Results 71 to 80 of about 292,283 (333)

A large, single pulmonary arteriovenous fistula presenting hours after birth [PDF]

, 2006
This article reports a case of a single, large pulmonary artery to left atrial fistula presenting within hours of birth. Symptomatic fistulas of this type are exceptionally rare in the neonatal period.
Gladstone, D.J., McBrien, Angela H., Sands, Andrew John   +2 more
core  

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia [PDF]

, 2001
BACKGROUND: Most patients with familial primary pulmonary hypertension have defects in the gene for bone morphogenetic protein receptor II (BMPR2), a member of the transforming growth factor beta (TGF-beta) superfamily of receptors. Because patients with
Alessandra Manes, Carl Atkinson, Cool CD, Cottingham RW, D'Alonzo GE, Gerald Simonneau, Ingrid Winship, James E. Loyd, Jennifer R. Thomson, Jonathan Berg, Julie McGaughran, Lisa Wheeler, Loyd JE, Makowski GS, Marc Humbert, Michael Pauciulo, Morse JH, Nazzareno Galie, Neil V. Morgan, Nicholas W. Morrell, Pietra GG, Rajiv D. Machado, Rich S, Richard C. Trembath, Whyte MK, William C. Nichols   +25 more
core   +1 more source

Arteriovenous Malformation of the Oral Cavity

Case Reports in Dentistry, 2014
Vascular anomalies are a heterogeneous group of congenital blood vessel disorders more typically referred to as birthmarks. Subcategorized into vascular tumors and malformations, each anomaly is characterized by specific morphology, pathophysiology ...
S. Manjunath, S. Shetty, N. Moon, Bhushan Sharma, K. Metta, N. Gupta, S. Goyal, Simranjit Singh   +7 more
semanticscholar   +1 more source

Coordinated expression of BMP10/ALK1/endoglin—proteins that drive embryonic cardiac and vascular morphogenesis—in patients with heart failure: The EMPEROR Program

European Journal of Heart Failure, EarlyView.
Aims Bone morphogenetic protein 10 (BMP10), activin receptor‐like kinase 1 (ALK1) and endoglin form a single transforming growth factor‐β family signalling complex that is the principal driver of cardiac and vascular morphogenesis and maturation during hypoxic embryonic development. These proteins are down‐regulated with the onset of normoxia at birth,
Milton Packer, Javed Butler, João Pedro Ferreira, Tariq Jamal Siddiqi, James L. Januzzi Jr, Naveed Sattar, Sandra González Maldonado, Marina Panova‐Noeva, Jürgen H. Prochaska, Mikhail Sumin, Serge Masson, Stuart J. Pocock, Gerasimos Filippatos, Stefan D. Anker, Faiez Zannad   +14 more
wiley   +1 more source

RASA1 Mutations and Associated Phenotypes in 68 Families with Capillary Malformation–Arteriovenous Malformation

Human Mutation, 2013
Capillary malformation–arteriovenous malformation (CM–AVM) is an autosomal‐dominant disorder, caused by heterozygous RASA1 mutations, and manifesting multifocal CMs and high risk for fast‐flow lesions.
N. Revencu, L. Boon, A. Mendola, M. Cordisco, J. Dubois, P. Clapuyt, F. Hammer, David J. Amor, A. Irvine, E. Baselga, A. Dompmartin, S. Syed, A. Martín-Santiago, L. Adès, F. Collins, Janine M. Smith, S. Sandaradura, V. Barrio, P. Burrows, F. Blei, M. Cozzolino, N. Brunetti‐Pierri, A. Vicente, M. Abramowicz, J. Désir, C. Vilain, W. Chung, Ashley Wilson, C. Gardiner, Y. Dwight, D. Lord, L. Fishman, C. Cytrynbaum, S. Chamlin, F. Ghali, Y. Gilaberte, S. Joss, M. D. C. Boente, C. Léauté-Labrèze, M. Delrue, Susan J. Bayliss, L. Martorell, M. González-Enseñat, J. Mazereeuw-Hautier, B. O'Donnell, D. Bessis, R. Pyeritz, A. Salhi, O. T. Tan, O. Wargon, J. Mulliken, M. Vikkula   +51 more
semanticscholar   +1 more source

Novel planning pipeline utilizing the Surgical Theater system for pediatric epilepsy surgery

Epilepsia Open, EarlyView.
Abstract Objective Advances in the analysis and collation of radiographic datasets have enhanced presurgical planning for various neurosurgical procedures, including clipping of cerebral aneurysms, surgical resection of tumors, and arteriovenous malformation management.
Lisa B. E. Shields, Hunain Abri, Cemal Karakas, Shannon D. Davis, Ian S. Mutchnick   +4 more
wiley   +1 more source

Diagnosis and treatment of hereditary hemorrhagic telangiectasia in a pediatric patient with chronic cyanosis. [PDF]

, 2016
Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder of vascular dysplasias that is characterized by mucocutaneous telangiectasias, gastrointestinal tract bleeding, and arteriovenous malformations (AVMs) of the ...
Johnson, B. V., Johnston, Thomas
core  

Pediatric intracranial dural arteriovenous fistulas: age-related differences in clinical features, angioarchitecture, and treatment outcomes. [PDF]

, 2016
OBJECTIVE Intracranial dural arteriovenous fistulas (DAVFs) are rare in children. This study sought to better characterize DAVF presentation, angioarchitecture, and treatment outcomes.
Amans, Matthew R, Cooke, Daniel L, Dowd, Christopher F, Fullerton, Heather J, Halbach, Van V, Hetts, Steven W, Higashida, Randall T, Maluste, Neil, Moftakhar, Parham   +8 more
core   +1 more source

From multi‐omics to precision medicine in intracranial aneurysm: Biomarker discovery and multimodal integration

Interdisciplinary Medicine, EarlyView.
This review explores intracranial aneurysm biomarker discovery through multi‐omics. It reveals key genes, proteins, and metabolites, and shows how machine‐learning‐based multi‐modal integration may aid diagnosis and treatment. Abstract Despite extensive research, currently, no biomarkers are available for clinical use in intracranial aneurysm (IA ...
Jiaxin Zhang, Yufei Yang, Bingxu Chen, Yanmeng Zhao, Haitao Sun   +4 more
wiley   +1 more source

Angioneogenese in cerebralen Arteriovernösen Malformationen [PDF]

, 2004
Arteriovenöse Malformationen werden in der Literatur meistens als angeborene und statische Gefäßmissbildungen beschrieben. Neuere Arbeiten und Erkenntnisse legen jedoch eine dynamische Biologie dieser Malformationen nahe.
Battenberg, Elmar, Sure, U. (PD Dr. med.)   +1 more
core   +1 more source