Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Oner

Showing results (41-50 of 120) with videos related to

Pageof 12
Sort By:
Pediatric Hematology and Oncology|March 1, 1996
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experienceA Gürgey, S Beksaç, E Gümrük, et al.
Acta Orthopaedica Scandinavica|October 1, 1995
Recurrent kyphosis after posterior stabilization of thoracolumbar fractures. 24 cases treated with a Dick internal fixator followed for 1.5-4 yearsM J Speth, F C Oner, M A Kadic, et al.
Hemoglobin|September 7, 2000
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levelsR Oner, E Birben, C Acar, et al.
British Journal of Haematology|October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.
The Turkish Journal of Pediatrics|April 1, 1997
Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutationA Gürgey, H Balkan, G Irken, et al.
Hemoglobin|January 1, 1991
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among TunisiansS Fattoum, F Guemira, C Oner, et al.
The Journal of Bone and Joint Surgery. American Volume|June 3, 2004
Histologic changes after vertebroplastyJ J Verlaan, F C Oner, P J Slootweg, et al.
Hemoglobin|May 1, 1995
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrowA Gürgey, C Altay, L H Gu, et al.
The Spine Journal : Official Journal of the North American Spine Society|September 3, 2013
Clinical outcome after traumatic spinal fractures in patients with ankylosing spinal disorders compared with control patientsL A Westerveld, J C van Bemmel, W J A Dhert, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|September 10, 2005
Transpedicular wedge resection osteotomy for the treatment of a kyphotic Andersson lesion-complicating ankylosing spondylitisB J Van Royen, R C A Kastelijns, D P Noske, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
Pediatric Hematology and Oncology|March 1, 1996
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experienceA Gürgey, S Beksaç, E Gümrük, et al.
Acta Orthopaedica Scandinavica|October 1, 1995
Recurrent kyphosis after posterior stabilization of thoracolumbar fractures. 24 cases treated with a Dick internal fixator followed for 1.5-4 yearsM J Speth, F C Oner, M A Kadic, et al.
Hemoglobin|September 7, 2000
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levelsR Oner, E Birben, C Acar, et al.
British Journal of Haematology|October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.
The Turkish Journal of Pediatrics|April 1, 1997
Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutationA Gürgey, H Balkan, G Irken, et al.
Hemoglobin|January 1, 1991
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among TunisiansS Fattoum, F Guemira, C Oner, et al.
The Journal of Bone and Joint Surgery. American Volume|June 3, 2004
Histologic changes after vertebroplastyJ J Verlaan, F C Oner, P J Slootweg, et al.
Hemoglobin|May 1, 1995
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrowA Gürgey, C Altay, L H Gu, et al.
The Spine Journal : Official Journal of the North American Spine Society|September 3, 2013
Clinical outcome after traumatic spinal fractures in patients with ankylosing spinal disorders compared with control patientsL A Westerveld, J C van Bemmel, W J A Dhert, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|September 10, 2005
Transpedicular wedge resection osteotomy for the treatment of a kyphotic Andersson lesion-complicating ankylosing spondylitisB J Van Royen, R C A Kastelijns, D P Noske, et al.
Pageof 12