Tamary H - Search Results

1

Molecular diagnosis of α-thalassemia in a multiethnic population.

Gilad O, Shemer OS, Dgany O, Krasnov T, Nevo M, Noy-Lotan S, Rabinowicz R, Amitai N, Ben-Dor S, Yaniv I, Yacobovich J, Tamary H. Gilad O, et al. Among authors: tamary h. Eur J Haematol. 2017 Jun;98(6):553-562. doi: 10.1111/ejh.12866. Epub 2017 Apr 6. Eur J Haematol. 2017. PMID: 28160324

2

The molecular biology of Fanconi anemia.

Tamary H, Bar-Yam R, Zemach M, Dgany O, Shalmon L, Yaniv I. Tamary H, et al. Isr Med Assoc J. 2002 Oct;4(10):819-23. Isr Med Assoc J. 2002. PMID: 12389351 Free article.

3

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H. Dgany O, et al. Among authors: tamary h. Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14. Am J Hum Genet. 2002. PMID: 12434312 Free PMC article.

4

CATSPER2, a human autosomal nonsyndromic male infertility gene.

Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, Zaizov R, Shalev H, Delaunay J, Fellous M, Lancet D, Beckmann JS. Avidan N, et al. Among authors: tamary h. Eur J Hum Genet. 2003 Jul;11(7):497-502. doi: 10.1038/sj.ejhg.5200991. Eur J Hum Genet. 2003. PMID: 12825070

5

High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis.

Tamary H, Aviner S, Freud E, Miskin H, Krasnov T, Schwarz M, Yaniv I. Tamary H, et al. J Pediatr Hematol Oncol. 2003 Dec;25(12):952-4. doi: 10.1097/00043426-200312000-00009. J Pediatr Hematol Oncol. 2003. PMID: 14663278

6

Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.

Tamary H, Dgany O, Toledano H, Shalev Z, Krasnov T, Shalmon L, Schechter T, Bercovich D, Attias D, Laor R, Koren A, Yaniv I. Tamary H, et al. Eur J Haematol. 2004 May;72(5):330-5. doi: 10.1111/j.1600-0609.2004.00240.x. Eur J Haematol. 2004. PMID: 15059067

7

Central venous line thrombosis in children and young adults with thalassemia major.

Finkelstein Y, Yaniv I, Berant M, Zilber R, Garty BZ, Epstein O, Lahav J, Tamary H. Finkelstein Y, et al. Among authors: tamary h. Pediatr Hematol Oncol. 2004 Jul-Aug;21(5):375-81. doi: 10.1080/08880010490457042. Pediatr Hematol Oncol. 2004. PMID: 15205080

8

Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn triplets.

Arnon S, Tamary H, Dgany O, Litmanovitz I, Regev R, Bauer S, Dolfin T, Yacobovich J, Wolach B, Jaber L. Arnon S, et al. Among authors: tamary h. Am J Hematol. 2004 Jul;76(3):263-6. doi: 10.1002/ajh.20094. Am J Hematol. 2004. PMID: 15224363 Free article.

9

A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I.

Shalev H, Kapelushnik J, Moser A, Dgany O, Krasnov T, Tamary H. Shalev H, et al. Among authors: tamary h. J Pediatr Hematol Oncol. 2004 Nov;26(11):746-8. doi: 10.1097/00043426-200411000-00011. J Pediatr Hematol Oncol. 2004. PMID: 15543010

10

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients.

Shalitin S, Carmi D, Weintrob N, Phillip M, Miskin H, Kornreich L, Zilber R, Yaniv I, Tamary H. Shalitin S, et al. Among authors: tamary h. Eur J Haematol. 2005 Feb;74(2):93-100. doi: 10.1111/j.1600-0609.2004.00371.x. Eur J Haematol. 2005. PMID: 15654898

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