galactose has been researched along with Aminoaciduria, Renal in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (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 |
|---|---|
| HARRIS, H | 1 |
| CARSON, NA; NEELY, RA | 1 |
| AKABANE, J; MINAGAWA, A; MIZUNO, T; MORIKAWA, T; OGASAWARA, J; OKAMURA, T; TADA, K; WADA, Y; YOSHIDA, T | 1 |
| Aperia, A; Bergqvist, G; Linné, T; Zetterström, R | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Berry, HK; Fogelson, MH | 1 |
| Kuttner, RE; Portoghese, AJ | 1 |
| Beyreiss, K; Theile, H | 1 |
| Hamilton, PB; Lou, MF | 1 |
9 other study(ies) available for galactose and Aminoaciduria, Renal
| Article | Year |
|---|---|
Renal aminoaciduria.
Topics: Amino Acids; Cystinuria; Galactose; Humans; Renal Aminoacidurias | 1957 |
DISACCHARIDE INTOLERANCE IN INFANCY.
Topics: Carbohydrate Metabolism; Chromatography; Disaccharides; Galactose; Humans; Infant; Infant Nutrition Disorders; Lactose; Renal Aminoacidurias; Sucrose; Urine | 1963 |
A SEX-LINKED DISORDER WITH MENTAL AND PHYSICAL RETARDATION CHARACTERIZED BY CEREBROCORTICAL ATROPHY AND INCREASE OF GLUTAMIC ACID IN THE CEREBROSPINAL FLUID.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Atrophy; Blood; Brain Diseases; Cerebrospinal Fluid; Chromosomes; Galactose; Genetics, Medical; Glutamates; Glutamic Acid; Glutamine; Growth; Humans; Intellectual Disability; Kidney; Renal Aminoacidurias; Urine | 1964 |
Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings.
Topics: Carbohydrate Metabolism, Inborn Errors; Fanconi Syndrome; Female; Galactose; Humans; Infant; Kidney; Malabsorption Syndromes; Male; Phosphotransferases; Renal Aminoacidurias; Transferases | 1981 |
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 |
Formation of experimental cataracts and urinary amino acids.
Topics: Animals; Cataract; Dietary Carbohydrates; Female; Galactose; Rats; Renal Aminoacidurias; Taurine; Xylose | 1967 |
[Studies on the etiology and pathogenesis of lactose intolerance].
Topics: Blood Glucose; Feces; Fructose; Galactose; Glucose Tolerance Test; Glycosuria; Humans; Infant; Lactose; Lactose Intolerance; Male; Renal Aminoacidurias | 1969 |
Hydroxylysine glycosides in human urine.
Topics: Adult; Blood Glucose; Bone and Bones; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Collagen; Electrophoresis; Galactose; Glycosides; Glycosuria; Humans; Hydrolysis; Kinetics; Lysine; Renal Aminoacidurias; Scoliosis; Spinal Fusion | 1971 |