galactose has been researched along with Brain Disorders in 25 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 22 (88.00) | 18.7374 |
1990's | 1 (4.00) | 18.2507 |
2000's | 1 (4.00) | 29.6817 |
2010's | 1 (4.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Gui, SH; Li, CL; Luo, DD; Mo, ZZ; Su, ZR; Sun, CY; Xie, JH; Xie, YL; Xu, LQ; Zhang, X; Zhang, ZB | 1 |
CROME, L | 1 |
AKABANE, J; MINAGAWA, A; MIZUNO, T; MORIKAWA, T; OGASAWARA, J; OKAMURA, T; TADA, K; WADA, Y; YOSHIDA, T | 1 |
Ahmad, S; Halim, MA; Khan, ZU; McGinnis, MR; Mokaddas, E; Nair, MP; Nampoory, MR; Said, T | 1 |
Kardel, T; Nörby Rasmussen, S; Ramsöe, K | 1 |
Cross, CA; Donnell, GN; Kaufman, FR; Nelson, MD; Wolff, JA | 1 |
Suzuki, K | 1 |
Eisenburg, J; Grunst, J; Krumpoch, B; Magerl, W; Munte, A; Schauer, S; Schmidt, S; Weinzierl, M | 1 |
Beretta, R; Cassi, E; Colombo, A; Cova, L; Ezechieli, S; Malacco, E; Massarotti, G; Pagani, C; Sala, E | 1 |
Holmer, GK; Lou, HC; Reske-Nielsen, E; Vagn-Hansen, P | 1 |
Brown, H; Goransky, L; McDermott, WV; Trey, C | 1 |
Brown, H; McDermott, WV; Trey, C | 2 |
Rorsman, G; Sulg, I | 1 |
Condon, RE | 1 |
Bircher, J; Haemmerli, UP; Largiader, F; Mocetti, T; Trabert, E | 1 |
Dawson, G; Matalon, R; Stein, AO | 1 |
EDGAR, GW | 1 |
FRICK, E | 1 |
COHEN, MG | 1 |
Brown, BD; Brunngraber, EG; Hof, H | 1 |
Brackenridge, CJ | 1 |
Brunngraber, EG | 1 |
Geffroy, PY; Geffroy, Y; Segrestin, M | 1 |
O'Brien, JS; Okada, S; Veath, ML | 1 |
1 review(s) available for galactose and Brain Disorders
Article | Year |
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Biochemistry, function, and neuropathology of the glycoproteins in brain tissue.
Topics: Aging; Animals; Brain; Brain Chemistry; Brain Diseases; Chromatography, Gel; Dialysis; Electrophoresis, Polyacrylamide Gel; Fucose; Gangliosides; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosamines; Hexoses; Humans; Molecular Weight; Nerve Tissue Proteins; Neuraminic Acids; Papain; Solubility; Spectrophotometry | 1972 |
2 trial(s) available for galactose and Brain Disorders
Article | Year |
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Lactulose treatment of hepatic encephalopathy: effects on carbohydrate metabolism and colonic hydrogen ion concentration.
Topics: Animals; Brain Diseases; Carbohydrate Metabolism; Clinical Trials as Topic; Colon; Dogs; Feces; Fructose; Galactose; Glucose; Glucose Tolerance Test; Humans; Hydrogen-Ion Concentration; Insulin; Iodine Isotopes; Liver; Liver Cirrhosis; Liver Diseases; Portacaval Shunt, Surgical | 1970 |
Lactulose treatment of hepatic encephalopathy in outpatients.
Topics: Adolescent; Aged; Alcoholism; Ambulatory Care; Ammonia; Brain Diseases; Colon; Diet Therapy; Dietary Proteins; Electroencephalography; Female; Fructose; Galactose; Humans; Hydrogen-Ion Concentration; Liver Cirrhosis; Male; Middle Aged; Nitrogen; Portacaval Shunt, Surgical; Sorbitol | 1971 |
22 other study(ies) available for galactose and Brain Disorders
Article | Year |
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Polydatin attenuates d-galactose-induced liver and brain damage through its anti-oxidative, anti-inflammatory and anti-apoptotic effects in mice.
