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Nejat Akar
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36
Akar, Ece
27
Cin, Sükrü
22
Tekin, Mustafa
18
Deda, Gülhis
16
Egin, Yonca
12
Cavdar, Ayhan
12
Yalçinkaya, Fatos
11
Uysal, Zümrüt
11
Ekim, Mesiha
10
Berberoglu, Merih
10
Cakar, Nilgün
10
Sipahi, Tansu
9
Ocal, Gönül
9
KEMAHLI, Sabri
8
Tümer, Necmiye
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All Publications
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2009: Yürürer Denizay; Teber Serap; Deda Gülhis; Egin Yonca; Akar Nejat
The relation between cytokines, soluble endothelial protein C receptor, and factor VIII levels in Turkish pediatric stroke patients.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009;15(5):545-51.
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2009: Kendirli Tanil; Ince Erdal; Ciftci Ergin; Dogru Ulker; Egin Yonca; Akar Nejat
Soluble endothelial protein C receptor level in children with sepsis.
Pediatric hematology and oncology 2009;26(6):432-8.
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2009: Eroglu Aydan; Cam Ragip; Egin Yonca; Akar Nejat
Factor V Leiden and prothrombin G20210A polymorphisms are not associated with disease-free survival in breast cancer.
Breast cancer research and treatment 2009;116(3):619-20.
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2009: Ozel Demiralp Duygu; Ekim Mesiha; Akar Nejat
The effect of plasminogen activator inhibitor-1 -675 4G/5G polymorphism on familial Mediterranean fever (FMF) disease.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009;15(4):443-7.
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2009: Cam Ragip; Eroglu Aydan; Egin Yonca; Akar Nejat
Dihydrofolate reductase (DHRF) 19-bp intron-1 deletion and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms in breast cancer.
Breast cancer research and treatment 2009;115(2):431-2.
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2009: Tras Serap Teber; Deda Gülhis; Akar Nejat
A note on homocysteine levels in children.
Thrombosis research 2009;123(5):799.
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2009: Unal Ozlem; Deda Gülhis; Teber Serap; Ertem Mehmet; Akar Nejat
Thrombophilic risk factors in epileptic children treated with valproic Acid.
Pediatric neurology 2009;40(2):102-6.
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2009: Oguzulgen I Kivilcim; Yilmaz E; Demirtas Senay; Erkekol Ferda Oner; Ekim Numan; Demir Nalan; Numanoglu Numan; Ozel Duygu; Ulu Arzu; Akar Nejat
The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolism.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009;15(1):73-7.
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2009: Eroglu Aydan; Egin Yonca; Cam Ragip; Akar Nejat
The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
Annals of hematology 2009;88(1):73-6.
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2009: Aytekin Caner; Dogu Figen; Ikinciogullari Aydan; Egin Yonca; Yüksek Mutlu; Bozdogan Günseli; Akar Nejat; Babacan Emel
[TGF-Beta1-915G/C and TNF-alpha-308G/A polymorphisms in children with asthma]
Tüberküloz ve toraks 2009;57(1):62-7.
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2008: Orhon F S; Ulukol B; Hanoluk A; Akar N
Serum pro-hepcidin levels in infants with iron deficiency anaemia.
International journal of laboratory hematology 2008;30(6):546-7.
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2008: Yalçindag F Nilüfer; Batioglu Figen; Ozdemir Ozden; Cansizoglu Esra; Egin Yonca; Akar Nejat
Soluble endothelial protein C receptor levels in Behçet patients with and without ocular involvement.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2008;246(11):1603-8.
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2008: Gulec Sukru; Ruchan Akar Ahmet; Akar Nejat
MEF2A sequence variants in Turkish population.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008;14(4):465-7.
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2008: Ozel Demiralp Duygu; Aktas Huseyin; Akar Nejat
The effect of plasminogen activator inhibitor-1 -675 4G/5G polymorphism on PAI-1 gene expression and adipocyte differentiation.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008;14(4):438-46.
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2008: Yildiz Zuleyha; Ulu Arzu; Incesulu Armagan; Ozkaptan Yalcin; Akar Nejat
The importance of thrombotic risk factors in the development of idiopathic sudden hearing loss.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008;14(3):356-9.
