نتایج جستجو برای: thalassemia minor

تعداد نتایج: 102111  

Journal: :Blood 1956
J HILLIER J F HOFFMAN A K PARPART I J WOLMAN

By J. F. HOFFMAN, I. J. WOLMAN, ,J. FIILLIER AND A. K. PAIuPART T HE ULTHASTRUCTURE of the isolated plasmssa nsemssbramses (ghosts) from nornsal hunsans erythrocytes has beers directly studied by Hillier ansd iloffmams5 umsimig the electrons mssicroscope. Thse reproducibility of the methods ensployed has beets further evaluated ansd the observationss extensded to the membramses of erythrocytes ...

2013
Samin Alavi Alieh Safari Elham Sadeghi Somayeh Amiri

which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Hematological malignancies complicating β-thalassemia syndromes: a single center experience TO THE EDITOR: Only few reports have addressed the occurrence of hematological malignancies in patients suffering from β-thalassemia. We herein report two patients wi...

2007
Biagio R. Di Iorio Pasquale Guastaferro Nicola Cillo Emanuele Cucciniello Vincenzo Bellizzi

BACKGROUND AND AIM Both thalassemia and carnitine deficiency represent independent causes of erythropoietin resistance, and thus anemia, in uremic patients. We evaluated the unknown long-term effects of L-carnitine administration in β-thalassemic on chronic hemodialysis. METHODS We studied twelve subjects (M = 8; F = 4) affected by β-thalassemia minor (β-thal; HbA2 level = 6.6 ± 0.6%) and for...

2015
Hassan Mottaghi Moghaddam Zahra Badiei Kambiz Eftekhari Reza Shakeri Hamid Farhangi

BACKGROUND There are various clinical symptoms of thalassemia intermedia, and they lie roughly between those of major and minor forms of the disease. Patients with thalassemia intermedia occasionally require blood transfusions. This renders them susceptible to pulmonary arterial hypertension (PAH) syndrome, which is one of the most significant complications in patients with thalassemia intermed...

2013
Y. Terry Lee Ki Soon Kim Colleen Byrnes Jaira F. de Vasconcellos Seung-Jae Noh Antoinette Rabel Emily R. Meier Jeffery L. Miller

Based upon the lack of clinical samples available for research in many laboratories worldwide, a significant gap exists between basic and clinical studies of beta-thalassemia major. To bridge this gap, we developed an artificially engineered model for human beta thalassemia by knocking down beta-globin gene and protein expression in cultured CD34+ cells obtained from healthy adults. Lentiviral-...

2015
Elahe Bordbar Mehdi Taghipour Beth E. Zucconi

OBJECTIVE Different indices and formulas of CBC parameters have been suggested as indicators of early stage screenings to detect couples with β-thalassemia minor (BTMi). In this study, we evaluated the accuracy of five previous published formulas and compared them to our new formula (│80-MCV│×│27-MCH│) in screening of β-thalassemia. METHODS All couples in the premarital β-thalassemia screenin...

طهزانی قدیم, سپیده, کلاهی, سوسن, کلاهی, علی اصغر,

Background & Objectives: Anemia is one of the most common disorders affecting all age groups. This cross-sectional study aimed to determine the prevalence of anemia and microcytic anemia in the population served by Asadabadi Health Center in Tabriz. Methods: We used a systematic sampling method to select 1623 subjects out of a total of 233000 persons aged above 12 years. Measurements of hemo...

Journal: :Journal of Anesthesiology and Clinical Research 2023

Introduction: One of the complications anesthesia that can be encountered in thalassemia patients is cardiovascular instability caused by chronic anemia, cardiomyopathy, and endocrinopathy. In addition, with preeclampsia may also experience postoperative risks such as sustained hypertension, stroke, venous thromboembolism, seizures. This case report will discuss anesthetic management pregnant w...

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