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.
2. 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]
3. 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]
4. 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]
5. Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease. Aerts JM; Van Weely S; Boot R; Hollak CE; Tager JM J Inherit Metab Dis; 1993; 16(2):288-91. PubMed ID: 8411983 [No Abstract] [Full Text] [Related]
12. [Gaucher disease]. Eto Y Nihon Rinsho; 2001 Mar; 59 Suppl 3():317-21. PubMed ID: 11347084 [No Abstract] [Full Text] [Related]
13. Competing for the treasure in exceptions. Cox TM Am J Hematol; 2013 Mar; 88(3):163-5. PubMed ID: 23400870 [No Abstract] [Full Text] [Related]
14. The clinical, molecular, and pathological characterisation of a family with two cases of lethal perinatal type 2 Gaucher disease. Sidransky E; Tayebi N; Stubblefield BK; Eliason W; Klineburgess A; Pizzolato GP; Cox JN; Porta J; Bottani A; DeLozier-Blanchet CD J Med Genet; 1996 Feb; 33(2):132-6. PubMed ID: 8929950 [TBL] [Abstract][Full Text] [Related]
15. Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S). Bodamer OA; Church HJ; Cooper A; Wraith JE; Scott CR; Scaglia F Am J Med Genet; 2002 May; 109(4):328-31. PubMed ID: 11992489 [TBL] [Abstract][Full Text] [Related]