galactose has been researched along with Deficiency Diseases in 20 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 20 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| FERNANDES, J; VAN DE KAMER, JH | 1 |
| Alleyne, GA; Scullard, GH | 1 |
| Kruas, H; Mönch, E | 1 |
| Sychlowy, A | 1 |
| Dipaolo, RV; Kanfer, JN; Newberne, PM | 1 |
| Britt, DG; Huber, JT | 1 |
| Peternel, WW | 1 |
| Linneweh, F | 1 |
| Gray, GM | 1 |
| Scheibenreiter, S; Thalhammer, O | 1 |
| Haschemian, G; Menne, F | 1 |
| Charuchinda, S; Valyasevi, A; Varavithya, W | 1 |
| Gitzelmann, R; Poley, JR; Prader, A | 1 |
| Holzel, A | 1 |
| Everson, GJ | 1 |
| Leach, RM; Muenster, AM; Wien, EM | 1 |
| SCHEFFLER, H | 1 |
| DUNKER, E; GARDEMANN, H | 1 |
| Rosman, NP | 1 |
| Bergen, WG; Johns, JT | 1 |
3 review(s) available for galactose and Deficiency Diseases
| Article | Year |
|---|---|
[Galactosemia: a hereditary galactose intolerance].
Topics: Age Factors; Cataract; Deficiency Diseases; Erythrocytes; Galactose; Galactosemias; Galactosidases; Genotype; Humans; Lactose; Nucleotidyltransferases; Phosphotransferases | 1972 |
Disaccharidase deficiency.
Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Colitis, Ulcerative; Crohn Disease; Deficiency Diseases; Diarrhea; Galactose; Glucose; Glycoside Hydrolases; Humans; Intestinal Absorption; Intestinal Mucosa; Kwashiorkor; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides; Peptic Ulcer; Sprue, Tropical; Sucrase | 1968 |
Intestinal digestion and maldigestion of dietary carbohydrates.
Topics: Biological Transport, Active; Deficiency Diseases; Dextranase; Dietary Carbohydrates; Digestion; Galactose; Glucose; Glycoside Hydrolases; Humans; Hydrolysis; Intestinal Absorption; Intestine, Small; Lactose Intolerance; Malabsorption Syndromes; Metabolism, Inborn Errors; Oligosaccharides; Sucrase | 1971 |
17 other study(ies) available for galactose and Deficiency Diseases
| Article | Year |
|---|---|
STUDIES ON THE UTILIZATION OF HEXOSES IN LIVER GLYCOGEN DISEASE.
Topics: Adolescent; Blood; Blood Glucose; Carbohydrate Metabolism; Child; Deficiency Diseases; Fatty Acids; Fructose; Galactose; Glucose; Glucose-6-Phosphatase; Hexoses; Humans; Lactates; Lactose Intolerance; Liver; Liver Glycogen; Metabolism; Metabolism, Inborn Errors; Phosphotransferases | 1965 |
Alterations in carbohydrate metabolism in Jamaican children with severe malnutrition.
Topics: Blood Glucose; Carbohydrate Metabolism; Deficiency Diseases; Galactose; Glucagon; Glucose Tolerance Test; Glucose-6-Phosphatase; Glucosyltransferases; Glycogen; Humans; Infant; Injections, Intravenous; Jamaica; Lactates; Liver; Liver Glycogen; Metabolic Clearance Rate; Muscles; Proteins; Pyruvates | 1969 |
[Enzymatic methods for the diagnosis of galactosemia and galactose deficiency].
Topics: Clinical Enzyme Tests; Deficiency Diseases; Galactose; Galactosemias; Glucokinase; Hexosyltransferases; Humans; Isomerases; NADP; Transferases | 1970 |
Copper deficiency and the central nervous system. Myelination in the rat: morphological and biochemical studies.
Topics: Animals; Brain; Brain Stem; Carbon Radioisotopes; Central Nervous System; Ceramides; Cerebellum; Cerebrosides; Cholesterol; Chromatography, Thin Layer; Copper; Deficiency Diseases; Disease Models, Animal; Female; Galactose; Gangliosides; Hexosyltransferases; Male; Movement Disorders; Myelin Sheath; Phosphatidylcholines; Phosphatidylethanolamines; Rats; Sphingomyelins; Sulfoglycosphingolipids | 1974 |
Effect of adding sugars to a carbohydrate-free diet on intestinal disaccharidase activities in the young calf.
