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Thorax|June 10, 2022
Ultra-low-dose CT versus chest X-ray for patients suspected of pulmonary disease at the emergency department: a multicentre randomised clinical trialInge A H van den Berk, Maadrika M N P Kanglie, Tjitske S R van Engelen, et al.Journal of Neuromuscular Diseases|May 26, 2019
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic ServiceDineke Westra, Meyke I Schouten, Bas C Stunnenberg, et al.American Journal of Obstetrics and Gynecology|November 20, 2022
Sexual functioning more than 15 years after premenopausal risk-reducing salpingo-oophorectomyLara Terra, Maarten J Beekman, Ellen G Engelhardt, et al.Nature Genetics|May 28, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16Heather J Cordell, Jamie Bentham, Ana Topf, et al.Physical Review Letters|May 2, 2015
Evidence of lensing of the cosmic microwave background by dark matter halosMathew Madhavacheril, Neelima Sehgal, Rupert Allison, et al.Neurology|August 4, 2017
Clinical phenotype and outcome of hepatitis E virus-associated neuralgic amyotrophyJeroen J J van Eijk, Harry R Dalton, Paolo Ripellino, et al.Circulation. Cardiovascular Genetics|July 24, 2013
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controlsChrysovalanto Mamasoula, R Reid Prentice, Tomasz Pierscionek, et al.The Journal of Clinical Investigation|November 1, 2019
KBTBD13 is an actin-binding protein that modulates muscle kineticsJosine M de Winter, Joery P Molenaar, Michaela Yuen, et al.BJOG : an International Journal of Obstetrics and Gynaecology|January 30, 2023
Long-term effects of premenopausal risk-reducing salpingo-oophorectomy on cognition in women with high familial risk of ovarian cancer: A cross-sectional studyLara Terra, Philippe R Lee Meeuw Kjoe, Joost A Agelink van Rentergem, et al.Brain : a Journal of Neurology|August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.Pageof 84