galactose has been researched along with Growth Disorders in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (66.67) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cerone, J; Rios, A | 1 |
| Milla, PJ; Pahari, A; van't Hoff, WG | 1 |
| Asano, M; Furukawa, K; Iwakura, Y; Kido, M; Kochibe, N; Matsumoto, S; Umesaki, Y | 1 |
| Gaifman, M; Nitzan, M; Vogel, R | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Holmer, GK; Lou, HC; Reske-Nielsen, E; Vagn-Hansen, P | 1 |
| Ford, JD; Haworth, JC; Younoszai, MK | 1 |
| Fekete, M; Gálfi, I; Mesty0N, J; Soltész, G | 1 |
| Stanescu, R; Stanescu, V; Szirmai, JA | 1 |
9 other study(ies) available for galactose and Growth Disorders
| Article | Year |
|---|---|
Galactosemia.
Topics: Bone Density; Bone Diseases, Metabolic; Developmental Disabilities; Female; Galactose; Galactosemias; Growth Disorders; Humans; Infant, Newborn; Neonatal Screening; Primary Ovarian Insufficiency | 2019 |
Neonatal nephrocalcinosis in association with glucose-galactose malabsorption.
Topics: Calcium; Diarrhea; Galactose; Glucose; Growth Disorders; Humans; Hypercalcemia; Infant, Newborn; Karyotyping; Kidney; Malabsorption Syndromes; Male; Nephrocalcinosis; Oxalates; Polyuria; Ultrasonography | 2003 |
Growth retardation and early death of beta-1,4-galactosyltransferase knockout mice with augmented proliferation and abnormal differentiation of epithelial cells.
Topics: alpha-Glucosidases; Animals; beta-Galactosidase; beta-N-Acetylglucosaminylglycopeptide beta-1,4-Galactosyltransferase; Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Cell Differentiation; Cell Division; Epithelium; Female; Galactose; Growth Disorders; Intestine, Small; Lactase; Male; Mice; Mice, Knockout; Microvilli; Molecular Sequence Data; N-Acetyllactosamine Synthase; Skin; Sucrase-Isomaltase Complex | 1997 |
Increased intracranial pressure in galactosemia. Consider this diagnosis with a bulging fontanel, hepatomegaly, and failure to thrive.
Topics: Diet Therapy; Galactose; Galactosemias; Growth Disorders; Hepatomegaly; Humans; Infant; Intracranial Pressure; Male; Neurologic Manifestations | 1976 |
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 |
Lipid composition in gray and white matter of the brain in Menkes' disease.
Topics: Brain; Brain Chemistry; Brain Diseases; Cholesterol; Chromatography, Gas; Chromatography, Thin Layer; Esters; Fatty Acids; Galactose; Glycolipids; Growth Disorders; Hair; Humans; Infant; Intellectual Disability; Lipid Metabolism; Phosphatidylcholines; Phosphatidylethanolamines; Plasmalogens; Sphingomyelins; Syndrome | 1974 |
Effect of galactose toxicity on growth of the rat fetus and brain.
Topics: Animals; Body Weight; Brain; Brain Chemistry; Dietary Carbohydrates; DNA; Embryonic and Fetal Development; Female; Galactose; Galactosemias; Gestational Age; Growth Disorders; Maternal-Fetal Exchange; Organ Size; Phosphates; Pregnancy; Pregnancy Complications; Proteins; Rats | 1969 |
Lactose absorption in growth retarded newborn infants.
Topics: Absorption; Female; Galactose; Gestational Age; Glucose; Growth; Growth Disorders; Humans; Infant Nutrition Disorders; Infant, Newborn; Infant, Premature; Lactose; Pregnancy | 1969 |
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 |