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Journal of Vascular and Interventional Radiology : JVIR|August 31, 2010
Percutaneous occlusion of the left subclavian and celiac arteries before or during endograft repair of thoracic and thoracoabdominal aortic aneurysms with detachable nitinol vascular plugsAshok Tholpady, Daniel E Hendricks, Ugur Bozlar, et al.
Seminars in Vascular Surgery|March 24, 2021
Fibromuscular dysplasia: A comprehensive review on evaluation and management and role for multidisciplinary comprehensive care and patient input modelKajal P Shah, Adithya Peruri, Manasa Kanneganti, et al.
Nature Communications|November 18, 2017
Methanogenesis in oxygenated soils is a substantial fraction of wetland methane emissionsJordan C Angle, Timothy H Morin, Lindsey M Solden, et al.
European Radiology|July 16, 2005
Magnetic resonance urography for the assessment of potential renal donors: comparison of the RARE technique with a low-dose gadolinium-enhanced magnetic resonance urography technique in the absence of pharmacological and mechanical interventionKlaus D Hagspiel, Sabah Butty, Kiran R Nandalur, et al.
Journal of Neurosurgery|April 9, 2013
Lateral hypothalamic area deep brain stimulation for refractory obesity: a pilot study with preliminary data on safety, body weight, and energy metabolismDonald M Whiting, Nestor D Tomycz, Julian Bailes, et al.
American Journal of Medical Genetics|December 23, 1999
Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and reviewE K Pivnick, B Angle, R A Kaufman, et al.
Current Neuropharmacology|February 20, 2025
Quantification of [11C]ABP688 Binding to mGluR5 in Human Brain using Cerebellum as Reference Region: Biological Interpretation and LimitationsMichele S Milella, Luciano Minuzzi, Chawki Benkelfat, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 17, 2011
Protection from UV-induced skin carcinogenesis by genetic inhibition of the ataxia telangiectasia and Rad3-related (ATR) kinaseMasaoki Kawasumi, Bianca Lemos, James E Bradner, et al.
Molecular Syndromology|April 20, 2013
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and MicrocephalyJ A Rosenfeld, K H Kim, B Angle, et al.
American Journal of Human Genetics|July 6, 2026
Bi-allelic variants in CDK20 cause a severe ciliopathy with midline brain and facial anomaliesGabrielle Lemire, Aren E Marshall, Tejan S Patel, et al.
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