Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Anette Drøhse Kjeldsen"'
Autor:
Anne Lørup Lyster, Signe Hedengran Biørn, Anette Drøhse Kjeldsen, Christian Nielsen, Bibi Lange, Annette Dam Fialla, Pernille Just Vinholt
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Patients with the rare disease; Hereditary haemorrhagic telangiectasia (HHT) often bleed from telangiectatic lesions in mucosal surfaces. Studies suggest that impaired platelet function may also play a role in their bleeding tende
Externí odkaz:
https://doaj.org/article/44cbc27a2e474faabe5ac85a0d591033
Autor:
Gunhild Nynke Thomsen, Mette Niemann Christoffersen, Hanne Merete Lindegaard, Jesper Rømhild Davidsen, Gitte Nyvang Hartmeyer, Kristian Assing, Charlotte G. Mortz, Raquel Martin-Iguacel, Michael Boe Møller, Anette Drøhse Kjeldsen, Troels Havelund, Daniel El Fassi, Sigurd Broesby-Olsen, Michael Maiborg, Sofie Lock Johansson, Christen Lykkegaard Andersen, Hanne Vestergaard, Ole Weis Bjerrum
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Eosinophilic granulocytes are normally present in low numbers in the bloodstream. Patients with an increased number of eosinophilic granulocytes in the differential count (eosinophilia) are common and can pose a clinical challenge because conditions
Externí odkaz:
https://doaj.org/article/2b8584069f364c14a011c10e2a0b3072
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by several clinical symptoms including epistaxis, arteriovenous malformations (AVM), and telangiectasia. In 2018, European Reference Netw
Externí odkaz:
https://doaj.org/article/1e19bdd8603046ffbfec40374191569f
Autor:
Anne Stockmann, Kenneth Lenhardt Larsen, Bibi Lange, Peter Darling, Gita Jørgensen, Lisbeth Høgedal, Anette Drøhse Kjeldsen
Publikováno v:
Rhinology Online, Vol 3, Pp 106-112 (2020)
Background: The significance of nasal septal deviations may be hard to evaluate. Patient history, clinical examination, nasal endoscopy and sinus CT scans contribute in the evaluation. We aimed to investigate the interrater agreement in the evaluatio
Externí odkaz:
https://doaj.org/article/b6cf3ae7606e4310b019d7780c3cf35e
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Background Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disorder with a wide variety of clinical manifestations due to the presence of multiple arteriovenous malformations in various tissues and organs. Objec
Externí odkaz:
https://doaj.org/article/5a0df3c75ff74c218812af0e088d9383
Publikováno v:
Ugeskrift for laeger. 184(20)
In this case report, it was suspected that a four-year-old girl had an impacted toy in her nose. Initially, she was refused consultation due to a COVID-19 positive parent. Three days later she presented with nasal secretion and facial oedema. At the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a03bd8e0f31b8372117ba3f31398cb6
https://pubmed.ncbi.nlm.nih.gov/35656602
https://pubmed.ncbi.nlm.nih.gov/35656602
Autor:
Justin P. McWilliams, Miles Conrad, Mary Porteous, Mary E. Meek, James R. Gossage, Jay F. Piccirillo, Masaki Komiyama, Elisabetta Buscarini, Carlo Sabbà, Andrea Lausman, Paul J. Rochon, Ketil Heimdal, Rose Pantalone, Claire L. Shovlin, Valerie A. Palda, Hanny Al-Samkari, Kevin Korenblatt, Marianne S. Clancy, Jamie McDonald, Katharine J. Henderson, Marie E. Faughnan, Claudia Crocione, Steven W. Hetts, Erik Deslandres, Urban W. Geisthoff, Ingrid Winship, Els de Gussem, Vivek N. Iyer, Daniel Cortes, Sophie Dupuis-Girod, Beth Plahn, Kelly Lang-Robertson, Patrick Foy, Mark S. Chesnutt, Ivan Radovanovic, Anette Drøhse Kjeldsen, Felix Ratjen, Johannes J. Mager, Carol Derksen, Adrienne M. Hammill, Sara Palmer, Marcelo M. Serra, Jack McMahon, Josanna Rodriguez-Lopez, Andrew J. White, Roberto Zarrabeitia, Raj S. Kasthuri, Marco C. Post, Jama M. Darling, Scott E. Olitsky, Dennis L. Sprecher, Murali M. Chakinala, Kevin J. Whitehead, David M. Poetker, Meir Mei-Zahav
