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Ece Akar

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Geographic Areas

Turkey

Disorders

Chemicals & Drugs

Procedures

Case-Control Studies

Physiology

Concepts & Ideas

Genes & Molecular Sequences

Alleles

Living Beings

Infant

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Co-Publications
Name
36
Akar, Nejat
8
Cin, Sükrü
8
Deda, Gülhis
7
Avcu, Ferit
7
Sipahi, Tansu
7
Yalçinkaya, Fatos
6
Yalçin, Atilla
5
Cakar, Nilgün
5
Tekin, Mustafa
4
Ozel, Duygu
4
Yilmaz, Erdal
3
Tümer, Necmiye
3
Ekim, Mesiha
3
Misirlioglu, Muge
2
Omürlü, K

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Publications

TOP 3
Akar Nejat; Hasipek Metis; Oztürk Aysenur; Akar Ece; Tekin Mustafa
Serum amyloid A1 -13 T/C alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.
Akar N; Ozturk A; Ozel D; Akar E; Ekim M
Is MEFV P706 polymorphism important in familial Mediterranean fever patients?
Karahan Zeynep C; Ozturk Aysenur; Akar Ece; Akar Nejat
Interleukin-6 (IL-6) -174 G/C polymorphism in familial Mediterranean fever patients with and without amyloidosis.