Topics: Amylases; Animal Nutritional Physiological Phenomena; Animals; Blood Glucose; Deficiency Diseases; Dietary Carbohydrates; Galactose; Galactosidases; Glucose; Glucosidases; Glycoside Hydrolases; Intestinal Mucosa; Intestine, Small; Lactose; Male; Organ Size; Pancreas; Structure-Activity Relationship | 1974 |
[Isotope use in the study of hereditary metabolic diseases].
Topics: Animals; Autoradiography; Blood Glucose; Brain Chemistry; Carbon Isotopes; Chromatography, Paper; Deficiency Diseases; Feces; Galactose; Glucokinase; Glucose; Glycosuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Malabsorption Syndromes; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Radioisotope Dilution Technique; Radioisotopes; Rats; Tritium | 1970 |
[Galactosemia, generally with a fulminating course. 10 cases found through an early detection program].
Topics: Austria; Blood Transfusion; Deficiency Diseases; Diagnosis, Differential; Diet Therapy; Dietary Carbohydrates; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Nucleotidyltransferases; Time Factors | 1972 |
[Mass testing of newborn infants for galactosemia and galactose deficiency].
Topics: Deficiency Diseases; Galactose; Galactosemias; Humans; Infant, Newborn; Mass Screening; Methods | 1970 |
Lactose malabsorption in Thai infants.
Topics: Blood Glucose; Body Weight; Child, Preschool; Deficiency Diseases; Diarrhea, Infantile; Follow-Up Studies; Galactose; Glucose; Humans; Infant; Infant Nutritional Physiological Phenomena; Lactose; Lactose Intolerance; Thailand | 1971 |
Partial galactose-1-phosphate uridyltransferase deficiency due to a variant enzyme.
Topics: Adult; Blood Glucose; Chromatography, Gas; Deficiency Diseases; Electrophoresis; Female; Galactose; Galactosemias; Gels; Humans; Infant, Newborn; Male; Nucleotidyltransferases; Pedigree; Starch | 1967 |
Defects of sugar absorption. Sugar malabsorption and sugar intolerance in childhood.
Topics: Blood Glucose; Child; Deficiency Diseases; Diarrhea; Female; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Male; Sucrase; Vomiting | 1968 |
Preliminary study of carbohydrates in the urine of manganese-deficient guinea pigs at birth.
Topics: Animals; Animals, Newborn; Arabinose; Carbohydrates; Chromatography, Paper; Creatinine; Deficiency Diseases; Female; Fructose; Fucose; Galactose; Glycosuria; Guinea Pigs; Inositol; Lactose; Manganese; Mannose; Maternal-Fetal Exchange; Pregnancy; Ribose; Uronic Acids; Xylose | 1968 |
Studies on the role of manganese in bone formation. II. Effect upon chondroitin sulfate synthesis in chick epiphyseal cartilage.
Topics: Animals; Bone and Bones; Carbon Isotopes; Cartilage; Chickens; Chondroitin; Deficiency Diseases; Diet; Epiphyses; Galactose; Glucuronates; Hexosamines; Magnesium; Manganese; Metals; Polysaccharides; Transferases; Uracil Nucleotides; Xylose | 1969 |
[Studies on the regulation of carbohydrate and water metabolism in malnutrition].
Topics: Carbohydrates; Deficiency Diseases; Drinking Behavior; Feeding and Eating Disorders; Hexoses; Humans; Malnutrition; Water | 1950 |
[Acid-base equilibrium of the blood in chronic malnutrition].
Topics: Acid-Base Equilibrium; Blood; Carbohydrates; Deficiency Diseases; Hexoses; Humans; Malnutrition; Metabolism; Sweetening Agents | 1950 |
The neuropathology of congenital hypothyroidism.
Topics: Age Factors; Animals; Animals, Newborn; Body Weight; Brain; Congenital Hypothyroidism; Deficiency Diseases; Female; Hexoses; Hypothyroidism; Iodine; Lipid Metabolism; Maternal-Fetal Exchange; Pregnancy; Pregnancy Complications; Rats; Thyroid Gland | 1972 |
Effect of essential fatty acid deficiency on amino acid uptake by the small intestine of rats.
Topics: Amino Acids; Analysis of Variance; Animals; Carbon Radioisotopes; Deficiency Diseases; Diet; Extracellular Space; Fatty Acids, Essential; Glucose; Hexoses; Intestinal Absorption; Intestinal Mucosa; Kinetics; Lysine; Male; Methionine; Rats | 1974 |