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Clinical Chemistry and Laboratory Medicine|October 7, 2020
IFCC Interim Guidelines on Biochemical/Hematological Monitoring of COVID-19 PatientsSimon Thompson, Mary Kathryn Bohn, Nicasio Mancini, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2011
Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literatureCsaba Siffel, Adolfo Correa, Emmanuelle Amar, et al.
Iscience|March 8, 2021
Moray eels are more common on coral reefs subject to higher human pressure in the greater CaribbeanGina M Clementi, Judith Bakker, Kathryn I Flowers, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2011
Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and ResearchOsvaldo M Mutchinick, Leonora Luna-Muñoz, Emmanuelle Amar, et al.
Cell Death & Disease|April 8, 2025
The SIRT1 activator SRT2104 exerts exercise mimetic effects and promotes Duchenne muscular dystrophy recoveryMatteo Giovarelli, Silvia Zecchini, Silvia Rosanna Casati, et al.
Heart, Lung and Vessels|July 16, 2014
Early molecular diagnosis of aspergillosis in a patient with acute myeloid leukaemiaR Greco, N Mancini, J Peccatori, et al.
European Journal of Human Genetics : EJHG|August 21, 2014
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndromeAlma Kuechler, Alexander M Zink, Thomas Wieland, et al.
Free Radical Biology & Medicine|September 26, 2024
Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signalingDavide Cervia, Silvia Zecchini, Luca Pincigher, et al.
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