Page last updated: 2024-08-17

galactose and Intellectual Disability

galactose has been researched along with Intellectual Disability in 31 studies

Research

Studies (31)

Timeframe	Studies, this research(%)	All Research%
pre-1990	30 (96.77)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (3.23)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Lee, PJ; Lilburn, M; Schadewaldt, P; Wendel, U	1
CARVER, MJ; WITTSON, C	1
CROME, L	1
GIELEN, W; KLENK, E; LIEDTKE, U	1
CALLERI, A; GIOVANNINI, M; TERZOLI, S	1
GOMMI, BW; WOOLLEY, DW	1
AKABANE, J; MINAGAWA, A; MIZUNO, T; MORIKAWA, T; OGASAWARA, J; OKAMURA, T; TADA, K; WADA, Y; YOSHIDA, T	1
Gommi, BW; Wild, G; Woolley, DW	1
Fornai, K; Osváth, P; Pozderka, B; Veres, B	1
Enzenauer, J; Matz, D; Menne, F	1
Miyashita, K; Miyatake, T; Miyatani, N; Tsuji, S; Yoshino, H	1
Jaeken, J	1
Lamberg, SI; Stoolmiller, AC	1
Dahlqvist, A; Hall, B; Källén, B	1
Bach, G; Berman, ER; Vered, J	1
Harvey, J; Robertson, WV	1
Bach, G; Cantz, M; Eisenberg, F; Neufeld, EF	1
Hambraeus, L; Holmgren, G	1
Berry, HK; Fogelson, MH	1
Pollitt, RJ; Pretty, KM	1
McKean, CM; Peterson, NA; Shah, SN	1
Dulaney, JT; Moser, HW; Sugita, M	1
Holmer, GK; Lou, HC; Reske-Nielsen, E; Vagn-Hansen, P	1
Kitagawa, T	1
Hansen, RG	1
Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW	1
Chen, PT; Cravey, CE; Hall, WK; Hollowell, JG; Ostendorff, ME; Thevaos, TG	1
Hager-Malecka, B; Sychlowy, A; Szczepański, Z	1
Dekaban, AS; Patton, VM	1
Dorfman, A; Matalon, R	1
Hovingh, P; Linker, A	1

Reviews

4 review(s) available for galactose and Intellectual Disability

Article	Year
[Late-infantile form galactosialidosis with psychomotor retardation and spastic paraparesis]. Rinsho shinkeigaku = Clinical neurology, 1989, Volume: 29, Issue:10 Topics: beta-Galactosidase; Carbohydrate Metabolism, Inborn Errors; Child; Galactose; Humans; Intellectual Disability; Male; Neuraminidase; Paraparesis, Tropical Spastic; Psychomotor Disorders; Sialic Acids	1989
Glycosaminoglycans. A biochemical and clinical review. The Journal of investigative dermatology, 1974, Volume: 63, Issue:6 Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chondroitin; Cornea; Corneal Opacity; Dermatan Sulfate; Fibroblasts; Galactose; Glucosamine; Glycosaminoglycans; Heparin; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Proteoglycans; Retinitis Pigmentosa; Skin; Staining and Labeling; Sulfatases; Testis	1974
[Congenital metabolic inborn errors, with the exception of amino acid metabolism]. Shinkei kenkyu no shimpo. Advances in neurological sciences, 1968, Volume: 12, Issue:1 Topics: Amino Acids; Carbohydrate Metabolism, Inborn Errors; Galactose; Humans; Hypercalcemia; Intellectual Disability; Kidney Function Tests; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Proline; Purine-Pyrimidine Metabolism, Inborn Errors; Renal Tubular Transport, Inborn Errors	1968
Hereditary galactosemia. JAMA, 1969, Jun-16, Volume: 208, Issue:11 Topics: Diet Therapy; Galactose; Galactosemias; Humans; Intellectual Disability	1969

