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Journal of Neurosurgery|December 25, 2007
Congenital supratentorial cystic hemangioblastoma. Case report and review of the literatureHakan Karabagli, Pinar Karabagli, Asude Alpman, et al.Fetal and Pediatric Pathology|April 4, 2012
A novel aspartoacylase (ASPA) gene mutation in Canavan diseaseAsude Alpman Durmaz, Haluk Akin, Huseyin Onay, et al.Developmental Medicine and Child Neurology|May 17, 2005
Ring chromosome 20 syndrome with intractable epilepsyAsude Alpman, Gul Serdaroglu, Ozgur Cogulu, et al.Allergy and Asthma Proceedings|October 18, 2008
Association of interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in Turkish children with atopic asthmaDost Zeyrek, Esen Demir, Asude Alpman, et al.Biomed Research International|April 16, 2015
Evolution of genetic techniques: past, present, and beyondAsude Alpman Durmaz, Emin Karaca, Urszula Demkow, et al.Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrowBurak Durmaz, Asude Alpman Durmaz, Emin Karaca, et al.Pediatric Neurology|January 13, 2009
Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphismsGul Serdaroğlu, Asude Alpman, Ayse Tosun, et al.Journal of Child Neurology|May 8, 2010
Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsyAsude Alpman, Ferda Ozkinay, Hasan Tekgul, et al.Genetic Testing and Molecular Biomarkers|April 18, 2009
The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, TurkeyBurak Durmaz, Asude Alpman, Erhan Pariltay, et al.Journal of Pediatric Hematology/Oncology|July 29, 2009
A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletionAsude Alpman Durmaz, Haluk Akin, Aslihan Yilmaz Ekmekci, et al.Pageof 2