Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M. E. Faughnan"'
Autor:
K. P. Thompson, J. Sykes, P. Chandakkar, P. Marambaud, N. T. Vozoris, D. A. Marchuk, M. E. Faughnan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022)
Abstract Background Vascular malformations in hereditary hemorrhagic telangiectasia (HHT) lead to chronic recurrent bleeding, hemorrhage, stroke, heart failure, and liver disease. There is great interest in identifying novel therapies for epistaxis i
Externí odkaz:
https://doaj.org/article/38df5068667a42a0b1a083e941b5304f
Autor:
K. P. Thompson, J. Nelson, H. Kim, S. M. Weinsheimer, D. A. Marchuk, M. T. Lawton, T. Krings, M. E. Faughnan, Brain Vascular Malformation Consortium HHT Investigator Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background Approximately 10% of hereditary hemorrhagic telangiectasia (HHT) patients harbour brain vascular malformations (VMs). Intracranial hemorrhage (ICH) from brain VMs can lead to death or morbidity, while treatment options for brain V
Externí odkaz:
https://doaj.org/article/77e8d90e8c0e4c73afa7b8b9cc4b5ae5
Autor:
T, Krings, H, Kim, S, Power, J, Nelson, M E, Faughnan, W L, Young, K G, terBrugge, William L, Young
Publikováno v:
American Journal of Neuroradiology. 36:863-870
BACKGROUND AND PURPOSE: Hereditary hemorrhagic telangiectasia is an autosomal dominant disease that presents in 10%–20% of patients with various brain vascular malformations. We aimed to report the radiologic features (phenotype) and the genotype-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a5d767e0dae622c78d8b938320c33c1
https://doi.org/10.3174/ajnr.a4210
https://doi.org/10.3174/ajnr.a4210
Publikováno v:
The European respiratory journal. 38(2)
Pulmonary arteriovenous malformations (PAVMs) can cause stroke, brain abscess or life-threatening haemorrhage. Most PAVMs are associated with hereditary haemorrhagic telangiectasia (HHT). The aim of the present study was to describe the clinical pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fa39a61ebec89ef658cb2c43639a265
https://pubmed.ncbi.nlm.nih.gov/21177836
https://pubmed.ncbi.nlm.nih.gov/21177836
Publikováno v:
The European respiratory journal. 33(5)
Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder, characterised by the presence of vascular malformations. The pulmonary vascular complications of HHT include pulmonary arteriovenous malformations, pulmonary hyperten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad5724bceb67f4ea6d058876eda260e
https://pubmed.ncbi.nlm.nih.gov/19407052
https://pubmed.ncbi.nlm.nih.gov/19407052
Autor:
C L, Shovlin, A E, Guttmacher, E, Buscarini, M E, Faughnan, R H, Hyland, C J, Westermann, A D, Kjeldsen, H, Plauchu
Publikováno v:
American journal of medical genetics. 91(1)
Hereditary Hemorrhagic Telangiectasia (HHT) is easily recognized in individuals displaying the classical triad of epistaxis, telangiectasia, and a suitable family history, but the disease is more difficult to diagnosis in many patients. Serious conse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96a87c44dfeaefb445ddecb87bff9a31
https://pubmed.ncbi.nlm.nih.gov/10751092
https://pubmed.ncbi.nlm.nih.gov/10751092
Publikováno v:
Chest. 117(1)
To study the clinical characteristics and prognosis of patients with diffuse pulmonary arteriovenous malformations (AVMs).Retrospective chart review of all patients (n = 16) with diffuse pulmonary AVMs seen at Yale New Haven Hospital, Johns Hopkins H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5121e363bf346481fbcbe609a84c1d23
https://pubmed.ncbi.nlm.nih.gov/10631195
https://pubmed.ncbi.nlm.nih.gov/10631195