نتایج جستجو برای: intermedia β

تعداد نتایج: 180489  

Journal: :iranian journal of blood and cancer 0
khadijeh arjmandi rafsanjani maryam razzaghy-azar leila zahedi-shoolami parvaneh vossough aliakbar modarres nima taheri

background: expansion of bone marrow cavity and decreased cortical and trabecular bone tissues and osteoporosis are resulted from beta-thalassemia. the aim of this study was to assess bone mineral density (bmd) in patients with β thalassemia major and intermedia, and to determine their biochemical and hormonal profiles that may affect bmd. materials and methods: in a cross sectional study from ...

Journal: :Blood cells, molecules & diseases 2013
Pooja Dabke Roshan B Colah K Ghosh Anita Nadkarni

The clinical and hematological course of β thalassemia intermedia is influenced by a number of genetic factors which play a role in increasing fetal haemoglobin levels. Several polymorphisms located in the promoters of β and γ globin gene are involved in influencing the disease severity. Our objective was to study the effect of cis-DNA haplotypes, motifs, or polymorphisms (Pre G γ globin gene h...

2017
Ayşegül Uǧur Kurtoǧllu Belkls Koçtekin Erdal Kurtoǧlu Mustafa Yildiz Selen Bozkurt

AIM OF THE STUDY β-thalassaemia (β-Thal) is considered a severe, progressive haemolytic anaemia, which needs regular blood transfusions for life expectancy. Complement-mediated erythrocyte destruction can cause both intravascular and extravascular haemolysis. Complement regulatory proteins protect cells from such effects of the complement system. We aimed to perform quantitative analysis of mem...

2014
MR El-Shanshory AA Hagag SS Shebl IM Badria AH Abd Elhameed ES Abd El-Bar Y Al-Tonbary A Mansour H Hassab M Hamdy M Alfy L Sherief E Sharaf

BACKGROUND The molecular defects resulting in a β-thalassemia phenotype, in the Egyptian population, show a clear heterogenic mutations pattern. PCR-based techniques, including direct DNA sequencing are effective on the molecular detection and characterization of these mutations. The molecular characterization of β-thalassemia is necessary for carrier screening, genetic counseling, and to offer...

Journal: :Revista Chapingo serie ciencias forestales y del ambiente 2023

Introducción: Schinus molle L. (Anacardiaceae), conocido como pirul en México, es una especie rica aceite esencial hojas y frutos.Objetivo: Caracterizar el perfil fitoquímico de obtenido S. mediante dos sistemas destilación distintos tiempos extracción.Materiales métodos: Se utilizó un destilador discontinuo Rayleigh escala intermedia para extraer colectadas la región central México. El product...

Journal: :Thorax 2010
Martina Ulrich Isabelle Beer Peter Braitmaier Michaela Dierkes Florian Kummer Bernhard Krismer Ulrike Schumacher Ute Gräpler-Mainka Joachim Riethmüller Peter Ø Jensen Thomas Bjarnsholt Niels Høiby Gabriel Bellon Gerd Döring

BACKGROUND Patients with cystic fibrosis (CF) with Pseudomonas aeruginosa lung infections produce endobronchial mucus plugs allowing growth of obligate anaerobes including Prevotella spp. Whether obligate anaerobes contribute to the pathophysiology of CF lung disease is unknown. METHODS The virulence of Prevotella intermedia and Ps aeruginosa was investigated in vitro and in mice, antibodies ...

2013
Ali Fettah Cengiz Bayram Nese Yarali Pamir Isik Abdurrahman Kara Vildan Culha Bahattin Tunc

INTRODUCTION The beta thalassemias are common genetic disorders in Turkey and in this retrospective study our aim was to evaluate β-globin chain mutations and the phenotypic severity of β-thalassemia patients followed-up in our hospital, a tertiary center which serves patients from all regions of Turkey. MATERIALS AND METHODS 106 pediatric patients were analysed for β-globin gene mutations by...

Journal: :Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2013
Mehran Karimi Sezaneh Haghpanah Nahid Ashjazadeh Abdolhamid Shariat Masoume Nazeri Sajad Emami Amin Abolhasani Forough Peyman Petramfar Ehsan Yaghoubi

We aimed to compare cerebral artery velocity and relevant clinical factors in patients with β-thalassemia intermedia (β-TI), β-thalassemia major (β-TM), and healthy individuals. For this study, 60 patients with β-TM and 64 with β-TI were randomly selected. Sixty healthy adults comprised the control group. Time average maximum mean velocity (TAMMV) was measured in large cerebral arteries with tr...

Journal: :Mediterranean Journal of Hematology and Infectious Diseases 2004

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