Tamary H - Search Results

1

The diverse molecular basis and mild clinical picture of HbH disease in Israel.

Tamary H, Klinger G, Shalmon L, Kirschmann H, Koren A, Bennet M, Zaizov R. Tamary H, et al. Ann N Y Acad Sci. 1998 Jun 30;850:432-5. doi: 10.1111/j.1749-6632.1998.tb10513.x. Ann N Y Acad Sci. 1998. PMID: 9668576 No abstract available.

2

Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations.

Tamary H, Surrey S, Kirschmann H, Shalmon L, Zaizov R, Schwartz E, Rappaport EF. Tamary H, et al. Am J Hematol. 1994 Jun;46(2):127-33. doi: 10.1002/ajh.2830460213. Am J Hematol. 1994. PMID: 8172179

3

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I.

Tamary H, Shalev H, Luria D, Shaft D, Zoldan M, Shalmon L, Gruinspan A, Stark B, Chaison M, Shinar E, Resnitzky P, Zaizov R. Tamary H, et al. Blood. 1996 Mar 1;87(5):1763-70. Blood. 1996. PMID: 8634422 Free article.

4

alpha-thalassemia caused by a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene including the first nucleotide of the poly A signal sequence.

Tamary H, Klinger G, Shalmon L, Attias D, Fortina P, Kobayashi M, Surrey S, Zaizov R. Tamary H, et al. Hemoglobin. 1997 Mar;21(2):121-30. doi: 10.3109/03630269708997516. Hemoglobin. 1997. PMID: 9101281

5

Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients.

Tamary H, Bar-Yam R, Shalmon L, Rachavi G, Krostichevsky M, Elhasid R, Barak Y, Kapelushnik J, Yaniv I, Auerbach AD, Zaizov R. Tamary H, et al. Br J Haematol. 2000 Oct;111(1):338-43. doi: 10.1046/j.1365-2141.2000.02323.x. Br J Haematol. 2000. PMID: 11091222 Free article.

6

Molecular characterization of four novel mutations causing factor VII deficiency.

Tamary H, Fromovich-Amit Y, Shalmon L, Zaizov R, Yaniv I, Klar A, Peretz H, Brenner B, Lanir N, Zivelin A, Seligsohn U. Tamary H, et al. Hematol J. 2000;1(6):382-9. doi: 10.1038/sj.thj.6200062. Hematol J. 2000. PMID: 11920218

7

Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.

Tamary H, Fromovich Y, Shalmon L, Reich Z, Dym O, Lanir N, Brenner B, Paz M, Luder AS, Blau O, Korostishevsky M, Zaizov R, Seligsohn U. Tamary H, et al. Thromb Haemost. 1996 Sep;76(3):283-91. Thromb Haemost. 1996. PMID: 8883260

8

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

Tamary H, Shalmon L, Shalev H, Halil A, Dobrushin D, Ashkenazi N, Zoldan M, Resnitzky P, Korostishevsky M, Bonne-Tamir B, Zaizov R. Tamary H, et al. Am J Hum Genet. 1998 May;62(5):1062-9. doi: 10.1086/301834. Am J Hum Genet. 1998. PMID: 9545404 Free PMC article.

9

Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP).

Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, Rappaport EF. Tamary H, et al. Blood Coagul Fibrinolysis. 1997 Sep;8(6):337-43. doi: 10.1097/00001721-199709000-00003. Blood Coagul Fibrinolysis. 1997. PMID: 9351523

10

No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type I.

Tamary H, Shalev H, Pinsk V, Zoldan M, Zaizov R. Tamary H, et al. Pediatr Hematol Oncol. 1999 Mar-Apr;16(2):165-8. doi: 10.1080/088800199277498. Pediatr Hematol Oncol. 1999. PMID: 10100277 Clinical Trial.

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