methionine has been researched along with Malabsorption Syndromes in 23 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 22 (95.65) | 18.7374 |
| 1990's | 1 (4.35) | 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 |
|---|---|
| Bamba, T; Ihara, T | 1 |
| Grävinghoff, J; Hütter, HJ | 1 |
| Cooper, BA | 1 |
| Mezey, E | 1 |
| Battesti, JP; Thuillier, A | 1 |
| Albot, G; Boisson, J; Leblanc, M | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Boisse, J; Moatti, N | 1 |
| Phillips, SF | 1 |
| Giorgio, AJ; Linarelli, LG; Macdonald, RR; Rubin, HM | 1 |
| Corcino, JJ; Herbert, V; Waxman, S | 1 |
| Rey, J | 1 |
| Dumitraşcu, D; Grigorescu, M; Tamás, S | 1 |
| Ellegaard, J; Esmann, V | 1 |
| Gibbins, JR; Jones, WO; Symons, LE | 1 |
| Carpenter, DG; Carter, CH | 1 |
| Althausen, TL; Doig, RK; Uyeyama, K; Weiden, S | 1 |
| Antener, I; Carton, D; Hooft, C; Snoeck, J; Timmermans, J; van den Hende, C | 1 |
| Schneider, C | 1 |
| Antener, I; Hooft, C | 1 |
| Domingo, EO; Warren, KS | 1 |
| Andrysek, O | 1 |
| Antener, I; Hooft, C; Oyaert, W; Snoeck, J; Timmermans, J; Van den Hende, C | 1 |
4 review(s) available for methionine and Malabsorption Syndromes
| Article | Year |
|---|---|
[Methionine malabsorption syndrome].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems; Animals; Biomarkers; Carrier Proteins; Diagnosis, Differential; Humans; Hydroxybutyrates; Malabsorption Syndromes; Methionine; Mutation; Prognosis | 1998 |
Megaloblastic anaemia and disorders affecting utilisation of vitamin B12 and folate in childhood.
Topics: Adolescent; Adult; Anemia, Hemolytic; Anemia, Macrocytic; Anemia, Megaloblastic; Anemia, Pernicious; Biological Transport; Bone Marrow; Bone Marrow Cells; Child; Child, Preschool; Female; Folic Acid; Folic Acid Deficiency; Homocystinuria; Humans; Infant; Intrinsic Factor; Malabsorption Syndromes; Male; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Orotic Acid; Phenylketonurias; Tetrahydrofolate Dehydrogenase; Transcobalamins; Vitamin B 12 | 1976 |
[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 |
Drugs, toxins and dietary amino acids affecting vitamin B12 or folic acid absorption or utilization.
Topics: Amino Acids; Anemia, Macrocytic; Contraceptives, Oral; Diet; DNA; Ethanol; Folic Acid; Folic Acid Antagonists; Folic Acid Deficiency; Glycine; Homocysteine; Humans; Malabsorption Syndromes; Methionine; Pharmacology; Serine; Toxins, Biological; Vitamin B 12 | 1970 |
19 other study(ies) available for methionine and Malabsorption Syndromes
| Article | Year |
|---|---|
[Acylase activity of human small intestinal mucosa in malabsorption syndrome].
Topics: Amidohydrolases; Anilides; Aspartic Acid; Celiac Disease; Child, Preschool; Humans; Infant; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Methionine | 1978 |
Intestinal function in chronic alcoholism.
Topics: Alcohol Oxidoreductases; Alcoholism; Chronic Disease; Diet Therapy; Digestive System; Dose-Response Relationship, Drug; Ethanol; Folic Acid; Gastrointestinal Motility; Humans; Intestinal Absorption; Intestines; Malabsorption Syndromes; Methionine; Nutrition Disorders; Thiamine; Vitamin B 12; Xylose | 1975 |
[Folic acid deficiencies. Etiology and biological diagnosis].
Topics: Alcoholic Intoxication; Anticonvulsants; Antimetabolites; Celiac Disease; Chromatography; Enterococcus faecalis; Female; FIGLU Test; Folic Acid; Folic Acid Deficiency; Humans; Jejunum; Lactobacillus; Liver Cirrhosis; Malabsorption Syndromes; Methionine; Methods; Nucleic Acids; Nutrition Disorders; Polarography; Pregnancy; Scleroderma, Systemic; Serine; Whipple Disease | 1968 |
[Digestive intolerance to cereal flour in adults and its prevention by a new method of flour predigestion].
Topics: Adolescent; Adult; Aged; Bilirubin; Cathartics; Child; Colonic Diseases; Constipation; Diarrhea; Diet Therapy; Digestive System; Dyspepsia; Edible Grain; Feces; Feeding Behavior; Female; Flour; Gastrointestinal Agents; Gastrointestinal Motility; Humans; Malabsorption Syndromes; Male; Mastication; Methionine; Middle Aged; Parasites; Phytotherapy; Psychophysiology; Radiography; Starch; Triticum; Trypsin Inhibitors; Yeasts | 1969 |
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 |
Relationship of diarrhea to maldigestion and malabsorption.
