tyrosine and Homocystinuria

tyrosine has been researched along with Homocystinuria in 42 studies

Research

Studies (42)

Timeframe	Studies, this research(%)	All Research%
pre-1990	39 (92.86)	18.7374
1990's	1 (2.38)	18.2507
2000's	2 (4.76)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Desilva, MA; Hainline, BE; Nagana Gowda, GA; Raftery, D; Raftery, MA; Shanaiah, N	1
di Spilimbergo, SS; Padula, E; Penzo, M; Rampazzo, A; Squaquara, R	1
Lee, EB	1
Meister, A; Wellner, D	1
Becker, K	1
Alm, J; Larsson, A; Rosenqvist, U	1
Mamunes, P	1
Milner, RD; Wirdnam, PK	1
Alm, J; Larsson, A	1
Bellisario, R; Pass, KA; Reilly, AA	1
Clayton, BE; Ersser, RS; Lilly, P; Seakins, JW; Whiteman, PD	1
Bickel, H	1
Jung, EG; Lutz, P; Paweletz, N; Wiest, LG	1
Reavey, PC; Yadav, GC	1
Leonard, JV; Michalski, A; Taylor, DS	1
Rigilano, JC; Stevens, MB; Wilson, CC	1
Irons, M; Levy, HL	1
Kawamura, M	1
Royer, P	1
Brissaud, HE	1
Bickel, H; Schmidt, H; Schürrle, L	1
Ampola, MG	1
Frimpter, GW	1
Levy, HL	1
Martin, JJ; Schlote, W	1
Kroll, S; Toussaint, W; Zebisch, P	2
Tomaszewski, L	1
Francis, MJ; Macmillan, DC; Smith, R	1
Schmid-Rüter, E	1
Ampola, MG; Efron, ML	1
Barbesier, J; Boisse, J; Charpentier, C; Lemonnier, A; Mozziconacci, P	1
Knoll, E; Scheibenreiter, S; Schmierer, G; Schön, R; Thalhammer, O	1
Tada, K	1
Barkin, E; Levy, HL	1
Clayton, BE	1
Hagge, W; Irtel von Brenndorff, A	1
Giovannini, M	1
Gjessing, LR; Seip, M; Vellan, EJ	1

Reviews

10 review(s) available for tyrosine and Homocystinuria

Article	Year
Metabolic diseases and the skin. Pediatric clinics of North America, 1983, Volume: 30, Issue:4 Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Biotin; Child; Child, Preschool; Hartnup Disease; Homocystinuria; Humans; Infant; Infant, Newborn; Phenylketonurias; Skin Diseases; Tyrosine; Tyrosine Transaminase	1983
A survey of inborn errors of amino acid metabolism and transport in man. Annual review of biochemistry, 1981, Volume: 50 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport; Cystinosis; Female; Glutathione; Glycine; Homocystinuria; Humans; Hydroxyproline; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Phenylalanine; Proline; Serine; Tyrosine; Urea; Valine	1981
Neonatal screening tests. Pediatric clinics of North America, 1980, Volume: 27, Issue:4 Topics: Adenosine Deaminase; Anemia, Sickle Cell; Biological Assay; Costs and Cost Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tyrosine; United States	1980
The eye and inherited metabolic disease: a review. Journal of the Royal Society of Medicine, 1988, Volume: 81, Issue:5 Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Eye Diseases; Homocystinuria; Humans; Metabolism, Inborn Errors; Ornithine; Tyrosine	1988
Metabolic syndromes with dermatologic manifestations. Clinical reviews in allergy, 1986, Volume: 4, Issue:1 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
Dietary treatment of inborn errors of amino acid and carbohydrate metabolism. Bibliotheca nutritio et dieta, 1973, Issue:18 Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Child; Child Development; Child Nutritional Physiological Phenomena; Child, Preschool; Cystinosis; Diet Therapy; Galactose; Glucose; Histidine; Homocystinuria; Humans; Infant; Infant Nutrition Disorders; Infant, Newborn; Lactose Intolerance; Malabsorption Syndromes; Maple Syrup Urine Disease; Phenylketonurias; Sucrose; Tyrosine	1973
Phenylketonuria and other disorders of amino acid metabolism. Pediatric clinics of North America, 1973, Volume: 20, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine	1973
Aminoacidurias due to inherited disorders of metabolism (first of two parts). The New England journal of medicine, 1973, Oct-18, Volume: 289, Issue:16 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child; Cystathionine; Cysteine; Cystine; Disulfides; Female; Homocystinuria; Humans; Infant, Newborn; Lactates; Male; Methionine; Oxidoreductases; Phenylalanine; Phenylketonurias; Pregnancy; Pyruvates; Sulfhydryl Compounds; Sulfites; Sulfur; Tyrosine	1973
Neonatal screening for inborn errors of amino acid metabolism. Clinics in endocrinology and metabolism, 1974, Volume: 3, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Biological Assay; Chromatography, Paper; Evaluation Studies as Topic; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Mass Screening; Methionine; Methods; Phenylalanine; Phenylketonurias; Pregnancy; Tyrosine	1974
The aminoacidurias. Pediatric clinics of North America, 1967, Volume: 14, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine	1967

