Pras E - Search Results

1

Clinical disease among patients heterozygous for familial Mediterranean fever.

Marek-Yagel D, Berkun Y, Padeh S, Abu A, Reznik-Wolf H, Livneh A, Pras M, Pras E. Marek-Yagel D, et al. Among authors: pras m, pras e. Arthritis Rheum. 2009 Jun;60(6):1862-6. doi: 10.1002/art.24570. Arthritis Rheum. 2009. PMID: 19479871 Free article.

2

Clinical differences between North African and Iraqi Jews with familial Mediterranean fever.

Pras E, Livneh A, Balow JE Jr, Pras E, Kastner DL, Pras M, Langevitz P. Pras E, et al. Among authors: pras m. Am J Med Genet. 1998 Jan 13;75(2):216-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<216::aid-ajmg20>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9450890

3

Clinical and diagnostic value of genetic testing in 216 Israeli children with Familial Mediterranean fever.

Padeh S, Shinar Y, Pras E, Zemer D, Langevitz P, Pras M, Livneh A. Padeh S, et al. Among authors: pras m, pras e. J Rheumatol. 2003 Jan;30(1):185-90. J Rheumatol. 2003. PMID: 12508410

4

Analysis of the three most common MEFV mutations in 412 patients with familial Mediterranean fever.

Zaks N, Shinar Y, Padeh S, Lidar M, Mor A, Tokov I, Pras M, Langevitz P, Pras E, Livneh A. Zaks N, et al. Among authors: pras m, pras e. Isr Med Assoc J. 2003 Aug;5(8):585-8. Isr Med Assoc J. 2003. PMID: 12929299 Free article.

5

An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis.

Zlotogorski A, Marek D, Horev L, Abu A, Ben-Amitai D, Gerad L, Ingber A, Frydman M, Reznik-Wolf H, Vardy DA, Pras E. Zlotogorski A, et al. Among authors: pras e. J Invest Dermatol. 2006 Jun;126(6):1292-6. doi: 10.1038/sj.jid.5700251. J Invest Dermatol. 2006. PMID: 16575393 Free article.

6

Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.

Abu A, Frydman M, Marek D, Pras E, Stolovitch C, Aviram-Goldring A, Rienstein S, Reznik-Wolf H, Pras E. Abu A, et al. Among authors: pras e. Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5283-7. doi: 10.1167/iovs.06-0206. Invest Ophthalmol Vis Sci. 2006. PMID: 17122114

7

A combined approach to the molecular analysis of cystinuria: from urinalysis to sequencing via genotyping.

Lotan D, Yoskovitz G, Bisceglia L, Gerad L, Reznik-Wolf H, Pras E. Lotan D, et al. Among authors: pras e. Isr Med Assoc J. 2007 Jul;9(7):513-6. Isr Med Assoc J. 2007. PMID: 17710781 Free article.

8

Human gene mutations. Gene symbol: SLC3A1. Disease: cystinuria.

Bisceglia L, Reznik-Wolf H, Di Perna M, Pras E. Bisceglia L, et al. Among authors: pras e. Hum Genet. 2007 Sep;122(2):215. Hum Genet. 2007. PMID: 18386386 No abstract available.

9

Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.

Abu A, Frydman M, Marek D, Pras E, Nir U, Reznik-Wolf H, Pras E. Abu A, et al. Among authors: pras e. Am J Hum Genet. 2008 May;82(5):1217-22. doi: 10.1016/j.ajhg.2008.04.001. Epub 2008 May 1. Am J Hum Genet. 2008. PMID: 18452888 Free PMC article.

10

Cone-rod dystrophy and a frameshift mutation in the PROM1 gene.

Pras E, Abu A, Rotenstreich Y, Avni I, Reish O, Morad Y, Reznik-Wolf H, Pras E. Pras E, et al. Mol Vis. 2009 Aug 28;15:1709-16. Mol Vis. 2009. PMID: 19718270 Free PMC article.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

307 results

Search Page

Filters