galactose has been researched along with Syndrome in 32 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 27 (84.38) | 18.7374 |
| 1990's | 1 (3.13) | 18.2507 |
| 2000's | 1 (3.13) | 29.6817 |
| 2010's | 1 (3.13) | 24.3611 |
| 2020's | 2 (6.25) | 2.80 |
| Authors | Studies |
|---|---|
| Lee, CJ; McGill, SK | 1 |
| Ayares, DL; Bianchi, JR; Choudhary, SK; Commins, SP; Kuravi, KV; Matheny, RG; Nellis, JR; Rahman, F; Sorrells, LT; Turek, JW; Walters, AH | 1 |
| Biedermann, T; Blank, S; Codreanu-Morel, F; Darsow, U; Eberlein, B; Fischer, J; Hilger, C; Mehlich, J; Morisset, M; Ollert, M; Schiener, M; Swiontek, K | 1 |
| Hartog, FE; Nijland, R; Wanders, RJ; Wevers, RA; Willemsen, WN | 1 |
| BICKEL, H; THURSBY-PELHAM, DC | 1 |
| POLAK, F | 2 |
| Freese, D | 1 |
| Fredrikzon, B; Keston, AS; Meeuwisse, GW | 1 |
| Cohn, RM; Segal, S; Yudkoff, M | 1 |
| Cornblath, M; Schwartz, R | 1 |
| DaCosta, H; Merchant, S; Shreeve, WW | 1 |
| Jaeken, J | 1 |
| Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Brady, RO | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Beyreiss, K | 1 |
| Berry, HK; Fogelson, MH | 1 |
| Agam, G; Cohen, T; Deckelbaum, RJ; Gutman, A; Russell, A; Shapira, E | 1 |
| Hiatt, W; Sattler, M; Wenger, DA | 1 |
| Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S | 1 |
| Anderson, CF; DeWeed, JH; Frohnert, PP; Holley, KE; Kazmier, FJ; Riley, FC; Suros, J; Woods, JE | 1 |
| Holmer, GK; Lou, HC; Reske-Nielsen, E; Vagn-Hansen, P | 1 |
| Milev, B | 1 |
| Jendryczko, A; Kucharz, E | 1 |
| Endo, H; Nagashima, K; Nakamura, N; Shimada, Y; Suzuki, Y; Yotsumoto, H | 1 |
| Dahr, W; Gunson, HH; Uhlenbruck, G; Van Der Hart, M | 1 |
| Cafferty, MS; Dimauro, S; Hays, AP; Lovelace, RE; Rowland, LP; Servidei, S | 1 |
| Embil, JA; Ripley, BA; Spence, MW; Tibbles, JA | 1 |
| Hall, CW; Neufeld, EF | 1 |
| Bach, G; Friedman, R; Neufeld, EF; Weissmann, B | 1 |
| Calne, DB; King, RH; Thomas, PK | 1 |
3 review(s) available for galactose and Syndrome
| Article | Year |
|---|---|
Food Allergies and Alpha-gal Syndrome for the Gastroenterologist.
Topics: Animals; Food Hypersensitivity; Galactose; Gastroenterologists; Humans; Immunoglobulin E; Mammals; Syndrome | 2023 |
Intracellular cholestatic syndromes of infancy.
Topics: Bacterial Infections; Bile Acids and Salts; Biopsy, Needle; Cholestasis, Intrahepatic; Fructose; Galactose; Glycogen Storage Disease; Hepatitis; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Liver; Metabolism, Inborn Errors; Prognosis; Syndrome; Tyrosine | 1982 |
Polyglucosan body disease.
Topics: Fecal Incontinence; Female; Hexoses; Humans; Middle Aged; Motor Neurons; Neuromuscular Diseases; Peripheral Nervous System Diseases; Peroneal Nerve; Sural Nerve; Syndrome; Urination Disorders | 1991 |
1 trial(s) available for galactose and Syndrome
| Article | Year |
|---|---|
The basophil activation test differentiates between patients with alpha-gal syndrome and asymptomatic alpha-gal sensitization.