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All Publications

2006: Akar Nejat; Hasipek Metis; Oztürk Aysenur; Akar Ece; Tekin Mustafa
Serum amyloid A1 -13 T/C alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.
Journal of nephrology 2006;19(3):318-21.
2006: Akar N; Ozturk A; Ozel D; Akar E; Ekim M
Is MEFV P706 polymorphism important in familial Mediterranean fever patients?
Journal of nephrology 2006;19(1):119-20.
2005: Karahan Zeynep C; Ozturk Aysenur; Akar Ece; Akar Nejat
Interleukin-6 (IL-6) -174 G/C polymorphism in familial Mediterranean fever patients with and without amyloidosis.
Journal of nephrology 2005;18(5):582-4.
2003: Akar Ece; Ozdemir Sibel; Hakki Timur Ismail; Akar Nejat
First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family.
American journal of hematology 2003;74(4):280-2.
2003: Akar Nejat; Hasipek Metis; Akar Ece; Ekim Mesiha; Yalçinkaya Fatos; Cakar Nilgün
Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2003;10(1):12-6.
2003: Akar Nejat; Akar Ece; Ozel Duygu; Tekin Mustafa; Ekim Mesiha; Yalçinkaya Fatos
A note on the mutation analysis in familial Mediterranean fever.
Pediatric nephrology (Berlin, Germany) 2003;18(2):196-7.
2002: Akar Nejat; Gökdemir Refik; Ozel Duygu; Akar Ece
Endothelial cell protein C receptor (EPCR) gene exon III, 23 bp insertion mutation in the Turkish pediatric thrombotic patients.
Thrombosis and haemostasis 2002;88(6):1068-9.
2002: Tekin Mustafa; Dogu F; Taçyíldiz N; Akar E; Ikinciogullari A; Ogur G; Yavuz G; Babacan E; Akar N
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.
Clinical genetics 2002;62(1):84-8.
2002: Tutar E; Akar N; Atalay S; Yilmaz E; Akar E; Yalçinkaya F
Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease.
Heart (British Cardiac Society) 2002;87(6):568-9.
2001: Cakar N; Yalçinkaya F; Ozkaya N; Tekin M; Akar N; Koçak H; Misirlioglu M; Akar E; Tümer N
Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome.
Clinical and experimental rheumatology 2001;19(5 Suppl 24):S63-7.
2001: Akar N; Akar E; Yalçinkaya F
E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients.
Pediatrics 2001;108(1):215.
2001: Akar N; Akar E; Yilmaz E; Deda G
Plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish children with cerebral infarct and effect on factor V 1691 A mutation.
Journal of child neurology 2001;16(4):294-5.
2001: Akar N; Duman T; Akar E; Deda G; Sipahi T
The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct.
Thrombosis research 2001;102(2):121-3.
2001: Akar N; Akar E; Ozel D; Deda G; Sipahi T
Common mutations at the homocysteine metabolism pathway and pediatric stroke.
Thrombosis research 2001;102(2):115-20.
2001: Tutar H E; Imamoglu A; Kendirli T; Akar E; Atalay S; Akar N
Isolated recurrent pericarditis in a patient with familial Mediterranean fever.
European journal of pediatrics 2001;160(4):264-5.
2001: Gülec S; Aras O; Akar E; Tutar E; Omürlü K; Avci F; Dinçer I; Akar N; Oral D
Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction.
Clinical cardiology 2001;24(4):281-4.
2001: Akar E; Yalcinkaya F; Akar N
Is the Ala138Gly alteration of MEFV gene important for amyloidosis?
Human mutation 2001;17(1):71.
2000: Avcu F; Akar E; Demirkiliç U; Yilmaz E; Akar N; Yalçin A
The role of prothrombotic mutations in patients with Buerger's disease.
Thrombosis research 2000;100(3):143-7.
2000: Yalçinkaya F; Tekin M; Cakar N; Akar E; Akar N; Tümer N
Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients.
QJM : monthly journal of the Association of Physicians 2000;93(10):681-4.
2000: Akar N; Akar E; Deda G; Sipahi T
No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke.
Neurology 2000;55(3):460-1.
2000: Akar N; Yilmaz E; Akar E; Deda G; Sipahi T
Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct.
Haemostasis 2000;30(3):118-22.
2000: Avcu F; Akar N; Akar E; Beyan C; Yalçin A
Prothrombin gene 20210 G-->A and Factor V Arg 506 to Gln mutation in a patient with Buerger's disease--a case report.
Angiology 2000;51(5):421-3.
2000: Akar N; Akar E; Deda G; Arsan S
Spina bifida and common mutations at the homocysteine metabolism pathway.
Clinical genetics 2000;57(3):230-1.
2000: Akar N; Akar E; Akçay R; Avcu F; Yalcin A; Cin S
Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients.
Thrombosis research 2000;97(3):163-7.
2000: Akar N; Yilmaz E; Akar E; Avcu F; Yalçin A; Cin S
Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A.
Thrombosis research 2000;97(4):227-30.
2000: Akar N; Misiroglu M; Yalcinkaya F; Akar E; Cakar N; Tümer N; Akcakus M; Tastan H; Matzner Y
MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever.
Human mutation 2000;15(1):118-9.
1999: Akar N; Yalçinkaya F; Akar E; Cakar N
MEFV mutation analysis in Turkish familial Mediterranean fever patients with amyloidosis.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 1999;6(4):301-2.
1999: Akar N; Akar E; Deda G; Sipahi T; Ezer U
Coexistence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients.
Pediatric hematology and oncology 1999;16(6):565-6.
1999: Akar N; Akar E; Deda G; Sipahi T; Orsal A
Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct.
Journal of child neurology 1999;14(11):749-51.
1999: Akar N; Akar E; Tastan H
Feasibility of restriction enzyme protocols for the molecular diagnosis of abnormal hemoglobins in Turkish population.
American journal of hematology 1999;62(3):198.
1999: Akar N; Akar E; Cin S; Deda G; Avcu F; Yalçin A
Endothelial nitric oxide synthase intron 4, 27 bp repeat polymorphism in Turkish patients with deep vein thrombosis and cerebrovascular accidents.
Thrombosis research 1999;94(1):63-4.
1999: Akar N; Akar E
Methylenetetrahydrofolate-dehydrogenase 1958 G-A (R653 Q) polymorphism in Turkish patients with venous thromboembolism.
Acta haematologica 1999;102(4):199-200.
1998: Akar N; Akar E; Misirlioglu M; Avcu F; Yalçin A; Cin S
Search for genetic factors favoring thrombosis in Turkish population.
Thrombosis research 1998;92(2):79-82.
1998: Akar N; Misirlioglu M; Akar E; Avcu F; Yalçin A; Sözüöz A
Prothrombin gene 20210 G-A mutation in the Turkish population.
American journal of hematology 1998;58(3):249.
1998: Akar N; Akar E
Further note for the discrimination of Hb C.
American journal of hematology 1998;57(2):181.
1997: Akar N; Akar E; Dalgin G; Sözüöz A; Omürlü K; Cin S
Frequency of Factor V (1691 G --> A) mutation in Turkish population.
Thrombosis and haemostasis 1997;78(6):1527-8.
1996: Akar N; Sipahi T; Akar E
Erythrocyte P antigen in beta thalassemia major patients with human parvovirus-B19 infection.
Pediatric hematology and oncology 1996;13(6):581-2.
1996: Akar N; Akar E; Tastan H; Cin S
Direct detection of Hb C (B6 Glu-Lys) by BseRI analysis.
American journal of hematology 1996;52(4):325-6.
1996: Akar N; Akar E; Tastan H; Cin S
Verification of Hb O-Arab [beta 121(GH4)Glu-->Lys] by dual restriction enzyme analysis.
Hemoglobin 1996;20(2):161-3.
1995: Akar N; Ozden A; Akar E; Cin S; Arcasoy A
Discrimination of Hb D Los Angeles (B121 Glu-Gln) and Hb Beograd (B121 Glu-Val) by dual restriction enzyme analysis.
American journal of hematology 1995;48(4):280-1.

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