methionine has been researched along with Amino Acid Transport Disorder, Neutral in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 16 (94.12) | 18.7374 |
| 1990's | 1 (5.88) | 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 |
|---|---|
| Efron, ML | 1 |
| Takita, H | 1 |
| Frimpter, GW | 1 |
| Tomaszewski, L | 2 |
| Bartsocas, CS; Crawford, JD | 1 |
| Boisse, J; Moatti, N | 1 |
| Silk, DB | 1 |
| Levy, HL | 1 |
| Ampola, MG; Efron, ML | 1 |
| Alpers, DH; Thier, SO | 1 |
| Menne, F | 1 |
| Milne, MD | 1 |
| Rey, J | 1 |
| Alpers, DH; Bartoscas, CS; Bixby, EM; Shih, VE; Thier, SO | 1 |
| Matthews, DM | 1 |
| Gershon, ES; Shader, RI | 1 |
8 review(s) available for methionine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
[Renal tubule transport defect of amino acids].
Topics: Cystinuria; Hartnup Disease; Humans; Imino Acids; Kidney Tubules; Methionine; Renal Aminoacidurias | 1997 |
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Cystine; Female; Glycine; Hartnup Disease; Humans; Infant; Lysine; Malabsorption Syndromes; Male; Methionine; Renal Tubular Transport, Inborn Errors; Tryptophan | 1973 |
Progress report. Peptide absorption in man.
Topics: Amino Acids; Betaine; Biological Transport, Active; Cystinuria; Dietary Proteins; Gelatin; Glycine; Hartnup Disease; Humans; Hydrolysis; Intestinal Absorption; Intestinal Mucosa; Kinetics; Methionine; Milk Proteins; Models, Biological; Nutritional Physiological Phenomena; Peptides; Phenylalanine; Structure-Activity Relationship | 1974 |
Neonatal screening for inborn errors of amino acid metabolism.
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.
Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine | 1967 |
Disorders of intestinal transport of amino acids.
Topics: Amino Acids; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Fructose; Galactosemias; Genes, Recessive; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Lysine; Methionine; Phenylketonurias; Proline; Renal Tubular Transport, Inborn Errors; Tryptophan | 1969 |
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine | 1968 |
Transport of amino acids and peptides in the gut and the kidney.
Topics: Adult; Alanine; Amino Acids; Animals; Biological Transport, Active; Digestive System; Glycine; Hartnup Disease; Histidine; Humans; Hydrolysis; Intestinal Absorption; Kidney; Kidney Tubules; Leucine; Lysine; Methionine; Peptides; Phenylalanine; Proteins; Rats; Serine; Threonine; Tryptophan; Valine | 1971 |
9 other study(ies) available for methionine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
Diet therapy for inborn errors of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child, Preschool; Coenzymes; Cystinuria; Diet Therapy; Hartnup Disease; Humans; Infant; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Tyrosine | 1967 |
Sulfur amino acids, hyperglycinemia, and certain possibly benign conditions.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Cystathionine; Diagnosis, Differential; Disulfides; Glycine; Hartnup Disease; Histidine; Histidine Ammonia-Lyase; Homocystinuria; Humans; Methionine; Proline; Sulfites | 1976 |
[Peptide transport].
Topics: Amino Acids; Animals; Biological Transport; Dogs; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Intestinal Mucosa; Methionine; Peptide Hydrolases; Peptides; Trypsin | 1976 |
Clinical phenotypes in kidney transport disorders.
Topics: Abnormalities, Multiple; Acidosis, Renal Tubular; Cerebrospinal Fluid Proteins; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria; Diabetes Insipidus; Galactose; Glucose; Glycosuria, Renal; Growth Disorders; Hartnup Disease; Humans; Hypophosphatemia, Familial; Kidney Tubules; Malabsorption Syndromes; Methionine; Phenotype; Pseudohypoparathyroidism; Pulmonary Heart Disease; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Seizures; Syndrome | 1974 |
[The inborn errors of metabolism of amino acids].
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 |
[Hereditary digestive enzyme defects].
Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chylomicrons; Cystinuria; Female; Hartnup Disease; Humans; Hypercalcemia; Indican; Lipid Metabolism, Inborn Errors; Lipoproteins; Malabsorption Syndromes; Male; Methionine | 1972 |
Studies of intestinal transport defect in Hartnup disease.
Topics: Adolescent; Biological Transport; Carbon Isotopes; Child; Culture Techniques; Feces; Genes, Recessive; Hartnup Disease; Humans; Intellectual Disability; Intestinal Mucosa; Jejunum; Leucine; Lysine; Male; Methionine; Phenylalanine; Proline; Tryptophan | 1971 |
Experimental approach in chemical pathology.
Topics: Adult; Amblyopia; Animals; Biological Transport; Cystinuria; Dipeptides; Female; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Nitrogen; Peptides; Proteins; Smoking; Tyrosine; Vitamin B 12 | 1971 |
Screening for aminoacidurias in psychiatric inpatients.
Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Brain Damage, Chronic; Depression; Drug Synergism; Hartnup Disease; Homocystinuria; Hospitals, Psychiatric; Humans; Intellectual Disability; Mass Screening; Massachusetts; Mental Disorders; Methionine; Monoamine Oxidase Inhibitors; Neurotic Disorders; Personality Disorders; Phenylketonurias; Schizophrenia; Substance-Related Disorders; Tryptophan | 1969 |