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2008: Sen Elif; Ulger Fusun; Kaya Akin; Akar Nejat; Gonullu Ugur
Serum endothelial monocyte-activating polypeptide-II: a novel biomarker in patients with non-small-cell lung cancer.
Clinical lung cancer 2008;9(3):166-70.
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2008: Ceyhan Seyit Temel; Beyan Cengiz; Bahce Muhterem; Baser Iskender; Kaptan Kursat; Ifran Ahmet; Egin Yonca; Akar Nejat
Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2008;101(2):188-9.
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2008: Ergür Ayça T; Ocal Gönül; Berberoglu Merih; Tekin Mustafa; Kiliç Birim G; Aycan Zehra; Kutlu Alev; Adiyaman Pelin; Siklar Zeynep; Akar Nejat; Sahin Aynur; Akçayöz Duygu
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(2):172-4.
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2008: Arisoy Münevver; Rad Abbas Yousefi; Akin Ali; Akar Nejat
Relationship between susceptibility to antimicrobials and virulence factors in paediatric Escherichia coli isolates.
International journal of antimicrobial agents 2008;31 Suppl 1():S4-8.
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2008: Tekeli Oya; Turacli M Erol; Egin Yonca; Akar Nejat; Elhan Atilla Halil
Tumor necrosis factor alpha-308 gene polymorphism and pseudoexfoliation glaucoma.
Molecular vision 2008;14():1815-8.
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2008: Tekeli Oya; Turaçli M Erol; Altinok Buket; Akar Nejat; Elhan Atilla Halil
No relation between angiotensin-converting enzyme gene polymorphism and pseudoexfoliation.
Ophthalmic research 2008;40(1):32-4.
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2007: Yalçinkaya Fatos; Ozçakar Z Birsin; Kasapçopur Ozgür; Oztürk Aysenur; Akar Nejat; Bakkaloglu Aysin; Arisoy Nil; Ekim Mesiha; Ozen Seza
Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa.
The Journal of pediatrics 2007;151(6):675-8.
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2007: Akar Nejat; Reisman Arnold; Oral Aysu
Albert Eckstein (1891-1950): modernizer of Turkey's paediatrics in exile.
Journal of medical biography 2007;15(4):213-8.
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2007: Eyileten Zeynep; Akar A Ruchan; Sirlak Mustafa; Ucanok Kemalettin; Akar Nejat
Off-pump coronary artery bypass graft surgery after stent implantation in a patient with combined thrombophilic risk factors.
The Canadian journal of cardiology 2007;23(13):1083-4.
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2007: Kendirli Tanil; Ciftçi Ergin; Ince Erdal; Yurdakul Engin; Kansu Aydan; Akar Nejat
Homozygous 23-bp insertion of endothelial protein c receptor gene in a child with fatal sepsis.
Pediatric hematology and oncology 2007;24(3):199-204.
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2007: Akar Nejat; Dönmez Buket; Deda Gülhis
FXIII gene Val34Leu polymorphism in Turkish children with cerebral infarct.
Journal of child neurology 2007;22(2):222-4.
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2007: Tekin Mustafa; Hismi Burcu Oztürk; Fitoz Suat; Ozdag Hilal; Cengiz Filiz Basak; Sirmaci Asli; Aslan Idil; Inceoglu Bora; Yüksel-Konuk E Berrin; Yilmaz Seda Tasir; Yasun Oztan; Akar Nejat
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.
American journal of human genetics 2007;80(2):338-44.
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2007: Ulukol Betul; Orhon Filiz Simsek; Hanoluk Ahmet; Akar Nejat
Serum pro-hepcidin levels and relationship with ferritin in healthy non-anaemic infants.
Acta haematologica 2007;118(2):70-2.
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2007: Ulu Arzu; Gunal Denizay; Tiras Serap; Egin Yonca; Deda Gülhis; Akar Nejat
EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients.
Thrombosis research 2007;120(1):47-52.
