galactose has been researched along with Abnormalities, Congenital in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| BIAGI, GL | 1 |
| Dahlqvist, A; Hall, B; Källén, B | 1 |
| Jaśkiewicz, J; Róg-Grochowska, E; Szafran, H | 1 |
| Dulaney, JT; Moser, HW; Sugita, M | 1 |
| Freinkel, N; Garcia-Palmer, FJ; Weigensberg, MJ | 1 |
1 review(s) available for galactose and Abnormalities, Congenital
| Article | Year |
|---|---|
[CONGENITAL ABNORMALITIES CAUSED BY CHEMICAL AGENTS AND DEFICIENCIES. I].
Topics: Abnormalities, Drug-Induced; Alkaloids; Amino Acids; Anti-Bacterial Agents; Antibodies; Congenital Abnormalities; Enzymes; Galactose; Hormones; Hypoglycemic Agents; Metals; Methylene Blue; Prochlorperazine; Sulfanilamide; Sulfanilamides; Sulfonamides; Thalidomide; Toxicology; Trypan Blue; Vitamin A | 1964 |
4 other study(ies) available for galactose and Abnormalities, Congenital
| Article | Year |
|---|---|
Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Abnormalities; Cri-du-Chat Syndrome; Down Syndrome; Female; Galactose; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Nucleotidyltransferases; Trisomy; Uracil Nucleotides | 1969 |
[Glucose and galactose absorption in infants with defects of the upper segment of the gastrointestinal tract during the operative period].
Topics: Age Factors; Congenital Abnormalities; Duodenal Obstruction; Female; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant; Infant, Newborn; Intestinal Absorption; Male; Postoperative Care; Preoperative Care; Pyloric Stenosis; Surgical Procedures, Operative | 1974 |
Ceramidase deficiency in Farber's disease (lipogranulomatosis).
Topics: Acid Phosphatase; Adult; Carbon Isotopes; Ceramides; Cerebellum; Cerebrosides; Child; Child, Preschool; Congenital Abnormalities; Female; Galactose; Galactosidases; Glucose; Glycoside Hydrolases; Heart Defects, Congenital; Hexosaminidases; Humans; Hydrolases; Infant; Infant, Newborn; Intellectual Disability; Kidney; Lipidoses; Liver Cirrhosis, Biliary; Male; Metabolism, Inborn Errors; Neuraminidase; Pigmentation Disorders; Respiratory Distress Syndrome, Newborn | 1972 |
Uptake of myo-inositol by early-somite rat conceptus. Transport kinetics and effects of hyperglycemia.
Topics: Animals; Biological Transport; Congenital Abnormalities; Culture Techniques; DNA; Embryo, Mammalian; Female; Glucose; Hexoses; Humans; Hyperglycemia; Inositol; Kinetics; Lipid Metabolism; Pregnancy; Proteins | 1990 |