Results 21 to 30 of about 588,958 (162)

Ischaemic strokes in patients with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia: associations with iron deficiency and platelets. [PDF]

, 2014
25/03/14 meb. OA paper , Ok to add.Background: Pulmonary first pass filtration of particles marginally exceeding ~7 µm (the size of a red blood cell) is used routinely in diagnostics, and allows cellular aggregates forming or entering the circulation in ...
John A Livesey, Michael A. Laffan (367175), Tighe Hannah C., Richard Manning (524799), James E Jackson, James E. Jackson (524802), Gillian Angus, Tighe, HC, Meek John, Jackson James E., Gillian Angus (367169), Claire L Shovlin, Livesey, J, Basel Chamali (524796), John A. Livesey (524798), Hannah C. Tighe (524801), Laffan, MA, Basel Chamali, Vatshalan Santhirapala (524797), Jackson, JE, Meek, J, Chamali Basel, Manning Richard, Chamali, B, Michael A Laffan, Hannah C Tighe, Claire L. Shovlin (367168), Manning, R, Livesey John A., Shovlin, CL, Angus Gillian, Santhirapala, V, Santhirapala Vatshalan, John Meek, Shovlin Claire L., Vatshalan Santhirapala, Richard Manning, Laffan Michael A., John Meek (524800)   +38 more
core   +1 more source

Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia

JACC: Case Reports, 2020
This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as ...
Gabriel Sánchez-Fernández, MD, Fernando García-López, MD, Isaac Martínez-Bendayán, MD, PhD, María José Bello-Peón, MD, Raquel Marzoa-Rivas, MD, PhD   +4 more
doaj   +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

Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformations. [PDF]

, 2014
01/04/14 MEB.
Hannah C Tighe, Tighe Hannah C., Williams Louisa C., James E Jackson, Shovlin, CL, Santhirapala, V, Santhirapala Vatshalan, Williams, LC, Tighe, HC, Jackson James E., Claire L Shovlin, Shovlin Claire L., Vatshalan Santhirapala, Jackson, JE, Louisa C Williams   +14 more
core   +1 more source

Pulmonary arteriovenous malformation: Case report [PDF]

Vojnosanitetski Pregled, 2021
Introduction. Pulmonary arteriovenous malformation (PAVM) is pathological communication between pulmonary artery and pulmonary vein, in way that it shunts normal alveolar capillary membrane resulting in inadequate blood oxygenation in this part of the ...
Sekulić Igor, Sagić Dragan, Rusović Siniša, Dulović Dragan, Pasovski Viktor, Bošković-Sekulić Jelena, Rančić Nemanja, Stevanović Jelena, Raičević Ranko   +8 more
doaj   +1 more source

Successful treatment of bilateral multiple pulmonary arteriovenous malformations in a patient with brain abscess and severe hypoxemia using a combination of transcatheter embolotherapy and surgical resection: a case report

Journal of Cardiothoracic Surgery, 2021
Background A pulmonary arteriovenous malformation is an abnormal dilated blood vessel that makes direct communication between a pulmonary artery and pulmonary vein and can be associated with hypoxemia or neurological complications, including brain ...
Takahiro Ochi, Masako Chiyo, Takamasa Ito, Hideharu Furumoto, Toshihiko Sugiura, Yukio Saitoh   +5 more
doaj   +1 more source

Pulmonary arteriovenous malformation causing lung sequestration and media infarction: a case report [PDF]

Frontiers in Medicine
Mark Kriegsmann, Raffaella Griffo
exaly   +2 more sources

Pulmonary Arteriovenous Malformations in a 18-months-old Child: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2022
Pulmonary Arteriovenous Malformation (PAVM) is a cardiovascular anomaly in which an anatomic communication between the pulmonary artery and pulmonary vein is formed, resulting in an additional cardiac shunt from right to left side.
Hesham Mohamad Fayad, Fatema Chowdhury, Godfred Antony Menezes, Shria Sadhu, Samiha Anjum Hossain   +4 more
doaj   +1 more source

Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report

Clinical Case Reports, 2022
Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat Ramanandafy, Finaritra Princy Parfait Andriamahenina, Michel Harison Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Razafimpihanina, Diamondra Andriarimanga, Jean Noêl Solohery Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana   +10 more
doaj   +1 more source

Impact of pulmonary arteriovenous malformations on respiratory-related quality of life in patients with hereditary haemorrhagic telangiectasia.

PLoS ONE, 2014
Fifteen to fifty percent of patients with hereditary haemorrhagic telangiectasia have pulmonary arteriovenous malformations. The objective of this study was to measure the effect of the presence of pulmonary arteriovenous malformations and of their ...
Sandra Blivet, Daniel Cobarzan, Alain Beauchet, Mostafa El Hajjam, Pascal Lacombe, Thierry Chinet   +5 more
doaj   +1 more source