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 *

155 related articles for article (PubMed ID: 6811161)

  • 21. Catalytically defective ganglioside neuraminidase in mucolipidosis IV.
    Ben-Yoseph Y; Momoi T; Hahn LC; Nadler HL
    Clin Genet; 1982 Jun; 21(6):374-81. PubMed ID: 6813002
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A case of adult type sialidosis with partial beta-galactosidase deficiency without myoclonus].
    Yamaguchi H; Okamoto K; Shooji M; Morimatsu M; Hirai S
    Rinsho Shinkeigaku; 1983 Jan; 23(1):1-8. PubMed ID: 6851348
    [No Abstract]   [Full Text] [Related]  

  • 23. Combined deficiency of beta-galactosidase and neuraminidase: three affected siblings in a French family.
    Maire I; Nivelon-Chevallier AR
    J Inherit Metab Dis; 1981; 4(4):221-3. PubMed ID: 6796775
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Turnover of beta-galactosidase in fibroblasts from patients with genetically different types of beta-galactosidase deficiency.
    Van Diggelen OP; Schram AW; Sinnott ML; Smith PJ; Robinson D; Galjaard H
    Biochem J; 1981 Oct; 200(1):143-51. PubMed ID: 6800355
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Oligosaccharide and ganglioside neuraminidase activities of mucolipidosis I (sialidosis) and mucolipidosis II (I-cell disease) fibroblasts.
    Cantz M; Messer H
    Eur J Biochem; 1979 Jun; 97(1):113-8. PubMed ID: 477659
    [No Abstract]   [Full Text] [Related]  

  • 26. Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.
    D'Azzo A; Hoogeveen A; Reuser AJ; Robinson D; Galjaard H
    Proc Natl Acad Sci U S A; 1982 Aug; 79(15):4535-9. PubMed ID: 6812049
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial characterization and studies of fibroblast and leucocyte neuraminidase activities towards sialyloligosaccharides in adult sialidosis and mucolipidosis II and III.
    Kuriyama M; Someya F; Miyatake T; Koseki M
    Biochim Biophys Acta; 1981 Dec; 662(2):220-5. PubMed ID: 7317438
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Galatosialidosis (beta-galactosidase-neuraminidase deficiency): clinical and biochemical studies on 13 patients.
    Suzuki Y; Fukuoka K; Sakuraba H; Hayashi K; Ko YM
    Adv Exp Med Biol; 1982; 152():241-51. PubMed ID: 6814202
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Enhanced proteolytic degradation of normal beta-galactosidase in the lysosomal storage disease with combined beta-galactosidase and neuraminidase deficiency.
    van Diggelen OP; Hoogeveen AT; Smith PJ; Reuser AJ; Galjaard H
    Biochim Biophys Acta; 1982 Apr; 703(1):69-76. PubMed ID: 6803839
    [No Abstract]   [Full Text] [Related]  

  • 30. Induction of beta-galactosidase in beta-galactosidase-alpha-neuraminidase deficiency: effects of leupeptin and sucrose.
    Kato T; Okada S; Yutaka T; Yabuuchi H
    Biochem Int; 1983 Feb; 6(2):267-73. PubMed ID: 6433925
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency.
    Kleijer WJ; Hoogeveen A; Verheijen FW; Niermeijer MF; Galjaard H; O'Brien JS; Warner TG
    Clin Genet; 1979 Jul; 16(1):60-1. PubMed ID: 477017
    [No Abstract]   [Full Text] [Related]  

  • 32. beta-Galactosidase-neuraminidase deficiency in adults: deficiency of a freeze-labile neuraminidase in leukocytes and fibroblasts.
    Suzuki Y; Sakuraba H; Potier M; Akagi M; Sakai M; Beppu H
    Hum Genet; 1981; 58(4):387-9. PubMed ID: 7327559
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mucolipidosis I (acid neuraminidase deficiency). Three cases and delineation of the variability of the phenotype.
    Kelly TE; Bartoshesky L; Harris DJ; McCauley RG; Feingold M; Schott G
    Am J Dis Child; 1981 Aug; 135(8):703-8. PubMed ID: 7270511
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case.
    Winter RM; Swallow DM; Baraitser M; Purkiss P
    Clin Genet; 1980 Sep; 18(3):203-10. PubMed ID: 6777097
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The complementation of beta-galactosidase in fused cells of mucolipidosis II with another variants of beta-galactosidase deficiency using new single cell enzyme assay.
    Okada S; Kato T; Yabuuchi H; Okada Y
    Biochem Biophys Res Commun; 1979 May; 88(2):559-62. PubMed ID: 111672
    [No Abstract]   [Full Text] [Related]  

  • 36. Neuraminidase studies in sialidosis.
    Cantz M
    Adv Exp Med Biol; 1980; 125():415-30. PubMed ID: 7189082
    [No Abstract]   [Full Text] [Related]  

  • 37. Ultrastructural study on a severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency).
    Yamano T; Shimada M; Sugino H; Dezawa T; Koike M; Okada S; Yabuuchi H
    Neuropediatrics; 1985 May; 16(2):109-12. PubMed ID: 3925363
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Neuraminidase in mucolipidoses: normal activity in frozen autopsy tissues from three patients with I-cell disease and adult beta-galactosidase deficiency.
    Suzuki Y; Fukuoka K
    Clin Chim Acta; 1979 Dec; 99(2):107-12. PubMed ID: 116781
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Adult type mucolipidosis with beta-galactosidase and sialidase deficiency. Histological and biochemical studies.
    Kobayashi T; Ohta M; Goto I; Tanaka Y; Kuroiwa Y
    J Neurol; 1979 Sep; 221(3):137-49. PubMed ID: 91667
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Mucolipidosis II (I cell disease): a sialidosis?].
    Farriaux JP; Strecker G
    Arch Fr Pediatr; 1979 Mar; 36(3):225-34. PubMed ID: 485767
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.