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.
116 related articles for article (PubMed ID: 18035560)
1. Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray. Ezgu F; Hasanoglu A; Okur I; Biberoglu G; Tumer L; Eminoglu T; Dogan H Blood Cells Mol Dis; 2008; 40(2):246-7. PubMed ID: 18035560 [No Abstract] [Full Text] [Related]
2. [Detection of the frequencies of GBA gene major mutations in patients with Gaucher disease in Ukraine]. Horovenko NH; Ol'khovych NV; Nedoboĭ AM; Pichkur NO Tsitol Genet; 2007; 41(4):41-7. PubMed ID: 18030725 [TBL] [Abstract][Full Text] [Related]
3. Gaucher disease among Chinese patients: review on genotype/phenotype correlation from 29 patients and identification of novel and rare alleles. Choy FY; Zhang W; Shi HP; Zay A; Campbell T; Tang N; Ferreira P Blood Cells Mol Dis; 2007; 38(3):287-93. PubMed ID: 17196853 [TBL] [Abstract][Full Text] [Related]
4. Identification of Gaucher disease mutations found in Saudi Arabia. Kaya N; Al-Zahrani F; Al-Odaib A; Rahbeeni Z; Al-Hassnan Z; Al-Sharif F; Ozand P; Al-Sayed M Blood Cells Mol Dis; 2008; 41(2):200-1. PubMed ID: 18586535 [No Abstract] [Full Text] [Related]
5. Gaucher disease in Tunisia: High frequency of the most common mutations. Cherif W; Ben Turkia H; Ben Rhouma F; Riahi I; Chemli J; Kefi R; Messai H; Amaral O; Miranda MC; Caillaud C; Tebib N; Ben Dridi MF; Abdelhak S Blood Cells Mol Dis; 2009; 43(2):161-2. PubMed ID: 19553144 [No Abstract] [Full Text] [Related]
6. 55-base pair deletion in certain patients with Gaucher disease complicates screening for common Gaucher alleles. Tayebi N; Stern H; Dymarskaia I; Herman J; Sidransky E Am J Med Genet; 1996 Dec; 66(3):316-9. PubMed ID: 8985494 [TBL] [Abstract][Full Text] [Related]
13. [From gene to disease; Gaucher disease]. Hollak CE; Boot RG; Poorthuis BJ; Aerts JM Ned Tijdschr Geneeskd; 2005 Sep; 149(39):2163-6. PubMed ID: 16223076 [TBL] [Abstract][Full Text] [Related]
14. Gaucher disease in Colombia: mutation identification and comparison to other Hispanic populations. Pomponio RJ; Cabrera-Salazar MA; Echeverri OY; Miller G; Barrera LA Mol Genet Metab; 2005 Dec; 86(4):466-72. PubMed ID: 16185907 [TBL] [Abstract][Full Text] [Related]
15. Detection of 12 new mutations in Gaucher disease Brazilian patients. Rozenberg R; Fox DC; Sobreira E; Pereira LV Blood Cells Mol Dis; 2006; 37(3):204-9. PubMed ID: 17059888 [TBL] [Abstract][Full Text] [Related]
16. Identification of a novel three-nucleotide insertion mutation (c.841-842insTGA) in the acid beta-glucosidase gene of a Taiwan Chinese patient with type II Gaucher disease. Wu JY; Wu MC; Lee CC; Tsai FJ Hum Mutat; 2001 Mar; 17(3):238. PubMed ID: 11241851 [No Abstract] [Full Text] [Related]
17. [Biochemical and molecular diagnosis of Gaucher disease in Tunisia]. Dandana A; Ferchichi S; Khedhiri S; Chkioua L; Jaidane Z; Monastiri K; Ben Khelifa S; Ben Mansour R; Maire I; Froissart R; Bonnet V; Laradi S; Miled A Ann Biol Clin (Paris); 2007; 65(6):647-52. PubMed ID: 18039610 [TBL] [Abstract][Full Text] [Related]
18. Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H;H255Q] double mutant allele. Santamaria R; Michelakakis H; Moraitou M; Dimitriou E; Dominissini S; Grossi S; Sánchez-Ollé G; Chabás A; Pittis MG; Filocamo M; Vilageliu L; Grinberg D Hum Mutat; 2008 Jun; 29(6):E58-67. PubMed ID: 18429048 [TBL] [Abstract][Full Text] [Related]
19. Gaucher disease: report of de novo GBA mutation in a Spanish family. Alfonso P; Pocovi M; Giraldo P Blood Cells Mol Dis; 2008; 40(3):444-5. PubMed ID: 18313951 [No Abstract] [Full Text] [Related]
20. Enzyme, substrate, and myeloma in Gaucher disease. Hughes DA Am J Hematol; 2009 Apr; 84(4):199-201. PubMed ID: 19291728 [No Abstract] [Full Text] [Related] [Next] [New Search]