Sidransky E - Search Results

1

Clinical evaluation of sibling pairs with gaucher disease discordant for parkinsonism.

Lopez G, Steward A, Ryan E, Groden C, Wiggs E, Segalà L, Monestime GM, Tayebi N, Sidransky E. Lopez G, et al. Among authors: sidransky e. Mov Disord. 2020 Feb;35(2):359-365. doi: 10.1002/mds.27916. Epub 2019 Nov 30. Mov Disord. 2020. PMID: 31785030

2

Gaucher's disease: advances and challenges.

Martin BM, Sidransky E, Ginns EI. Martin BM, et al. Among authors: sidransky e. Adv Pediatr. 1989;36:277-306. Adv Pediatr. 1989. PMID: 2675571 Review. No abstract available.

3

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

4

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.

5

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

6

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

7

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.

8

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.

9

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

10

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.

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