Zobrazeno 1 - 10
of 24
pro vyhledávání: '"L, Tillyer"'
Publikováno v:
Journal of Clinical Pathology. 56:243-248
With the ever increasing demands for pathology testing within the National Health Service there is a need to manage the demand for these tests. This review discusses strategies for the demand management of requests made by clinicians in the disciplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0359d263f27ce8b74578cd75f82c116
https://doi.org/10.1136/jcp.56.4.243
https://doi.org/10.1136/jcp.56.4.243
Publikováno v:
Journal of Thrombosis and Haemostasis. 10:730-732
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10470cd75147e7e3ae8433aecd86eb6
https://doi.org/10.1111/j.1538-7836.2012.04659.x
https://doi.org/10.1111/j.1538-7836.2012.04659.x
Publikováno v:
European Journal of Pediatrics. 154:534-538
Two unrelated female infants with homozygous protein C (Pr C) deficiency are reported. Both are of U.K. Pakistani origin and in each case the parents are consanguinous. A previous sibling had died in each family. Both sets of parents were shown to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f17550d8354f848a7cd31eb3534146
https://doi.org/10.1007/bf02074829
https://doi.org/10.1007/bf02074829
Autor:
M L Tillyer, C R Tillyer
Publikováno v:
Journal of Clinical Pathology. 47:205-208
AIMS--To determine the value of the red cell distribution width (RDW) and erythrocyte zinc protoporphyrin (ZPP) concentration in discriminating between iron deficiency, and beta and alpha thalassaemia in a mixed urban Asian population. METHODS--The R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85bd43f050991354c1661d810e025df
https://doi.org/10.1136/jcp.47.3.205
https://doi.org/10.1136/jcp.47.3.205
Publikováno v:
Immunohematology. 23(4)
Anti-hrB and anti-HrB are rare alloantibodies found predominantly in people of Black African descent. It has been assumed that strongly reacting examples of anti-hrB may cause hemolytic transfusion reactions, but precise information is limited. Anti-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca6661e02f3e3c7cc6720bbcb9028ff2
https://pubmed.ncbi.nlm.nih.gov/18284303
https://pubmed.ncbi.nlm.nih.gov/18284303
Publikováno v:
Journal of Medical Screening. 5:31-33
Objectives To determine the prevalence and molecular basis of α thalassaemia in the British South Asian population, and the implications for genetic screening for haemoglobin disorders. Methods 397 South Asian subjects were screened for haemoglobino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c6fb0f7ca47e012881ab85560031524
https://doi.org/10.1136/jms.5.1.31
https://doi.org/10.1136/jms.5.1.31
Autor:
T, Ng, M L, Tillyer
Publikováno v:
Clinical and laboratory haematology. 23(4)
Thrombotic events are rare complications during anticoagulation therapy. The thrombosis varies from localized cutaneous involvement to catastrophic thromboembolism and is usually associated with an underlying thrombophilia. We describe a patient who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::358148290912112a3b3fd5c407feee4b
https://pubmed.ncbi.nlm.nih.gov/11683790
https://pubmed.ncbi.nlm.nih.gov/11683790
Publikováno v:
European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery. 19(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d99220bd8a700e71126a51bf9755ec59
https://pubmed.ncbi.nlm.nih.gov/10828239
https://pubmed.ncbi.nlm.nih.gov/10828239
Autor:
E. L. Gladigau, Richard W. Farndale, Willem H. Ouwehand, L. W. Davies, Kate Campbell, Peter A. Smethurst, L. Tillyer, R. Yusuf, Stephen F. Garner, Angela Rankin
Publikováno v:
Transfusion Medicine. 16:45-46
Background Studies of cases of acquired and inherited GPVI deficiency have made critical contributions to the understanding of the pivotal role of GPVI in collagen mediated platelet signaling. Aim To characterize the first UK case of GPVI deficiency.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4c7f547923e2666919986deb918ff45
https://doi.org/10.1111/j.1365-3148.2006.00694_49.x
https://doi.org/10.1111/j.1365-3148.2006.00694_49.x
Publikováno v:
The Journal of infection. 34(2)
Five cases of Salmonella osteomyelitis are presented in children with sickle cell disease living in the East End of London. Four of these had involvement of the long bones and one (an infant) presented with hand-foot syndrome. Four required surgical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f26d5a76168a79390f3b5adaa65d062
https://pubmed.ncbi.nlm.nih.gov/9138136
https://pubmed.ncbi.nlm.nih.gov/9138136