Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ghaniah Hassan‐Smith"'
Autor:
Syed Rizvi, Muhammad Khakwani, Shivan Pancham, Dimitris Tsitsikas, Zbigniew Rudzki, Ghaniah Hassan‐Smith, Michael Bowen, Christine Wright, Daniel Park
Publikováno v:
eJHaem, Vol 4, Iss 1, Pp 207-210 (2023)
Abstract Fat embolism syndrome (FES) is a rare life‐threatening condition that is particularly seen in milder forms of sickle cell disease (SCD). Widespread systemic fat emboli are generated in the context of extensive bone marrow necrosis. Multi
Externí odkaz:
https://doaj.org/article/979445b1e8aa4370968517b09f8a8df8
Autor:
Gavin Giovannoni, Eli Silber, Ruth Dobson, Riffat Tanveer, Jade Harris, Tarunya Arun, Miriam Mattoscio, Ghaniah Hassan-Smith, Huw Morris, Rod Middleton, Emma Tallantyre, David Rog, Nikos Evangelou, Benjamin M Jacobs, Antonio Scalfari, Waqar Rashid, Helen L Ford, Charles A Mein, Stephen Sawcer, Cord Spilker, Bruno Gran, Martin O'Malley, Ashwini Nandoskar, Emeka Uzochukwu, Katila George, Sadid Hoque, Luisa Schalk, Angie Dunne, Charlotte Sellers, Elisa Visentin, Elizabeth Lindsey Bezzina, Eva Wozniak, Eve Sacre, Joan Bradley, Joshua Breedon, Judith Brooke, Karim L Kreft, Katherine Tuite Dalton, Maria Papachatzaki, Michelle Peter, Neisha Rhule, Nimisha Vinod, Outi Quinn, Ramya Shamji, Rashmi Kaimal, Rebecca Boulton, Roxanne Murray, Ruth Bellfield, Shakeelah Patel, Sonia Raj, Stephanie Gumus, Stephanie Mitchell, Tatiana Pogreban, Terri-Louise Brown, Thamanna Begum, Veronica Antoine
Publikováno v:
BMJ Open, Vol 13, Iss 5 (2023)
Purpose Genetic studies of multiple sclerosis (MS) susceptibility and severity have focused on populations of European ancestry. Studying MS genetics in other ancestral groups is necessary to determine the generalisability of these findings. The gene
Externí odkaz:
https://doaj.org/article/dfaa829aa3244981a9b0642497517dd8
Autor:
Syed Rizvi, Muhammad Khakwani, Shivan Pancham, Dimitris Tsitsikas, Zbigniew Rudzki, Ghaniah Hassan‐Smith, Michael Bowen, Christine Wright, Daniel Park
Publikováno v:
eJHaem. 4:207-210
Autor:
Benjamin M Jacobs, Luisa Schalk, Angie Dunne, Antonio Scalfari, Ashwini Nandoskar, Bruno Gran, Charles A Mein, Charlotte Sellers, Cord Spilker, David Rog, Elisa Visentin, Elizabeth Lindsey Bezzina, Emeka Uzochukwu, Emma Tallantyre, Eva Wozniak, Eve Sacre, Ghaniah Hassan-Smith, Helen L Ford, Jade Harris, Joan Bradley, Joshua Breedon, Judith Brooke, Karim L Kreft, Katherine Tuite Dalton, Katila George, Maria Papachatzaki, Martin O'Malley, Michelle Peter, Miriam Mattoscio, Neisha Rhule, Nikos Evangelou, Nimisha Vinod, Outi Quinn, Ramya Shamji, Rashmi Kaimal, Rebecca Boulton, Riffat Tanveer, Rod Middleton, Roxanne Murray, Ruth Bellfield, Sadid Hoque, Shakeelah Patel, Sonia Raj, Stephanie Gumus, Stephanie Mitchell, Stephen Sawcer, Tarunya Arun, Tatiana Pogreban, Terri-Louise Brown, Thamanna Begum, Veronica Antoine, Waqar Rashid, Alastair J Noyce, Eli Silber, Huw Morris, Gavin Giovannoni, Ruth Dobson
Publikováno v:
BMJ Open. 13:e071656
PurposeGenetic studies of multiple sclerosis (MS) susceptibility and severity have focused on populations of European ancestry. Studying MS genetics in other ancestral groups is necessary to determine the generalisability of these findings. The genet
Autor:
Richard J Perry, Arina Tamborska, Bhagteshwar Singh, Brian Craven, Richard Marigold, Peter Arthur-Farraj, Jing Ming Yeo, Liqun Zhang, Ghaniah Hassan-Smith, Matthew Jones, Christopher Hutchcroft, Esther Hobson, Dana Warcel, Daniel White, Phillip Ferdinand, Alastair Webb, Tom Solomon, Marie Scully, David J Werring, Christine Roffe, Sara Al-izzi, Aravindhan Baheerathan, Soma Banerjee, Gary Benson, Claudia Boshier, Sandeep Buddha, Nathan Burley, Ruaridh Cameron Smail, Arvind Chandratheva, Pavel Chudakou, Philip Clatworthy, Alasdair Coles, Thomas Cox, Ranjit Dasgupta, Richard Davenport, Darrell Devine, Stephen Fenlon, Carolyn Gabriel, Rita Ghatala, Claire Hall, Milan Hargovan, Kirsty Harkness, Ian Harvey, Lucy Hicken, Laura Howaniec, Abubaker Ibnouf, Luis Idrovo, Gordon Ingle, Yong Kyan Lee, Ailidh Lang, Simon McBride, Malcolm McLeod, Ruth Medlock, Puja Mehta, Ian Morrison, Girish Muddegowda, Sharon Muzerengi, Donald Pang, Gopinath Periyasamy, Gavin Preston, Naomi Priestley, Lydia Revicka, Sadia Saber, Elliott Smith, Youssef Sorour, Oliver Spooner, Jon Stone, Laszlo Sztriha, Narmathey Thambirajah, Rhys Thomas, David Veale, Jasmine Wall, Sarah White, James White, Syarah Yusoff, Laura Zambreanu
