Microfluidic point-of-care testing: commercial landscape and future directions

S Sachdeva, RW Davis, AK Saha - Frontiers in Bioengineering and …, 2021 - frontiersin.org
Point-of-care testing (POCT) allows physicians to detect and diagnose diseases at or near
the patient site, faster than conventional lab-based testing. The importance of POCT is …

Sickle cell disease

GJ Kato, FB Piel, CD Reid, MH Gaston… - Nature reviews Disease …, 2018 - nature.com
Sickle cell disease (SCD) is a group of inherited disorders caused by mutations in HBB,
which encodes haemoglobin subunit β. The incidence is estimated to be between 300,000 …

Point-of-care diagnostics: recent developments in a connected age

S Nayak, NR Blumenfeld, T Laksanasopin… - Analytical …, 2017 - ACS Publications
The field of point-of-care (POC) diagnostics offers the tantalizing possibility of providing
rapid diagnostic results in nonlaboratory settings. Here, we review progress in this research …

Sickle cell disease

FB Piel, MH Steinberg, DC Rees - New England Journal of …, 2017 - Mass Medical Soc
Sickle cell disease is caused by an alteration in a single DNA base, but its clinical
manifestations are influenced by other genes and behavioral and environmental factors …

Techniques for the detection of sickle cell disease: a review

WA Arishi, HA Alhadrami, M Zourob - Micromachines, 2021 - mdpi.com
Sickle cell disease (SCD) is a widespread disease caused by a mutation in the beta-globin
gene that leads to the production of abnormal hemoglobin called hemoglobin S. The …

Paper microfluidics for point-of-care blood-based analysis and diagnostics

H Li, AJ Steckl - Analytical chemistry, 2018 - ACS Publications
Blood is the most intensely studied human biofluid and is used as the main indicator of the
health status of an individual. Blood is a very complex fluid, containing a multiplicity of …

Sickle cell anemia and its phenotypes

TN Williams, SL Thein - Annual review of genomics and human …, 2018 - annualreviews.org
In the 100 years since sickle cell anemia (SCA) was first described in the medical literature,
studies of its molecular and pathophysiological basis have been at the vanguard of scientific …

Sickle cell disease: clinical presentation and management of a global health challenge

ME Houwing, PJ De Pagter, EJ Van Beers, BJ Biemond… - Blood reviews, 2019 - Elsevier
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by
chronic haemolytic anaemia, painful episodes of vaso-occlusion, progressive organ failure …

Point‐of‐care screening for sickle cell disease in low‐resource settings: A multi‐center evaluation of HemoTypeSC, a novel rapid test

C Steele, A Sinski, J Asibey… - American journal of …, 2019 - Wiley Online Library
Sickle cell disease (SCD) is a common, life‐threatening genetic disorder that is best
managed when diagnosed early by newborn screening. However, SCD is most prevalent in …

Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care

K Esoh, E Wonkam-Tingang, A Wonkam - The Lancet Haematology, 2021 - thelancet.com
Sickle cell disease can be life-threatening or chronically debilitating for both children and
adults. Worldwide, more than 300 000 children are born with sickle cell disease every year …