Compounds > galactose
Page last updated: 2024-08-17

galactose and Autosomal Chromosome Disorders

galactose has been researched along with Autosomal Chromosome Disorders in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dahlqvist, A; Hall, B1
Dahlqvist, A; Hall, B; Källén, B1
Elsas, LJ1
Handmaker, S; Kampine, JP; Kanfer, JN; Richards, R; Yankee, RA1
Calne, DB; King, RH; Thomas, PK1

Other Studies

5 other study(ies) available for galactose and Autosomal Chromosome Disorders

ArticleYear
Enzyme activity in D trisomies.
    Lancet (London, England), 1971, Oct-23, Volume: 2, Issue:7730

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Galactose; Humans; Nucleotidyltransferases; Phosphates; Trisomy; Uracil Nucleotides

1971
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
Glucose reabsorption in familial renal glycosuria and glucose-galactose malabsorption.
    Birth defects original article series, 1970, Volume: 6, Issue:3

    Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Galactose; Genes, Recessive; Glucose; Glycosuria, Renal; Humans; Jejunum; Kidney; Kidney Concentrating Ability; Kidney Tubules; Malabsorption Syndromes; Male

1970
Alteration of e sphingolipid content in leucocytes from patients with Chediak-Higashi syndrome.
    Life sciences, 1967, Dec-15, Volume: 6, Issue:24

    Topics: Amides; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Hexoses; Humans; Leukocytes; Lipids; Phosphates; Sphingomyelins

1967
Autosomal dominant forms of hereditary hypertrophic neuropathy.
    Monographs in human genetics, 1972, Volume: 6

    Topics: Age Factors; Ceramides; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Hexoses; Humans; Hypertrophy; Metabolism, Inborn Errors; Muscular Atrophy; Neuritis; Syndrome

1972