Publikováno v:
Lancet (London, England)
LANCET
LANCET
Background: A new syndrome of vaccine-induced immune thrombotic thrombocytopenia (VITT) has emerged as a rare side-effect of vaccination against COVID-19. Cerebral venous thrombosis is the most common manifestation of this syndrome but, to our knowle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd9fef3e16362f6577bc8d3cd07ae55
https://www.repository.cam.ac.uk/handle/1810/327808
https://www.repository.cam.ac.uk/handle/1810/327808
Autor:
Prisca Singh, Ghaniah Hassan-Smith
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:e2.209
The novel SARS-CoV-2 virus has affected healthcare services across the world, with the impact on neurology services being no exception to the global disruption. There is variable reporting of neurological conditions during the pandemic. This work exp
Autor:
Maria Uldall, Ghaniah Hassan-Smith, Hannah Botfield, Ana M. Gonzalez, Alexandra J Sinclair, Mohammed A.L. Miah, Rigmor Jensen, Liam D Cato, Keira Markey
Publikováno v:
Journal of Pain Research
Markey, K A, Uldall, M, Botfield, H, Cato, L D, Miah, M A L, Hassan-Smith, G, Jensen, R H, Gonzalez, A M & Sinclair, A J 2016, ' Idiopathic intracranial hypertension, hormones, and 11β-hydroxysteroid dehydrogenases ', Journal of Pain Research, vol. 9, pp. 223-232 . https://doi.org/10.2147/JPR.S80824
Markey, K A, Uldall, M, Botfield, H, Cato, L D, Miah, M A L, Hassan-Smith, G, Jensen, R H, Gonzalez, A M & Sinclair, A J 2016, ' Idiopathic intracranial hypertension, hormones, and 11β-hydroxysteroid dehydrogenases ', Journal of Pain Research, vol. 9, pp. 223-232 . https://doi.org/10.2147/JPR.S80824
Idiopathic intracranial hypertension (IIH) results in raised intracranial pressure (ICP) leading to papilledema, visual dysfunction, and headaches. Obese females of reproductive age are predominantly affected, but the underlying pathological mechanis
Autor:
Emma, Rathbone, Lindsay, Durant, James, Kinsella, Antony R, Parker, Ghaniah, Hassan-Smith, Michael R, Douglas, S John, Curnow
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 89(10)
To determine whether the ratio of cerebrospinal fluid (CSF) immunoglobulin kappa to lambda light chains at time of multiple sclerosis (MS) diagnosis predicts disease progression and whether this was intrinsic to CSF plasmablasts.CSF and peripheral bl
Autor:
Susan P, Mollan, Brendan, Davies, Nick C, Silver, Simon, Shaw, Conor L, Mallucci, Benjamin R, Wakerley, Anita, Krishnan, Swarupsinh V, Chavda, Satheesh, Ramalingam, Julie, Edwards, Krystal, Hemmings, Michelle, Williamson, Michael A, Burdon, Ghaniah, Hassan-Smith, Kathleen, Digre, Grant T, Liu, Rigmor Højland, Jensen, Alexandra J, Sinclair
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry
The aim was to capture interdisciplinary expertise from a large group of clinicians, reflecting practice from across the UK and further, to inform subsequent development of a national consensus guidance for optimal management of idiopathic intracrani
Autor:
Michael R. Douglas, S. Kalra, J.M. Faint, S.J. Curnow, L.K. Assi, Ghaniah Hassan-Smith, A. Tsentemeidou, Lindsay Durant
Publikováno v:
Journal of Neuroimmunology. 276:175-179
Cerebrospinal fluid (CSF) analysis is routinely used in the diagnostic work-up of multiple sclerosis (MS), by detecting CSF-specific oligoclonal bands (OCB). More recently, several studies have reported CSF free light chains (FLC) as an alternative.