000725655 000__ 03348cam\a2200457Ii\4500
000725655 001__ 725655
000725655 005__ 20230306140650.0
000725655 006__ m\\\\\o\\d\\\\\\\\
000725655 007__ cr\cn\nnnunnun
000725655 008__ 150216s2015\\\\enka\\\\ob\\\\001\0\eng\d
000725655 020__ $$a9781447124733$$qelectronic book
000725655 020__ $$a1447124731$$qelectronic book
000725655 020__ $$z9781447124726
000725655 0247_ $$a10.1007/978-1-4471-2473-3$$2doi
000725655 035__ $$aSP(OCoLC)ocn903489969
000725655 035__ $$aSP(OCoLC)903489969
000725655 040__ $$aGW5XE$$beng$$erda$$epn$$cGW5XE$$dDKU$$dUPM$$dCOO$$dE7B$$dEBLCP$$dYDXCP$$dSTJ
000725655 049__ $$aISEA
000725655 050_4 $$aRC641.7.S5
000725655 08204 $$a616.152706$$223
000725655 1001_ $$aHoward, Jo,$$eauthor.
000725655 24510 $$aSickle cell disease in clinical practice$$h[electronic resource] /$$cJo Howard, Paul Telfer.
000725655 264_1 $$aLondon :$$bSpringer,$$c2015.
000725655 300__ $$a1 online resource.
000725655 336__ $$atext$$btxt$$2rdacontent
000725655 337__ $$acomputer$$bc$$2rdamedia
000725655 338__ $$aonline resource$$bcr$$2rdacarrier
000725655 4901_ $$aIn clinical practice
000725655 504__ $$aIncludes bibliographical references and index.
000725655 5050_ $$aOverview of sickle cell disease -- Laboratory tests used in diagnosis and monitoring -- Organization of care -- Overview and general principles -- Pain in sickle cell disease -- Respiratory and cardiac complications -- Neurological complications -- Renal and urological complications -- Bone and joint complications in sickle cell disease -- Ophthalmological complications -- The spleen -- Infection and infection prophylaxis -- Gastroenterological complications -- Anemia and sickle cell disease -- Leg ulceration -- Management of pregnancy -- Surgical management -- Treatment of sickle cell disease -- Out-patient management.
000725655 506__ $$aAccess limited to authorized users.
000725655 520__ $$aThis practical clinical handbook reveals that sickle cell disease (SCD) is an increasingly common condition to manage in Europe and North America. SCD demands clinical expertise and experience as well as sensitivity to its social and cultural context. This book is designed to broaden readersℓ́ℓ knowledge in this challenging condition by describing the acute and long-term complications unique to SCD and that affect nearly every system of the body. Critically, it also details the significant recent advances in understanding the pathophysiology of SCD that are leading to novel treatment modalities. ℗ℓ Sickle Cell Disease in Clinical Practice promotes higher quality care by outlining the clinical problems as they arise, and covering essential background information, including up-to-date research, and useful points to guide management. As such, the intended target audience is broad and includes general physicians, general practitioners, hematologists, pediatricians, emergency medicine physicians, surgeons, medical students, nurse specialists and commissioners.
000725655 588__ $$aDescription based on print version record.
000725655 650_0 $$aSickle cell anemia$$xTreatment.
000725655 7001_ $$aTelfer, Paul,$$eauthor.
000725655 77608 $$iPrint version:$$aHoward, Jo.$$tSickle cell disease in clinical practice$$z9781447124726$$w(OCoLC)819520352
000725655 830_0 $$aIn clinical practice (Springer (Firm))
000725655 852__ $$bebk
000725655 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-1-4471-2473-3$$zOnline Access$$91397441.1
000725655 909CO $$ooai:library.usi.edu:725655$$pGLOBAL_SET
000725655 980__ $$aEBOOK
000725655 980__ $$aBIB
000725655 982__ $$aEbook
000725655 983__ $$aOnline
000725655 994__ $$a92$$bISE