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Even if the terms “forensic sciences” and “legal medicine” seem to be synonymous, they could be defined as two sides of the same coin. It has been demonstrated that they are different components of the application of medical knowledge upon the legal system. Legal medicine has greater relevance to civil and tort law, impacting upon patient care, whereas forensic medicine relates to criminal law and damage to (or by) patients. This Special Issue, entitled “Forensic Science and Legal Medicine: A Multidisciplinary Puzzle!”, collected accurate and up-to-date scientific information on all aspects of this theme, publishing original investigations, case series and case reports, and reviews in all forensic and medico-legal branches.

senility --- Jointpoint analysis --- coefficient of variation --- AASs --- anabolic androgenic steroids --- organ damage --- toxicity --- injury --- chronic administration --- anaphylactic death --- diagnostic workflow --- immunohistochemical investigation --- blood tryptase level --- COVID-19 --- mortality --- RT-PCR --- chest computed tomography --- phorate --- acute toxicity --- chronic toxicity --- histopathological kidney --- toxicological examination --- primary cerebral melanoma --- sudden death --- clinical signs --- pathological observations --- forensic pathology --- glycophorin A investigation --- vitality --- sudden death (SD) --- sudden cardiac death (SCD) --- autopsy --- molecular autopsy --- genetics --- post-mortem investigation --- practical flowchart in SD --- microbiome --- human identification --- biobank --- forensic --- homicidal --- case series --- malingering --- feigned --- threat --- risk assessment --- psychiatric evaluation

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Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality associated with the undiagnosed disease. Newborn screening helps to make the diagnosis early and to prevent fatal complications and diagnostic odysseys. This book gives an overview of diagnostic standards in newborn screening for sickle cell disease and examples of existing newborn screening programs.

glucose-6-phosphate dehydrogenase --- hydroxyurea/hydroxycarbamide --- n/a --- cord blood --- screening --- hemoglobin pattern --- capillary electrophoresis --- sickle cell disease --- (recommended) screening panel --- vaso-occlusive crisis --- Guthrie spots --- newborn screening) --- foetal haemoglobin --- harmonisation --- review --- birth prevalence --- G6PD deficiency --- prevention --- end-organ damage --- thalassemia --- MALDI-TOF --- IEF --- acute chest syndrome --- India --- sickle cell and thalassaemia screening programme --- ‘Getting to Outcomes’ --- newborn screening --- hemoglobinopathy --- service users --- public health engagement --- automated HPLC --- Kaduna State --- gene therapy for haemoglobinopathies --- ?-globin gene --- methods --- neonatal screening program --- malaria --- Plasmodium vivax --- sub-Saharan Africa --- patient organisations --- health policy --- pathophysiology --- Sickle Cell Disease --- mass spectrometry --- sickle cell disorder --- neonatal screening --- non-tribal --- Nigeria --- point-of-care --- HPLC --- laboratory methods --- registry --- patient advocacy --- bone marrow transplant --- anaemia --- hemoglobinopathies --- tribal --- newborn --- burden of disease --- patient representatives --- diagnostics --- policy making --- haemolysis --- Caribbean --- high performance liquid chromatography (HPLC) --- sickle cell disease (SCD) --- implementation science --- 'Getting to Outcomes'