Topics: Adult; Anaphylaxis; Basophils; Female; Galactose; Humans; Immunoglobulin E; Male; Middle Aged; Skin Tests; Syndrome | 2019 |
28 other study(ies) available for galactose and Syndrome
| Article | Year |
|---|---|
Allergic response to medical products in patients with alpha-gal syndrome.
Topics: Anaphylaxis; Animals; Food Hypersensitivity; Galactose; Humans; Immunoglobulin E; Mammals; Swine; Syndrome | 2022 |
Galactose-1-phosphate uridyl transferase deficiency is not associated with Müllerian aplasia in Dutch patients.
Topics: Adult; Case-Control Studies; Female; Galactose; Humans; Middle Aged; Mullerian Ducts; Netherlands; Polymorphism, Single Nucleotide; Pregnancy; Syndrome; UTP-Hexose-1-Phosphate Uridylyltransferase; Young Adult | 2009 |
Hyperamino-aciduria in Lignac-Fanconi disease, in galactosaemia and in an obscure syndrome.
Topics: Amino Acids; Galactose; Galactosemias; Humans; Metabolic Diseases; Syndrome; Urine | 1954 |
[Reactibility of the liver function shown by a galactose test in posthepatitic syndrome].
Topics: Galactose; Hepatitis; Humans; Liver Function Tests; Syndrome | 1955 |
[Work galactose test in posthepatic syndrome].
Topics: Galactose; Hepatitis; Humans; Liver Function Tests; Syndrome | 1956 |
Evidence for participation of mutarotase in sugar transport: absence of the enzyme in a case of glucose galactose malabsorption.
Topics: Adult; Biological Transport; Carbohydrate Epimerases; Child; Female; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Jejunum; Kinetics; Malabsorption Syndromes; Male; Syndrome | 1982 |
Errors of carbohydrate metabolism in infants and children: a survey.
Topics: Carbohydrate Metabolism, Inborn Errors; Diarrhea; Fructokinases; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactokinase; Galactose; Galactosemias; Glucose; Humans; Lactose Intolerance; Malabsorption Syndromes; Sucrase-Isomaltase Complex; Syndrome; Transferases; Uridine Diphosphate Galactose | 1978 |
Disorders of carbohydrate metabolism in infancy.
Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Diabetes Mellitus, Type 1; Female; Fructose Intolerance; Galactose; Glucose; Glycogen; Homeostasis; Humans; Hydrocortisone; Hypoglycemia; Infant; Infant, Newborn; Malabsorption Syndromes; Male; Metabolic Diseases; Pregnancy; Pregnancy in Diabetics; Syndrome | 1976 |
Radiorespirometric study of carbohydrate metabolism in childhood liver disease.
Topics: Carbon Dioxide; Carbon Radioisotopes; Child; Child, Preschool; Fatty Liver; Galactose; Glucose; Humans; India; Infant; Liver Cirrhosis; Syndrome | 1976 |
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins].
Topics: Acetylglucosamine; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Demyelinating Diseases; Diseases in Twins; Female; Galactose; Glucosamine; Humans; Intellectual Disability; Sialic Acids; Syndrome; Twins, Monozygotic | 1989 |
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 |
The adnormal biochemistry of inherited disorders of lipid metabolism.
Topics: Brain; Ceramides; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Female; Fibroblasts; Galactose; Galactosidases; Gaucher Disease; Glucose; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Humans; Intestines; Kidney; Leukocytes; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Muscles; Niemann-Pick Diseases; Phosphoric Diester Hydrolases; Sphingomyelins; Spleen; Sulfoglycosphingolipids; Syndrome | 1973 |
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 |
[Exocrine pancreatic insufficiency, neutropenia, metaphyseal dysostosis and growth retardation (Shwachman syndrome) with transient disturbances of carbohydrate metabolism].
Topics: Acidosis; Agranulocytosis; Blood Glucose; Carbohydrate Metabolism; Child, Preschool; Dwarfism; Galactose; Glucose Tolerance Test; Humans; Insulin; Male; Neutropenia; Osteochondrodysplasias; Pancreatic Diseases; 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 |
Type 3 glycogenosis: atypical enzyme activities in blood cells in two siblings.
