Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Sorena Kiani‑Alikhan"'
Autor:
Marcus Maurer, Markus Magerl, Emel Aygören-Pürsün, Konrad Bork, Henriette Farkas, Hilary Longhurst, Sorena Kiani‑Alikhan, Laurence Bouillet, Isabelle Boccon-Gibod, Mauro Cancian, Andrea Zanichelli, David Launay
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 18, Iss 1, Pp 1-12 (2022)
Abstract Background Hereditary angioedema (HAE) is characterized by potentially severe and life-threatening attacks of localized swelling. Prophylactic therapies are available, including attenuated androgens. Efficacy of attenuated androgens has not
Externí odkaz:
https://doaj.org/article/5c2ad1d8ea544b7b9d2fa3693dc729cb
Autor:
Matthew S. Buckland, James B. Galloway, Caoimhe Nic Fhogartaigh, Luke Meredith, Nicholas M. Provine, Stuart Bloor, Ane Ogbe, Wioleta M. Zelek, Anna Smielewska, Anna Yakovleva, Tiffeney Mann, Laura Bergamaschi, Lorinda Turner, Frederica Mescia, Erik J. M. Toonen, Carl-Philipp Hackstein, Hossain Delowar Akther, Vinicius Adriano Vieira, Lourdes Ceron-Gutierrez, Jimstan Periselneris, Sorena Kiani-Alikhan, Sofia Grigoriadou, Devan Vaghela, Sara E. Lear, M. Estée Török, William L. Hamilton, Joanne Stockton, Josh Quick, Peter Nelson, Michael Hunter, Tanya I. Coulter, Lisa Devlin, CITIID-NIHR COVID-19 BioResource Collaboration, MRC-Toxicology Unit COVID-19 Consortium, John R. Bradley, Kenneth G. C. Smith, Willem H. Ouwehand, Lise Estcourt, Heli Harvala, David J. Roberts, Ian B. Wilkinson, Nick Screaton, Nicholas Loman, Rainer Doffinger, Paul A. Lyons, B. Paul Morgan, Ian G. Goodfellow, Paul Klenerman, Paul J. Lehner, Nicholas J. Matheson, James E. D. Thaventhiran
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Remdesivir is under evaluation for treatment of COVID-19 in clinical trials. Here, the authors report results of remdesivir treatment in a patient with COVID-19 and the genetic antibody deficiency XLA. They show a temporally correlated clinical and v
Externí odkaz:
https://doaj.org/article/c14cbd11e914499b8bdaf50363c87805
Autor:
Marcus Maurer, MD, Markus Magerl, MD, Stephen Betschel, MD, Werner Aberer, MD, Ignacio J. Ansotegui, MD, PhD, Emel Aygören-Pürsün, MD, Aleena Banerji, MD, Noémi-Anna Bara, MD, Isabelle Boccon-Gibod, MD, Konrad Bork, MD, Laurence Bouillet, Pr, MD, PhD, Henrik Balle Boysen, Nicholas Brodszki, MD, PhD, Paula J. Busse, MD, Anette Bygum, MD, DMSci, Teresa Caballero, MD, PhD, Mauro Cancian, MD, PhD, Anthony J. Castaldo, Danny M. Cohn, MD, PhD, Dorottya Csuka, MD, Henriette Farkas, MD, PhD, DSc, Mark Gompels, MBBS, BSc, MD, Richard Gower, MD, Anete S. Grumach, MD, PhD, Guillermo Guidos-Fogelbach, MD, PhD, Michihiro Hide, MD, PhD, Hye-Ryun Kang, MD, PhD, Allen P. Kaplan, MD, Constance H. Katelaris, MBBS, PhD, Sorena Kiani-Alikhan, PhD, Wei-Te Lei, MD, Richard F. Lockey, MD, Hilary Longhurst, PhD, William Lumry, MD, Andrew MacGinnitie, MD, PhD, Alejandro Malbran, MD, PhD, Inmaculada Martinez Saguer, MD, Juan José Matta Campos, MD, Alexander Nast, MD, Dinh Nguyen, MD, PhD, Sandra A. Nieto-Martinez, MD, Ruby Pawankar, MD, PhD, Jonathan Peter, MB ChB, MMed, FCP (SA), PhD, Grzegorz Porebski, MD, Nieves Prior, MD, PhD, Avner Reshef, MD, Marc Riedl, MD, Bruce Ritchie, MD, Farrukh Rafique Sheikh, MBBS, William B. Smith, MBBS, PhD, Peter J. Spaeth, PhD, Marcin Stobiecki, MD, Elias Toubi, MD, Lilian Agnes Varga, PhD, Karsten Weller, MD, Andrea Zanichelli, MD, Yuxiang Zhi, MD, Bruce Zuraw, MD, Timothy Craig, MD
Publikováno v:
World Allergy Organization Journal, Vol 15, Iss 3, Pp 100627- (2022)
Hereditary Angioedema (HAE) is a rare and disabling disease for which early diagnosis and effective therapy are critical. This revision and update of the global WAO/EAACI guideline on the diagnosis and management of HAE provides up-to-date guidance f
Externí odkaz:
https://doaj.org/article/8b9e359b6d224c3ca799a778ade61235
Autor:
Henriette Farkas, Marcin Stobiecki, Jonny Peter, Tamar Kinaciyan, Marcus Maurer, Emel Aygören‐Pürsün, Sorena Kiani‐Alikhan, Adrian Wu, Avner Reshef, Anette Bygum, Olivier Fain, David Hagin, Aarnoud Huissoon, Miloš Jeseňák, Karen Lindsay, Vesna Grivcheva Panovska, Urs C. Steiner, Celia Zubrinich, Jessica M. Best, Melanie Cornpropst, Daniel Dix, Sylvia M. Dobo, Heather A. Iocca, Bhavisha Desai, Sharon C. Murray, Eniko Nagy, William P. Sheridan
Publikováno v:
Clinical and Translational Allergy, Vol 11, Iss 4, Pp n/a-n/a (2021)
Abstract Background Berotralstat (BCX7353) is an oral, once‐daily inhibitor of plasma kallikrein recently approved for prevention of angioedema attacks in adults and adolescents with hereditary angioedema (HAE). The objective of this report is to s
Externí odkaz:
https://doaj.org/article/857745995f5542e9849cc3caa86d3acb
Autor:
Ching Lam, Gehanjali Amarasinghe, Natalia Zarate-Lopez, Asma Fikree, Peter Byrne, Sorena Kiani-Alikhan, Simon Gabe, Peter Paine
Publikováno v:
Frontline Gastroenterol
Patients diagnosed with hypermobile Ehlers-Danlos syndrome and hypermobile spectrum disorders are increasingly presenting to secondary and tertiary care centres with gastrointestinal (GI) symptoms and nutritional issues. Due to the absence of specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14b590f61f97991ef6b3cebf6aadeb1b
https://doi.org/10.1136/flgastro-2022-102088
https://doi.org/10.1136/flgastro-2022-102088
Autor:
Emel Aygören-Pürsün, Andrea Zanichelli, Danny M Cohn, Mauro Cancian, Roman Hakl, Tamar Kinaciyan, Markus Magerl, Inmaculada Martinez-Saguer, Marcin Stobiecki, Henriette Farkas, Sorena Kiani-Alikhan, Vesna Grivcheva-Panovska, Jonathan A Bernstein, H Henry Li, Hilary J Longhurst, Paul K Audhya, Michael D Smith, Christopher M Yea, Andreas Maetzel, Daniel K Lee, Edward P Feener, Richard Gower, William R Lumry, Aleena Banerji, Marc A Riedl, Marcus Maurer
Publikováno v:
The Lancet, 401(10375), 458-469. Elsevier Limited
Background: Guidelines recommend effective on-demand therapy for all individuals with hereditary angioedema. We aimed to assess the novel oral plasma kallikrein inhibitor, sebetralstat, which is in development, for on-demand treatment of hereditary a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecd222b086018bb478d12029297cd21f
https://ruj.uj.edu.pl/xmlui/handle/item/309592
https://ruj.uj.edu.pl/xmlui/handle/item/309592
Autor:
Manisha Ahuja, Anthony Dorr, Eniola Bode, Anne P. R. Boulton, Matthew Buckland, Samuel Chee, Claire Dalley, Sarah Denman, Anjali Ekbote, Shuayb Elkhalifa, Tariq El‐Shanawany, Efrem Eren, Archana Herwadkar, Tomaz Garcez, Harichandana Ghanta, Alexandros Grammatikos, Sofia Grigoriadou, Rashmi Jain, Lorena Lorenzo, Ania Manson, Emily Moon, Sai Murng, Aveen Murphy, Leman Mutlu, Nicholas Peters, Kavitha Sooriyakumar, Catherine Stroud, Katie Townsend, Robert L. Yellon, Patrick Yong, Sorena Kiani‐Alikhan
Publikováno v:
Allergy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc9de74ceee69b8c3acc9f792fb1565
https://pubmed.ncbi.nlm.nih.gov/36609839
https://pubmed.ncbi.nlm.nih.gov/36609839
Autor:
Anthony D. Dorr, Charu Chopra, Tanya I. Coulter, John Dempster, Magdalena Dziadzio, Tariq El‐Shanawany, Tomaz Garcez, Mark Gompels, Richard Herriot, Rashmi Jain, Marcel Levi, Lorena Lorenzo, Inas Makki, Elizabeth Mapazire, Sai H. K. Murng, Sadia Noorani, Sinisa Savic, Cathal L. Steele, Christine Symons, Michael Tarzi, Patrick F. K. Yong, Sorena Kiani‐Alikhan
Publikováno v:
Allergy: European Journal of Allergy and Clinical Immunology. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1716e146afad47a5730b4b44d0d32a55
https://doi.org/10.22541/au.166295883.36707256/v1
https://doi.org/10.22541/au.166295883.36707256/v1
Autor:
Manisha Ahuja, Anthony Dorr, Eniola Bode, Anne Pacita Rosillo Boulton, Matthew Buckland, Samuel Chee, Claire Dalley, Sarah Denman, Anjali Ekbote, Shuayb Elkhalifa, Tariq El-Shanawany, Efrem Eren, Archana Herwadkar, Tomaz Garcez, Harichandana Ghanta, Alexandros Grammatikos, Sofia Grigoriadou, Rashmi Jain, Lorena Lorenzo, Ania Manson, Emily Moon, Sai Murng, Aveen Murphy, Leman Mutlu, Nicholas Peters, Kavitha Sooriyakumar, Catherine Stroud, Katie Townsend, Patrick Yong, Sorena Kiani-Alikhan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45903811bbbd436bb8869cf6f30eb7d2
https://doi.org/10.22541/au.165466812.28629415/v1
https://doi.org/10.22541/au.165466812.28629415/v1
Publikováno v:
Obstet Med
Hereditary angioedema (HAE) is a rare genetic condition associated with episodic swelling due to dysfunction of bradykinin regulation pathways. This is most frequently caused by low level and/or function of the C1-esterase inhibitor protein (C1INH) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42fbfc30b34ee36c95a11243732fd54d
https://doi.org/10.1177/1753495x20958225
https://doi.org/10.1177/1753495x20958225