Other Studies

27 other study(ies) available for galactose and Intellectual Disability

Article	Year
A woman with untreated galactosaemia. Lancet (London, England), 2003, Aug-09, Volume: 362, Issue:9382 Topics: Adult; Female; Food, Formulated; Galactose; Galactosemias; Humans; Intellectual Disability	2003
Metabolic errors and mental retardation. Clinical medicine (Northfield, Ill.), 1961, Volume: 8 Topics: Biochemical Phenomena; Galactose; Hepatolenticular Degeneration; Humans; Intellectual Disability; Phenylketonurias	1961
A case of galactosaemia with the pathological and neuropathological findings. Archives of disease in childhood, 1962, Volume: 37 Topics: Brain; Brain Diseases; Galactose; Galactosemias; Humans; Intellectual Disability; Nervous System Diseases; Neurologic Manifestations	1962
[BRAIN GANGLIOSIDES IN INFANTILE AMAUROTIC IDIOCY OF THE TAY-SACHS TYPE]. Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1963, Volume: 334 Topics: Brain; Chromatography; Fatty Acids; Galactose; Gangliosides; Glucose; Humans; Intellectual Disability; Lipidoses; Tay-Sachs Disease	1963
[METABOLIC STUDIES IN A GROUP OF CHILDREN WITH MENTAL DEFICIENCY: URINARY ELIMINATION OF AMINO ACIDS, CARBOHYDRATES, TRYPTOPHAN METABOLITES AND ABNORMAL METABOLITES]. Minerva pediatrica, 1964, Mar-24, Volume: 16 Topics: Amino Acids; Body Fluids; Carbohydrates; Child; Galactose; Glycosaminoglycans; Humans; Imidazoles; Infant; Intellectual Disability; Kynurenine; Metabolism; Tryptophan; Urine; Xanthurenates	1964
SEROTONIN RECEPTORS. IV. SPECIFIC DEFICIENCY OF RECEPTORS IN GALACTOSE POISONING AND ITS POSSIBLE RELATIONSHIP TO THE IDIOCY OF GALACTOSEMIA. Proceedings of the National Academy of Sciences of the United States of America, 1964, Volume: 52 Topics: Acetylcholine; Brain Chemistry; Cerebrosides; Dietary Carbohydrates; Epinephrine; Galactose; Galactosemias; Gangliosides; Glucose; Intellectual Disability; Lipids; Pharmacology; Phenylketonurias; Rats; Receptors, Serotonin; Research; Serotonin; Stomach; Toxicology; Transferases	1964
A SEX-LINKED DISORDER WITH MENTAL AND PHYSICAL RETARDATION CHARACTERIZED BY CEREBROCORTICAL ATROPHY AND INCREASE OF GLUTAMIC ACID IN THE CEREBROSPINAL FLUID. The Tohoku journal of experimental medicine, 1964, Aug-25, Volume: 83 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
Effects of experimental galactosemia on the measured serotonin receptor activity of rat brain. Biochemistry, 1967, Volume: 6, Issue:6 Topics: Animals; Brain Chemistry; Chromatography; Chromatography, Thin Layer; Female; Galactose; Galactosemias; Gangliosides; Glucose; Glycolipids; Hexosamines; Humans; Intellectual Disability; Rats; Serotonin; Stomach	1967
[Galactose loading test in infants and small children suffering in recurrent bronchitis and other chronic illness (author's transl)]. Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1981, Volume: 129, Issue:8 Topics: Bronchitis; Child; Child, Preschool; Diarrhea; Eclampsia; Female; Galactokinase; Galactose; Galactosemias; Heterozygote; Humans; Infant; Intellectual Disability; Male; Pregnancy; Recurrence; Respiratory Tract Infections	1981
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2]. Medizinische Klinik, 1976, Apr-30, Volume: 71, Issue:18 Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases	1976
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins]. Verhandelingen - Koninklijke Academie voor Geneeskunde van Belgie, 1989, Volume: 51, Issue:4 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
Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations. Human heredity, 1969, Volume: 19, Issue:6 Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Abnormalities; Cri-du-Chat Syndrome; Down Syndrome; Female; Galactose; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Nucleotidyltransferases; Trisomy; Uracil Nucleotides	1969
A reliable spot test for mucopolysaccharidoses. Clinical chemistry, 1971, Volume: 17, Issue:9 Topics: Adult; Bone Diseases, Developmental; Carbazoles; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Coloring Agents; Corneal Opacity; Dialysis; Dwarfism; Female; Galactose; Glucosamine; Glycosaminoglycans; Hexosamines; Humans; Indicators and Reagents; Infant; Intellectual Disability; Male; Methods; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Onium Compounds; Paper; Peptide Hydrolases; Phenols; Retinitis Pigmentosa; Sulfuric Acids; Toluene; Uronic Acids	1971
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine. Biochemical medicine, 1972, Volume: 6, Issue:3 Topics: Achondroplasia; Adolescent; Adult; Aged; Aging; Arthritis, Rheumatoid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Colorimetry; Dermatomyositis; Female; Galactose; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Infant, Newborn; Intellectual Disability; Lipid Metabolism, Inborn Errors; Male; Methods; Middle Aged; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfuric Acids	1972
