Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 1
1971 1
1973 1
1975 1
1978 1
1979 1
1980 1
1982 1
1984 2
1985 2
1987 1
1990 3
1993 2
1995 1
2000 1
2001 1
2002 1
2004 1
2005 1
2007 2
2011 1
2012 5
2013 1
2014 1
2015 3
2016 5
2026 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

41 results

Results by year

Citations

1 article found by citation matching

Search results

Filters applied: . Clear all
Page 1
Beta-thalassemia in Turkey.
Oner R, Altay C, Gurgey A, Aksoy M, Kilinç Y, Stoming TA, Reese AL, Kutlar A, Kutlar F, Huisman TH. Oner R, et al. Hemoglobin. 1990;14(1):1-13. doi: 10.3109/03630269009002250. Hemoglobin. 1990. PMID: 2200760 Review.
A review is presented of the various beta-thalassemia alleles observed in nearly 191 patients with beta-thalassemia major and their 182 heterozygous relatives. ...Combinations of different mutations were present in many patients; some were mildly affected because of …
A review is presented of the various beta-thalassemia alleles observed in nearly 191 patients with beta-thalassemia major and …
Prevalence and molecular analysis of beta-thalassemia in Adiyaman, Turkey.
Genc A, Tastemir Korkmaz D, Buyukleyla M, Celiker M. Genc A, et al. Hemoglobin. 2012;36(2):131-8. doi: 10.3109/03630269.2012.658128. Epub 2012 Feb 22. Hemoglobin. 2012. PMID: 22356097
Thalassemia is one of the most common hereditary disorders in the Mediterranean region. We report here the results of a premarital screening carried out in Adiyaman in the southeastern region of Turkey, a region with a hitherto unknown incidence of beta-th
Thalassemia is one of the most common hereditary disorders in the Mediterranean region. We report here the results of a premarital sc
Prevalence of beta-thalassemia trait and abnormal hemoglobins in the province of Adiyaman, Turkey.
Genc A, Tastemir Korkmaz D, Urhan Kucuk M, Rencuzogullari E, Atakur S, Bayram S, Onderci M, Koc T, Aslan S, Mutalip A, Faruk M, Sevgiler Y, Tuncdemir A. Genc A, et al. Pediatr Hematol Oncol. 2012 Oct;29(7):620-3. doi: 10.3109/08880018.2012.713085. Epub 2012 Aug 16. Pediatr Hematol Oncol. 2012. PMID: 22897698
BACKGROUND/AIMS: Thalassemia is one of the most common hereditary disorders in Turkey. The aim of this study was to determine the prevalence of the beta-thalassemia trait and abnormal hemoglobins in the province of Adiyaman in Turkey. ... …
BACKGROUND/AIMS: Thalassemia is one of the most common hereditary disorders in Turkey. The aim of this study was to determine …
The Hematological and Molecular Spectrum of alpha-Thalassemias in Turkey: The Hacettepe Experience.
Ünal Ş, Gümrük F. Ünal Ş, et al. Turk J Haematol. 2015 Jun;32(2):136-43. doi: 10.4274/tjh.2014.0200. Turk J Haematol. 2015. PMID: 26316481 Free PMC article.
RESULTS: Supporting the previous data from Turkey, -alpha3.7 was the most common mutation among patients with Hb H disease (62.8%) and in the other 78 subjects (39.7%). ...CONCLUSION: This study indicated that Hb H disease is not rare in Turkey and its genotype is q …
RESULTS: Supporting the previous data from Turkey, -alpha3.7 was the most common mutation among patients with Hb H disease (62.8%) an …
Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey.
Irken G, Oren H, Undar B, Duman M, Gülen H, Uçar C, Sanli N. Irken G, et al. Turk J Pediatr. 2002 Jan-Mar;44(1):21-4. Turk J Pediatr. 2002. PMID: 11858374
Turkey is located in a geographic area of the world where thalassemia syndromes and abnormal hemoglobins are common. In this study we aimed to evaluate the thalassemia syndromes and abnormal hemoglobins in patients from the Aegean
Turkey is located in a geographic area of the world where thalassemia syndromes and abnormal hemoglobins are com
Hemoglobinopathies in Turkey.
Aksoy M. Aksoy M. Hemoglobin. 1985;9(2):209-16. doi: 10.3109/03630268508997007. Hemoglobin. 1985. PMID: 4030383 No abstract available.
Hemoglobinopathies in the district of Antalya, Turkey.
Bircan I, Sişli S, Güven A, Cali S, Yeğin O, Ertuğ H, Güven AG, Akar N. Bircan I, et al. Pediatr Hematol Oncol. 1993 Jul-Sep;10(3):289-91. doi: 10.3109/08880019309029499. Pediatr Hematol Oncol. 1993. PMID: 8217548
A screening program was conducted to ascertain the incidence of hemoglobinopathies in the district of Antalya, Turkey. The survey sample was selected from the household registration forms of health centers by systematic random sampling. ...The prevalence of abnor
A screening program was conducted to ascertain the incidence of hemoglobinopathies in the district of Antalya, Turkey. The sur …
Prenatal diagnosis of beta-thalassemia and other hemoglobinopathies in southwestern Turkey.
Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G. Mendilcioglu I, et al. Hemoglobin. 2011;35(1):47-55. doi: 10.3109/03630269.2010.544607. Hemoglobin. 2011. PMID: 21250881
Our aim was to evaluate the prenatal diagnosis of beta-thalassemia (beta-thal) and other hemoglobinopathies in a region with high frequency. After detection by premarital or antenatal screening, 312 patients underwent 420 prenatal diagnostic procedures for 407 fetuses in a …
Our aim was to evaluate the prenatal diagnosis of beta-thalassemia (beta-thal) and other hemoglobinopathies in a region with high fre …
Prevalence of beta-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.
Incebiyik A, Genc A, Hilali NG, Camuzcuoglu A, Camuzcuoglu H, Kilic A, Vural M. Incebiyik A, et al. Hemoglobin. 2014;38(6):402-4. doi: 10.3109/03630269.2014.978008. Hemoglobin. 2014. PMID: 25405917 Clinical Trial.
Thalassemia is one of the most common hereditary disorders in Turkey, especially in the Mediterranean region of the country. The purpose of this study was to determine the frequency of the beta-thalassemia (beta-thal) trait and abnormal hemoglobins
Thalassemia is one of the most common hereditary disorders in Turkey, especially in the Mediterranean region of the country. T
41 results