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 *

174 related articles for article (PubMed ID: 11336404)

  • 21. Sixteen years of prenatal consultations for the N370S/N370S Gaucher disease genotype: what have we learned?
    Eitan Y; Abrahamov A; Phillips M; Elstein D; Zimran A
    Prenat Diagn; 2010 Oct; 30(10):924-7. PubMed ID: 20721872
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Frequency of the Gaucher mutation among recent Russian immigrants].
    Hodish I; Elstein D; Abrahamov A; Lonshakova N; Zimran A
    Harefuah; 1995 Jun; 128(12):757-8, 824. PubMed ID: 7557682
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Look before you leap. Carrier screening for type 1 Gaucher disease: difficult questions.
    Borry P; Clarke A; Dierickx K
    Eur J Hum Genet; 2008 Feb; 16(2):139-40. PubMed ID: 18043719
    [No Abstract]   [Full Text] [Related]  

  • 24. Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?
    Fares F; Badarneh K; Abosaleh M; Harari-Shaham A; Diukman R; David M
    Prenat Diagn; 2008 Mar; 28(3):236-41. PubMed ID: 18264947
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Gaucher's and Fabry's diseases: biochemical and genetic aspects].
    Caillaud C; Poenaru L
    J Soc Biol; 2002; 196(2):135-40. PubMed ID: 12360742
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.
    Peleg L; Frisch A; Goldman B; Karpaty M; Narinsky R; Bronstein S; Frydman M
    Eur J Hum Genet; 1998; 6(2):185-6. PubMed ID: 9781065
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela.
    Eblan MJ; Nguyen J; Ziegler SG; Lwin A; Hanson M; Gallardo M; Weiser R; De Lucca M; Singleton A; Sidransky E
    Mov Disord; 2006 Feb; 21(2):282-3. PubMed ID: 16261622
    [No Abstract]   [Full Text] [Related]  

  • 28. Development and performance of a comprehensive targeted sequencing assay for pan-ethnic screening of carrier status.
    Tanner AK; Valencia CA; Rhodenizer D; Espirages M; Da Silva C; Borsuk L; Caldwell S; Gregg E; Grimes E; Lichanska AM; Morris L; Purkayastha A; Weslowski B; Tibbetts C; Lorence MC; Hegde M
    J Mol Diagn; 2014 May; 16(3):350-60. PubMed ID: 24517888
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Increased incidence of Parkinson disease among relatives of patients with Gaucher disease.
    Halperin A; Elstein D; Zimran A
    Blood Cells Mol Dis; 2006; 36(3):426-8. PubMed ID: 16651014
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation analysis of 28 Gaucher disease patients: the Australasian experience.
    Lewis BD; Nelson PV; Robertson EF; Morris CP
    Am J Med Genet; 1994 Jan; 49(2):218-23. PubMed ID: 8116672
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Frequency of carriers of chronic (type I) Gaucher disease in Ashkenazi Jews.
    Matoth Y; Chazan S; Cnaan A; Gelernter I; Klibansky C
    Am J Med Genet; 1987 Jul; 27(3):561-5. PubMed ID: 3631130
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Antenatal screening for cystic fibrosis: a trial of the couple model.
    Livingstone J; Axton RA; Gilfillan A; Mennie M; Compton M; Liston WA; Calder AA; Gordon AJ; Brock DJ
    BMJ; 1994 Jun; 308(6942):1459-62. PubMed ID: 8019277
    [TBL] [Abstract][Full Text] [Related]  

  • 33. ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent.
    Obstet Gynecol; 2009 Oct; 114(4):950. PubMed ID: 19888064
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Carrier testing for autosomal-recessive disorders.
    Vallance H; Ford J
    Crit Rev Clin Lab Sci; 2003 Aug; 40(4):473-97. PubMed ID: 14582604
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases.
    Scott SA; Edelmann L; Liu L; Luo M; Desnick RJ; Kornreich R
    Hum Mutat; 2010 Nov; 31(11):1240-50. PubMed ID: 20672374
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation analysis of an Ashkenazi Jewish family with Gaucher disease in three successive generations.
    Kolodny EH; Firon N; Eyal N; Horowitz M
    Am J Med Genet; 1990 Aug; 36(4):467-72. PubMed ID: 2117855
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The molecular characterization of Gaucher disease in South Africa.
    Morar B; Lane AB
    Clin Genet; 1996 Aug; 50(2):78-84. PubMed ID: 8937765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new diagnostic test for Gaucher disease suitable for population screening.
    Sakallah SA; Sansieri C; Kopp DW; Cooper DL; Barranger JA
    PCR Methods Appl; 1994 Aug; 4(1):1-5. PubMed ID: 9018309
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?
    Holtkamp KC; van Maarle MC; Schouten MJ; Dondorp WJ; Lakeman P; Henneman L
    Eur J Hum Genet; 2016 Feb; 24(2):171-7. PubMed ID: 25966636
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gaucher disease: gene frequencies in the Ashkenazi Jewish population.
    Beutler E; Nguyen NJ; Henneberger MW; Smolec JM; McPherson RA; West C; Gelbart T
    Am J Hum Genet; 1993 Jan; 52(1):85-8. PubMed ID: 8434610
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.