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2015-03-10
Sickle Cell Disease in Clinical Practice - de Jo Howard (Author)
Details Sickle Cell Disease in Clinical Practice
Le paragraphe suivant répertorie les données communes relatives aux Sickle Cell Disease in Clinical Practice
Le Titre Du Livre | Sickle Cell Disease in Clinical Practice |
Date de publication | 2015-03-10 |
Traducteur | Dayyan Ming |
Chiffre de Pages | 714 Pages |
Taille du fichier | 69.15 MB |
Langage | Français & Anglais |
Éditeur | Hodder Headline |
ISBN-10 | 7210647137-IRV |
Type de e-Book | PDF AMZ EPub FDX WPS |
Auteur | Jo Howard |
Digital ISBN | 412-3754423729-ERW |
Nom de Fichier | Sickle-Cell-Disease-in-Clinical-Practice.pdf |
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Sickle Cell Disease is the most common genetic disease world wide and in the UK It has marked geographical variation in its distribution in the UK with a concentration in London and other major conurbations Birmingham and Manchester
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An investigational drug for the treatment of sickle cell disease is showing early promise in clinical trials for impacting biomarkers of the disease in patients reported UConn School of Medicine
Sickle Cell Disease
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Sickle cell disease is the most frequent hereditary haemoglobin disease and as a result its prevalence is not common Osteoarticular pain in patients with acute vasoocclusive crisis is the major clinical problem prompting emergency department visit of patients with sickle cell disease Such acute painful episodes require potent analgesic combination approaches along with additional measures
Sickle Cell Unit Caribbean Institute for Health Research University of the West Indies Mona Campus Kingston 7 Jamaica Introduction Sickle cell disease can result in visually threatening eye disease proliferative sickle cell retinopathy