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Clinical Orthopaedics and Related Research|November 21, 2024
Robotic Assistance Is Not Associated With Decreased Early Revisions in Cementless TKA: An Analysis of the American Joint Replacement RegistryGregory J Kirchner, Jeffrey B Stambough, Emily Jimenez, et al.
Frontiers in Microbiology|November 7, 2024
Use of transcriptomics and genomics to assess the effect of disinfectant exposure on the survival and resistance of Escherichia coli O157:H7, a human pathogenMiranda Kirchner, Javier Nunez-Garcia, Nicholas Duggett, et al.
Journal of Cardiothoracic Surgery|November 3, 2024
Atrial appendage closure is associated with increased risk for postoperative atrial fibrillationJeffrey H Shuhaiber, Mostafa Abbas, Thomas Morland, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 27, 2024
Endoplasmic Reticulum and Mitochondrial Calcium Handling Dynamically Shape Slow Afterhyperpolarizations in Vasopressin Magnocellular NeuronsMatthew K Kirchner, Ferdinand Althammer, Elba Campos-Lira, et al.
European Journal of Human Genetics : EJHG|April 18, 2006
Sequence variations in the 5' upstream regions of the FBN1 gene associated with Marfan syndromeKrishna Kumar Singh, Praphulla Chandra Shukla, Kathrin Rommel, et al.
International Journal of Nephrology and Renovascular Disease|December 4, 2012
Death and cardiovascular events after bacteriuria among adult women with chronic kidney diseaseSusmitha Dhanyamraju, Michael A Foltzer, Xiaoqin Tang, et al.
Klinische Padiatrie|September 1, 1992
[The anion gap--screening for hyperlactatemia in critically ill children?]C Aufricht, M Ties, I Hartl, et al.
Indoor Air|May 6, 2017
Perceived indoor air quality and its relationship to air pollutants in French dwellingsS Langer, O Ramalho, E Le Ponner, et al.
Nature Communications|August 6, 2020
Daylight space debris laser rangingMichael A Steindorfer, Georg Kirchner, Franz Koidl, et al.
Neuroradiology|February 20, 2009
Performance of a new quantitative method for assessing dural ectasia in patients with FBN1 mutations and clinical features of Marfan syndromeBahar Söylen, Kerstin Hinz, Jana Prokein, et al.
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