Topics: Animals; Bile Acids and Salts; Diarrhea; Digestion; Fatty Acids; Glycols; Humans; Intestinal Absorption; Lactose Intolerance; Malabsorption Syndromes; Methionine; Water-Electrolyte Balance | 1973 |
Selective malabsorption of vitamin B 12: report of a case with metabolic studies.
Topics: Alanine; Amino Acids; Anemia, Macrocytic; Child; Chromatography, Gas; Glycine; Hemoglobins; Histidine; Humans; Isoleucine; Leucine; Malabsorption Syndromes; Male; Malonates; Methionine; Proteinuria; Renal Tubular Transport, Inborn Errors; Reticulocytes; Serine; Taurine; Threonine; Tyrosine; Valine; Vitamin B 12; Vitamin B 12 Deficiency | 1974 |
[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 |
[Malabsorption in chronic nonspecific enteropathy].
Topics: Carbon Isotopes; Chronic Disease; Enteritis; Feces; Gastrectomy; Humans; Intestinal Diseases; Iodine Radioisotopes; Lipid Metabolism; Malabsorption Syndromes; Methionine; Oleic Acids; Protein-Losing Enteropathies; Proteins; Serum Albumin, Radio-Iodinated; Stearic Acids; Triolein | 1972 |
Folate deficiency in malnutrition, malabsorption, and during phenytoin treatment diagnosed by determination of serine synthesis in lymphocytes.
Topics: Adult; Aged; Anemia; Carbon Isotopes; Epilepsy; Erythrocytes; Female; Folic Acid; Folic Acid Deficiency; Humans; Lymphocytes; Malabsorption Syndromes; Male; Methionine; Middle Aged; Nutrition Disorders; Phenytoin; Proteins; RNA; Serine; Time Factors | 1972 |
Jejunal malabsorption in the rat infected by the nematode Nippostrongylus brasiliensis.
Topics: Animals; Carbon Isotopes; Epithelial Cells; Epithelium; Glucose; Histidine; Hookworm Infections; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Male; Methionine; Microscopy, Electron; Mitochondria; Oxygen Consumption; Palmitic Acids; Rats; Serum Albumin, Bovine; Sodium Chloride; Sulfobromophthalein | 1971 |
Inborn errors of metabolism associated with unusual odors.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Malabsorption Syndromes; Maple Syrup Urine Disease; Methionine; Odorants; Phenylalanine; Tryptophan; Valerates | 1970 |
Digestion and absorption after massive resection of the small intestine. II. Recovery of the absorptive function as shown by intestinal absorption tests in two patients and a consideration of compensatory mechanisms.
Topics: Animals; Celiac Disease; Crohn Disease; Galactose; Glucose; Humans; Hypocalcemia; Intestinal Absorption; Intestine, Small; Malabsorption Syndromes; Methionine; Neomycin; Osteomalacia; Postgastrectomy Syndromes; Rats; Vitamin A | 1968 |
Further investigations in the methionine malabsorption syndrome.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Height; Body Weight; Child; Child, Preschool; Diarrhea; Feces; Female; Humans; Hydroxybutyrates; Intellectual Disability; Keto Acids; Malabsorption Syndromes; Methionine; Pedigree; Seizures | 1968 |
[Scintigraphy of the liver, gallbladder and pancreas].
Topics: Arteriovenous Fistula; Gallbladder; Humans; Iodine Radioisotopes; Liver; Liver Cirrhosis; Liver Neoplasms; Malabsorption Syndromes; Methionine; Neoplasm Metastasis; Pancreas; Pancreatitis; Radioisotopes; Radionuclide Imaging; Selenium | 1968 |
Methionine malabsorption syndrome.
Topics: Amino Acids; Diarrhea; Diet Therapy; Feces; Female; Homocystinuria; Humans; Hydroxybutyrates; Intellectual Disability; Malabsorption Syndromes; Male; Methionine; Pedigree; Seizures | 1968 |
Pathology and pathophysiology of the small intestine in murine schistosomiasis mansoni, including a review of the literature.
Topics: Animals; Glucose; Hepatomegaly; Hypertension, Portal; Intestinal Absorption; Intestinal Diseases, Parasitic; Intestine, Small; Malabsorption Syndromes; Methionine; Mice; Propionates; Schistosomiasis; Splenomegaly | 1969 |
[Use of isotopes in pancreatic diseases].
Topics: Animals; Diagnosis, Differential; Fatty Acids, Nonesterified; Humans; Iodine Radioisotopes; Malabsorption Syndromes; Methionine; Pancreatic Diseases; Pancreatitis; Radiography; Radionuclide Imaging; Rats | 1965 |
[Methionine malabsorption].
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Humans; Intellectual Disability; Malabsorption Syndromes; Methionine | 1966 |