tyrosine has been researched along with Growth Disorders in 20 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 12 (60.00) | 18.7374 |
1990's | 4 (20.00) | 18.2507 |
2000's | 2 (10.00) | 29.6817 |
2010's | 2 (10.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Arberas, C; Armando, R; Ballerini, MG; Barros, ÁC; Bergadá, I; Braslavsky, D; Casali, B; Cassinelli, H; Castro, JF; Del Rey, G; Domené, H; Domené, S; Gutiérrez, M; Jasper, H; Keselman, AC; Landi, E; Lapunzina-Badía, P; Martin, A; Nevado Blanco, J; Pennisi, PA; Ramirez, L; Rey, RA; Ropelato, MG; Sanguineti, NM; Scaglia, PA | 1 |
Walenkamp, MJE; Wit, JM | 1 |
Debrabander, A; Dobbelaere, D; Farriaux, JP; Gottrand, F; Michaud, L; Turck, D; Vanderbecken, S | 1 |
Dunger, DB; Firth, H; Fukushima, T; O'Rahilly, S; Okubo, Y; Petry, CJ; Saukkonen, T; Siddle, K; Stanhope, R; Takahashi, S; Willatt, L; Wilson, LC | 1 |
Benevenga, NJ; Steele, RD | 1 |
El-Harith, EA; Hiller, A; Ter Meulen, U | 1 |
Holmberg, C; Jalanko, H; Laine, J; Sarna, S; Sipilä, I | 1 |
Abe, H; Arisaka, O; Chihara, K; Kaji, H; Koga, J; Okimura, Y; Shirono, H; Takahashi, K; Takahashi, Y; Tanaka, T; Yagi, T | 1 |
Engelke, U; Lehnert, W; Stögmann, W; van den Berg, GB; Wevers, RA | 1 |
Goldsmith, LA; Reed, J | 1 |
Danks, DM; Rogers, J; Tippett, P | 1 |
Bakker, HD; van Sprang, FJ; Wadman, SK | 1 |
Boling, JA; Hall, JB; Hileman, SM; Schillo, KK | 1 |
O'Halloran, MT; Yu, JS | 1 |
Baden, HP; Bienfang, DC; Gerald, P; Goldsmith, LA; Jimbow, K; Kang, E | 1 |
Bost, M; Boucharlat, J; Favier, A; Ledru, J; Ratel, M; Serre, JC | 1 |
Berry, HK; Light, IJ; Sutherland, JM | 1 |
Benevenga, NJ; Harper, AE; Wohlhueter, RM | 1 |
Hsia, DY | 1 |
Ersser, RS; Harries, JT; Lloyd, JK; Seakins, JW | 1 |
3 review(s) available for tyrosine and Growth Disorders
Article | Year |
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Adverse effects of excessive consumption of amino acids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Cattle; Diet; Disease Models, Animal; Ethionine; Fenclonine; Glycine; Growth Disorders; Histidine; Humans; Methionine; Nerve Tissue Proteins; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pneumonia, Atypical Interstitial, of Cattle; Serine; Stereoisomerism; Sulfhydryl Compounds; Tissue Distribution; Tryptophan; Tyrosine; Vitamin A | 1984 |
Effects of ingestion of disproportionate amounts of amino acids.
Topics: Adaptation, Physiological; Age Factors; Amino Acids; Ammonia; Animals; Cystine; Deficiency Diseases; Feeding Behavior; Glycine; Growth Disorders; Histidine; Homeostasis; Humans; Leucine; Liver; Lysine; Methionine; Nicotinic Acids; Nutrition Disorders; Phenylalanine; Rats; Threonine; Tryptophan; Tyrosine | 1970 |
Phenylketonuria and its variants.
Topics: Adult; Child, Preschool; Congenital Abnormalities; Female; Gene Frequency; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Mixed Function Oxygenases; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine | 1970 |
1 trial(s) available for tyrosine and Growth Disorders
Article | Year |
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Evaluation of nutritional status and pathophysiology of growth retardation in patients with phenylketonuria.
Topics: Aging; Anthropometry; Body Composition; Body Height; Body Weight; Child; Child, Preschool; Chromatography, Gas; Cross-Sectional Studies; Diet; Erythrocytes; Female; Growth Disorders; Hormones; Humans; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Male; Nutritional Status; Phenylalanine; Phenylketonurias; Thyroid Hormones; Trace Elements; Tyrosine | 2003 |
16 other study(ies) available for tyrosine and Growth Disorders
Article | Year |
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A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Topics: Abnormalities, Multiple; Cell Proliferation; Computational Biology; Computer Simulation; Fetal Growth Retardation; Growth Disorders; Hearing Loss, Sensorineural; HEK293 Cells; Homozygote; Humans; Infant; Insulin-Like Growth Factor I; Male; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Receptor, IGF Type 1; Receptors, Somatomedin; Tyrosine | 2019 |
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Topics: Growth Disorders; Hearing Loss, Sensorineural; Humans; Insulin-Like Growth Factor I; Mutation; Tyrosine | 2019 |
Cell proliferation activities on skin fibroblasts from a short child with absence of one copy of the type 1 insulin-like growth factor receptor (IGF1R) gene and a tall child with three copies of the IGF1R gene.
