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Journal of Parkinson'S Disease|July 26, 2014
In a rush to decide: deep brain stimulation and dopamine agonist therapy in Parkinson's diseaseAtbin Djamshidian, Sean S O'Sullivan, Alessandro Tomassini, et al.
Cancer|June 6, 2025
Racial and ethnic variation in body composition and prognosis of nonmetastatic breast cancerIjeamaka A Fumagalli, Erica T Warner, Adana A M Llanos, et al.
Breast Cancer Research and Treatment|July 25, 2016
Impact of race, ethnicity, and BMI on achievement of pathologic complete response following neoadjuvant chemotherapy for breast cancer: a pooled analysis of four prospective Alliance clinical trials (A151426)Erica T Warner, Karla V Ballman, Carrie Strand, et al.
Brain Research|July 29, 2018
Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson's disease brains with Lewy body pathologyAdamantios Mamais, Claudia Manzoni, Iqra Nazish, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.
Neurology|May 17, 2024
Neuropathologic Validation and Diagnostic Accuracy of Presynaptic Dopaminergic Imaging in the Diagnosis of ParkinsonismAlexandra Hastings, Patrick Cullinane, Sarah Wrigley, et al.
Cancer Research|August 18, 2016
Plasma 25-Hydroxyvitamin D and Risk of Breast Cancer in Women Followed over 20 YearsA Heather Eliassen, Erica T Warner, Bernard Rosner, et al.
The Journal of Extra-Corporeal Technology|February 6, 2023
COVID-19 and Blood Clots: A Report of Massive Pulmonary Embolism in COVID-19 Patient Supported on Veno-Venous ECMO and the Utility of ThrombolysisBindu Akkanti, Joseph Zwischenberger, Mark T Warner, et al.
Acta Neuropathologica|July 12, 2024
DNA methylation patterns in the frontal lobe white matter of multiple system atrophy, Parkinson's disease, and progressive supranuclear palsy: a cross-comparative investigationMegha Murthy, Katherine Fodder, Yasuo Miki, et al.
Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
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