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Cell Death & Disease|November 21, 2022
Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndromeElisa Maria Turco, Angela Maria Giada Giovenale, Laura Sireno, et al.
World Neurosurgery|December 1, 2018
A Survey on Pituitary Surgery in ItalyDomenico Solari, Francesco Zenga, Filippo F Angileri, et al.
Circulation|October 22, 2025
Advanced Life Support: 2025 International Liaison Committee on Resuscitation Consensus on Science With Treatment RecommendationsIan R Drennan, Katherine M Berg, Bernd W Böttiger, et al.
Science Bulletin|December 22, 2022
Global wood anatomical perspective on the onset of the Late Antique Little Ice Age (LALIA) in the mid-6th century CEUlf Büntgen, Alan Crivellaro, Dominique Arseneault, et al.
Genes|September 28, 2023
Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in <i>CHD3</i> and Literature ReviewPatricia Pascual, Jair Tenorio-Castano, Cyril Mignot, et al.
Neurology. Genetics|February 12, 2020
Clinical spectrum of POLR3-related leukodystrophy caused by biallelic <i>POLR1C</i> pathogenic variantsLaurence Gauquelin, Ferdy K Cayami, László Sztriha, et al.
Resuscitation|October 21, 2025
Advanced Life Support: 2025 International Liaison Committee on Resuscitation Consensus on Science With Treatment RecommendationsIan R Drennan, Katherine M Berg, Bernd W Böttiger, et al.
Seizure|April 8, 2021
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European studyFederico Raviglione, Sofia Douzgou, Marcello Scala, et al.
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