These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 5016302)

  • 1. Glycosphingolipid levels in an unusual neurovisceral storage disease characterized by lactosylceramide galactosyl hydrolase deficiency: lactosylceramidosis.
    Dawson G
    J Lipid Res; 1972 Mar; 13(2):207-19. PubMed ID: 5016302
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts.
    Dawson G; Matalon R; Stein AO
    J Pediatr; 1971 Sep; 79(3):423-9. PubMed ID: 5567965
    [No Abstract]   [Full Text] [Related]  

  • 3. Detection of glycosphingolipids in small samples of human tissue.
    Dawson G
    Ann Clin Lab Sci (1971); 1972; 2(4):274-84. PubMed ID: 5072682
    [No Abstract]   [Full Text] [Related]  

  • 4. Generalized accumulation of neutral glycosphingolipids with G M2 ganglioside accumulation in the brain.
    Snyder PD; Krivit W; Sweeley CC
    J Lipid Res; 1972 Jan; 13(1):128-36. PubMed ID: 5059190
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Studies on neural and visceral glycolipids in a case of infantile form of Gaucher's disease.
    Kubota M
    Jpn J Exp Med; 1972 Dec; 42(6):513-26. PubMed ID: 4540903
    [No Abstract]   [Full Text] [Related]  

  • 6. Lipid changes in Niemann-Pick disease type C brain: personal experience and review of the literature.
    Vanier MT
    Neurochem Res; 1999 Apr; 24(4):481-9. PubMed ID: 10227680
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Glycosphingolipids in cultured human skin fibroblasts. II. Characterization and metabolism in fibroblasts from patients with inborn errors of glycosphingolipid and mucopolysaccharide metabolism.
    Dawson G; Matalon R; Dorfman A
    J Biol Chem; 1972 Sep; 247(18):5951-8. PubMed ID: 5057092
    [No Abstract]   [Full Text] [Related]  

  • 8. Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease.
    Nilsson O; Svennerholm L
    J Neurochem; 1982 Sep; 39(3):709-18. PubMed ID: 7097276
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glycolipids isolated from the spleen of Gaucher's disease.
    Makita A; Suzuki C; Yosizawa Z; Konno T
    Tohoku J Exp Med; 1966 Mar; 88(3):277-88. PubMed ID: 5956509
    [No Abstract]   [Full Text] [Related]  

  • 10. Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage disease.
    Bradová V; Smíd F; Ulrich-Bott B; Roggendorf W; Paton BC; Harzer K
    Hum Genet; 1993 Sep; 92(2):143-52. PubMed ID: 8370580
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further developments in studies in sphingolipidoses: "missing enzymes".
    Brady RO
    Riv Patol Nerv Ment; 1970 Oct; 91(5):263-73. PubMed ID: 5525771
    [No Abstract]   [Full Text] [Related]  

  • 12. [Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue].
    Pilz H; Heipertz R
    Fortschr Neurol Psychiatr Grenzgeb; 1975 Nov; 43(11):602-17. PubMed ID: 53174
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gangliosides and neutral glycolipids in guinea pig adrenal glands.
    Sekine M; Ariga T; Miyatake T; Kase R; Suzuki A; Yamakawa T
    J Biochem; 1984 Jul; 96(1):237-44. PubMed ID: 6490601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of Gaucher's disease.
    Nilsson O; Månsson JE; Håkansson G; Svennerholm L
    Biochim Biophys Acta; 1982 Sep; 712(3):453-63. PubMed ID: 7126619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lactosyl ceramidosis: catabolic enzyme defect of glycosphingolipid metabolism.
    Dawson G; Stein AO
    Science; 1970 Oct; 170(3957):556-8. PubMed ID: 5507210
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cerebral and visceral organ gangliosides and related glycolipids in gm1-gangliosidosis type 1, type 2 and chronic type.
    Taketomi T; Hara A; Kasama T
    Adv Exp Med Biol; 1984; 174():419-29. PubMed ID: 6430048
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Farber's lipogranulomatosis. Report of a case and demonstration of an excess of free ceramide and ganglioside.
    Moser HW; Prensky AL; Wolfe HJ; Rosman NP
    Am J Med; 1969 Dec; 47(6):869-90. PubMed ID: 5395479
    [No Abstract]   [Full Text] [Related]  

  • 18. [Sphingolipidoses. Biochemistry and enzymatic mechanisms].
    Gajdos A
    Nouv Presse Med; 1972 Jun; 1(26):1789-92. PubMed ID: 5054020
    [No Abstract]   [Full Text] [Related]  

  • 19. Characterization and quantitative determination of gangliosides and neutral glycosphingolipids in human liver.
    Nilsson O; Svennerholm L
    J Lipid Res; 1982 Feb; 23(2):327-34. PubMed ID: 7077147
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A lysosomal storage disorder in mice characterized by the accumulation of several sphingolipids.
    Pentchev PG; Gal AE; Boothe AD; Fouks J; Omodeo-Sale F; Brady RO
    Birth Defects Orig Artic Ser; 1980; 16(1):225-30. PubMed ID: 7448355
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.