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Military Medicine|March 15, 2003
Sentinel cases of community-acquired methicillin-resistant Staphylococcus aureus onboard a naval shipJames E LaMar, Russell B Carr, Craig Zinderman, et al.
Journal of National Black Nurses' Association : JNBNA|September 16, 2015
A Postpartum Community-Based Weight Management Intervention Designed for Low-Income Women: Feasibility and Initial Efficacy TestingDiane Berry, Sarah Verbiest, Emily Gail Hall, et al.
Journal of the American College of Emergency Physicians Open|December 16, 2025
Trends and Predictors of Emergency Department Outcomes in Atrial Fibrillation: A Statewide Analysis from North Carolina-2016 to 2023Shantanu Srivatsa, Parsa Pazooki, Benjamin K Lau, et al.
European Journal of Medical Genetics|March 6, 2019
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disordersElena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 30, 2022
Biallelic variants in CENPF causing a phenotype distinct from Strømme syndromeGerarda Cappuccio, Simona Brillante, Roberta Tammaro, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2024
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42NDLeila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
European Journal of Human Genetics : EJHG|May 15, 2023
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individualsHenrike L Sczakiel, Max Zhao, Brigitte Wollert-Wulf, et al.
Brain : a Journal of Neurology|June 8, 2022
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasisRenzo Guerrini, Davide Mei, Katalin Kerti-Szigeti, et al.
Nature Communications|May 8, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorderSukhleen Kour, Deepa S Rajan, Tyler R Fortuna, et al.
European Journal of Human Genetics : EJHG|October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlationsAngela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
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