Joshua Kriger

Correlating the Bethesda System for Reporting Thyroid Cytopathology with Histology and Extent of Surgery: A Review of 21,746 Patients from Four Endocrine Surgery Registries Across Two Continents

W. Inabnet, G. Doherty, J. Sosa, 2020, World Journal of Surgery.

Preprocedural Ultrasound for Infant Lumbar Puncture: A Randomized Clinical Trial

P. Dayan, D. Kessler, V. Pahalyants, 2018, Academic emergency medicine : official journal of the Society for Academic Emergency Medicine.

Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapy.

S. Dimauro, John L.P. Thompson, D. Egli, 2016, Human reproduction.

Retrospective natural history of thymidine kinase 2 deficiency

Robert W. Taylor, S. Dimauro, P. Chinnery, 2018, Journal of Medical Genetics.

Optimal Volume of Administration of Intranasal Midazolam in Children: A Randomized Clinical Trial

P. Dayan, B. Levin, John Babineau, 2017, Annals of emergency medicine.

Mitochondrial diseases in North America

Marni J. Falk, Kathryn M. Camp, J. Ganesh, 2020, Neurology: Genetics.

Prevalence of and Risk Factors for Intracranial Abnormalities in Unprovoked Seizures

W. Hauser, P. Dayan, G. Conners, 2015, Pediatrics.

Predictors of Low Weight and Tube Feedings in Children With Congenital Diaphragmatic Hernia at 1 Year of Age

J. Wynn, G. Aspelund, U. Krishnan, 2014, Journal of pediatric gastroenterology and nutrition.

Use of High-Sensitivity Troponin T to Identify Patients With Acute Heart Failure at Lower Risk for Adverse Outcomes: An Exploratory Analysis From the RELAX-AHF Trial.

P. Ponikowski, G. Filippatos, G. Felker, 2016, JACC. Heart failure.

Mitochondrial disease patients' perception of dietary supplements' use.

S. Parikh, M. Hirano, A. Karaa, 2016, Molecular genetics and metabolism.