Publikováno v:
Faughnan, M E, Mager, J J, Hetts, S W, Palda, V A, Lang-Robertson, K, Buscarini, E, Deslandres, E, Kasthuri, R S, Lausman, A, Poetker, D, Ratjen, F, Chesnutt, M S, Clancy, M, Whitehead, K J, Al-Samkari, H, Chakinala, M, Conrad, M, Cortes, D, Crocione, C, Darling, J, de Gussem, E, Derksen, C, Dupuis-Girod, S, Foy, P, Geisthoff, U, Gossage, J R, Hammill, A, Heimdal, K, Henderson, K, Iyer, V N, Kjeldsen, A D, Komiyama, M, Korenblatt, K, McDonald, J, McMahon, J, McWilliams, J, Meek, M E, Mei-Zahav, M, Olitsky, S, Palmer, S, Pantalone, R, Piccirillo, J F, Plahn, B, Porteous, M E M, Post, M C, Radovanovic, I, Rochon, P J, Rodriguez-Lopez, J, Sabba, C, Serra, M, Shovlin, C, Sprecher, D, White, A J, Winship, I & Zarrabeitia, R 2020, ' Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia ', Annals of Internal Medicine, vol. 173, no. 12, pp. 989-1001 . https://doi.org/10.7326/M20-1443
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of vascular malformations (VMs). These result in chronic bleeding, acute hemorrhage, and comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ee4994475518c545cc94de43b382bf
https://doi.org/10.7326/m20-1443
https://doi.org/10.7326/m20-1443
Autor:
Anna Trier Heiberg, Brix, Pernille Mathiesen, Tørring, Anette Drøhse, Kjeldsen, Anette, Bygum, Annette, Schuster, Troels Halfeld, Nielsen
Publikováno v:
Ugeskrift for laeger. 184(19)
Capillary malformations - arteriovenous malformation, hereditary hemorrhagic telangiectasia and Sturge-Weber syndrome - are rare diseases in which cutaneous capillary malformations (CM) may be associated with cerebral vascular malformations. The clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c545e7da13b3ba15dd50e264d2b8803f
https://pubmed.ncbi.nlm.nih.gov/35593371
https://pubmed.ncbi.nlm.nih.gov/35593371
Publikováno v:
International journal of dermatologyReferences. 61(12)
The diagnostic criteria for hereditary hemorrhagic telangiectasia (HHT) include the presence of telangiectatic lesions in common sites (nose, fingers, oral cavity, and lips). Telangiectatic lesions are described as red spots in the skin, but this des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08808ab336fd18adbc435be3035e1070
https://pubmed.ncbi.nlm.nih.gov/35792874
https://pubmed.ncbi.nlm.nih.gov/35792874
Autor:
Pernille Hahn, Anne-Louise Christensen, Camilla Andersen, Tejs Ehlers Klug, Helle Døssing, Sophie Mikkelsen, Thomas Greve, Christian Sander Danstrup, Maria Rusan, Niels Krintel Petersen, Anette Drøhse Kjeldsen
Publikováno v:
Klug, T E, Andersen, C, Hahn, P, Danstrup, C S, Petersen, N K, Mikkelsen, S, Døssing, H, Christensen, A-L, Rusan, M, Kjeldsen, A & Greve, T 2022, ' Clinical evaluation of antibiotic regimens in patients with surgically verified parapharyngeal abscess : a prospective observational study ', European Archives of Oto-Rhino-Laryngology, vol. 279, no. 4, pp. 2057-2067 . https://doi.org/10.1007/s00405-021-06962-8
PURPOSE: We aimed to evaluate the effectiveness of different antibiotic regimens for the treatment of parapharyngeal abscess (PPA) and characterize patients, who suffered potentially preventable complications (defined as death, abscess recurrence, sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5ad7be5d4c7bb89b8d5b01124bc75c
https://portal.findresearcher.sdu.dk/da/publications/171dc2b6-3cfa-421f-b1b5-9624ea7ffb83
https://portal.findresearcher.sdu.dk/da/publications/171dc2b6-3cfa-421f-b1b5-9624ea7ffb83