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2006: Ekmekci Yakup; Keven Kenan; Akar Nejat; Egin Yonca; Sengul Sule; Kutlay Sim; Erturk Sehsuvar; Erbay Bulent
Thrombophilia and avascular necrosis of femoral head in kidney allograft recipients.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2006;21(12):3555-8.
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2006: Adiyaman Pelin Bilir; Ocal Gonul; Cetinkaya Ergun; Akar Nejat; Uysal Ali; Duman Turker; Evliyaoglu Olcay; Aycan Zehra; Lumbroso Serge; Sultan Charles; Berberoglu Merih
5 alpha steroid reductase deficiency in Turkey.
Pediatric endocrinology reviews : PER 2006;3 Suppl 3():462-9.
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2006: Tekin Mustafa; Hismi Burcu Oztürk; Fitoz Suat; Yalçinkaya Fatos; Ekim Mesiha; Kansu Aydan; Ertem Mehmet; Deda Gülhis; Tutar Ercan; Arsan Saadet; Zhou Xiao-Ping; Pilarski Robert; Eng Charis; Akar Nejat
A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus.
American journal of medical genetics. Part A 2006;140(13):1472-5.
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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.
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2006: Berberoglu M; Evliyaoglu O; Adiyaman P; Ocal G; Ulukol B; Simsek F; Siklar Z; Törel A; Ozel D; Akar N
Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children.
Journal of pediatric endocrinology & metabolism : JPEM 2006;19(5):741-8.
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2006: Arisoy M; Aysev D; Ekim M; Ozel D; Köse S K; Ozsoy E D; Akar N
Detection of virulence factors of Escherichia coli from children by multiplex polymerase chain reaction.
International journal of clinical practice 2006;60(2):170-3.
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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.
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2006: Erkekol Ferda Oner; Ulu Arzu; Numanoglu Numan; Akar Nejat
High plasma levels of factor VIII: an important risk factor for isolated pulmonary embolism.
Respirology (Carlton, Vic.) 2006;11(1):70-4.
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2006: Karahan Z Ceren; Mumcuoglu Ipek; Guriz Haluk; Tamer Deniz; Balaban Neriman; Aysev Derya; Akar Nejat
PCR evaluation of false-positive signals from two automated blood-culture systems.
Journal of medical microbiology 2006;55(Pt 1):53-7.
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2006: Ozdag Hilal; Egin Yonca; Akar Nejat
Prothrombin gene 20209 C >T along with the first description of a homozygous polymorphism at the 3' downstream region +4 C >T in the Turkish population.
Laboratory hematology : official publication of the International Society for Laboratory Hematology 2006;12(3):131-3.
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2005: Turaçli M Erol; Tekeli Oya; Ozdemir Filiz; Akar Nejat
Methylenetetrahydrofolate reductase 677 C-T and homocysteine levels in Turkish patients with pseudoexfoliation.
Clinical & experimental ophthalmology 2005;33(5):505-8.
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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.
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2005: Tekin Mustafa; Akcayoz Duygu; Ucar Canan; Gulen Huseyin; Akar Nejat
657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.
Human biology; an international record of research 2005;77(3):393-7.
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2005: Kurekci A Emin; Aydin H Ibrahim; Atay A Avni; Akar Nejat; Cetan Turker; Ozcan Okan; Gokcay Erdal
Familial high factor VIII level in a child with necrotizing fasciitis complicating primary varicella infection.
Pediatric hematology and oncology 2005;22(3):219-22.
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2005: Aycan Zehra; Berberoglu Merih; Ocal Gönül; Evliyaoglu Olcay; Adiyaman Pelin; Deda Gülhis; Caksen Hüseyin; Akar Nejat; Karahan Ceren; Cinas Peyami; Bideci Aysun
Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese children.
Journal of pediatric endocrinology & metabolism : JPEM 2005;18(3):275-84.
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2005: Oguzulgen I Kivilcim; Ekim Numan; Erkekol Ferda Oner; Altinok Buket; Akar Nejat
Is tissue-plasminogen activator gene polymorphism a risk factor for venous thromboembolism in every population?
Journal of thrombosis and thrombolysis 2005;19(1):61-3.
