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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.Biochimica Et Biophysica Acta|June 5, 1986
Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identificationT H Huisman, J B Wilson, A Kutlar, et al.Transplantation Proceedings|April 15, 2019
The Analysis of Posthepatectomy Liver Failure Incidence and Risk Factors Among Right Liver Living Donors According to International Study Group of Liver Surgery DefinitionT Egeli, T Unek, C Agalar, et al.Hemoglobin|January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newbornsY J Fei, F Kutlar, H F Harris, et al.Diabetic Medicine : a Journal of the British Diabetic Association|January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutationsT Demir, H Onay, D B Savage, et al.Pageof 16