نتایج جستجو برای: sickle

تعداد نتایج: 16277  

Journal: :The Journal of the American Board of Family Practice 2001
M Cooper-Effa W Blount N Kaslow R Rothenberg J Eckman

BACKGROUND Patients with sickle cell disease cope with their disease in various ways, such as psychological counseling, hypnosis, medication, and prayer. Spirituality is a coping mechanism in a variety of diseases. This study evaluates the role of spirituality in patients coping with the pain of sickle cell disease. METHODS Seventy-one patients from the Georgia Sickle Cell Clinic completed a ...

Journal: :The Journal of clinical investigation 1986
U Galili M R Clark S B Shohet

A large proportion of sickle erythrocytes is removed from the circulation by the macrophages of the reticuloendothelial system. In view of the proposed role for natural antibodies in the destruction of normal senescent erythrocytes, we looked for a possible similarity in the antibodies that bind in situ to senescent and sickle cells. Bound IgG molecules were detected by a highly sensitive roset...

2018
Laura Dell'Arti Giulio Barteselli Lorenzo Riva Elisa Carini Giovanna Graziadei Eleonora Benatti Alessandro Invernizzi Maria D Cappellini Francesco Viola

PURPOSE To identify systemic risk factors for sickle cell maculopathy, and to analyze the microstructure of the macula of Sickle Cell Disease (SCD) patients by using automated segmentation of individual retinal layers. METHODS Thirty consecutive patients with SCD and 30 matched controls underwent spectral-domain optical coherence tomography (SD-OCT) and automated thickness measurement for eac...

2004

Gadolinium (Gd), an element that possesses a character similar to that of calcium or magnesium, is known to have a strong hemolytic effect on erythrocytes (RBC) at even very low concentrations. 3, 5 One of the major characteristics of sickle cell disease is hemolysis of the abnormal RBC. Therefore, concerns have been raised that Gadolinium, as an MRI contrast agent for clinical use, should not ...

Journal: :Transplantation 2000
S Emre K Kitibayashi M E Schwartz J Ahn A Birnbaum S N Thung C M Miller

BACKGROUND Sickle cell intrahepatic cholestasis is a potentially catastrophic complication of sickle cell anemia Once acute liver failure develops, transplantation is the only option. We describe a patient with sickle cell intrahepatic cholestasis who underwent liver transplantation. METHODS Data were obtained from the chart. Serial hemoglobin S levels were monitored, and measures were taken ...

Journal: :Annals of African medicine 2010
M A Emokpae P O Uadia A A Gadzama

BACKGROUND Reactive oxygen species have been shown to mediate inflammatory process and may be involved in lipid peroxidation. METHODS This study evaluates superoxide dismutase, glutathione peroxidase, catalase, malondialdehyde, C- reactive protein and fibrinogen in the serum of patients with sickle cell disease and their correlation with renal insufficiency. Superoxide dismutase, glutathione ...

2017
Gökhan Özgür Musa Barış Aykan Murat Yıldırım Selim Sayın Ahmet Uygun Cengiz Beyan

included. References 1. Almeida A, Roberts I. Bone involvement in sickle cell disease. Br J Haematol 2005;129:482-490. 2. Booth C, Inusa B, Obaro SK. Infection in sickle cell disease: a review. Int J Infect Dis 2010;14:e2-e12. 3. Atkins BL, Price EH, Tillyer L, Novelli V, Evans J. Salmonella osteomyelitis in sickle cell disease children in the East End of London. J Infect 1997;34:133-138. 4. Bu...

2014
Erica M. Sparkenbaugh Pichika Chantrathammachart Jacqueline Mickelson Joanne van Ryn Robert P. Hebbel Dougald M. Monroe Nigel Mackman Nigel S. Key Rafal Pawlinski

• Inhibition of FXa or thrombin might be considered to reduce thrombotic complications and vascular inflammation in sickle cell patients. • PAR-2 could be a potential target to inhibit vascular pathology associated with sickle cell disease. Activation of coagulation and vascular inflammation are prominent features of sickle cell disease (SCD). Previously, we have shown that inhibition of tissue...

Journal: :The Journal of clinical investigation 1996
S C Liu S J Yi J R Mehta P E Nichols S K Ballas P W Yacono D E Golan J Palek

In red cells from patients with sickle cell anemia, hemoglobin S denatures and forms Heinz bodies. Binding of Heinz bodies to the inner surface of the sickle cell membrane promotes clustering and colocalization of the membrane protein band 3, outer surface-bound autologous IgG and, to some extent, the membrane proteins glycophorin and ankyrin. Loss of transbilayer lipid asymmetry is also found ...

Journal: :Clinical science 1983
M A Zago C Bottura

Studies of splenic function were carried out on patients with sickle-cell diseases by the measurement of the clearance of autologous heat-damaged 99mTc-labelled erythrocytes from circulation and into the spleen, the spleen area by a scintillation scanning, the enumeration of pitted erythrocytes by direct-interference microscopy, and the percentage of irreversibly sickled cells (ISC) and of cell...

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