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2005: Tekin M; Bogoclu G; Arican S T; Orman M N; Tastan H; Elsobky E; Elsayed S; Akar N
Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia.
Clinical genetics 2005;67(1):31-7.
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2005: Sen Elif; Gönüllü Ugur; Akar Nejat
The detection of quantitative serum p53 protein in lung cancer.
Tüberküloz ve toraks 2005;53(3):231-7.
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2005: Karahan Z C; Akar N
Subtypes of genotype A Candida albicans isolates determined by restriction endonuclease and sequence analyses.
Microbiological research 2005;160(4):361-6.
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2005: Karahan Zeynep Ceren; Akar Nejat
Restriction endonuclease analysis as a solution for determining rifampin resistance mutations by automated DNA sequencing in heteroresistant Mycobacterium tuberculosis strains.
Microbial drug resistance (Larchmont, N.Y.) 2005;11(2):137-40.
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2005: Karahan Zeynep Ceren; Deda Gülhis; Sipahi Tansu; Elhan Atilla H; Akar Nejat
TNF-alpha -308G/A and IL-6 -174 G/C polymorphisms in the Turkish pediatric stroke patients.
Thrombosis research 2005;115(5):393-8.
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2004: Karahan Z C; Güriz H; Agirbasli H; Balaban N; Göçmen J S; Aysev D; Akar N
Genotype distribution of Candida albicans isolates by 25S intron analysis with regard to invasiveness.
Mycoses 2004;47(11-12):465-9.
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2004: Akar Nejat
Albert Eckstein: a pioneer in pediatrics in Turkey.
The Turkish journal of pediatrics 2004;46(4):295-7.
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2004: Tekin Mustafa; Kavaz Asli; Berberoglu Merih; Fitoz Suat; Ekim Mesiha; Ocal Gönül; Akar Nejat
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype.
American journal of medical genetics. Part A 2004;130A(3):284-7.
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2004: Ekim Numan; Oguzulgen I Kivilcim; Demir Nalan; Altinok Buket; Akar Nejat
The role of angiotensin-converting enzyme gene polymorphism in pulmonary thromboembolism.
Thrombosis and haemostasis 2004;92(2):432-3.
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2004: Arsan Saadet; Atasay Begüm; Akar Nejat
Thrombophilia and neonatal complications in preterm infants.
Thrombosis and haemostasis 2004;92(1):212-3; author reply 213.
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2004: Adiyaman P; Ocal G; Berberoglu M; Evliyaoglu O; Aycan Z; Cetinkaya E; Bulca Y; Ersöz G; Akar N
Alterations in serum growth hormone (GH)/GH dependent ternary complex components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 molar ratio) and the influence of these alterations on growth pattern in female rhythmic gymnasts.
Journal of pediatric endocrinology & metabolism : JPEM 2004;17(6):895-903.
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2004: Ulukol Betül; Tezcan Sabahat; Akar Nejat; Gökçe Hafize; Cin Sükrü
Evaluation of erythropoiesis by serum transferrin receptor and ferritin in infants aged 0-6 months.
Pediatric hematology and oncology 2004;21(4):293-305.
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2004: Ocaktan Esin; Ozyurda Ferda; Akar Nejat
Natural immunity to Haemophilus influenzae type B in children of Ankara, Turkey.
Pediatrics international : official journal of the Japan Pediatric Society 2004;46(3):280-4.
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2004: Cangöz Emel; Deda Gülhis; Akar Nejat
Effect of factor VIIIc levels in pediatric stroke patients.
Pediatric hematology and oncology 2004;21(3):255-60.
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2004: Karahan Zeynep Ceren; Atalay Figen; Uzun Meltem; Erturan Zayre; Atasever Melike; Akar Nejat
Sequence analysis of rpoB mutations in rifampin-resistant clinical Mycobacterium tuberculosis isolates from Turkey.
Microbial drug resistance (Larchmont, N.Y.) 2004;10(4):325-33.
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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.
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2003: Atasay Begüm; Arsan Saadet; Günlemez Ayla; Kemahli Sabri; Akar Nejat
Factor V Leiden and prothrombin gene 20210A variant in neonatal thromboembolism and in healthy neonates and adults: a study in a single center.
