نتایج جستجو برای: sickle cell syndrome scs

تعداد نتایج: 2226393  

Journal: :world journal of plastic surgery 0
akbar vahdati department of biology, fars science and research branch, islamic azad university, fars, iran; and department of biology, shiraz branch, islamic azad university, shiraz, iran alireza fathi department of biology, fars science and research branch, islamic azad university, fars, iran; and department of biology, shiraz branch, islamic azad university, shiraz, iran mehrdokht hajihoseini department of biology, fars science and research branch, islamic azad university, fars, iran; and department of biology, shiraz branch, islamic azad university, shiraz, iran ghaem aliborzi department of biology, fars science and research branch, islamic azad university, fars, iran; and department of biology, shiraz branch, islamic azad university, shiraz, iran

background infertility is a serious social problem in advanced nations, with male factor in half of all cases of infertility. this study was conducted to determine the regenerative effect of bone marrow-derived stem cells in spermatogenesis of infertile hamster. methods twelve adult male hamsters were equally divided into azoospermic and control groups. busulfan was intraperitoneally used for i...

Journal: :Anales de pediatria 2015
A I Gutiérrez Díaz E Svarch A Arencibia Núñez V Sabournin Ferrier S Machín García A Menendez Veitía L Ramón Rodriguez J Serrano Mirabal T García Peralta L G López Martin

INTRODUCTION Total splenectomy in sickle cell disease is related to a high risk of fulminant sepsis and increased incidence of other events, which have not been reported in patients with partial splenectomy. In this study we examined the patients with sickle cell disease and partial splenectomy and compared the clinical and laboratory results with non-splenectomized patients. MATERIAL AND MET...

Journal: :Chest 2002
Joshua P Needleman Lennette J Benjamin Joseph A Sykes Thomas K Aldrich

STUDY OBJECTIVES To determine the effect of sickle cell pain and its treatment on patients' breathing patterns, and to compare the effect of thoracic cage pain to pain at other sites. DESIGN Prospective, observational study. SETTING Sickle Cell Center Day Hospital. PATIENTS Twenty-five patients with sickle cell disease admitted to the Sickle Cell Center Day Hospital for treatment of vaso-...

Journal: :Respiratory Research 2001
Elizabeth S Klings Harrison W Farber

Acute chest syndrome (ACS) of sickle cell disease (SCD) is characterized pathologically by vaso-occlusive processes that result from abnormal interactions between sickle red blood cells (RBCs), white blood cells (WBCs) and/or platelets, and the vascular endothelium. One potential mechanism of vascular damage in ACS is by generation of oxygen-related molecules, such as superoxide (O2-), hydrogen...

2009
Maha M. Maher Amany H. Mansour

BACKGROUND Hepatic lesions in sickle cell disease were studied essentially in autopsy specimens. We investigated chronic hepatopathy in living adults with sickle cell disease and report the clinical, biochemical, and hepatic histological findings in these patients. METHODS A total of 170 adult patients with sickle cell syndrome were prospectively investigated. Clinical and laboratory investig...

Journal: :Tuberkuloz ve toraks 2006
Cenk Babayiğit Ismet Murat Melek Taşkin Duman Abdurrahman Senyiğit Edip Gali

Sickle cell anemia is a disease caused by production of abnormal hemoglobin. Infection, acute splenic sequestration crisis, aplastic crises, acute chest syndrome, stroke, cholelithiasis, renal disease and pain are the major complications. Unilateral or bilateral diaphragm paralysis maybe seen following phrenic nerve injury and with a variety of motor-neuron diseases, myelopathies, neuropathies,...

2017
Jian Wang Yuanlin Song

Single cell sequencing (SCS) has become a new approach to study biological heterogeneity. The advancement in technologies for single cell isolation, amplification of genome/transcriptome and next-generation sequencing enables SCS to reveal the inherent properties of a single cell from the large scale of the genome, transcriptome or epigenome at high resolution. Recently, SCS has been widely app...

Journal: :iranian journal of medical sciences 0
zohreh rahimi a. vaisi-raygani a. merat m. haghshenass m. rezaei

background: molecular genetic factors regulating hemoglobin f (hb f) expression are important modifiers of the severity of sickle cell anemia (ss).   methods: the prevalence of xmni polymorphic site, the g g: a g ratio and the hb f level were determined using pcr-rflp procedure, hplc and alkaline denaturation method, respectively, in various haplotypes of 52 patients with ss, 18 patients with s...

2017
Angela B. Snyder Peter A. Lane Mei Zhou Susan T. Paulukonis Mary M. Hulihan

Sickle cell disease affects more than 100,000 individuals in the United States, among whom disease severity varies considerably. One factor that influences disease severity is the sickle cell disease genotype. For this reason, clinical prevention and treatment guidelines tend to differentiate between genotypes. However, previous research suggests caution when using a claimsbased determination o...

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