Sidransky E - Search Results

1

Danilov SM, Tikhomirova VE, Metzger R, Naperova IA, Bukina TM, Goker-Alpan O, Tayebi N, Gayfullin NM, Schwartz DE, Samokhodskaya LM, Kost OA, Sidransky E. Danilov SM, et al. Among authors: sidransky e. Mol Genet Metab. 2018 Apr;123(4):501-510. doi: 10.1016/j.ymgme.2018.02.007. Epub 2018 Feb 17. Mol Genet Metab. 2018. PMID: 29478818 Free PMC article.

2

DNA mutation analysis of Gaucher patients.

Sidransky E, Tsuji S, Martin BM, Stubblefield B, Ginns EI. Sidransky E, et al. Am J Med Genet. 1992 Feb 1;42(3):331-6. doi: 10.1002/ajmg.1320420315. Am J Med Genet. 1992. PMID: 1536173

3

Gaucher patients with oculomotor abnormalities do not have a unique genotype.

Sidransky E, Tsuji S, Stubblefield BK, Currie J, FitzGibbon EJ, Ginns EI. Sidransky E, et al. Clin Genet. 1992 Jan;41(1):1-5. doi: 10.1111/j.1399-0004.1992.tb03618.x. Clin Genet. 1992. PMID: 1633639

4

Diagnosing Gaucher disease. Early recognition, implications for treatment, and genetic counseling.

Sidransky E, Tayebi N, Ginns EI. Sidransky E, et al. Clin Pediatr (Phila). 1995 Jul;34(7):365-71. doi: 10.1177/000992289503400705. Clin Pediatr (Phila). 1995. PMID: 7554686

5

Clinical heterogeneity among patients with Gaucher's disease.

Sidransky E, Ginns EI. Sidransky E, et al. JAMA. 1993 Mar 3;269(9):1154-7. JAMA. 1993. PMID: 8433471 No abstract available.

6

Congenital ichthyosis preceding neurologic symptoms in two sibs with type 2 Gaucher disease.

Fujimoto A, Tayebi N, Sidransky E. Fujimoto A, et al. Among authors: sidransky e. Am J Med Genet. 1995 Nov 20;59(3):356-8. doi: 10.1002/ajmg.1320590315. Am J Med Genet. 1995. PMID: 8599361

7

Genotype D399N/R463C in a patient with type 3 Gaucher disease previously assigned genotype N370S/R463C.

Tayebi N, Herman J, Ginns EI, Sidransky E. Tayebi N, et al. Among authors: sidransky e. Biochem Mol Med. 1996 Apr;57(2):149-51. doi: 10.1006/bmme.1996.0021. Biochem Mol Med. 1996. PMID: 8733893

8

Differentiation of the glucocerebrosidase gene from pseudogene by long-template PCR: implications for Gaucher disease.

Tayebi N, Cushner S, Sidransky E. Tayebi N, et al. Among authors: sidransky e. Am J Hum Genet. 1996 Sep;59(3):740-1. Am J Hum Genet. 1996. PMID: 8751878 Free PMC article. No abstract available.

9

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. Sidransky E, et al. J Med Genet. 1996 Feb;33(2):132-6. doi: 10.1136/jmg.33.2.132. J Med Genet. 1996. PMID: 8929950 Free PMC article.

10

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. Among authors: sidransky e. 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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

289 results

Search Page