Pediatric hematology and oncology 2003;20(8):627-34.
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2003: Tekin M; Akçayöz D; Comak E; Bogoçlu G; Duman T; Fitoz S; Ilhan I; Akar N
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
Clinical genetics 2003;64(4):371-4.
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2003: Ates Askin; Düzgün Nursen; Ulu Arzu; Tiryaki A Olcay Aydintug; Akar Nejat
Factor V gene (1691A and 4070G) and prothrombin gene 20210A mutations in patients with Behçet's disease.
Pathophysiology of haemostasis and thrombosis 2003;33(3):157-63.
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2003: Tekin Mustafa; Duman Türker; Bogoçlu Gönül; Incesulu Armagan; Comak Elif; Ilhan Inci; Akar Nejat
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating.
Human mutation 2003;21(5):552-3.
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2003: Kurekci A Emin; Gokce Hafize; Akar Nejat
Factor VIII levels in children with thrombosis.
Pediatrics international : official journal of the Japan Pediatric Society 2003;45(2):159-62.
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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.
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2003: Tekin M; Duman T; Bogoçlu G; Incesulu A; Comak E; Fitoz S; Yilmaz E; Ilhan I; Akar N
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.
European journal of pediatrics 2003;162(3):154-8.
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2003: Gözdasoglu Sevgi; Akar Nejat
The strong correlation between serum copper level and the copper/zinc ratio to histopathological changes, clinical stage, and prognosis of Hodgkin's disease.
Biological trace element research 2003;91(2):191-2.
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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.
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2003: Tekin M; Duman T; Bogoçlu G; Incesulu A; Cin S; Akar N
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene.
Genetic counseling (Geneva, Switzerland) 2003;14(4):379-86.
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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.
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2002: Akar Nejat; Gökçe Hafize
High levels of FVIII and FIX in a pediatric patient with retinal artery occlusion.
Pediatric hematology and oncology 2002;19(8):593-5.
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2002: Akar Nejat; Gökçe Hafize
Red blood cell indexes in patients in patients with hereditary spherocytosis and beta-thalassemia combination.
Pediatric hematology and oncology 2002;19(8):569-73.
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2002: Ermis Cengiz; Tsai Micheal Y; Hanson Naomi Q; Akar Nejat; Aras Omer
Angiotensin I converting enzyme, angiotensin II type 1 receptor and angiotensinogen polymorphisms and early myocardial infarction in Turkish population.
Thrombosis and haemostasis 2002;88(4):693-4.
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2002: Bakkaloglu Sevcan A; Ekim Mesiha; Tümer Necmiye; Akar Nejat; Uysal Zümrüt
Soluble transferrin receptor is not a reliable marker of iron deficiency in pediatric CAPD patients.
Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis 2002;22(5):621-5.
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2002: Deda Gülhis; Içagasioglu Dilara; Caksen Hüseyin; Akar Nejat
Combined genetic defects in a child with ischemic stroke: case report.
Journal of child neurology 2002;17(7):533-4.
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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.
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2002: Gözdasoglu Sevgi; Uysal Zümrüt; Ertem Mehmet; Akar Nejat
Three risk factors--high lipoprotein (a), elevated FVIII, and FV Leiden--in a pediatric Behçet's disease patient with deep vein thrombosis.
Thrombosis research 2002;106(4-5):263.
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2002: Atasay Begüm; Günlemez Ayla; Akar Nejat; Arsan Saadet
Does early erythropoietin therapy decrease transfusions in anemia of prematurity?
Indian journal of pediatrics 2002;69(5):389-91.
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2002: Ince Erdal; Cakar Nilgün; Tekin Mustafa; Kendirli Tanil; Ozkaya Nuray; Akar Nejat; Yalçinkaya Fatos
Arthritis in children with familial Mediterranean fever.
Rheumatology international 2002;21(6):213-7.
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2002: Ocal G; Adiyaman P; Berberoglu M; Cetinkaya E; Akar N; Uysal A; Duman T; Evliyaoglu O; Aycan Z; Lumbroso S; Sultan C;
Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village.
