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C Altay

Showing results (131-140 of 160) with videos related to

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Acta Endocrinologica (Bucharest, Romania : 2005)|May 8, 2023
NIVOLUMAB ASSOCIATED ENDOCRINE ABNORMALITIES: CHALLENGING CASES FROM A REFERENCE CLINICM C Unal, G Güngör Semiz, O Ozdoğan, et al.
The Turkish Journal of Pediatrics|April 19, 2000
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 casesA Gürgey, I Yenicesu, T Kanra, et al.
Hemoglobin|January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemiaR Oner, S Agarwal, A J Dimovski, et al.
Hemoglobin|January 1, 1981
Hb E and Hb E-like variants in individuals from TurkeyV Prozorova-Zamani, S Ozsoylu, M Aksoy, et al.
Journal of Chromatography|July 5, 1991
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetusesF Kutlar, H Moscoso, C R Kiefer, et al.
Journal of Pediatric Urology|June 23, 2016
Evaluation of ureteral jet dynamics in pediatric kidney stone formers: A cross-sectional studyS Celik, O Bozkurt, C Altay, et al.
Acta Haematologica|January 1, 1992
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observationsY J Fei, R Oner, G Bözkurt, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
Hemoglobin|January 1, 1989
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemiaA Kutlar, F Kutlar, M Aksoy, et al.
Pediatric Research|February 1, 1977
Hemoglobin alpha chain deficiency in black children with variable quantities of hemoglobin Bart's at birthC Altay, B Ringelhann, G I Yawson, et al.
Pageof 16

Showing results (131-140 of 160) with videos related to

Sort By:
Pageof 16
Acta Endocrinologica (Bucharest, Romania : 2005)|May 8, 2023
NIVOLUMAB ASSOCIATED ENDOCRINE ABNORMALITIES: CHALLENGING CASES FROM A REFERENCE CLINICM C Unal, G Güngör Semiz, O Ozdoğan, et al.
The Turkish Journal of Pediatrics|April 19, 2000
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 casesA Gürgey, I Yenicesu, T Kanra, et al.
Hemoglobin|January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemiaR Oner, S Agarwal, A J Dimovski, et al.
Hemoglobin|January 1, 1981
Hb E and Hb E-like variants in individuals from TurkeyV Prozorova-Zamani, S Ozsoylu, M Aksoy, et al.
Journal of Chromatography|July 5, 1991
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetusesF Kutlar, H Moscoso, C R Kiefer, et al.
Journal of Pediatric Urology|June 23, 2016
Evaluation of ureteral jet dynamics in pediatric kidney stone formers: A cross-sectional studyS Celik, O Bozkurt, C Altay, et al.
Acta Haematologica|January 1, 1992
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observationsY J Fei, R Oner, G Bözkurt, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
Hemoglobin|January 1, 1989
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemiaA Kutlar, F Kutlar, M Aksoy, et al.
Pediatric Research|February 1, 1977
Hemoglobin alpha chain deficiency in black children with variable quantities of hemoglobin Bart's at birthC Altay, B Ringelhann, G I Yawson, et al.
Pageof 16