Showing results (11-20 of 81) with videos related to
Sort By:
Pageof 9
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 1, 2015
Alpha-thalassemia mutations in adana province, southern Turkey: genotype-phenotype correlationSevcan Tug Bozdogan, Ozge Ozalp Yuregir, Nurhilal Buyukkurt, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 17, 2023
Ethylmalonic Encephalopathy: a literature review and two new cases of mild phenotypeIsobel Platt, Atil Bisgin, Sebile KilavuzMetabolic Brain Disease|September 24, 2018
MEDNIK syndrome with a frame shift causing mutation in AP1S1 gene and literature review of the clinical featuresFaruk Incecik, Atil Bisgin, Mustafa YılmazJournal of Pediatric Neurosciences|October 2, 2018
Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish ChildFaruk Incecik, Ozlem M Hergüner, Atil BisginHemoglobin|March 6, 2012
Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish casesSevcan Tug Bozdogan, Cagatay Unsal, Hakan Erkman, et al.Clinical Case Reports|September 28, 2020
Identification of a novel homozygous variant in the alkaline phosphate (<i>ALPL</i>) gene associated with hypophosphatasiaAtil Bisgin, Ibrahim Boga, Cihan Cetin, et al.Annals of Indian Academy of Neurology|March 10, 2021
Mitochondrial Membrane Protein-Associated Neurodegeneration: A Case Series of Six ChildrenFaruk Incecik, Ozlem M Herguner, Atil BisginMediators of Inflammation|January 15, 2013
IL-8, IL-10, TGF-β, and GCSF levels were increased in severe persistent allergic asthma patients with the anti-IgE treatmentArzu D Yalcin, Atil Bisgin, Reginald M GorczynskiScientific Reports|April 16, 2021
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID)Atil Bisgin, Ozge Sonmezler, Ibrahim Boga, et al.Archives of Medical Science : AMS|October 12, 2012
β-Globin chain abnormalities with coexisting α-thalassemia mutationsBirol Guvenc, Abdullah Canataroglu, Cagatay Unsal, et al.Pageof 9