Journal of pediatric endocrinology & metabolism : JPEM 2002;15(4):411-21.
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2002: Oguzulgen I K; Ekim N N; Akar N; Demirel K; Kitapci M
The role of thrombophilic risk factors in the severity of pulmonary thromboembolism.
The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology 2002;19(4):709-11.
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2002: Uysal Zümrüt; Dogu Figen; Kürekçi A Emin; Culha Vildan Kosan; Deda Gülhis; Ekim Mesiha; Akar Nejat; Erterm Mehmet; Ikinciogullari Aydan; Babacan Emel; Gözdasoglu Sevgi
Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndrome.
Pediatric hematology and oncology 2002;19(1):59-66.
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2002: Atalay S; Akar N; Tutar H E; Yilmaz E
Factor V 1691 G-A mutation in children with intracardiac thrombosis: a prospective study.
Acta paediatrica (Oslo, Norway : 1992) 2002;91(2):168-71.
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2001: Atalay S; Akar N; Tutar H E; Gökçe H; Uçar T
Is high levels of factor VIII a possible risk factor for intracardiac thrombosis?
International journal of cardiology 2001;81(2-3):289-90.
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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.
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2001: Berberoglu M; Aycan Z; Ocal G; Begeot M; Naville D; Akar N; Adiyaman P; Evliyaoglu O; Penhoat A
Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients.
Journal of pediatric endocrinology & metabolism : JPEM 2001;14(8):1113-8.
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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.
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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.
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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.
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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.
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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.
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2001: Tekin D; Yavuzer S; Tekin M; Akar N; Cin S
Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemia.
Pediatrics international : official journal of the Japan Pediatric Society 2001;43(1):74-7.
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2001: Akar E; Yalcinkaya F; Akar N
Is the Ala138Gly alteration of MEFV gene important for amyloidosis?
Human mutation 2001;17(1):71.
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2000: Cakir M; Gurkan O U; Savas I; Numanoglu N; Ataman S; Ekinci C; Akar N
Extensive jugular and upper limb thrombosis in a patient with factor V Leiden mutation and non-Hodgkin's lymphoma.
Australian and New Zealand journal of medicine 2000;30(6):735-6.
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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.
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2000: Akar H; Keven K; Nergizoglu G; Erturk S; Ates K; Erbay B; Akar N; Duman N; Karatan O
Renal amyloidosis in a patient with homozygous sickle cell anemia and M694V/M694V mutation.
Nephron 2000;86(3):383-4.
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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.
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2000: Tekin M; Yalçinkaya F; Cakar N; Akar N; Misirlioglu M; Tastan H; Tümer N
MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?
Clinical genetics 2000;57(6):430-4.
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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.
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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.
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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.
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2000: Tekin M; Yalçinkaya F; Tümer N; Akar N; Misirlioglu M; Cakar N
Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis.
Acta paediatrica (Oslo, Norway : 1992) 2000;89(2):177-82.
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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.
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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.
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2000: Yalçinkaya F; Cakar N; Misirlioglu M; Tümer N; Akar N; Tekin M; Tastan H; Koçak H; Ozkaya N; Elhan A H
Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis.
Rheumatology (Oxford, England) 2000;39(1):67-72.
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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.
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1999: Arcasoy A; Ocal G; Kemahli S; Berberoglu M; Yildirmak Y; Canatan D; Akçurin S; Akar N; Uysal Z; Adiyaman P; Cetinkaya E
Recombinant human growth hormone treatment in children with thalassemia major.
Pediatrics international : official journal of the Japan Pediatric Society 1999;41(6):655-61.
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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.
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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.
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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.
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1999: Akar N; Egin Y
A further case of homozygous G20210A prothrombin gene mutation without thromboembolic events.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 1999;5(4):284.
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1999: Nergizoglu G; Keven K; Gürses M A; Aras O; Ertürk S; Duman N; Ates K; Akar H; Akar N; Karatan O; Erbay B; Ertug A E
Carotid intima-media thickness and ACE-gene polymorphism in hemodialysis patients.
Journal of nephrology 1999;12(4):261-5.
