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 Altay

Showing results (81-90 of 160) with videos related to

Pageof 16
Sort By:
The Turkish Journal of Pediatrics|April 19, 2000
Changes of hemostatic factors in patients with hemoglobinopathiesA F Oner, A Gürgey, H Okur, et al.
Cancer|February 1, 1985
Acute leukemia in two patients with hemophiliaC Altay, G Hicsonmez, V P Zamani, et al.
Hemoglobin|January 1, 1987
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish familyC Altay, A Kutlar, J B Wilson, et al.
Biochimica Et Biophysica Acta|May 20, 1976
Hemoglobin Hacettepe or alpha 2 beta 2 127 (H5) Gln replaced by GluC Altay, N Altinöz, J B Wilson, et al.
Pediatric Hematology and Oncology|January 1, 1995
Anemia associated with diabetes mellitusA Gürgey, N Bilginturan, N Yordam, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1988
Poor prognosis in children with acute nonlymphoblastic leukemia in TurkeyG Hiçsönmez, A Gürgey, V P Zamani, et al.
Hemoglobin|January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation siteC Altay, A Gurgey, R Oner, et al.
Transplantation Proceedings|May 19, 2019
Comparison of Patients With and Without Anterior Sector Venous Drainage in Right Lobe Liver Transplantation From Live Donors in Terms of Complications, Rejections, and Graft Survival: Single-Center ExperienceM Ozbilgin, T Unek, T Egeli, et al.
British Journal of Haematology|November 28, 2001
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap siteR Oner, C Oner, E Birben, et al.
Hematology and Cell Therapy|October 30, 1999
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patientA Koç, R Oner, C Oner, et al.
Pageof 16

Showing results (81-90 of 160) with videos related to

Sort By:
Pageof 16
The Turkish Journal of Pediatrics|April 19, 2000
Changes of hemostatic factors in patients with hemoglobinopathiesA F Oner, A Gürgey, H Okur, et al.
Cancer|February 1, 1985
Acute leukemia in two patients with hemophiliaC Altay, G Hicsonmez, V P Zamani, et al.
Hemoglobin|January 1, 1987
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish familyC Altay, A Kutlar, J B Wilson, et al.
Biochimica Et Biophysica Acta|May 20, 1976
Hemoglobin Hacettepe or alpha 2 beta 2 127 (H5) Gln replaced by GluC Altay, N Altinöz, J B Wilson, et al.
Pediatric Hematology and Oncology|January 1, 1995
Anemia associated with diabetes mellitusA Gürgey, N Bilginturan, N Yordam, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1988
Poor prognosis in children with acute nonlymphoblastic leukemia in TurkeyG Hiçsönmez, A Gürgey, V P Zamani, et al.
Hemoglobin|January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation siteC Altay, A Gurgey, R Oner, et al.
Transplantation Proceedings|May 19, 2019
Comparison of Patients With and Without Anterior Sector Venous Drainage in Right Lobe Liver Transplantation From Live Donors in Terms of Complications, Rejections, and Graft Survival: Single-Center ExperienceM Ozbilgin, T Unek, T Egeli, et al.
British Journal of Haematology|November 28, 2001
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap siteR Oner, C Oner, E Birben, et al.
Hematology and Cell Therapy|October 30, 1999
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patientA Koç, R Oner, C Oner, et al.
Pageof 16