Haluk Akin
Haluk Akin
Professor of Medical Genetics, Ege University
ege.edu.tr üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Association between Ala–9Val polymorphism of Mn-SOD gene and schizophrenia
O Akyol, M Yanik, H Elyas, M Namli, H Canatan, H Akin, H Yuce, ...
Progress in Neuro-Psychopharmacology and Biological Psychiatry 29 (1), 123-131, 2005
1142005
Bireylerin mutluluk düzeylerinin ordinal lojistik regresyon analizi ile incelenmesi-analysing levels of happiness of individuals with ordinal logistic analysis
HB AKIN, E Şentürk
Öneri Dergisi 10 (37), 183-193, 2012
972012
MEFV mutations in patients with Familial Mediterranean Fever from the Aegean region of Turkey
H Akin, H Onay, E Turker, O Cogulu, F Ozkinay
Molecular biology reports 37 (1), 93-98, 2010
672010
OECD ülkelerinin eğitim göstergelerinin kümeleme analizi ve çok boyutlu ölçekleme analizi ile karşılaştırmalı analizi
HB Akın, Ö Eren
Öneri Dergisi 10 (37), 175-181, 2012
302012
Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients
H Akin, H Onay, E Turker, F Ozkinay
Journal of assisted reproduction and genetics 28 (5), 419-423, 2011
272011
A severe α thalassemia case compound heterozygous for Hb Adana in α1 gene and 20.5 kb double gene deletion
AA Durmaz, H Akin, AY Ekmekci, H Onay, B Durmaz, O Cogulu, ...
Journal of pediatric hematology/oncology 31 (8), 592-594, 2009
242009
The activities of purine catabolizing enzymes in plasma and bronchial washing fluid in patients with lung cancer and pneumonia
Ö Akyol, I Gökbulut, N Köksal, H Akin, H Özyurt, Z Yildirim
Clinical biochemistry 34 (3), 251-254, 2001
242001
Adenosine deaminase and xanthine oxidase activities in bladder washing fluid from patients with bladder cancer: a preliminary study
M Güleç, H Akın, H üseyin Yüce, E Ergin, H Elyas, O Yalçın, Ö Akyol
Clinical biochemistry 36 (3), 193-196, 2003
232003
Interferon-γ gene and interferon-γ receptor-1 gene polymorphisms in children with tuberculosis from Turkey
H Onay, A Ekmekci, B Durmaz, E Sayin, H Cosar, N Bayram, D Can, ...
Scandinavian journal of infectious diseases 42 (1), 39-42, 2010
172010
Molecular analysis and clinical findings of Griscelli syndrome patients
A Durmaz, F Ozkinay, H Onay, M Tombuloglu, A Atay, O Gursel, E Peker, ...
Journal of pediatric hematology/oncology 34 (7), 541-544, 2012
132012
The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey
E Ataman, O Cogulu, A Durmaz, E Karaca, B Durmaz, H Akin, F Ozkinay
Genetic testing and molecular biomarkers 16 (2), 150-153, 2012
132012
Fragile X syndrome and cerebral perfusion abnormalities: single-photon emission computed tomographic study
N Kabakus, M Aydin, H Akin, TA Balci, A Kurt, E Kekilli
Journal of child neurology 21 (12), 1040-1046, 2006
132006
The Ala-9Val polymorphism in the mitochondrial targeting sequence (MTS) of the manganese superoxide dismutase gene is not associated with juvenile-onset asthma
A Gurel, N Tomac, HR Yilmaz, I Tekedereli, O Akyol, F Armutcu, H Yuce, ...
Clinical biochemistry 37 (12), 1117-1120, 2004
122004
Multiple pterygium syndrome
FF Özkinay, C Özkinay, H Akin, S Azarsiz, C Gündüz
The Indian Journal of Pediatrics 64 (1), 113-116, 1997
101997
Bilateral familial elastofibroma dorsi: is genetic abnormality essential?
Tİ Akçam, U Çağırıcı, A Çakan, H Akın
The Annals of thoracic surgery 98 (2), e31-e32, 2014
92014
OECD ÜLKELERİNİN EĞİTİM GÖSTERGELERİNİN KÜMELEME ANALİZİ VE ÇOK BOYUTLU ÖLÇEKLEME ANALİZİ İLE KARŞILAŞTIRMALI ANALİZİ-OECD COUNTRIES WITH EDUCATION INDICATORS COMPARATIVE …
HB AKIN, E Özge
Öneri Dergisi 10 (37), 175-181, 2012
72012
Reactive oxygen species
C Boreera, O Akyol, M Yanik, H Elyas, M Namli, H Canatan, H Akin, ...
Biol Psychiatry 32, 1123-31, 2015
62015
Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven‐Year Period
O Cogulu, F Ozkinay, H Akin, H Onay, E Karaca, AA Durmaz, B Durmaz, ...
Journal of genetic counseling 20 (3), 287-293, 2011
52011
Genomik imprinting, uniparental dizomi, mikrodelesyon sendromları
H Akın, F Özkınay
Türkiye Klinikleri J Pediatr Sci 1, 61-7, 2005
52005
The role of 99Tcm-tetrofosmin myocardial perfusion scintigraphy in the assessment of patients with previous myocardial infarction: a comparative study with 201Tl.
Z Burak, H Akin, S Buket, A Sagcan, M Argon, Y Atay, I Durmaz, Y Duman
Nuclear medicine communications 19 (2), 127-136, 1998
51998
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20