Topics: Aging; Animals; Anti-Inflammatory Agents; Antioxidants; Apoptosis; Brain Diseases; Chemical and Drug Induced Liver Injury; Cytokines; Dose-Response Relationship, Drug; Galactose; Glucosides; Liver; Malondialdehyde; Mice; Molecular Structure; Oxidative Stress; Stilbenes | 2016 |
A case of galactosaemia with the pathological and neuropathological findings.
Topics: Brain; Brain Diseases; Galactose; Galactosemias; Humans; Intellectual Disability; Nervous System Diseases; Neurologic Manifestations | 1962 |
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 |
Cerebral aspergillosis diagnosed by detection of Aspergillus flavus-specific DNA, galactomannan and (1-->3)-beta-D-glucan in clinical specimens.
Topics: Amphotericin B; Antifungal Agents; Aspergillosis; Aspergillus flavus; beta-Glucans; Brain; Brain Diseases; Caspofungin; Diagnosis, Differential; DNA, Fungal; Echinocandins; Electrophoresis, Agar Gel; Galactose; Humans; Lipopeptides; Male; Mannans; Middle Aged; Peptides, Cyclic; Polymerase Chain Reaction | 2007 |
Preoperative liver function tests correlated with encephalopathy after porta-caval anastomosis.
Topics: Adult; Age Factors; Aged; Alcoholism; Bilirubin; Brain Diseases; Esophageal and Gastric Varices; Female; Galactose; Gastrointestinal Hemorrhage; Humans; Liver; Liver Cirrhosis; Liver Function Tests; Male; Middle Aged; Portacaval Shunt, Surgical; Preoperative Care; Prognosis; Prothrombin Time; Serum Albumin | 1975 |
Galactosemia: evaluation with MR imaging.
Topics: Adolescent; Adult; Age Factors; Brain Diseases; Child; Child, Preschool; Diagnosis, Differential; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Phosphotransferases; Racemases and Epimerases; Transferases | 1992 |
Cerebral GM1-gangliosidosis: chemical pathology of visceral organs.
Topics: Brain Diseases; Chromatography, Thin Layer; Galactose; Gangliosides; Glycosaminoglycans; Hexosamines; Humans; Lipidoses; Liver; Polysaccharides; Spleen | 1968 |
[Therapeutic effect of lactulose on shunt encephalopathy and blood ammonia concentration in cirrhosis patients].
Topics: Adult; Ammonia; Brain Diseases; Female; Fructose; Galactose; Humans; Ketones; Lactose; Liver Circulation; Liver Cirrhosis; Male; Middle Aged; Portacaval Shunt, Surgical; Portal System | 1972 |
[Treatment of chronic portal-systemic encephalopathy with lactulose (synthetic disaccharide: one molecule of galactose and one of fructose)].
Topics: Adult; Aged; Ascites; Brain Diseases; Chronic Disease; Disaccharides; Female; Fructose; Galactose; Humans; Liver Cirrhosis; Male; Middle Aged; Portal System | 1972 |
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 |
Encephalopathy after portacaval shunting managed with lactulose.
Topics: Aged; Brain Diseases; Disaccharides; Female; Fructose; Galactose; Humans; Liver Cirrhosis; Male; Middle Aged; Portacaval Shunt, Surgical; Postoperative Complications | 1970 |
Lactulose treatment of chronic hepatoportal encephalopathy. A clinical and electroencephalographic study.
Topics: Adult; Aged; Biopsy; Brain Diseases; Dietary Proteins; Disaccharides; Electroencephalography; Esophageal and Gastric Varices; Female; Fructose; Galactose; Hepatic Encephalopathy; Humans; Liver Cirrhosis; Male; Middle Aged; Portacaval Shunt, Surgical; Postoperative Complications | 1970 |
Effect of dietary protein on symptoms and survival in dogs with an Eck fistula.