Topics: Autoradiography; Blood Glucose; Carbon Isotopes; Erythrocytes; Female; Galactose; Glucagon; Glucosidases; Glycogen; Glycogen Storage Disease; Humans; Infant; Leukocytes; Liver; Liver Diseases; Male; Muscles; Pedigree; Syndrome; Transferases | 1972 |
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.
Topics: Adult; Brain; Ceramides; Female; Galactose; Galactosidases; Gangliosides; Humans; Infant; Lactose; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Liver; Male; Niemann-Pick Diseases; Skin; Spleen; Syndrome | 1974 |
Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration | 1974 |
A kidney transplant patient with Fabry's disease. Unusual features.
Topics: Adult; Cadaver; Ceramides; Galactose; Galactosidases; Glycolipids; Heparin; Humans; Kidney Failure, Chronic; Kidney Transplantation; Leukocytes; Lipid Metabolism, Inborn Errors; Male; Pulmonary Embolism; Subclavian Vein; Syndrome; Thrombophlebitis; Transplantation, Homologous; Vena Cava, Inferior | 1973 |
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 |
[Disorders of liver function in endemic nephropathy].
Topics: Bilirubin; Disease Reservoirs; Europe, Eastern; Galactose; Glomerulonephritis; Humans; Liver Diseases; Liver Function Tests; Nephritis; Pyelonephritis; Sulfobromophthalein; Syndrome; Urobilinogen | 1972 |
Aldehyde content of collagen from liver of rats with collagen-like syndrome.
Topics: Aldehydes; Animals; Collagen; Collagen Diseases; Hexoses; Hydroxyproline; Liver; Male; Rats; Syndrome | 1983 |
Macular cherry-red spots and beta-galactosidase deficiency in an adult. An autopsy case with progressive cerebellar ataxia, myoclonus, thrombocytopathy, and accumulation of polysaccharide in liver.
Topics: Adult; Blood Platelet Disorders; Brain; Cerebellar Ataxia; Epilepsies, Myoclonic; G(M1) Ganglioside; Galactosidases; Hexoses; Humans; Liver; Lysosomes; Male; Mucolipidoses; Mucopolysaccharidoses; Polysaccharides; Skin; Skin Manifestations; Spinal Cord; Syndrome | 1977 |
Molecular basis of Tn-polyagglutinability.
Topics: Anemia, Hemolytic; Antibodies, Heterophile; Blood Glucose; Blood Protein Electrophoresis; Cell Membrane; Chromatography, Gas; Electrophoresis, Polyacrylamide Gel; Erythrocytes; Glycopeptides; Hemagglutination; Hemagglutination Tests; Hexoses; Humans; Leukopenia; Molecular Weight; Sialic Acids; Sodium Dodecyl Sulfate; Syndrome; Thrombocytopenia; Trypsin | 1975 |
A new variant of Sandhoff's disease.
Topics: Appendix; Aspartate Aminotransferases; Cholesterol; Developmental Disabilities; Fibroblasts; Ganglia; Gangliosides; Hexosaminidases; Hexoses; Humans; Isoenzymes; L-Lactate Dehydrogenase; Leukocytes; Liver; Male; Neuraminic Acids; Phospholipids; Seizures; Sphingolipidoses; Syndrome; Temperature; Uronic Acids | 1974 |
Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.
Topics: Adult; Amniotic Fluid; Cells, Cultured; Child; Corneal Opacity; Female; Fibroblasts; Galactosidases; Glucuronidase; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Hexoses; Humans; Mucopolysaccharidoses; Pregnancy; Retinitis Pigmentosa; Skin; Syndrome; Uronic Acids | 1973 |
The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.
Topics: Carbohydrate Metabolism, Inborn Errors; Cell Fractionation; Chromatography, Gas; Corneal Opacity; Fibroblasts; Glycosaminoglycans; Glycoside Hydrolases; Hexoses; Humans; Lysosomes; Methods; Mucopolysaccharidosis I; Retinitis Pigmentosa; Syndrome; Uronic Acids | 1972 |
Autosomal dominant forms of hereditary hypertrophic neuropathy.
Topics: Age Factors; Ceramides; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Hexoses; Humans; Hypertrophy; Metabolism, Inborn Errors; Muscular Atrophy; Neuritis; Syndrome | 1972 |