Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Beatrice Emmanouil"'
Autor:
Dorothy Halliday, Joshua James Brown, Anne May, Rose Crabtree, Beatrice Emmanouil, Allyson Parry, Samuel Mackeith
Publikováno v:
BMJ Open Quality, Vol 10, Iss 1 (2021)
Externí odkaz:
https://doaj.org/article/61ab76cc6ddd4b549fe57949c1ba5dc6
Publikováno v:
BMC Anesthesiology, Vol 17, Iss 1, Pp 1-9 (2017)
Abstract Background It is important to inform medical educators and workforce planners in Anaesthesia about early career choices for the specialty, factors that influence them and to elucidate how recent choices of men and women doctors relate to the
Externí odkaz:
https://doaj.org/article/5d8675e58f844607b942da05fbeb653a
Autor:
Martin Wasik, Beatrice Emmanouil, Srilakshmi M. Sharma, Allyson Parry, Peter Charbel Issa, Dorothy Halliday
Publikováno v:
Ophthalmic Research. 65:77-85
Introduction: This case-control study seeks to systematically characterize the central retinal findings in a large cohort of patients with neurofibromatosis type 2 (NF2) using spectral domain optical coherence tomography (SD-OCT) as well as the exami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99b41a24d68690d6febf56625d901b0
https://doi.org/10.1159/000519143
https://doi.org/10.1159/000519143
Autor:
Beatrice Emmanouil, Sean Cox, Rachel Halford, Georgia Threadgold, Mark Gillyon-Powell, Graham Foster
Publikováno v:
Journal of Hepatology. 77:S44-S45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2834351b00971ca4cd4ab25259e60108
https://doi.org/10.1016/s0168-8278(22)00499-8
https://doi.org/10.1016/s0168-8278(22)00499-8
Autor:
Zuzana Sipkova, Sally L Painter, Dorothy Halliday, John S. Elston, Beatrice Emmanouil, Allyson Parry
Publikováno v:
Journal of Neuro-Ophthalmology. 39:44-49
Objective Neurofibromatosis type 2 (NF2) is an uncommon but well-recognized disorder characterized by multiple schwannomas and meningiomas. Adults typically present with hearing loss and balance disturbance, and children with ocular, dermatological,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d21e92523ec2499a6c3dbee0bbc2e93
https://doi.org/10.1097/wno.0000000000000675
https://doi.org/10.1097/wno.0000000000000675
Autor:
James D. Ramsden, Beatrice Emmanouil, Rory Houston, Samuel MacKeith, Allyson Parry, Anne May, C Oliver Hanemann, Dorothy Halliday
Publikováno v:
The Laryngoscope. 129:974-980
Objectives/hypothesis This study set out to describe the progression of hearing loss in patients with neurofibromatosis type 2 (NF2), treated in a quaternary multidisciplinary clinic. It also aimed to compare hearing loss across patients grouped acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f337000ea1337a868b84ba8db0f37ee9
https://doi.org/10.1002/lary.27586
https://doi.org/10.1002/lary.27586
Publikováno v:
Disability and Rehabilitation. 41:1632-1638
Patients with Neurofibromatosis type 2 often experience debilitating neuro-otological problems which affect their mobility and balance. This study examined the efficacy of a personalised program of vestibular rehabilitation for patients with Neurofib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::993f0f79d4dd1ba4323f01f473fa12f1
https://doi.org/10.1080/09638288.2018.1442505
https://doi.org/10.1080/09638288.2018.1442505
Autor:
Pieter M. Pretorius, Sally Painter, Helen Tomkins, Beatrice Emmanouil, D. Gareth Evans, Allyson Parry, Dorothy Halliday, Samuel MacKeith
Publikováno v:
Halliday, D, Emmanouil, B, Pretorius, P, MacKeith, S, Painter, S, Tomkins, H, Evans, D & Parry, A 2017, ' GENETIC SEVERITY SCORE PREDICTS CLINICAL PHENOTYPE IN NF2 ', Journal of Medical Genetics . https://doi.org/10.1136/jmedgenet-2017-104519
Journal of Medical Genetics
Journal of Medical Genetics
Background The clinical severity of disease in neurofibromatosis type 2 (NF2) is variable. Patients affected with a constitutional truncating NF2 mutation have severe disease, while missense mutations or mosaic mutations present with a milder atte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e026b7e3316f672d1034994409a453f1
https://doi.org/10.1136/jmedgenet-2017-104519
https://doi.org/10.1136/jmedgenet-2017-104519
Autor:
Gabriella Rands, Rachel Clarke, Dorothy Halliday, Allyson Parry, Louise May Quarmby, Louise Dalton, Beatrice Emmanouil, Sonia Patel, Rachel A. Woolrich
Publikováno v:
Psycho-oncology. 28(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d82cc92a3fcb8bec96eac55ff3304107
https://pubmed.ncbi.nlm.nih.gov/31033096
https://pubmed.ncbi.nlm.nih.gov/31033096
Autor:
Pieter M. Pretorius, Grace Vassallo, Saleel Chandratre, Beatrice Emmanouil, D. Gareth Evans, James Nicholson, Karine Lascelles, Allyson Parry, Martin Wasik, Dorothy Halliday, Geetha Anand
Publikováno v:
Halliday, D, Emmanouil, B, Vassallo, G, Lascelles, K, Nicholson, J, Chandratre, S, Anand, G, Wasik, M, Pretorius, P & Evans, D G 2019, ' Trends in phenotype in the English paediatric Neurofibromatosis Type 2 cohort stratified by genetic severity ', Clinical Genetics . https://doi.org/10.1111/cge.13551
Childhood onset neurofibromatosis type 2 can be severe and genotype dependent. We present a retrospective phenotypic analysis of all ascertained children in Englandage 18 (N = 87; male 61%). Mean age at last review was 13.9 years with mean follow-up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07c7b7142d4f6c4d41f0607c33875470
https://www.research.manchester.ac.uk/portal/en/publications/trends-in-phenotype-in-the-english-paediatric-neurofibromatosis-type-2-cohort-stratified-by-genetic-severity(e6bfb523-9c8c-4da2-b233-60769097ae2c).html
https://www.research.manchester.ac.uk/portal/en/publications/trends-in-phenotype-in-the-english-paediatric-neurofibromatosis-type-2-cohort-stratified-by-genetic-severity(e6bfb523-9c8c-4da2-b233-60769097ae2c).html
