galactose has been researched along with Abnormalities, Multiple in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (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 |
|---|---|
| Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Berry, HK; Fogelson, MH | 1 |
3 other study(ies) available for galactose and Abnormalities, Multiple
| Article | Year |
|---|---|
Brain sphingolipids in I cell disease (mucolipidosis II).
Topics: Abnormalities, Multiple; Ceramides; Cerebrosides; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Cytoplasmic Granules; Fibroblasts; Galactose; Gangliosides; Glucose; Humans; Lactose; Lipidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Neuraminic Acids; Retinitis Pigmentosa; Sphingolipids; Sphingomyelins; Sulfoglycosphingolipids; Syndrome | 1974 |
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 |
Nutritional investigations in the oculocerebrorenal syndrome of Lowe.
Topics: Abnormalities, Multiple; Amino Acids; Animals; Dehydration; Eye Diseases; Female; Galactose; Hospitalization; Humans; Infant, Newborn; Intellectual Disability; Male; Meat; Milk; Nucleotidyltransferases; Pregnancy; Protein Hydrolysates; Proteinuria; Renal Aminoacidurias; Syndrome | 1974 |