Showing results (471-480 of 628) with videos related to
Sort By:
Pageof 63
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|February 11, 2017
Region-specific vulnerability to lipid peroxidation and evidence of neuronal mechanisms for polyunsaturated fatty acid biosynthesis in the healthy adult human central nervous systemAlba Naudí, Rosanna Cabré, Mayelin Dominguez-Gonzalez, et al.Diabetologia|February 11, 2012
Delaying progression to type 2 diabetes among high-risk Spanish individuals is feasible in real-life primary healthcare settings using intensive lifestyle interventionB Costa, F Barrio, J-J Cabré, et al.BMC Public Health|November 15, 2011
Effectiveness of a structured motivational intervention including smoking cessation advice and spirometry information in the primary care setting: the ESPITAP studyFrancisco Martin-Lujan, Josep L I Piñol-Moreso, Nuria Martin-Vergara, et al.Free Radical Biology & Medicine|December 17, 2016
Sixty years old is the breakpoint of human frontal cortex agingRosanna Cabré, Alba Naudí, Mayelin Dominguez-Gonzalez, et al.Journal of Inflammation Research|February 10, 2025
Inflammatory and Redox Blood Gene Expression Fingerprint of Severe Obstructive Sleep Apnoea in Patients With Mild Alzheimer's DiseaseLeila Romero-ElKhayat, Farida Dakterzada, Raquel Huerto, et al.Frontiers in Aging Neuroscience|October 27, 2025
Clinical validation of a plasma-based antibody-free LC-MS method for identifying CSF amyloid positivity in mild cognitive impairmentJosé Antonio Allué, Leticia Sarasa, Noelia Fandos, et al.Revista De Neurologia|July 28, 2005
[Differential diagnosis of intracranial calcifications]G Piñol-Ripoll, J A Mauri-Llerda, I de la Puerta Martínez-Miró, et al.Journal of Neuropathology and Experimental Neurology|August 16, 2012
Phenotypic variability within the inclusion body spectrum of basophilic inclusion body disease and neuronal intermediate filament inclusion disease in frontotemporal lobar degenerations with FUS-positive inclusionsEllen Gelpi, Albert Lladó, Jordi Clarimón, et al.Frontiers in Cell and Developmental Biology|July 24, 2024
Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophyEsther Fernández-Simón, Patricia Piñol-Jurado, Rasya Gokul-Nath, et al.Journal of Inherited Metabolic Disease|January 10, 2024
Tetrahydrobiopterin (BH4) treatment stabilizes tyrosine hydroxylase: Rescue of tyrosine hydroxylase deficiency phenotypes in human neurons and in a knock-in mouse modelKunwar Jung-Kc, Alba Tristán-Noguero, Altanchimeg Altankhuyag, et al.Pageof 63