Zoekresultaten - "thalassemia"

Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China door Zeyan Zhong, Zhiyang Guan, Dina Chen, Guoxing Zhong, Hailin He, Kunxiang Yang, Jianhong Chen

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Reporting two hemoglobin J Iran cases, molecular follow-up, or is it insignificant? door Amin Solouki, Tahereh Manoochehrabadi, Farzaneh Korani, Mohammadreza Farshchi

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Lipid Peroxidation and Antioxidant Status in β-Thalassemic Patients: Effect of Iron Overload door Bassm N. Aziz, Mohammad A. Al-Kataan, Wasan K. Ali

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Efikasi Diri Anak Usia 6-18 Tahun Yang Mengalami Thalasemia door Stella Pramasita, Lina Dewi Anggraeni

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TALASEMIA ASOCIADA A EMBARAZO door Gregorio Evans M., Ronald Poulsen R., Juan Carlos Canahuate, José Luis Pastor

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Prevalence Of Common Hemoglobinopathies in Gujarat: An Analysis of a Large Population Screening Program door Ashwin P Patel, Madhuben R Naik, Nilam M Shah, Narmadeshwar P Sharma, Prakash H Parmar

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Evaluation of Orofacial Manifestations in 50 Thalassemic Patients: A Clinical Study door Preeti Girinath, Sonal P Vahanwala, Vasavi Krishnamurthy, Sandeep S Pagare

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Spectrum of hemoglobinopathies in a tertiary care centre door Nisha Sharma, Anil Dev Pant, Usha Manandhar

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GAMBARAN POLA ASUH ORANG TUA PADA REMAJA DENGAN THALASEMIA DI RSUD SUMEDANG door Febriani, Penni

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Clinical features of patients with hemolytic anemia due to red blood cells membrane defect door Pustika Amalia W, Djajadiman Gatot, Teny Tjitrasari, Iswari Setianingsih, Nanis Sacharis Marzuki

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Psychosocial Problems of Thalassemic in A Tertiary Care Centre, Indore door Sameer Inamdar, Anila Gangrade

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RESIKO REMAJA THALASEMIA TERHADAP PERUBAHAN PERILAKU door Halimah -, Allenidekania -, Fajar Tri Waluyanti

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To study the quality of life and its relation with socioeconomic status in thalassemic adolescents in a tertiary care center door Navjot Kaur Grewal, Candy Sodhi, Praveen Sobti

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Influence of Oxidative Stress Biomarkers and Genetic Polymorphisms on the Clinical Severity of Hydroxyurea-Free Senegalese Children with Sickle Cell Anemia door Fatou Gueye Tall, Cyril Martin, El hadji Malick Ndour, Camille Faes, Indou Déme Ly, Vincent Pialoux, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Céline Renoux, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall, Philippe Joly

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Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay door Katarzyna Rawa, Roman J. Szczesny, Ewelina P. Owczarek, Anna Adamowicz-Salach, Anna Klukowska, Urszula Demkow, Danuta Plochocka, Pawel Szczesny, Monika Gora, Andrzej Dziembowski, Beata Burzynska

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Spinal cord compression secondary to intraspinal extramedullary hematopoiesis door Foziah J AlShamrani, Noor M AlMohish, Fahad A AlDawsari, Jaafer J AlObaid, Ibrahim A AlGhanimi, Abdullah A AlNahdi

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Inherited haemoglobin disorders: an increasing global health problem door Weatherall D.J, Clegg J.B

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Synthesis of Deferiprone as a Widely Used Iron-Chelating Drug for the Treatment of Iron-Overload Diseases door Sara Sadeghian, Fateme Zare, Lotfollah Saghaie, Razieh Sabet

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Anthropometric measurements of peri-oral region in a sample of Iraqi thalassemic patients door Riad Al-Taee, Aqeel Ibrahim Lazim Al-Saedi, Mohammed Nahidh

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A HOSPITAL-BASED STUDY ON UTILISING HPLC TO DETECT HB-VARIANTS AND HEMOGLOBINOPATHIES: A RETROSPECTIVE DESCRIPTIVE STUDY. door Satish Kumar, Rawi Agrawal, Kaushal Kumar, Vijayanand Choudhary

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