Shalmon L - Search Results

1

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. Among authors: shalmon l. Am J Hematol. 1994 Jun;46(2):127-33. doi: 10.1002/ajh.2830460213. Am J Hematol. 1994. PMID: 8172179

2

A new deletional alpha-thalassemia detected in Yemenites with hemoglobin H disease.

Shalmon L, Kirschmann C, Zaizov R. Shalmon L, et al. Am J Hematol. 1994 Mar;45(3):201-4. doi: 10.1002/ajh.2830450302. Am J Hematol. 1994. PMID: 8296789

3

Alpha-thalassemia genes in Israel: deletional and nondeletional mutations in patients of various origins.

Shalmon L, Kirschmann C, Zaizov R. Shalmon L, et al. Hum Hered. 1996 Jan-Feb;46(1):15-9. doi: 10.1159/000154319. Hum Hered. 1996. PMID: 8825457

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. Among authors: shalmon l. Hemoglobin. 1997 Mar;21(2):121-30. doi: 10.3109/03630269708997516. Hemoglobin. 1997. PMID: 9101281

5

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. Among authors: shalmon l. Blood Coagul Fibrinolysis. 1997 Sep;8(6):337-43. doi: 10.1097/00001721-199709000-00003. Blood Coagul Fibrinolysis. 1997. PMID: 9351523

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. Among authors: shalmon l. Hematol J. 2000;1(6):382-9. doi: 10.1038/sj.thj.6200062. Hematol J. 2000. PMID: 11920218

7

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. Among authors: shalmon l. 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.

8

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. Among authors: shalmon l. Blood. 1996 Mar 1;87(5):1763-70. Blood. 1996. PMID: 8634422 Free article.

9

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. Among authors: shalmon l. Am J Hum Genet. 1998 May;62(5):1062-9. doi: 10.1086/301834. Am J Hum Genet. 1998. PMID: 9545404 Free PMC article.

10

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. Among authors: shalmon l. Thromb Haemost. 1996 Sep;76(3):283-91. Thromb Haemost. 1996. PMID: 8883260

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