|
|
|
|
LEADER |
00000cam a2200000 i 4500 |
001 |
EBSCO_ocn952337010 |
003 |
OCoLC |
005 |
20231017213018.0 |
006 |
m o d |
007 |
cr ||||||||||| |
008 |
160212s2016 nyu ob 001 0 eng |
010 |
|
|
|a 2020676668
|
040 |
|
|
|a DLC
|b eng
|e rda
|c DLC
|d YDXCP
|d N$T
|d OCLCF
|d EBLCP
|d SNK
|d DKU
|d AUW
|d IGB
|d D6H
|d VTS
|d AGLDB
|d G3B
|d S8J
|d S9I
|d STF
|d OCLCO
|d OCLCQ
|
020 |
|
|
|a 9781634848503
|q (ebook)
|
020 |
|
|
|a 1634848500
|
020 |
|
|
|z 9781634847049
|q (hardcover)
|
029 |
1 |
|
|a AU@
|b 000058458299
|
035 |
|
|
|a (OCoLC)952337010
|
050 |
0 |
0 |
|a RC641.7.S5
|
072 |
|
7 |
|a HEA
|x 039000
|2 bisacsh
|
072 |
|
7 |
|a MED
|x 014000
|2 bisacsh
|
072 |
|
7 |
|a MED
|x 022000
|2 bisacsh
|
072 |
|
7 |
|a MED
|x 112000
|2 bisacsh
|
072 |
|
7 |
|a MED
|x 045000
|2 bisacsh
|
082 |
0 |
0 |
|a 616.1/527
|2 23
|
049 |
|
|
|a UAMI
|
100 |
1 |
|
|a Waked, Intsar S.
|q (Intsar Salim),
|e author.
|
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]
|
300 |
|
|
|a 1 online resource.
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
347 |
|
|
|a data file
|2 rda
|
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
|
590 |
|
|
|a eBooks on EBSCOhost
|b EBSCO eBook Subscription Academic Collection - Worldwide
|
650 |
|
0 |
|a Sickle cell anemia
|x Treatment.
|
650 |
|
6 |
|a Drépanocytose
|x Traitement.
|
650 |
|
7 |
|a HEALTH & FITNESS / Diseases / General
|2 bisacsh
|
650 |
|
7 |
|a MEDICAL / Clinical Medicine
|2 bisacsh
|
650 |
|
7 |
|a MEDICAL / Diseases
|2 bisacsh
|
650 |
|
7 |
|a MEDICAL / Evidence-Based Medicine
|2 bisacsh
|
650 |
|
7 |
|a MEDICAL / Internal Medicine
|2 bisacsh
|
650 |
|
7 |
|a Sickle cell anemia
|x Treatment.
|2 fast
|0 (OCoLC)fst01118106
|
700 |
1 |
|
|a Alotaibi, Amal A.,
|e author.
|
776 |
0 |
8 |
|i Print version:
|t Sickle cell anemia
|d New York : Nova Biomedical, [2016]
|z 9781634847049 (hardcover)
|w (DLC) 2016933379
|
830 |
|
0 |
|a Recent advances in hematology research.
|
856 |
4 |
0 |
|u https://ebsco.uam.elogim.com/login.aspx?direct=true&scope=site&db=nlebk&AN=1258666
|z Texto completo
|
938 |
|
|
|a YBP Library Services
|b YANK
|n 12882145
|
938 |
|
|
|a EBSCOhost
|b EBSC
|n 1258666
|
938 |
|
|
|a ProQuest Ebook Central
|b EBLB
|n EBL4591511
|
994 |
|
|
|a 92
|b IZTAP
|