Topics: Alkaline Phosphatase; Amino Acids; Ammonia; Animals; Aspartate Aminotransferases; Blood Chemical Analysis; Blood Urea Nitrogen; Body Weight; Brain Diseases; Dietary Proteins; Dogs; Fish Products; Galactose; Liver Function Tests; Meat; Milk; Neurologic Manifestations; Portacaval Shunt, Surgical; Quaternary Ammonium Compounds; Seizures; Serum Albumin; Sulfobromophthalein; Transaminases | 1971 |
The mechanism of action of lactulose in portal-systemic encephalopathy. Non-ionic diffusion of ammonia in the canine colon.
Topics: Ammonia; Animals; Biological Transport; Brain Diseases; Colon; Diffusion; Disaccharides; Dogs; Feces; Fructose; Galactose; Hydrogen-Ion Concentration | 1971 |
Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts.
Topics: Brain Diseases; Cerebrosides; Chromatography, Gas; Chromatography, Thin Layer; Culture Techniques; Fibroblasts; Galactose; Glycoside Hydrolases; Heterozygote; Lactose; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Sphingolipids | 1971 |
[Biochemical approach to types of lipoidosis and leukodystrophy].
Topics: Brain; Brain Diseases; Hexoses; Humans; Lipid Metabolism; Lipidoses; Lysosomal Storage Diseases; Phospholipids | 1955 |
[Studies on the protein-bound carbohydrates and lipids in the cerebrospinal fluid].
Topics: Brain Diseases; Carbohydrates; Cerebrospinal Fluid; Cerebrospinal Fluid Proteins; Hexoses; Lipids; Spinal Cord | 1962 |
PSEUDOTUMOR CEREBRI FOLLOWING ACUTE RHEUMATIC FEVER.
Topics: Adolescent; Brain Diseases; Diet, Sodium-Restricted; Hexoses; Humans; Hydrochlorothiazide; Intracranial Pressure; Papilledema; Penicillins; Pseudotumor Cerebri; Rheumatic Fever; Urea | 1963 |
Determination of gangliosides, glycoproteins, and glycosaminoglycans in brain tissue.
Topics: Acetates; Adult; Animals; Brain Chemistry; Brain Diseases; Cattle; Cerebral Cortex; Chemical Precipitation; Child; Child, Preschool; Chloroform; Chromatography, Gel; Dialysis; Electrophoresis; Fucose; Galactosemias; Gangliosides; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosamines; Hexoses; Humans; Hydrogen-Ion Concentration; Lipidoses; Methanol; Methods; Myelin Sheath; Neuraminic Acids; Papain; Peptide Hydrolases; Pyridinium Compounds; Rats; Solubility; Subacute Sclerosing Panencephalitis; Temperature | 1971 |
The fractionation of some plasma constituents by exclusion chromatography, with application to neuropsychiatric disorders.
Topics: Acute Disease; Adolescent; Adult; Aged; Blood Proteins; Brain Diseases; Cerebrospinal Fluid Proteins; Child; Child, Preschool; Chromatography, Gel; Dementia; Female; Hexoses; Humans; Huntington Disease; Hydrogen-Ion Concentration; Male; Mathematics; Mental Disorders; Methods; Molecular Weight; Parietal Lobe; Psychotic Disorders; Schizophrenia | 1970 |
[Value of lactulose in the treatment of chronic porto-cave encephalopathy (20 cases)].
Topics: Adult; Aged; Ammonia; Brain Diseases; Female; Hexoses; Humans; Liver Cirrhosis; Male; Middle Aged | 1970 |
Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A.
Topics: Amidohydrolases; Brain Diseases; Cerebral Cortex; Child, Preschool; Female; Gangliosides; Genes, Recessive; Hexoses; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Skin | 1970 |