Literature DB >> 6629831

Hemoglobinopathies in Israel.

R Eliakim, E A Rachmilewitz.   

Abstract

A survey of the various hemoglobinopathies in Israel is reported. The information was supplied from 13 hematology services throughout the country and from the Ministry of Health. The common hemoglobinopathies encountered were the thalassemias and sickle cell anemia. In addition, hemoglobin C and O Arab were found in isolated communities. Sporadic cases of hemoglobin Hasharon, hemoglobin D, hemoglobin NYU were also found. The thalassemic patients originated mainly from Kurdistan, Yemen and Iraq, while the sickle cell patients were mainly Moslem Arabs or Bedouins.

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Year:  1983        PMID： 6629831     DOI： 10.3109/03630268309038420

Source DB:  PubMed          Journal:  Hemoglobin        ISSN： 0363-0269            Impact factor:   0.849


  3 in total

1.  The origin of sickle cell alleles in Israel.

Authors:  D Rund; N Kornhendler; O Shalev; A Oppenheim
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

2.  Inadequate utilization of routine electronic RBC counts to identify beta thalassemia carriers.

Authors:  O Shalev; E Yehezkel; E A Rachmilewitz
Journal:  Am J Public Health       Date:  1988-11       Impact factor: 9.308

3.  Sero-prevalence of Helicobacter pylori CagA immunoglobulin G antibody, serum pepsinogens and haemoglobin levels in adults.

Authors:  Khitam Muhsen; Ronit Sinnreich; Gany Beer-Davidson; Hisham Nassar; Daniel Cohen; Jeremy D Kark
Journal:  Sci Rep       Date:  2018-12-04       Impact factor: 4.379
  3 in total

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