A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22‐23

Por Pras, E, Mahler, O, Kumar, V, Frydman, M, Gefen, N, Pras, E, Hejtmancik, J F
Publicado em 2006

Yersinia enterocolitica endocarditis on a prosthetic valve.

Por Pras, E., Arber, N., Pinkhas, J., Sidi, Y.
Publicado em 1992

Close association of HLA-B51 and B52 in Israeli patients with Behçet's syndrome.

Por Arber, N, Klein, T, Meiner, Z, Pras, E, Weinberger, A
Publicado em 1991

Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology

Por Achiron, R., Katorza, E., Reznik-Wolf, H., Pras, E., Kidron, D., Berkenstadtt, M.
Publicado no Ultrasound Int Open (2016)

NOD2/CARD 15 gene mutations in patients with Familial Mediterranean Fever

Por Bujanover Y, Livneh A, Lidar M, Pras E, Shinar Y, Padeh S, Karban A, Berkun Y
Publicado em 2011-09-01

NOD2/CARD 15 gene mutations in patients with Familial Mediterranean Fever

Por Berkun, Y, Karban, A, Padeh, S, Shinar, Y, Pras, E, Lidar, M, Livneh, A, Bujanover, Y
Publicado em 2011

Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19q.

Por Wartenfeld, R, Golomb, E, Katz, G, Bale, S J, Goldman, B, Pras, M, Kastner, D L, Pras, E
Publicado em 1997

Over representation of the A allele in the IL23R rs1004819 polymorphism in M694V homozygote non-responsive FMF patients

Por Pras, E, Dahan, S, Epstein, A, Zvi, I Ben, Marek-Yagel, D, Shinar, Y, Lidar, M, Livneh, A
Publicado no Pediatr Rheumatol Online J (2015)

Hepatic Iron Overload following Liver Transplantation from a C282Y/H63D Compound Heterozygous Donor

Por Veitsman, E., Pras, E., Pappo, O., Arish, A., Eshkenazi, R., Feray, C., Calderaro, J., Azoulay, D., Ari, Z. Ben
Publicado no Case Reports Hepatol (2018)

A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts

Por Shinar, Y, Ben-Zeev, B, Brand, N, Lahat, H, Gross-Zur, V, MacGregor, D, Bahan, T, Kastner, D, Pras, E
Publicado em 2002

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

Por Stratakis, C A, Carney, J A, Lin, J P, Papanicolaou, D A, Karl, M, Kastner, D L, Pras, E, Chrousos, G P
Publicado em 1996

Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi...

Por Aksentijevich, I, Torosyan, Y, Samuels, J, Centola, M, Pras, E, Chae, J J, Oddoux, C, Wood, G, Azzaro, M P, Palumbo, G, Giustolisi, R, Pras, M, Ostrer, H, Kastner, D L
Publicado em 1999

Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

Por Levy, E. N., Shen, Y., Kupelian, A., Kruglyak, L., Aksentijevich, I., Pras, E., Balow, J. E., Linzer, B., Chen, X., Shelton, D. A., Gumucio, D., Pras, M., Shohat, M., Rotter, J. I., Fischel-Ghodsian, N., Richards, R. I., Kastner, D. L.
Publicado em 1996

OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN)

Por Levy-Lahad, E, Elkan-Navon, P, Segel, R, Pierce, SB, Walsh, T, Barash, J, Padeh, S, Zlotogorski, A, Berkun, YY, Press, JJ, Mukamel, M, Hashkes, PJ, Harel, LL, Tekin, M, Yalcinkaya, F, Kasapcopur, O, Emirogullari, EF, Lee, MK, Klevit, RE, Renbaum, PF, Weinberg-Shukron, A, Zeligson, S, Marek-Yagel, D, Shohat, M, Singer, A, Pras, E, Rubinow, AA, Anikster, Y, King, M-C
Publicado em 2013