Other Studies

32 other study(ies) available for tyrosine and Homocystinuria

Article	Year
Class selection of amino acid metabolites in body fluids using chemical derivatization and their enhanced 13C NMR. Proceedings of the National Academy of Sciences of the United States of America, 2007, Jul-10, Volume: 104, Issue:28 Topics: Amino Acids; Argininosuccinic Acid; Carbon Isotopes; Homocystinuria; Humans; Magnetic Resonance Spectroscopy; Phenylketonurias; Tyrosine	2007
Hypercoagulability due to homocystinuria in a case of head and neck reconstruction resolved with combined systemic therapy. Plastic and reconstructive surgery, 2008, Volume: 121, Issue:4 Topics: Carcinoma, Squamous Cell; Fibrinolytic Agents; Head and Neck Neoplasms; Homocystinuria; Humans; Male; Platelet Aggregation Inhibitors; Postoperative Complications; Surgical Flaps; Thrombophilia; Tirofiban; Tissue Plasminogen Activator; Tyrosine	2008
[Phaenotypic aspects of hereditary aminoacidopathies (author's transl)]. Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1981, Volume: 129, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Germany, West; Homocystinuria; Humans; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Mass Screening; Phenotype; Phenylketonurias; Time Factors; Tyrosine	1981
Health economic analysis of the Swedish neonatal metabolic screening programme. A method of optimizing routines. Medical decision making : an international journal of the Society for Medical Decision Making, 1982, Volume: 2, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Cost-Benefit Analysis; Galactosemias; Histidine; Homocystinuria; Humans; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Sweden; Tyrosine	1982
The pancreatic beta cell fraction in children with errors of amino acid metabolism. Pediatric research, 1982, Volume: 16, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Homocystinuria; Humans; Infant; Infant, Newborn; Islets of Langerhans; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine	1982
Evaluation of a nation-wide neonatal metabolic screening programme in Sweden 1965-1979. Acta paediatrica Scandinavica, 1981, Volume: 70, Issue:5 Topics: Evaluation Studies as Topic; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Sweden; Tyrosine	1981
Multivariate discrimination for phenylketonuria (PKU) and non-PKU hyperphenylalaninemia after analysis of newborns' dried blood-spot specimens for six amino acids by ion-exchange chromatography. Clinical chemistry, 1998, Volume: 44, Issue:2 Topics: Amino Acids; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; False Positive Reactions; Genetic Testing; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Multivariate Analysis; New York; Phenylalanine; Phenylketonurias; Tyrosine	1998
Changing incidence of neonatal hypermethioninaemia: implications for the detection of homocystinuria. Archives of disease in childhood, 1979, Volume: 54, Issue:8 Topics: Amino Acid Metabolism, Inborn Errors; Bottle Feeding; England; Female; Homocystinuria; Humans; Infant, Newborn; Male; Mass Screening; Methionine; Milk Proteins; Tyrosine	1979
Dietary restriction in inborn errors of amino acid metabolism. Current concepts in nutrition, 1979, Volume: 8 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Food, Formulated; Histidine; Homocystinuria; Humans; Infant; Infant Food; Infant, Newborn; Intelligence; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Tyrosine	1979
American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism. Pediatrics, 1976, Volume: 57, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cysteine; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Nutritional Requirements; Phenylalanine; Phenylketonurias; Risk; Tyrosine; Valine	1976
[Morphological and biochemical investigations of hairs in inborn errors of amino acid metabolism (author's transl)]. Archives for dermatological research = Archiv fur dermatologische Forschung, 1976, Jul-26, Volume: 256, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Cystine; Hair; Homocystinuria; Humans; Keratins; Phenylketonurias; Tyrosine	1976
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study. Humangenetik, 1975, Dec-23, Volume: 30, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Australia; Cystinuria; Ethnicity; Europe; Galactosemias; Genetics, Population; Hartnup Disease; Histidine; Homocystinuria; Humans; Inbreeding; Infant, Newborn; Israel; Japan; Maple Syrup Urine Disease; Mass Screening; New Zealand; North America; Phenylketonurias; Tyrosine	1975
Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital. Journal of inherited metabolic disease, 1988, Volume: 11, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Citrulline; Cystinuria; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Kuwait; Male; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1988
State screening for metabolic disorders in newborns. American family physician, 1988, Volume: 37, Issue:4 Topics: Adrenal Hyperplasia, Congenital; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Biotinidase; Congenital Hypothyroidism; Cystic Fibrosis; Galactosemias; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine; United States	1988
[Laboratory examinations for inborn errors of metabolism]. Rinsho byori. The Japanese journal of clinical pathology, 1986, Volume: 34, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Computers; Congenital Hypothyroidism; Galactosemias; Gas Chromatography-Mass Spectrometry; Homocystinuria; Humans; Japan; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine	1986