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1999: Tutar H E; Imamoglu A; Atalay S; Gümüs H; Akar N
Plasma endothelin-1 levels in patients with left-to-right shunt with or without pulmonary hypertension.
International journal of cardiology 1999;70(1):57-62.
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1999: Küçük N O; Aras G; Sipahi T; Ibis E; Akar N; Soylu A; Erbay G
Evaluation of cardiac functions in patients with thalassemia major.
Annals of nuclear medicine 1999;13(3):175-9.
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1999: Sipahi T; Duru F; Ciftçi E; Sahin F; Akar N
Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence.
European journal of haematology 1999;62(4):281-3.
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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.
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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.
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1998: Pasin M; Yavuzer S; Tekin M; Akar N; Violi F
Oxygen free radical-dependent increased platelet function in beta-thalassemia major patients.
Thrombosis research 1998;92(6):283-6.
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1998: Akar N; Kemahli S; Uysal Z; Cin S
Thromboembolism in beta-thalassemia major.
Acta haematologica 1998;100(3):166.
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1998: Akar N; Aras O; Omürlü K; Cin S
Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease.
Scandinavian journal of clinical and laboratory investigation 1998;58(6):491-5.
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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.
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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.
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1998: Tekin M; Akar N; Egin Y; Cin S
Serum superoxide dismutase levels of beta thalassemia patients and effects of high dosage of intravenous desferrioxamine treatment on superoxide dismutase levels.
Pediatric hematology and oncology 1998;15(4):371-4.
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1998: Kemahli S; Alhenc-Gelas M; Gandrille S; Aiach M; Akar N; Cin S
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1998;9(4):351-4.
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1998: Uysal Z; Yildirmak Y; Akar N; Basak N; Cin S
alpha-Thalassemia and hereditary spherocytosis in the same patient: the interaction of two diseases.
Pediatric hematology and oncology 1998;15(3):271-6.
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1998: Akar N; Akar E
Further note for the discrimination of Hb C.
American journal of hematology 1998;57(2):181.
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1998: Sipahi T; Akar N; Egin Y; Cin S
Serum interleukin-2 and interleukin-6 levels in iron deficiency anemia.
Pediatric hematology and oncology 1998;15(1):69-73.
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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.
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1997: Cakar N; Ekim M; Tümer N; Yalçinkaya F; Akar N; Onaran H O
Pharmacokinetics of recombinant human erythropoietin in children with chronic renal failure.
International urology and nephrology 1997;29(3):377-83.
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1996: Loudianos G; Dessì V; Angius A; Lovicu M; Loi A; Deiana M; Akar N; Vajro P; Figus A; Cao A; Pirastu M
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients.
Human genetics 1996;98(6):640-2.
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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.
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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.
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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.
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1996: Yildirmak Y; Kemahli S; Akar N; Uysal Z; Cin S; Arcasoy A
A case of severe thrombocytopenia due to parvovirus B19 virus.
Pediatric hematology and oncology 1996;13(2):183-5.
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1995: Akar N; Sipahi T; Egin Y; Cin S; Arcasoy A
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey.
Pediatric hematology and oncology 1995;12(5):507-9.
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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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1995: Uysal Z; Cin S; Arcasoy A; Akar N
Interferon treatment of hepatitis B and C in beta-thalassemia.
Pediatric hematology and oncology 1995;12(1):87-9.
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1995: Canatan D; Akar N; Arcasoy A
Effects of calcitonin therapy on osteoporosis in patients with thalassemia.
Acta haematologica 1995;93(1):20-4.
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1994: Kemahli S; Canatan D; Uysal Z; Akar N; Cin S; Arcasoy A
GM-CSF in the treatment of Fanconi's anaemia.
British journal of haematology 1994;87(4):871-2.
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1994: Akar N; Ozden A
Rapid diagnosis of two beta-thalassemia mutations: frameshift codon 5 (-CT) and codon 6 (-A)
Pediatric hematology and oncology 1994;11(4):459-60.
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1994: Tuncer R; Sipahi T; Erkaya S; Akar N K; Baysar N S; Erçevik S
Primary twin ovarian pregnancy.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 1994;46(1):57-9.
