tyrosine has been researched along with ALDOB Deficiency in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (80.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mowat, AP | 1 |
| Katz, AJ | 1 |
| Igarashi, T | 1 |
| Engelke, U; Lehnert, W; Stögmann, W; van den Berg, GB; Wevers, RA | 1 |
| Grand, RJ; Katz, AJ; Watkins, JB | 1 |
| Finegold, MJ | 1 |
| Dimmick, JE; Hardwick, DF | 1 |
| Beaufils, F; Bourrillon, A; Mercier, JC; Odievre, M | 1 |
| Bulovich, D; Filipovich, D; Khaĭdukovich, R; Zagorka, S | 1 |
| Mowat, A | 1 |
5 review(s) available for tyrosine and ALDOB Deficiency
| Article | Year |
|---|---|
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Cystic Fibrosis; Female; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactosemias; Glycogen Storage Disease; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Polycystic Kidney Diseases; Porphyrias; Tyrosine; Urea | 1982 |
[Fanconi syndrome].
Topics: Acidosis; Amino Acids; Cystine; Cytochrome-c Oxidase Deficiency; Fanconi Syndrome; Fructose Intolerance; Galactosemias; Glycogen Storage Disease; Humans; Kidney Tubules, Proximal; Oculocerebrorenal Syndrome; Tyrosine | 1998 |
Neonatal hepatitis: a diagnostic approach.
Topics: alpha 1-Antitrypsin Deficiency; Biliary Tract; Cholestasis; Fructose Intolerance; Galactosemias; Hepatitis; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infections; Jaundice, Neonatal; Parenteral Nutrition; Tyrosine | 1977 |
Cholestatic syndromes in infancy.
Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine | 1976 |
Metabolic cirrhoses of infancy and early childhood.
Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine | 1976 |
5 other study(ies) available for tyrosine and ALDOB Deficiency
| Article | Year |
|---|---|
Diagnostic procedures in the evaluation of hepatic diseases. Metabolic errors.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Child; Fructose Intolerance; Galactosemias; Hepatolenticular Degeneration; Humans; Infant, Newborn; Liver Diseases; Metabolism, Inborn Errors; Phenotype; Tyrosine | 1983 |
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 |
[Hereditary fructose intolerance with early onset].
Topics: Alanine Transaminase; Blood Coagulation Disorders; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Exchange Transfusion, Whole Blood; Female; Fructose Intolerance; Fructose-Bisphosphate Aldolase; Galactosemias; Hemorrhage; Hepatomegaly; Humans; Hypoglycemia; Infant; Infant, Newborn; Jaundice; Liver; Liver Function Tests; Neurologic Manifestations; Prognosis; Respiratory Insufficiency; Tyrosine | 1976 |
[Congenital disorders of metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Fructose Intolerance; Glutathione Reductase; Humans; Infant; Male; Metabolism, Inborn Errors; Tyrosine | 1975 |
The management of metabolic disorders of the liver.
Topics: alpha 1-Antitrypsin Deficiency; Child, Preschool; Fructose Intolerance; Galactosemias; Genetic Counseling; Glycogen Storage Disease; Hepatolenticular Degeneration; Humans; Hydrolases; Infant; Infant, Newborn; Liver Diseases; Metabolic Diseases; Phenotype; Prognosis; Tyrosine | 1985 |