepinephrine; Pyridoxine; Serotonin; Tranylcypromine; Twins, Monozygotic; Tyrosine	1990
[4 cases of Richner-Hanhart syndrome (tyrosinemia type II) with neurological symptomatology in a Yugoslav family]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1988, Volume: 39, Issue:3 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
Ultraviolet fluorescence spectra of the cerebrospinal fluid in tyrosinaemia. Acta paediatrica Academiae Scientiarum Hungaricae, 1972, Volume: 13, Issue:1 Topics: Diseases in Twins; Female; Fluorometry; Humans; Infant, Newborn; Infant, Premature, Diseases; Male; Metabolism, Inborn Errors; Seizures; Tyrosine	1972