BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 1672707)

  • 1. A case of nonneurologic Gaucher's disease that biochemically resembles the neurologic types.
    Glew RH; Gopalan V; Hubbell CA; Beutler E; Geil JD; Lee RE
    J Neuropathol Exp Neurol; 1991 Mar; 50(2):108-17. PubMed ID: 1672707
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enzymic differentiation of neurologic and nonneurologic forms of Gaucher's disease.
    Glew RH; Daniels LB; Clark LS; Hoyer SW
    J Neuropathol Exp Neurol; 1982 Nov; 41(6):630-41. PubMed ID: 6813430
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of N-acyl phosphatidylethanolamines with different N-acyl groups as activators of glucocerebrosidase in various forms of Gaucher's disease.
    Basu A; Prence E; Garrett K; Glew RH; Ellingson JS
    Arch Biochem Biophys; 1985 Nov; 243(1):28-34. PubMed ID: 3933429
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease.
    Tsuji S; Choudary PV; Martin BM; Stubblefield BK; Mayor JA; Barranger JA; Ginns EI
    N Engl J Med; 1987 Mar; 316(10):570-5. PubMed ID: 2880291
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Activators of spleen glucocerebrosidase from controls and patients with various forms of Gaucher's disease.
    Basu A; Glew RH; Daniels LB; Clark LS
    J Biol Chem; 1984 Feb; 259(3):1714-9. PubMed ID: 6693432
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sucrose gradient analysis of phospholipid-activated beta-glucosidase in type 1 and type 2 Gaucher's disease.
    Garrett KO; Prence EM; Glew RH
    Arch Biochem Biophys; 1985 Apr; 238(1):344-52. PubMed ID: 3920967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gaucher's disease in Lithuania: its diagnosis and treatment.
    Kleinotienė G; Tylki-Szymanska A; Czartoryska B
    Medicina (Kaunas); 2011; 47(7):405-11. PubMed ID: 22112991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coincidence of Gaucher's disease due to a private mutation and Ph' positive chronic myeloid leukemia.
    Petrides PE; leCoutre P; Müller-Höcker J; Magin E; Harzer K; Demina A; Beutler E
    Am J Hematol; 1998 Sep; 59(1):87-90. PubMed ID: 9723584
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's disease.
    Tayebi N; Reissner KJ; Lau EK; Stubblefield BK; Klineburgess AC; Martin BM; Sidransky E
    Pediatr Res; 1998 May; 43(5):571-8. PubMed ID: 9585001
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of the 1226 (Jewish) mutation for Gaucher's disease by color PCR. A means for studying the gene frequency of the disorder.
    Zimran A; Kuhl WC; Beutler E
    Am J Clin Pathol; 1990 Jun; 93(6):788-91. PubMed ID: 2346136
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gaucher's disease.
    Patel AL; Shaikh WA; Khobragade AK; Soni HG; Joshi AS; Sahasrabudhe GS; Chole PV
    J Assoc Physicians India; 2009 May; 57():410-1. PubMed ID: 19634291
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Type I Gaucher's disease with homozygous R463C mutation without neurological involvement.
    Bolaman Z; Kadikoylu G; Levi E; Barutca S; Temucin K
    Haematologia (Budap); 2002; 32(4):487-93. PubMed ID: 12803123
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Gaucher's disease suspected by abdominal echography findings].
    Castellano G; Yela MC; Martín A; Manzano ML; Colina F; Solís JA
    Gastroenterol Hepatol; 1998 Apr; 21(4):184-7. PubMed ID: 9633179
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Imprint cytology of Gaucher's disease presenting as a splenic mass. A case report with molecular approaches.
    Kobayashi TK; Tamagaki T; Yoneyama C; Watanabe S; Sugihara H; Ida H
    Acta Cytol; 1998; 42(2):419-24. PubMed ID: 9568149
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidase.
    Dahl N; Erikson A; Hammarström-Heeroma K; Pettersson U
    Genomics; 1988 Nov; 3(4):296-8. PubMed ID: 2468600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic diagnosis of Gaucher's disease.
    Mistry PK; Smith SJ; Ali M; Hatton CS; McIntyre N; Cox TM
    Lancet; 1992 Apr; 339(8798):889-92. PubMed ID: 1348297
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Glucocerebrosidase deficiency--Gaucher's disease].
    Tsuji S
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):728-33. PubMed ID: 2908399
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patient.
    Choy FY; Humphries ML; Ferreira P
    Am J Med Genet; 1997 Jan; 68(2):211-5. PubMed ID: 9028460
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prediction of severity of Gaucher's disease by identification of mutations at DNA level.
    Zimran A; Sorge J; Gross E; Kubitz M; West C; Beutler E
    Lancet; 1989 Aug; 2(8659):349-52. PubMed ID: 2569551
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gaucher's disease and pregnancy.
    Fasouliotis SJ; Ezra Y; Schenker JG
    Am J Perinatol; 1998 May; 15(5):311-8. PubMed ID: 9643638
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.