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Journal of Clinical Medicine|April 23, 2022
Non-Invasive Assessment of Arterial Stiffness: Pulse Wave Velocity, Pulse Wave Analysis and Carotid Cross-Sectional Distensibility: Comparison between MethodsPaolo Salvi, Filippo Valbusa, Anna Kearney-Schwartz, et al.
Frontiers in Neurology|March 10, 2015
Salicylate-induced hearing loss and gap detection deficits in ratsKelly E Radziwon, Daniel J Stolzberg, Maxwell E Urban, et al.
Cureus|September 13, 2021
Testosterone Replacement Therapy in Hypogonadal Men and Myocardial Infarction Risk: Systematic Review & Meta-AnalysisJun Hee Lee, Prutha H Shah, Davuluri Uma, et al.
Eye (London, England)|June 20, 2020
Optic nerve sheath fenestration via a supero-medial eyelid skin crease approach for the treatment of idiopathic intracranial hypertension in a UK populationJ M Jefferis, R A Littlewood, I M Pepper, et al.
The American Journal of Emergency Medicine|May 1, 2021
Predictors of readmission requiring hospitalization after discharge from emergency departments in patients with COVID-19Vincenzo G Menditto, Francesca Fulgenzi, Martina Bonifazi, et al.
Clinical Implant Dentistry and Related Research|September 10, 2023
Long-term treatment outcomes of single maxillary buccal peri-implant soft tissue dehiscences: A 10-year prospective studyAndrea Roccuzzo, Leonardo Mancini, Crystal Marruganti, et al.
Trends in Plant Science|February 24, 2024
Genetic regulation of the root angle in cerealsGwendolyn K Kirschner, Frank Hochholdinger, Silvio Salvi, et al.
Scientific Reports|May 21, 2026
A multi-level attention CNN-transformer based framework for the detection of brain tumor using regional dual-score explainabilityAryaman Kaprekar, Anjan Gudigar, U Raghavendra, et al.
International Journal of Molecular Sciences|December 11, 2022
N-Linked Glycosylation in Chinese Hamster Ovary Cells Is Critical for Insulin-like Growth Factor 1 SignalingRupashree Salvi, Chandan Kumar, Krupanshi Brahmbhatt, et al.
American Journal of Medical Genetics|May 30, 1998
Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosisM C Patrosso, F Salvi, D De Grandis, et al.
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