Search Results - "thalassemia"

Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene def... by Kainaz Sidhwa, Manisha Ramani Daruwalla, Ravikiran Pawar, Anita Nadkarni, Priya Hariharan, Pallavi Mehta, Amar Das Gupta

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Technology forecast: advanced therapies in late clinical research, EMA approval or clinical application via hospital exemption by Claudia Eder, Claudia Wild

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Primary Health Care: An Approach to Community Control of Genetic and Congenital Disorders by H Aghajani, A Samavat, M Haghazali, F Valizadeh, G Sarbazi

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Update on the use of deferasirox in the management of iron overload by Ali Taher, Maria Domenica Cappellini

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A Preliminary Report on Prevalence of Antibody Response to GBV-C, E2 Protein in Iranian Blood Donors and Multitrans-fused Patients by H Rezvan, M Sharafi, H Shams, M Mahmoodian Shooshtari

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Primary Health Care: An Approach to Community Control of Genetic and Congenital Disorders by H Aghajani, A Samavat, M Haghazali, F Valizadeh, G Sarbazi

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Deferasirox-induced hyperammonemia and Fanconi syndrome: a case report by Houfu Zhou, Daoxue Xiong, Yan Feng, Jianyu Jiang

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Anabolic therapy in b-thalassaemia major induced osteoporosis: case report and literature review by F.P. Cantatore, A. Corrado, A. Trotta

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Kidney Tubular Damage Secondary to Deferasirox: Systematic Literature Review by Martin Scoglio, Maria Domenica Cappellini, Emanuela D'Angelo, Mario G. Bianchetti, Sebastiano A. G. Lava, Carlo Agostoni, Gregorio P. Milani

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Study Of Hemoglobinopathies in Patients of Anemia Using High Performance Liquid Chromatography (HPLC) In Western India by Jignasa N Bhalodia, Haren V Oza, Palak J Modi, Ami M Shah, Kinara A Patel, Himani B Patel

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Investigating the Relationship between miR210 Upregulation and Hemoglobin Gamma Chain Expression by Seyed Amir Hossein Emami, Shahin Mohammadi, Saeed Kavyani, Masud Soleimani, Shaban Alizadeh, Ehteram Dejbakhsh, Fatemeh Kouhkan, Majid Mossahebi, Hossein Dargahi

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Case report: Effect of Hb E heterozygosity on HbA1c value by the Tosoh HLC-723G11 by Wei Gao, Wenyu Li, Qian Zheng, Nenggang Jiang, Huairong Tang

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Evaluation of pulmonary function in Egyptian children with sickle cell disease: a single center study by Abla S. Mostafa, Dina H. Hamed, Basma B ELSayed, Amina M Kholeif, Ilham Youssry

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A Preliminary Report on Prevalence of Antibody Response to GBV-C, E2 Protein in Iranian Blood Donors and Multitrans-fused Patients by H Rezvan, M Sharafi, H Shams, M Mahmoodian Shooshtari

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Applications of gene modification technologies in the treatment of inherited diseases by Maciej Superson, Katarzyna Szmyt, Klaudia Wilk-Trytko, Julia Krasnoborska, Sylwia Samojedny, Katarzyna Szymańska, Kamil Walczak

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Genetic determinants and stroke in children with sickle cell disease, by Daniela O.W. Rodrigues, Luiz C. Ribeiro, Lysla C. Sudário, Maria T.B. Teixeira, Marina L. Martins, Anuska M.O.L. Pittella, Irtis de O. Fernandes Junior

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Effect On Alpha Hemoglobin Chain Expression In K562 Cell Line by Sh Alizadeh, S Kaviani, M Soleimani, AA Pourfathollah, N Amirizadeh, F Kouhkan, S Abroun, M Noruzinia

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Efficient and in situ correction of hemoglobin Constant Spring mutation by prime editing in human hematopoietic cells by Congwen Shao, Qing Liu, Jinchao Xu, Jianxiang Zhang, Chengpeng Zhang, Ye Xin, Yuhua Ye, Bin Lin, Xinhua Zhang, Li Cheng, Xiangmin Xu, Peng Xu

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The Impact of Vitamin K2 (Menaquionones) in Children's Health and Diseases: A Review of the Literature by Agnieszka Kozioł-Kozakowska, Katarzyna Maresz

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Screening of Iron Deficiency Anemia in Children Using Mentzer Index in Pakistan: A Cross Sectional Study by Atika Sherali FCPS, Abdul Ahad FCPS, Shiyam Sunder Tikmani MSc, Suman Sohail FCPS

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