tyrosine has been researched along with alpha 1-Antitrypsin Deficiency in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (75.00) | 18.7374 |
| 1990's | 3 (25.00) | 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 |
| Groth, CG; Ringdén, O | 1 |
| Katz, AJ | 1 |
| Rabinowitz, JG | 1 |
| Perlmutter, DH; Teckman, J | 1 |
| Kane, PA; Karani, JB; Meili-Vergani, G; Williams, R | 1 |
| Kohgo, Y; Ono, M | 1 |
| Gerbeaux, J; Labrune, B; Tournier, G | 1 |
| Hill, GN; Pollard, AC; Robertson, EF | 1 |
| Grand, RJ; Katz, AJ; Watkins, JB | 1 |
| Allende, H; Boix-Ochoa, J; Infante, D; Margarit, C; Martínez Ibáñez, V; Sanchís, L; Tormo, R | 1 |
| Mowat, A | 1 |
6 review(s) available for tyrosine and alpha 1-Antitrypsin 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 |
Transplantation in relation to the treatment of inherited disease.
Topics: alpha 1-Antitrypsin Deficiency; Amyloidosis; Bone Marrow Transplantation; Fabry Disease; Gaucher Disease; Genetic Diseases, Inborn; Gout; Granulomatous Disease, Chronic; Hemoglobinopathies; Hemophilia A; Hepatolenticular Degeneration; Humans; Immunologic Deficiency Syndromes; Kidney Transplantation; Leukodystrophy, Metachromatic; Liver Transplantation; Lymphocytes; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nephritis, Hereditary; Niemann-Pick Diseases; Osteopetrosis; Oxalates; Oxalic Acid; Transplantation; Tyrosine; Uremia | 1984 |
Conceptual advances in the pathogenesis and treatment of childhood metabolic liver disease.
Topics: alpha 1-Antitrypsin Deficiency; Child; Gaucher Disease; Hepatolenticular Degeneration; Humans; Liver Diseases; Metabolism, Inborn Errors; Tyrosine | 1995 |
[Liver cirrhosis associated with metabolic disorders].
Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Galactosemias; Glycogen Storage Disease; Hemochromatosis; Hepatolenticular Degeneration; Humans; Liver Cirrhosis; Metabolism, Inborn Errors; Tyrosine | 1995 |
[Pediatrics in 1976].
Topics: Adolescent; alpha 1-Antitrypsin Deficiency; Body Weight; Carcinoma, Hepatocellular; Catheterization; Child; Child, Preschool; Glycine max; Haemophilus Infections; Humans; Huntington Disease; Infant; Infant, Newborn; Levamisole; Liver Neoplasms; Malabsorption Syndromes; Mucocutaneous Lymph Node Syndrome; Nitrites; Obesity; Pediatrics; Pericarditis; Sepsis; Splenectomy; Tyrosine; Urinary Tract Infections | 1977 |
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 |
6 other study(ies) available for tyrosine and alpha 1-Antitrypsin 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 |
Abnormalities of the liver and other organs.
Topics: Abnormalities, Multiple; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Colitis; Colon; Cystinosis; Heart Failure; Hemochromatosis; Hepatolenticular Degeneration; Humans; Liver; Liver Diseases; Necrosis; Radiography; Sclerosis; Tyrosine | 1980 |
Pseudotumours of hepatic imaging.
Topics: Adolescent; Adult; Aged; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Gaucher Disease; Humans; Infant; Liver Diseases; Liver Failure; Liver Transplantation; Tomography, X-Ray Computed; Tyrosine | 1996 |
Evaluation of a state-wide neonatal screening programme.
Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Australia; Evaluation Studies as Topic; Follow-Up Studies; Galactosemias; Histidine; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine | 1979 |
[New perspectives in liver-based metabolic errors: liver transplantation].
Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycogen Storage Disease Type II; Humans; Hyperlipoproteinemia Type II; Infant, Newborn; Liver; Liver Cirrhosis; Liver Transplantation; Male; Metabolism, Inborn Errors; Tyrosine | 1989 |
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 |