Results 121 to 130 of about 654,931 (251)

Pulmonary arteriovenous malformations in children with hereditary hemorrhagic telangiectasia: a longitudinal study

Pulmonary Circulation, 2018
Pulmonary arteriovenous malformations (PAVMs) often occur in children with hereditary hemorrhagic telangiectasia (HHT). A 14-year longitudinal study of PAVMs in children with HHT was undertaken to assess the prevalence, the clinical impact, and ...
Katie L. Mowers, L. Sekarski, Andrew J. White, R. Grady   +3 more
semanticscholar   +1 more source

Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia. [PDF]

, 2003
BACKGROUND\ud \ud Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).
Flanagan, J A, Gruenig, E, Sankelo, M, Halme, M, Elliott, C G, Laitinen, T, Morrell, N W, Trembath, R C, Räisänen-Sokolowski, A, Olschewski, H, Harrison, R E, Robbins, I M, Kermeen, F, Abdalla, S A, Rowell, J, Machado, R D, McLaughlin, V   +16 more
core   +1 more source

Detachable coiling for embolotherapy of high-flow pulmonary arteriovenous malformation: case report and review of the literature

Journal of the Belgian Society of Radiology, 2010
Pulmonary arteriovenous malformations (PAVMs) are very rare anomalies of the lung parenchyma. Although many patients are asymptomatic, it carries a high risk of severe cerebral complications, and rarely fatal outcome due to rupture of the malformation ...
M Laureys, P Mendes da Costa, L Divano
doaj   +1 more source

Giant pulmonary arteriovenous malformations

Case Reports in Clinical Practice, 2016
No ...
Farnoosh Larti, Soheil Peiman, Shima Molaee, Morteza Foroumandi   +3 more
doaj  

Pulmonary Arteriovenous Malformation can be Associated with Embolic Stroke of Undetermined Source (ESUS)

European Journal of Case Reports in Internal Medicine, 2019
Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies. Alternative designations are pulmonary arteriovenous fistulae or aneurysms. Although mostly asymptomatic, PAVMs can cause respiratory symptoms due to right-to-left shunt.
Mariana Barros Cruz, Nuno Palma, Joao Rocha, Ricardo Meireles   +3 more
doaj   +1 more source

Pulmonary Arteriovenous Malformations and Cerebral Abscess Recurrence in a Child With Hereditary Hemorrhagic Telangiectasia.

, 2015
BACKGROUND: A 17-year-old boy was referred to our center with a history of brain abscess (BA) recurring after 9 years. The patient reported 2 previous treatments for pulmonary arteriovenous malformations, sporadic nosebleeds, and familial history for ...
GIORDANO, Paola, Lastella P, Attolini E, FIORELLA, Maria Luisa, Sangerardi M, Suppressa P, SABBA', Carlo, Valente F, Lenato GM   +8 more
core   +1 more source

Usefulness of Hydrogel-Coated Coils in Embolization of Pulmonary Arteriovenous Malformations

Cardiovascular and Interventional Radiology, 2018
PurposeTo evaluate the usefulness of hydrogel-coated coils for preventing recanalization after coil embolization of pulmonary arteriovenous malformations (PAVMs).Materials and MethodsThirty-seven consecutive patients with 57 untreated PAVMs underwent ...
M. Shimohira, T. Kawai, Takuya Hashizume, M. Muto, M. Kitase, Y. Shibamoto   +5 more
semanticscholar   +1 more source

Long-Term Follow-up After Embolization of Pulmonary Arteriovenous Malformations with Detachable Silicone Balloons

, 2008
Long-term follow-up results after embolization of 13 pulmonary arteriovenous malformations in 10 patients by use of 14 detachable silicone balloons are given. Patients were followed for a mean of 99 months (range, 63-123 months) with chest x-rays and for
Andersen, Poul Erik, Kjeldsen, Anette D; id_orcid   +1 more
core   +1 more source

Pulmonary Arteriovenous Malformations: an uncharacterized phenotype of Dyskeratosis Congenita and related Telomere Biology Disorders

European Respiratory Journal, 2017
The telomere biology disorder (TBD) dyskeratosis congenita (DC) is a multisystem inherited bone marrow failure syndrome and cancer predisposition syndrome caused by germline mutations in telomere biology genes (DKC1, TINF2, TERC, TERT, NOP10, NHP2, CTC1,
Payal P. Khincha, A. Bertuch, Suneet Agarwal, D. Townsley, N. Young, S. Keel, A. Shimamura, F. Boulad, T. Simoneau, H. Justino, Christin S. Kuo, S. Artandi, Charles A. McCaslin, D. Cox, S. Chaffee, B. Collins, N. Giri, B. Alter, G. Raghu, S. Savage   +19 more
semanticscholar   +1 more source

Novel approach to complex pulmonary arteriovenous malformation embolization using detachable coils and Amplatzer vascular plugs

, 2012
We evaluated the feasibility of a modified embolization technique of pulmonary arteriovenous malformations (PAVM) using venous sac embolization with detachable coils combined with the feeding artery embolization with the Amplatzer vascular plug (AVP)
Steinbach, Silke, Hundt, Walter, Kalinowski, Mark, Klose, Klaus Jochen, Burbelko, Mykhaylo, Kiessling, Andreas, Heverhagen, Johannes T, Eivazi, Behfar, Werner, Jochen   +8 more
core   +1 more source