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1994: Kemahli S; Canatan D; Uysal Z; Akar N; Cin S; Arcasoy A
DDAVP shortens bleeding time in Bernard-Soulier syndrome.
Thrombosis and haemostasis 1994;71(5):675.
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1993: Uysal Z; Akar N; Kemahli S; Dincer N; Arcasoy A
Desferrioxamine and urinary zinc excretion in beta-thalassemia major.
Pediatric hematology and oncology 1993;10(3):257-60.
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1993: Cavdar A O; Gözdasoglu S; Yavuz G; Babacan E; Unal E; Uluoglu O; Yücesan S; Magrath I T; Akar N
Burkitt's lymphoma between African and American types in Turkish children: clinical, viral (EBV), and molecular studies.
Medical and pediatric oncology 1993;21(1):36-42.
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1992: Canatan D; Erden I; Aytac S; Akar N; Kemahli S; Arcasoy A
Doppler color flow imaging for the evaluation of postsplenectomy portal vein thrombosis in pediatric hematological diseases.
Pediatric hematology and oncology 1992;9(4):397-9.
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1992: Akar N; Berberoglu M; Arcasoy A
Effects of zinc supplementation on somatomedin-C level, in beta thalassemia.
American journal of hematology 1992;41(2):142-3.
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1991: Cavdar A O; Bahçeci M; Akar N; Dinçer F N; Erten J
Maternal hair zinc concentration in neural tube defects in Turkey.
Biological trace element research 1991;30(1):81-5.
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1991: Cavdar A O; Bahçeci M; Akar N; Erten J; Yavuz H
Effect of zinc supplementation in a Turkish woman with two previous anencephalic infants.
Gynecologic and obstetric investigation 1991;32(2):123-5.
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1988: Cavdar A O; Bahçeci M; Akar N; Erten J; Bahçeci G; Babacan E; Arcasoy A; Yavuz H
Zinc status in pregnancy and the occurrence of anencephaly in Turkey.
Journal of trace elements and electrolytes in health and disease 1988;2(1):9-14.
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1988: Akar N; Cavdar A O; Arcasoy A
High incidence of neural tube defects in Bursa, Turkey.
Paediatric and perinatal epidemiology 1988;2(1):89-92.
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1988: Cin S; Akar N; Arcasoy A; Cavdar A O
Abnormal hemoglobins in Turkish Cypriots.
Hemoglobin 1988;12(4):423-5.
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1987: Akar N; Cavdar A O; Dessi E; Loi A; Pirastu M; Cao A
Beta thalassaemia mutations in the Turkish population.
Journal of medical genetics 1987;24(6):378-9.
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1987: Arcasoy A; Cavdar A; Cin S; Erten J; Babacan E; Gözdasoglu S; Akar N
Effects of zinc supplementation on linear growth in beta-thalassemia (a new approach).
American journal of hematology 1987;24(2):127-36.
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1984: Cin S; Akar N; Arcasoy A; Cavdar A O; Dedeoglu S
Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population.
Journal of medical genetics 1984;21(2):158.
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1984: Akar N; Gözdasoglu S
Spectrum of anomalies in Fanconi anaemia.
Journal of medical genetics 1984;21(1):75-6.
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1984: Cin S; Akar N; Arcasoy A; Dedeoglu S; Cavdar A O
Prevalence of thalassemia and G6PD deficiency in North Cyprus.
Acta haematologica 1984;71(1):69-70.
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1983: Cavdar A O; Babacan E; Asik S; Arcasoy A; Ertem U; Himmetoglu O; Bayçu T; Akar N
Zinc levels of serum, plasma, erythrocytes and hair in Turkish women with anencephalic babies.
Progress in clinical and biological research 1983;129():99-106.
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1983: Cin S; Akar N; Cavdar A O; Arcasoy A; Dedeoglu S; Webber B; Lam H; Huisman T H
Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.
Hemoglobin 1983;7(5):467-70.
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1982: Gözdasoglu S; Cavdar A O; Arcasoy A; Akar N
Serum copper and zinc levels and copper/zinc ratio in pediatric non-Hodgkin's lymphoma.
Acta haematologica 1982;67(1):67-70.
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