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proceedings of the National Academy of Sciences of the United States of America, 1973, Volume: 70, Issue:7 Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Galactose; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycosides; Humans; Iduronic Acid; Intellectual Disability; Mannose; Mucopolysaccharidosis II; Retinitis Pigmentosa; Skin; Sulfatases; Sulfur Isotopes; Sulfuric Acids; Tritium; Uronic Acids	1973
Urinary metabolic screening in children with psycho-neurological diseases. Evaluation of different screening tests. Upsala journal of medical sciences. Supplement, 1974, Volume: 15 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Paper; Electrophoresis, Paper; Evaluation Studies as Topic; Female; Galactose; Glycosaminoglycans; Humans; Indicators and Reagents; Infant; Infant, Newborn; Intellectual Disability; Male; Mass Screening; Methods; Reagent Strips; Renal Tubular Transport, Inborn Errors	1974
Nutritional investigations in the oculocerebrorenal syndrome of Lowe. Birth defects original article series, 1974, Volume: 10, Issue:10 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
Glycoasparagines in the urine of patients with aspartylglycosaminuria. The Biochemical journal, 1972, Volume: 128, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Chromatography; Chromatography, Ion Exchange; Fucose; Galactose; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Molecular Weight	1972
Lipid composition of human cerebral white matter and myelin in phenylketonuria. Journal of neurochemistry, 1972, Volume: 19, Issue:10 Topics: Adolescent; Adult; Aged; Autopsy; Brain; Brain Chemistry; Cholesterol; Female; Galactose; Glycolipids; Humans; Intellectual Disability; Lipids; Male; Myelin Sheath; Phenylketonurias	1972
Ceramidase deficiency in Farber's disease (lipogranulomatosis). Science (New York, N.Y.), 1972, Dec-08, Volume: 178, Issue:4065 Topics: Acid Phosphatase; Adult; Carbon Isotopes; Ceramides; Cerebellum; Cerebrosides; Child; Child, Preschool; Congenital Abnormalities; Female; Galactose; Galactosidases; Glucose; Glycoside Hydrolases; Heart Defects, Congenital; Hexosaminidases; Humans; Hydrolases; Infant; Infant, Newborn; Intellectual Disability; Kidney; Lipidoses; Liver Cirrhosis, Biliary; Male; Metabolism, Inborn Errors; Neuraminidase; Pigmentation Disorders; Respiratory Distress Syndrome, Newborn	1972
Lipid composition in gray and white matter of the brain in Menkes' disease. Journal of neurochemistry, 1974, Volume: 22, Issue:3 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
Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis. Pediatric research, 1969, Volume: 3, Issue:6 Topics: Biopsy; Bone Marrow; Bone Marrow Cells; Brain; Culture Media; Culture Techniques; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glycolipids; Humans; Infant; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Niemann-Pick Diseases; Rheumatic Heart Disease; Skin	1969
An evaluation of galactosuria. The Journal of pediatrics, 1970, Volume: 77, Issue:4 Topics: Adolescent; Adult; Animals; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Child; Chromatography; Diet; Dietary Carbohydrates; Galactose; Humans; Intellectual Disability; Methods; Middle Aged; Milk; Nucleotidyltransferases	1970
[Galactosemia as based on the records of Department I of Pediatrics of the Silesian Medical Academy]. Pediatria polska, 1971, Volume: 46, Issue:2 Topics: Body Weight; Cataract; Child, Preschool; Female; Galactose; Galactosemias; Hepatomegaly; Heterozygote; Homozygote; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Pedigree; Splenomegaly	1971
Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry. Archives of pathology, 1971, Volume: 91, Issue:5 Topics: Amides; Brain; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Child; Chromatography, Thin Layer; Female; Gangliosides; Glycosaminoglycans; Hexoses; Histocytochemistry; Humans; Intellectual Disability; Lipids; Male; Mucopolysaccharidosis I; Nerve Degeneration	1971
Hurler's syndrome, an -L-iduronidase deficiency. Biochemical and biophysical research communications, 1972, May-26, Volume: 47, Issue:4 Topics: Amnion; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Female; Fibroblasts; Galactosidases; Genes; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Hexoses; Humans; Intellectual Disability; Liver; Lysosomes; Mucopolysaccharidosis I; Phenols; Retinitis Pigmentosa; Skin; Uronic Acids	1972
The heparitin sulfates (heparan sulfates). Carbohydrate research, 1973, Volume: 29, Issue:1 Topics: Amyloidosis; Animals; Aorta; Carbohydrate Metabolism, Inborn Errors; Cattle; Chromatography, Ion Exchange; Dialysis; Electrophoresis; Galactosamine; Glucuronates; Glycosaminoglycans; Heparitin Sulfate; Hexosamines; Hexoses; Humans; Intellectual Disability; Intestines; Liver; Lung; Methods; Molecular Weight; Optical Rotation; Proteins; Uronic Acids	1973