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Pediatric Radiology|June 4, 2023
Comparison of phase contrast magnetic resonance imaging and scintigraphy for determination of split pulmonary blood flow in children and young adults with congenital heart diseaseRawan Hafiz, Murat Kocaoglu, Andrew T Trout
Journal of Pediatric Orthopedics. Part B|October 9, 2008
Congenital agenesis of pubic bones: a case reportCemil Yildiz, Yuksel Yurttas, Murat Oto, et al.
The Journal of Laryngology and Otology|June 14, 2005
Agenesis of the unilateral parotid gland associated with pleomorphic adenoma of the contralateral parotid glandOmer Karakoc, Tímur Akcam, Murat Kocaoglu, et al.
The Pan African Medical Journal|April 15, 2015
Unusual presentation of multiple nerve entrapment: a case reportVeli Citisli, Murat Kocaoglu, Selcuk Göcmen, et al.
West African Journal of Medicine|April 4, 2007
An unusual complication of the use of stapler after Hartmann's procedureNihat Kaymakcioglu, Gokhan Yagci, Mehmet Fatih Can, et al.
Japanese Journal of Radiology|September 13, 2012
Magnetic resonance imaging predictors of surgical outcome in degenerative lumbar spinal stenosisBanu Alicioglu, Baris Yilmaz, Nail Bulakbasi, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Spoiled gradient recalled acquisition in the steady state technique is superior to conventional postcontrast spin echo technique for magnetic resonance imaging detection of adrenocorticotropin-secreting pituitary tumorsNicholas Patronas, Nail Bulakbasi, Constantine A Stratakis, et al.
Auris, Nasus, Larynx|November 18, 2005
A rare cause of parotid swelling: primary hydatid cystSerdar Karahatay, Timur Akcam, Murat Kocaoglu, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|October 19, 2021
Quantitative assessment of velocity and flow using compressed SENSE in children and young adults with adequate acquired temporal resolutionMurat Kocaoglu, Amol Pednekar, Jean A Tkach, et al.
Acta Orthopaedica|March 21, 2009
Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndromeFaysal Gok, Ilana Chefetz, Margarita Indelman, et al.
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