galactose has been researched along with Hypophosphatemia, Familial in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bartsocas, CS; Crawford, JD | 1 |
| Hasegawa, H; Mitarai, T; Takayanagi, K | 1 |
| Stanescu, R; Stanescu, V; Szirmai, JA | 1 |
1 review(s) available for galactose and Hypophosphatemia, Familial
| Article | Year |
|---|---|
[Disorders of renal tubular transport of amino acids, hexose and phosphate].
Topics: Amino Acids; Biological Transport; Cystinuria; Glycosuria, Renal; Hartnup Disease; Hexoses; Humans; Hypophosphatemia, Familial; Kidney Tubules; Osteomalacia; Phosphates; Renal Tubular Transport, Inborn Errors | 2006 |
2 other study(ies) available for galactose and Hypophosphatemia, Familial
| Article | Year |
|---|---|
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 |
Microchemical analysis of human tibial growth cartilage in various forms of dwarfism.
Topics: Achondroplasia; Adolescent; Biopsy; Carbohydrate Metabolism, Inborn Errors; Cartilage; Child; Chondroitin; Collagen; Dwarfism; Dwarfism, Pituitary; Female; Galactosamine; Glycosaminoglycans; Growth Disorders; Hexosamines; Hexoses; Histocytochemistry; Humans; Hydroxyproline; Hypophosphatemia, Familial; Male; Myxedema; Proteins; Pyridinium Compounds; Tibia; Turner Syndrome | 1972 |