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Ali Dursun
Ali Dursun
Verified email at hacettepe.edu.tr
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Cited by
Cited by
Year
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency
S Kölker, SF Garbade, CR Greenberg, JV Leonard, JM Saudubray, ...
Pediatric research 59 (6), 840-847, 2006
2992006
Hypoxia inducible factor 1 (HIF-1) and cardioprotection
D Tekin, AD Dursun, L Xi
Acta Pharmacologica Sinica 31 (9), 1085-1094, 2010
2132010
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
N Akizu, V Cantagrel, MS Zaki, L Al-Gazali, X Wang, RO Rosti, E Dikoglu, ...
Nature genetics 47 (5), 528-534, 2015
1372015
Newborn PKU screening in Turkey: at present and organization for future.
I Ozalp, T Coşkun, A Tokatli, HS Kalkanoğlu, A Dursun, S Tokol, G Köksal, ...
The Turkish journal of pediatrics 43 (2), 97-101, 2001
1322001
Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype–phenotype correlation in 38 classical citrullinemia patients
HZ Gao, K Kobayashi, A Tabata, H Tsuge, M Iijima, T Yasuda, ...
Human mutation 22 (1), 24-34, 2003
1102003
The molecular basis of familial hypercholesterolaemia in Turkish patients
MM Sözen, R Whittall, C Öner, A Tokatlı, HS Kalkanoğlu, A Dursun, ...
Atherosclerosis 180 (1), 63-71, 2005
602005
Hearing loss in biotinidase deficiency: genotype-phenotype correlation
HSK Sivri, GA Genç, A Tokatlı, A Dursun, T Coşkun, Hİ Aydın, ...
The Journal of pediatrics 150 (4), 439-442, 2007
572007
Mutations in the G6PC3 gene cause Dursun syndrome
S Banka, WG Newman, RK Özgül, A Dursun
American Journal of Medical Genetics Part A 152 (10), 2609-2611, 2010
562010
Secondary hemophagocytosis in 3 patients with organic acidemia involving propionate metabolism
M Gokce, O Unal, B Hismi, F Gumruk, T Coskun, G Balta, S Unal, M Cetin, ...
Pediatric hematology and oncology 29 (1), 92-98, 2012
532012
Transient nonketotic hyperglycinemia: two case reports and literature review
D Aliefendioğlu, T Coşkun, A Dursun, FN Çakmak, M Kesimer
Pediatric neurology 28 (2), 151-155, 2003
492003
Pamukkale Üniversitesi öğrencilerinde alkol ve sigara bağımlılığı taraması
H Alaçam, A Korkmaz, M Efe, CŞ Balcı, C Şengül
Pamukkale Tıp Dergisi, 2015
442015
The prevalence, molecular analysis and HLA typing of late-onset 21-hydroxylase deficiency in Turkish woman with hirsutism and polycystic ovary
S Yarman, A Dursun, F Oguz, F ALAGÖL
Endocrine journal 51 (1), 31-36, 2004
432004
Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screening
M Karaca, RK Özgül, Ö Ünal, D Yücel-Yılmaz, M Kılıç, B Hişmi, A Tokatlı, ...
European journal of pediatrics 174, 1077-1084, 2015
392015
Methylmalonic acidemia mimicking diabetic ketoacidosis in an infant.
FB Guven A, Cebeci N, Dursun A, Aktekin E, Baumgartner M
Pediatr Diabetes. 13 (6), e22-5, 2012
382012
Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria?
H Gokmen Ozel, T Kucukkasap, G Koksal, HS Kalkanoglu Sivri, A Dursun, ...
Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2008
382008
Effects of exercise training on anxiety in diabetic rats
H Caliskan, F Akat, Y Tatar, N Zaloglu, AD Dursun, M Bastug, H Ficicilar
Behavioural brain research 376, 112084, 2019
362019
Audiologic findings in children with biotinidase deficiency in Turkey
GA Genc, HS Sivri-Kalkanoğlu, A Dursun, HI Aydın, A Tokatlı, ...
International journal of pediatric otorhinolaryngology 71 (2), 333-339, 2007
362007
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency
M Kilic, RK Özgül, T Coşkun, D Yücel, M Karaca, HS Sivri, A Tokatli, ...
JIMD Reports-Case and Research Reports, 2011/3, 17-23, 2012
332012
Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: a probable new familial syndrome with multisystem involvement
A Dursun, RK Ozgul, A Soydas, T Tugrul, A Gurgey, A Celiker, RJ Barst, ...
Clinical Dysmorphology 18 (1), 19-23, 2009
332009
Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiency
N Kandemir, DY Yilmaz, EN Gonc, A Ozon, A Alikasifoglu, A Dursun, ...
The Journal of steroid biochemistry and molecular biology 165, 57-63, 2017
312017
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