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Hydrops fetalis: lysosomal storage disorders in extremis.
Stone DL, Sidransky E. Stone DL, et al. Adv Pediatr. 1999;46:409-40. Adv Pediatr. 1999. PMID: 10645471 Review.
Gaucher's disease: advances and challenges.
Martin BM, Sidransky E, Ginns EI. Martin BM, et al. Adv Pediatr. 1989;36:277-306. Adv Pediatr. 1989. PMID: 2675571 Review. No abstract available.
Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease.
Sidransky E, Fartasch M, Lee RE, Metlay LA, Abella S, Zimran A, Gao W, Elias PM, Ginns EI, Holleran WM. Sidransky E, et al. Pediatr Res. 1996 Jan;39(1):134-41. doi: 10.1203/00006450-199601000-00020. Pediatr Res. 1996. PMID: 8825398
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. Tayebi N, et al. Am J Med Genet. 1996 Dec 18;66(3):316-9. doi: 10.1002/(SICI)1096-8628(19961218)66:3<316::AID-AJMG15>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8985494
New perspectives in type 2 Gaucher disease.
Sidransky E. Sidransky E. Adv Pediatr. 1997;44:73-107. Adv Pediatr. 1997. PMID: 9265968 Review. No abstract available.
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. Tayebi N, et al. Pediatr Res. 1998 May;43(5):571-8. doi: 10.1203/00006450-199805000-00003. Pediatr Res. 1998. PMID: 9585001
Type 2 Gaucher disease with hydrops fetalis in an Ashkenazi Jewish family resulting from a novel recombinant allele and a rare splice junction mutation in the glucocerebrosidase locus.
Reissner K, Tayebi N, Stubblefield BK, Koprivica V, Blitzer M, Holleran W, Cowan T, Almashanu S, Maddalena A, Karson EM, Sidransky E. Reissner K, et al. Mol Genet Metab. 1998 Apr;63(4):281-8. doi: 10.1006/mgme.1998.2675. Mol Genet Metab. 1998. PMID: 9635296
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