[Dietetics in hereditary enzyme deficiencies]. La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1970, Feb-26, Volume: 46, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970
[Dietetics of amino acid metabolism disorders]. La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1971, Feb-08, Volume: 47, Issue:7 Topics: Amino Acid Metabolism, Inborn Errors; Diet Therapy; Glycine; Histidine; Homocystinuria; Humans; Isoleucine; Leucine; Phenylketonurias; Tryptophan; Tyrosine; Valine	1971
Neuropathological study of aminoacidurias. Monographs in human genetics, 1972, Volume: 6 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Central Nervous System; Cystathionine; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Maple Syrup Urine Disease; Middle Aged; Phenylketonurias; Renal Tubular Transport, Inborn Errors; Sex Factors; Tyrosine; Urea	1972
[Hereditary amino acid metabolism disorders. Indications for early diagnosis]. Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11 Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine	1972
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods]. Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11 Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine	1972
[The inborn errors of metabolism of amino acids]. Postepy biochemii, 1973, Volume: 19, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chemical Phenomena; Chemistry; Cystinuria; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Sarcosine; Tyrosine; Valine	1973
Polymeric collagen of skin in normal sunjects and in patients with inherited connective tissue disorders. Clinical science, 1973, Volume: 44, Issue:5 Topics: Acromegaly; Adolescent; Adult; Aged; Child; Child, Preschool; Collagen; Collagen Diseases; Female; Hexosamines; Homocystinuria; Hot Temperature; Humans; Hyperparathyroidism; Male; Microscopy, Electron; Middle Aged; Myositis Ossificans; Osteitis Deformans; Osteogenesis Imperfecta; Osteopetrosis; Pseudoxanthoma Elasticum; Skin; Tyrosine; Werner Syndrome	1973
[Screening results for inborn errors of metabolism in Western Europe]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:5 Topics: Denmark; Europe; Evaluation Studies as Topic; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; International Cooperation; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Preventive Medicine; Switzerland; Tyrosine; United Kingdom	1973
Collective results of mass screening for inborn metabolic errors in eight European countries. Acta paediatrica Scandinavica, 1973, Volume: 62, Issue:4 Topics: Belgium; Denmark; France; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Ireland; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Netherlands; Phenylketonurias; Switzerland; Tyrosine; United Kingdom	1973
[Mass screening of phenylketonuria. Report on a screening center (October 1967-December 1968)]. La Presse medicale, 1969, Sep-13, Volume: 77, Issue:37 Topics: Adolescent; Adult; Amino Acids; Bacteriological Techniques; Child; Child, Preschool; Chromatography, Paper; Fluorometry; France; Homocystinuria; Humans; Infant; Infant, Newborn; Mass Screening; Methionine; Phenylalanine; Phenylketonurias; Sampling Studies; Tyrosine	1969
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]. Wiener klinische Wochenschrift, 1972, Volume: 84 Topics: Amino Acid Metabolism, Inborn Errors; Austria; Child, Preschool; Chromatography, Thin Layer; Diet Therapy; Economics, Medical; Follow-Up Studies; Galactosemias; Glycine; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Multiphasic Screening; Phenylketonurias; Proline; Time Factors; Tyrosine	1972
[Treatment of amino acid metabolism anomalies]. Horumon to rinsho. Clinical endocrinology, 1971, Volume: 19, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Homocystinuria; Humans; Phenylketonurias; Tyrosine	1971
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders. The Journal of laboratory and clinical medicine, 1971, Volume: 78, Issue:4 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine	1971
Experience with a screening service, using the Guthrie test, in the north-west and north-east metropolitan regions. Archives of disease in childhood, 1971, Volume: 46, Issue:250 Topics: Amino Acid Metabolism, Inborn Errors; Biological Assay; Homocystinuria; Humans; Infant; Mass Screening; Methionine; Phenylalanine; Phenylketonurias; Tyrosine	1971
[Experiences with a new amino acid analyzer for a rapid analysis]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Amino Acids; Autoanalysis; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Premature, Diseases; Isoleucine; Leucine; Maple Syrup Urine Disease; Metabolic Diseases; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970
[Current views on therapy of some dysmetabolic oligophrenias]. Minerva pediatrica, 1967, Dec-22, Volume: 19, Issue:51 Topics: Child, Preschool; Diet Therapy; Galactosemias; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine	1967
Hair amino acids in cystinosis, homocystinuria, Fölling's disease and tyrosinosis. Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:3 Topics: Amino Acids; Autoanalysis; Citrulline; Cystine; Cystinosis; Female; Hair; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Male; Metabolic Diseases; Methionine; Methods; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1969