 Turkey
"Turkey" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
No definition found.
| Descriptor ID |
D014421
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| MeSH Number(s) |
Z01.252.245.500.850 Z01.586.500.850
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Turkey".
Below are MeSH descriptors whose meaning is more specific than "Turkey".
This graph shows the total number of publications written about "Turkey" by people in this website by year, and whether "Turkey" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 | | 2004 | 0 | 2 | 2 | | 2005 | 0 | 1 | 1 | | 2006 | 0 | 1 | 1 | | 2010 | 0 | 1 | 1 | | 2014 | 0 | 2 | 2 | | 2015 | 0 | 2 | 2 |
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Below are the most recent publications written about "Turkey" by people in Profiles.
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Özoguz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Saygi C, Sapp PC, Keagle P, Parman Y, Tan E, Koç F, Deymeer F, Oflazer P, Hanagasi H, Gürvit H, Bilgiç B, Durmus H, Ertas M, Kotan D, Akalin MA, Güllüoglu H, Zarifoglu M, Aysal F, Dösoglu N, Bilguvar K, Günel M, Keskin Ö, Akgün T, Özçelik H, Landers JE, Brown RH, Basak AN. The distinct genetic pattern of ALS in Turkey and novel mutations. Neurobiol Aging. 2015 Apr; 36(4):1764.e9-18.
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Keskin EY, Gürsel T, Kaya Z, Dai L, Koçak Ü, Yenicesu I, Belen FB, Mitchell M. Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. Blood Coagul Fibrinolysis. 2015 Jan; 26(1):63-8.
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Wahid FI, Khan A, Khan IA. Complications of chronic suppurative otitis media: challenge for a developing country. Kulak Burun Bogaz Ihtis Derg. 2014 Sep-Oct; 24(5):265-70.
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Browne EP, Dinc SE, Punska EC, Agus S, Vitrinel A, Erdag GC, Anderton DL, Arcaro KF, Yilmaz B. Promoter methylation in epithelial-enriched and epithelial-depleted cell populations isolated from breast milk. J Hum Lact. 2014 Nov; 30(4):450-7.
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Cengiz FB, Duman D, Sirmaci A, Tokgöz-Yilmaz S, Erbek S, Oztürkmen-Akay H, Incesulu A, Edwards YJ, Ozdag H, Liu XZ, Tekin M. Recurrent and private MYO15A mutations are associated with deafness in the Turkish population. Genet Test Mol Biomarkers. 2010 Aug; 14(4):543-50.
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Bozkurt G, Sackesen C, Civelek E, Kalayci O, Akalan N, Cataltepe O. Latex sensitization and allergy in children with spina bifida in Turkey. Childs Nerv Syst. 2010 Dec; 26(12):1735-42.
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Arikan R, Appelbaum PS, Sercan M, Turkcan S, Satmis N, Polat A. Civil commitment in Turkey: reflections on a bill drafted by psychiatrists. Int J Law Psychiatry. 2007 Jan-Feb; 30(1):29-35.
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Duman BS, Türkoglu C, Akpinar B, Güden M, Vertii A, Cagatay P, Günay D, Sevim Büyükdevrim A. Genetic variations of the apolipoprotein B gene in Turkish patients with coronary artery disease. Ann Hum Biol. 2005 Sep-Oct; 32(5):620-9.
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Duman BS, Türkoglu C, Akpinar B, Güden M, Vertii A, Dak E, Cagatay P, Günay D, Büyükdevrim AS. Lipoprotein lipase gene polymorphism and lipid profile in coronary artery disease. Arch Pathol Lab Med. 2004 Aug; 128(8):869-74.
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Tamer L, Tanriverdi K, Ercan B, Unlu A, Sucu N, Pekdemir H, Atik U. Apolipoprotein B gene polymorphisms in people in the east Mediterranean area of Turkey. East Mediterr Health J. 2004 Jan-Mar; 10(1-2):125-30.
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