Topics: Body Height; Cell Division; Cells, Cultured; Child; Child, Preschool; Cytogenetic Analysis; Female; Fibroblasts; Gene Dosage; Growth Disorders; Humans; In Situ Hybridization, Fluorescence; Insulin-Like Growth Factor I; Kinetics; Male; Phosphorylation; Receptor, IGF Type 1; Recombinant Proteins; Skin; Tyrosine | 2003 |
The effect of administration of glycine and tyrosine on the growth depression caused by mimosine in rats.
Topics: Animals; Glycine; Growth Disorders; Male; Mimosine; Pyridones; Rats; Rats, Inbred Strains; Tyrosine | 1983 |
Factors affecting growth after pediatric liver transplantation.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Biliary Atresia; Carcinoma, Hepatocellular; Child; Child, Preschool; Female; Growth; Growth Disorders; Growth Hormone; Humans; Hydrocortisone; Infant; Insulin-Like Growth Factor I; Liver Neoplasms; Liver Transplantation; Male; Methylprednisolone; Time Factors; Tyrosine | 1994 |
Biologically inactive growth hormone caused by an amino acid substitution.
Topics: Child, Preschool; Dimerization; Female; Growth Disorders; Human Growth Hormone; Humans; Mutation; Phosphorylation; Receptors, Somatotropin; Tyrosine | 1997 |
Long-term follow up of a new case of hawkinsinuria.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acidosis, Renal Tubular; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Cyclohexenes; Diagnosis, Differential; Follow-Up Studies; Fructose Intolerance; Growth Disorders; Humans; Infant; Liver Diseases; Male; Tyrosine | 1999 |
Tyrosine-induced eye and skin lesions. A treatable genetic disease.
Topics: Female; Growth Disorders; Humans; Infant; Intellectual Disability; Keratoderma, Palmoplantar; Syndrome; Tyrosine | 1976 |
A new form of prolonged transient tyrosinemia presenting with severe metabolic acidosis.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Breast Feeding; Dietary Proteins; Female; Growth Disorders; Humans; Infant; Infant Food; Peptides; Tyrosine | 1975 |
[Tyrosinosis].
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Ascorbic Acid; Chronic Disease; Female; Growth Disorders; Hematuria; Humans; Infant, Newborn; Liver; Liver Diseases; Male; Methionine; Pregnancy; Tyrosine | 1976 |
Does tyrosine act as a nutritional signal mediating the effects of increased feed intake on luteinizing hormone patterns in growth-restricted lambs?
Topics: Animals; Dose-Response Relationship, Drug; Eating; Female; Growth Disorders; Hypothalamus; Luteinizing Hormone; Ovariectomy; Radioimmunoassay; Sheep; Tyrosine | 1992 |
Children of mothers with phenylketonuria.
Topics: Adolescent; Adult; Child; Child, Preschool; Diet Therapy; Family Planning Services; Female; Growth Disorders; Heart Defects, Congenital; Heterozygote; Homozygote; Humans; Intellectual Disability; Male; Microcephaly; Middle Aged; Phenylalanine; Phenylketonurias; Seizures; Strabismus; Tyrosine | 1970 |
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 |
[2 new cases of microcephalic children with intrauterine growth retardation born of phenylketonuric mothers].
Topics: Birth Weight; Chromatography, Ion Exchange; Female; Growth Disorders; Humans; Infant; Male; Mental Disorders; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine | 1972 |
Clinical significance of tyrosinemia of prematurity.
Topics: Amino Acid Metabolism, Inborn Errors; Ascorbic Acid; Child Development; Chromatography, Paper; Diet Therapy; Fatigue; Feeding Behavior; Female; Growth Disorders; Humans; Infant, Newborn; Infant, Premature, Diseases; Intelligence; Intelligence Tests; Phenylalanine; Pregnancy; Pregnancy Complications; Tyrosine | 1973 |
Recovery after dietary treatment of an infant with features of tyrosinosis.
Topics: Amino Acid Metabolism, Inborn Errors; Cholestasis; Diet Therapy; Female; Growth Disorders; Humans; Hypophosphatemia, Familial; Infant; Methionine; Phenylalanine; Phosphates; Renal Aminoacidurias; Rickets; Tyrosine | 1969 |