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Sickle cell anemia : modern trends in treatment /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Waked, Intsar S. (Intsar Salim) (Autor), Alotaibi, Amal A. (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York : Nova Biomedical/Nova Science Publishers, Inc., [2016]
Colección:Recent advances in hematology research.
Temas:
Acceso en línea:Texto completo

MARC

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245 1 0 |a Sickle cell anemia :  |b modern trends in treatment /  |c Intsar S. Waked and Dr. Amal A. Alotaibi. 
264 1 |a New York :  |b Nova Biomedical/Nova Science Publishers, Inc.,  |c [2016] 
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490 1 |a Recent advances in hematology research 
504 |a Includes bibliographical references (pages 87-107) and index. 
588 |a Description based on print version record and CIP data provided by publisher. 
505 0 |a SICKLE CELL ANEMIA MODERN TRENDS IN TREATMENT ; SICKLE CELL ANEMIA MODERN TRENDS IN TREATMENT ; Contents ; Preface ; Introduction ; Definition of Terms ; Sickle Cell Anemia ; Sickle Cell Trait ; Sickle Cell -- Hemoglobin SC Disease ; Sickle Cell -- Hemoglobin E Disease ; Hemoglobin S-Beta-Thalassemia ; Chapter 1 Epidemiology and Distribution ; Chapter 2 Anatomy and Physiology ; Physiology; Chapter 3 Genetic Inheritance ; Genotypes ; Chapter 4 Pathophysiology of SCD ; The Basic Pathophysiological Mechanism: Hemoglobin S Polymerization and Red Blood Cell Alteration 
505 8 |a Increased Adhesion of Sickle Red Blood Cells to the Endothelium All the Cells in the Blood Vessel Are Implicated ; Sickle Red Blood Cells Are Activable and Activated ; Importance of Haemolysis as One of the Primary Pathophysiological Factor in SCD; The Role of Whole Blood Viscosity in the Pathophysiology of Sickle Cell Disease ; The Viscosity of Individual Red Cells ; The Role of Hematocrit; The Effects of Increased Viscosity ; Clinical Complications Made Worse by Increased Viscosity ; Chapter 5 Diagnosis of SCA ; Diagnostic Test ; Neonatal Screening and Routine Management 
505 8 |a Chapter 6 Signs and Symptoms of Sickle Cell Anemia Signs ; Symptoms ; Pain ; Infection ; Anaemia ; Childhood Symptoms ; Potential Symptoms in Teenagers and Adults ; Chapter 7 Sickle Cell Disease Complications ; Acute Complications of Sickle Cell Disease ; Vaso-Occlusive Crisis (VOC) or Sickle Cell Crisis ; Hand-Foot Syndrome; Fever- Infections ; Stroke ; Transcranial Doppler Scanning (TCD) in Stroke Prevention ; Meningitis ; Cerebral Infarction ; Intracranial Hemorrhage ; Seizures ; Asthma ; Acute Renal Failure ; Hepatobiliary Complications ; Acute Hepatic Sequestration 
505 8 |a Acute Intrahepatic Cholestasis Acute Anemia ; Acute Splenic Sequestration (ASS) ; Aplastic Crisis; Acute Chest Syndrome (ACS) ; Priapism ; Gall Stones; Multisystem Organ Failure ; Chronic Complications of Sickle Cell Disease ; 1. Chronic Pain ; 2. Avascular Necrosis ; 3. Leg Ulcers ; 4. Pulmonary Hypertension ; 5. Renal Complications ; Stuttering/Recurrent Priapism; Ophthalmologic Complications ; Adult SCD ; Chapter 8 Imaging of SCA ; Musculoskeletal Complications ; Neurological Complications ; Cardiovascular Complications ; Pulmonary Complications; Renal Complications 
505 8 |a Abdominal Complications Spleen ; Liver ; Gall Bladder ; Sequestration Syndrome; Less Common Complications ; Chapter 9 Prevention and Treatment of Sickle Cell Anemia ; Prevention of Complications ; Treatment of Complications ; Cure ; General Principles and Guidelines ; Infection Prevention; Immunizations ; Pneumococcal Disease ; Influenza ; Meningococcus ; Other Standard Vaccinations; Prophylactic Penicillin ; Variant Sickle Cell Syndromes ; 1. Hgb SC ; 2. Sickle Cell-Beta-Thalassemia ; Infection Management ; Nutrition; Routine Evaluation and Treatment; 1. Retinopathy 
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650 7 |a Sickle cell anemia  |x Treatment.  |2 fast  |0 (OCoLC)fst01118106 
700 1 |a Alotaibi, Amal A.,  |e author. 
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