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The Journal of Clinical Endocrinology and Metabolism|July 25, 2014
Maternal perchlorate levels in women with borderline thyroid function during pregnancy and the cognitive development of their offspring: data from the Controlled Antenatal Thyroid StudyPeter N Taylor, Onyebuchi E Okosieme, Rhian Murphy, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|March 24, 2021
Nerve transfer for restoration of lower motor neuron-lesioned bladder function. Part 1: attenuation of purinergic bladder smooth muscle contractionsNagat Frara, Dania Giaddui, Alan S Braverman, et al.
Molecular Genetics and Metabolism|May 27, 2003
Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trapS Harvey Mudd, Nancy Braverman, Martin Pomper, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 9, 2022
Neurological event rates and associated risk factors in acute type B aortic dissections treated by thoracic aortic endovascular repairBenedikt Reutersberg, Thomas Gleason, Nimesh Desai, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Advanced Functional Materials|August 2, 2021
Surface engineered polymersomes for enhanced modulation of dendritic cells during cardiovascular immunotherapySijia Yi, Xiaohan Zhang, Hussain Sangji, et al.
Molecular Neurobiology|February 29, 2012
Neuropsychopharmacology and neurogenetic aspects of executive functioning: should reward gene polymorphisms constitute a diagnostic tool to identify individuals at risk for impaired judgment?Abdalla Bowirrat, Thomas J H Chen, Marlene Oscar-Berman, et al.
American Heart Journal|June 7, 2016
Shock complicating type A acute aortic dissection: Clinical correlates, management, and outcomesEduardo Bossone, Reed E Pyeritz, Alan C Braverman, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Altered oscillatory coupling reflects possible inhibitory interneuron dysfunction in Rett syndromeDevorah Kranz, Yael Braverman, Michelle McCarthy, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
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