نتایج جستجو برای: platelet disorder

تعداد نتایج: 699157  

Journal: :iranian journal of medical sciences 0
soghra bahmanpour laboratory for stem cell research, department of anatomical sciences, school of medicine, shiraz university of medical sciences, shiraz, iran maryam ghasemi phd student in anatomical sciences, school of medicine, shiraz university of medical sciences, shiraz, iran mohsen sadeghi-naini tehran university of medical science, tehran, iran iraj ragerdi kashani department of anatomical sciences, school of medicine, tehran university of medical sciences, tehran, iran

background: the purpose of this study was to create biomaterial scaffolds like platelet-rich plasma (prp) and platelet-rich fibrin (prf) containing stromal cell-derived factor-1 (sdf1) as a chemokine to induce hyaline cartilage regeneration of rabbit knee in a full thickness defect. methods: we created a full thickness defect in the trochlear groove of thirty-six bilateral knees of eighteen mat...

Journal: :iranian journal of pediatric hematology and oncology 0
a hashemi tayer department of hematology, university of medical sciences, arak , iran sh alizadeh department of surgery, university of medical sciences, arak , iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی اراک (arak university of medical sciences) m heidari bateni department of surgery, university of medical sciences, arak , iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی اراک (arak university of medical sciences)

abstract background autologus platelet gel is easy to prepare and is relatively low cost. the aim of this study was to prepare and evaluate in vitro efficacy of autologus platelet gel. materials and methods in this experimental study, platelet concentrate and platelet poor plasma were prepared with aphaeresis method. thrombin was prepared by mixing the plasma with calcium. thrombin activity lev...

2001
Shinji Kunishima Tetsuhito Kojima Tadashi Matsushita Toshihiro Tanaka Masahito Tsurusawa Yoshio Furukawa Yukitsugu Nakamura Takashi Okamura Norihiko Amemiya Takayuki Nakayama Tadashi Kamiya Hidehiko Saito

Macrothrombocytopenia with leukocyte inclusions is a rare autosomal dominant platelet disorder characterized by a triad of giant platelets, thrombocytopenia, and characteristic Döhle body-like leukocyte inclusions. A previous study mapped a locus for the disease on chromosome 22q12.3-q13.2 by genome-wide linkage analysis. In addition, the complete DNA sequence of human chromosome 22 allowed a p...

2011
Efthymia Vlachaki Vaia Papageorgiou Filippos Klonizakis Maria Spandonidou Sofia Chisan Evaggelia Vetsiou Elissavet Ioannidou

Immune thrombocytopenia (ITP) in adults is an acquired chronic immune-mediated disorder defined by isolated thrombocytopenia. In recent years, an improved understanding of the pathophysiology of ITP has been achieved and it is now accepted that the disorder is due to increased platelet destruction and decreased platelet production from megakary-ocytes. Thrombopoietin (TPO)-receptor agonists (ro...

Journal: :Progress in neuro-psychopharmacology & biological psychiatry 2014
Jan Pláteník Zdeněk Fišar Richard Buchal Roman Jirák Eva Kitzlerová Martina Zvěřová Jiří Raboch

BACKGROUND Glycogen synthase kinase-3β (GSK3β), cAMP-response element-binding protein (CREB) and brain-derived neurotrophic factor (BDNF) play critical roles in neuronal survival, synaptic plasticity and memory and participate in the pathophysiology of both depressive disorder and Alzheimer's disease (AD). METHODS This study was designed to determine the association of GSK3β activity, CREB ac...

Journal: : 2021

AIM This study aims to investigate whether there is a relationship between attention-deficit/hyperactivity disorder (ADHD) and inflammation, using hematologic inflammatory parameters in large sample of children adolescents. METHOD retrospective comprises 347 adolescents with ADHD 6 17 years age who met the inclusion criteria as well 205 healthy control group. Serum such white blood cell (WBC), ...

Journal: :Physical review letters 2012
Zaiwang Huang Xiaodong Li

Understanding nacre's bottom-up biomineralization mechanism, particularly, how individual aragonite platelets are formed, has long remained elusive due to its crystallographic peculiarity and structural complexity. Here we report that crystallographic order-disorder transition can be triggered within individual aragonite platelets in pristine nacre by means of heat treatment and/or inelastic de...

Journal: :Clinical advances in hematology & oncology : H&O 2005
Douglas B Cines Robert McMillan

Idiopathic thrombocytopenic purpura (ITP) is a common hematologic disorder manifested by immune-mediated thrombocytopenia. The diagnosis remains one of exclusion, after other thrombocytopenic disorders are ruled out based on history, physical examination, and laboratory evaluation. The goal of treatment is to raise the platelet count into a hemostatically safe range. The disorder is usually chr...

Journal: :Blood 2001
S Kunishima T Kojima T Matsushita T Tanaka M Tsurusawa Y Furukawa Y Nakamura T Okamura N Amemiya T Nakayama T Kamiya H Saito

Macrothrombocytopenia with leukocyte inclusions is a rare autosomal dominant platelet disorder characterized by a triad of giant platelets, thrombocytopenia, and characteristic Döhle body-like leukocyte inclusions. A previous study mapped a locus for the disease on chromosome 22q12.3-q13.2 by genome-wide linkage analysis. In addition, the complete DNA sequence of human chromosome 22 allowed a p...

2012
Naga Purnachand Meka Yahya Osman Malik

BACKGROUND Hyperkalemia is a potentially life-threatening medical condition; on the other hand pseudohyperkalemia is a benign entity, which should be suspected when serum potassium is elevated without concomitant electrolyte imbalances or remarkable degree of renal dysfunction. Patients seldom have the classical manifestations of hyperkalemia. Failure to recognize this condition causes anxiety ...

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