Filon D - Search Results

1

Gaucher-like cells in beta-thalassemia patient after bone marrow transplantation.

Gesundheit B, Or R, Amar A, Filon D, Gail A. Gesundheit B, et al. Among authors: filon d. J Pediatr Hematol Oncol. 2006 Apr;28(4):203-4. doi: 10.1097/01.mph.0000210403.36309.57. J Pediatr Hematol Oncol. 2006. PMID: 16679915 No abstract available.

2

New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F.

Ghoti H, Fibach E, Rachmilewitz EA, Jeadi H, Filon D. Ghoti H, et al. Among authors: filon d. Hemoglobin. 2017 Mar;41(2):144-146. doi: 10.1080/03630269.2017.1339611. Epub 2017 Jul 3. Hemoglobin. 2017. PMID: 28670942

3

An unexpectedly high frequency of heterozygosity for alpha-thalassemia in Ashkenazi Jews.

Rund D, Filon D, Jackson N, Asher N, Oron-Karni V, Sacha T, Czekalska S, Oppenheim A. Rund D, et al. Among authors: filon d. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):1-3. doi: 10.1016/j.bcmd.2004.04.009. Blood Cells Mol Dis. 2004. PMID: 15223003

4

Haplotype analysis of α-thalassemia chromosomes reveals heterogeneity and multiple founders in Ashkenazi Jews.

Shaulov A, Filon D, Rund D. Shaulov A, et al. Among authors: filon d. Eur J Med Genet. 2016 Nov;59(11):555-558. doi: 10.1016/j.ejmg.2016.10.008. Epub 2016 Oct 19. Eur J Med Genet. 2016. PMID: 27771472

5

[The prevention programs for beta thalassemia in the Jezreel and Eiron valleys: results of fifteen years experience].

Koren A, Zalman L, Palmor H, Ekstein E, Schneour Y, Schneour A, Shalev S, Rachmilewitz EA, Filon D, Openhaim A. Koren A, et al. Among authors: filon d. Harefuah. 2002 Nov;141(11):938-43, 1210. Harefuah. 2002. PMID: 12476624 Hebrew.

6

Y chromosome evidence for a founder effect in Ashkenazi Jews.

Nebel A, Filon D, Faerman M, Soodyall H, Oppenheim A. Nebel A, et al. Among authors: filon d. Eur J Hum Genet. 2005 Mar;13(3):388-91. doi: 10.1038/sj.ejhg.5201319. Eur J Hum Genet. 2005. PMID: 15523495

7

The beta+-IVS-I-6 (T-->C) mutation accounts for half of the thalassemia chromosomes in the Palestinian populations of the mountain regions.

El-Latif MA, Filon D, Rund D, Oppenheim A, Kanaan M. El-Latif MA, et al. Among authors: filon d. Hemoglobin. 2002 Feb;26(1):33-40. doi: 10.1081/hem-120002938. Hemoglobin. 2002. PMID: 11939510

8

Genetic evidence for the expansion of Arabian tribes into the Southern Levant and North Africa.

Nebel A, Landau-Tasseron E, Filon D, Oppenheim A, Faerman M. Nebel A, et al. Among authors: filon d. Am J Hum Genet. 2002 Jun;70(6):1594-6. doi: 10.1086/340669. Am J Hum Genet. 2002. PMID: 11992266 Free PMC article. No abstract available.

9

Hb TAYBE: clinical and morphological findings IN 43 patients.

Koren A, Levin C, Zalman L, Palmor H, Filon D, Chubar E, Resnitzky P, Bennett M. Koren A, et al. Among authors: filon d. Eur J Haematol. 2016 Aug;97(2):137-44. doi: 10.1111/ejh.12694. Epub 2015 Dec 15. Eur J Haematol. 2016. PMID: 26519868

10

Sickle cell anemia in northern Israel: screening and prevention.

Koren A, Zalman L, Palmor H, Zamir RB, Levin C, Openheim A, Daniel-Spiegel E, Shalev S, Filon D. Koren A, et al. Among authors: filon d. Isr Med Assoc J. 2009 Apr;11(4):229-34. Isr Med Assoc J. 2009. PMID: 19603597 Free 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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

44 results

Search Page