FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2500896969> ?p ?o ?g. }

• W2500896969 abstract "Hereditary Hemochromatosis (HH) is a disorder where iron and ferritin concentrations in a patient's blood are much higher than normal healthy levels. The main therapeutic intervention for individuals with HH is removing 300-500 mL of blood every few months to maintain ferritin concentration within acceptable ranges. The blood collected during these venesections is usually discarded as there is a belief that blood with high levels of ferritin are not suitable for blood transfusion purposes. Australian Red Cross Blood Services voluntarily collects blood from donors for subsequent use in blood transfusion. Annually more than 700 thousand units are transfused within Australia and there is a constant need for new donors given the significant imbalance between supply and demand of blood products. Besides red cell transfusions, the Red Cross also issues donor blood for development of many other blood products essential for patient health care. The HH blood can currently be used for other blood products if not for red cell transfusion. However, there is evidence to suggest that there is no significant difference between the red cells of the normal healthy population compared to those from HH patients. Australian Red Cross has developed a mobile computer application (High Ferritin “app”) as they have started collecting blood from HH patients. Though there is little or no awareness about the existence and use of this High Ferritin app in general HH population, their doctors and nurses collecting their blood for therapeutic purposes. This chapter describes possibility of saving and utilizing the blood collected from hemochromatosis patients for therapeutic purposes. A national hemochromatosis patients registry, in collaboration with High Ferritin app (HFa) developed by Australian Red Cross Blood Services, accessible to the patients, their doctors and Red Cross Blood Collection Sservices 24 hours a day anywhere in the country can allow the patients to donate the blood collected for therapeutic purposes at any affiliated blood collection center in the country after they automatically get a message either by email or text message after their blood results have been reviewed by their doctor and they are required to go for venesection." @default.
• W2500896969 created "2016-08-23" @default.
• W2500896969 creator A5030655906 @default.
• W2500896969 creator A5049560493 @default.
• W2500896969 creator A5052746457 @default.
• W2500896969 date "2016-01-01" @default.
• W2500896969 modified "2023-09-27" @default.
• W2500896969 title "Developing a National Registry for Hemochromatosis" @default.
• W2500896969 cites W1963797525 @default.
• W2500896969 cites W1979792970 @default.
• W2500896969 cites W2008371779 @default.
• W2500896969 cites W2020218579 @default.
• W2500896969 cites W2020337134 @default.
• W2500896969 cites W2032280527 @default.
• W2500896969 cites W2067242321 @default.
• W2500896969 cites W2080594514 @default.
• W2500896969 cites W2103062509 @default.
• W2500896969 cites W2103433121 @default.
• W2500896969 cites W2114015514 @default.
• W2500896969 cites W2114952318 @default.
• W2500896969 cites W2121221073 @default.
• W2500896969 cites W2124377321 @default.
• W2500896969 cites W2124893310 @default.
• W2500896969 cites W2126742636 @default.
• W2500896969 cites W2141657484 @default.
• W2500896969 cites W2143199657 @default.
• W2500896969 cites W2149354967 @default.
• W2500896969 cites W2151254759 @default.
• W2500896969 cites W2161972035 @default.
• W2500896969 cites W4232187658 @default.
• W2500896969 cites W4236442175 @default.
• W2500896969 cites W65987205 @default.
• W2500896969 doi "https://doi.org/10.4018/978-1-4666-9432-3.ch007" @default.
• W2500896969 hasPublicationYear "2016" @default.
• W2500896969 type Work @default.
• W2500896969 sameAs 2500896969 @default.
• W2500896969 citedByCount "0" @default.
• W2500896969 crossrefType "book-chapter" @default.
• W2500896969 hasAuthorship W2500896969A5030655906 @default.
• W2500896969 hasAuthorship W2500896969A5049560493 @default.
• W2500896969 hasAuthorship W2500896969A5052746457 @default.
• W2500896969 hasConcept C126322002 @default.
• W2500896969 hasConcept C187212893 @default.
• W2500896969 hasConcept C2776590208 @default.
• W2500896969 hasConcept C2908964109 @default.
• W2500896969 hasConcept C71924100 @default.
• W2500896969 hasConceptScore W2500896969C126322002 @default.
• W2500896969 hasConceptScore W2500896969C187212893 @default.
• W2500896969 hasConceptScore W2500896969C2776590208 @default.
• W2500896969 hasConceptScore W2500896969C2908964109 @default.
• W2500896969 hasConceptScore W2500896969C71924100 @default.
• W2500896969 hasLocation W25008969691 @default.
• W2500896969 hasOpenAccess W2500896969 @default.
• W2500896969 hasPrimaryLocation W25008969691 @default.
• W2500896969 hasRelatedWork W1497937236 @default.
• W2500896969 hasRelatedWork W1996312039 @default.
• W2500896969 hasRelatedWork W2017032242 @default.
• W2500896969 hasRelatedWork W2086338786 @default.
• W2500896969 hasRelatedWork W2091331340 @default.
• W2500896969 hasRelatedWork W2173804760 @default.
• W2500896969 hasRelatedWork W2279634835 @default.
• W2500896969 hasRelatedWork W2296026731 @default.
• W2500896969 hasRelatedWork W2332774184 @default.
• W2500896969 hasRelatedWork W2425136375 @default.
• W2500896969 hasRelatedWork W2471091278 @default.
• W2500896969 hasRelatedWork W2581150207 @default.
• W2500896969 hasRelatedWork W2785742798 @default.
• W2500896969 hasRelatedWork W2891448553 @default.
• W2500896969 hasRelatedWork W2916745822 @default.
• W2500896969 hasRelatedWork W3118136942 @default.
• W2500896969 hasRelatedWork W3148486613 @default.
• W2500896969 hasRelatedWork W3162560384 @default.
• W2500896969 hasRelatedWork W2226934872 @default.
• W2500896969 hasRelatedWork W3032536894 @default.
• W2500896969 isParatext "false" @default.
• W2500896969 isRetracted "false" @default.
• W2500896969 magId "2500896969" @default.
• W2500896969 workType "book-chapter" @default.