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A Ozel

Showing results (21-30 of 25) with videos related to

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JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|April 7, 2011
Hepatic alveolar echinococcosis: a diagnostic challengeO Yapici, S M Erturk, M Ulusay, et al.
Journal of Ultrasound|February 12, 2013
Cysts of the canal of Nuck: ultrasound and magnetic resonance imaging findingsA Ozel, O Kirdar, A M Halefoglu, et al.
Clinical Nephrology|February 28, 2002
Renal function in children with sickle cell anemiaA Karabay Bayazit, A Noyan, B Aldudak, et al.
Pediatric Nephrology (Berlin, Germany)|November 30, 2000
Renal function in pediatric patients with beta-thalassemia majorB Aldudak, A Karabay Bayazit, A Noyan, et al.
Archives of Endocrinology and Metabolism|February 8, 2018
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingFernanda A Correa, Marcela M França, Qing Fang, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|April 7, 2011
Hepatic alveolar echinococcosis: a diagnostic challengeO Yapici, S M Erturk, M Ulusay, et al.
Journal of Ultrasound|February 12, 2013
Cysts of the canal of Nuck: ultrasound and magnetic resonance imaging findingsA Ozel, O Kirdar, A M Halefoglu, et al.
Clinical Nephrology|February 28, 2002
Renal function in children with sickle cell anemiaA Karabay Bayazit, A Noyan, B Aldudak, et al.
Pediatric Nephrology (Berlin, Germany)|November 30, 2000
Renal function in pediatric patients with beta-thalassemia majorB Aldudak, A Karabay Bayazit, A Noyan, et al.
Archives of Endocrinology and Metabolism|February 8, 2018
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingFernanda A Correa, Marcela M França, Qing Fang, et al.
Pageof 3