Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maren Khan"'
Publikováno v:
Public Health Genomics. 3:144-147
The objective of genetic screening is informed choice. The UK Confidential Enquiry into Genetic Counselling by Non-Geneticists (CEGEN) aims to assess the attainment of this objective at the community level. Antenatal screening for thalassaemias and s
Publikováno v:
Prenatal Diagnosis. 20:469-474
Prospective risk detection with availability of prenatal diagnosis is the best service currently available for couples at high genetic risk Here we describe the long term effect of this service on the reproductive life of 102 couples at risk of thala
Autor:
R. Nagar, Raj Raghupathy, Abu Salim Mustafa, Anmol Mathur, A. Misra, R. Agarwal, Maren Khan, U. C. Chaturvedi, H. Al-Sayer, Fawaz Azizieh, H. Nusrat, S. Kapoor, E.A. Elbishbishi
Publikováno v:
Journal of Medical Virology. 56:280-285
Dengue virus causes dengue fever, a mild febrile illness, and at times dengue hemorrhagic fever (DHF), a severe illness the pathogenesis of which is not fully understood. Given the crucial roles played by interleukin-8 (IL-8) as a chemoattractant cyt
Autor:
Michael Modell, Beatrix Wonke, Michael Lloyd, Maren Khan, Elizabeth Anionwu, Sharon See Tai, Bernadette Modell
Publikováno v:
BMJ. 317:788-791
Objective: To investigate the feasibility of improving screening for carriers of haemoglobin disorders in general practice by using a nurse facilitator to work with primary care teams and the relevant haematology laboratories; to identify problems in
Publikováno v:
Lancet (London, England). 355(9220)
Summary About 50% of UK patients with β-thalassaemia major die before the age of 35 years, mainly because conventional iron-chelation therapy is too burdensome for full adherence. Patients require an idividually-tailored treatment plan incorporating
Autor:
Maren Khan, Beverley Lane, L. Varnavides, Mary Petrou, Bernadette Modell, Matthew Darlison, Mark Layton, John M. Old, Rodney Harris
Publikováno v:
BMJ (Clinical research ed.). 320(7231)
Objective: National audit of informed choice in antenatal screening for thalassaemia. Design: Audit from the UK Confidential Enquiry into Counselling for Genetic Disorders. Setting: Thalassaemia module of the UK Confidential Enquiry into Counselling
Autor:
M. Zamiri, W. S. Douglas, W. N. Missaoui, Michael Norman Badminton, Sharon D. Whatley, Harry A. Dailey, Nicola G. Mason, N. J. Wainwright, Maren Khan, George H. Elder, Tamara A. Dailey
Publikováno v:
Journal of Medical Genetics. 41:e105-e105
Erythropoietic protoporphyria (EPP; MIM 177000) is an inherited disorder of haem biosynthesis characterised by the onset in early childhood of lifelong acute photosensitivity of sun-exposed skin.1 It results from partial deficiency of ferrochelatase
Autor:
Maren Khan, Bernadette Modell, Dudley J. Pennell, Mark Westwood, Matthew Darlison, David Ingram
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 10, Iss 1, p 42 (2008)
Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance
Background The UK Thalassaemia Register records births, deaths and selected clinical data of patients with thalassaemia who are resident in the UK. A study of survival and causes of death was undertaken which aimed to include the possible impact of T