Showing results (81-90 of 411) with videos related to

Sort By:
Pageof 42
Archives of Gerontology and Geriatrics|May 22, 2007
Cross-sectional observations of thyroid function in geriatric Mexican outpatients with and without dementiaLilia Cárdenas-Ibarra, José A Solano-Velázquez, Ricardo Salinas-Martínez, et al.
Revista De Neurologia|December 31, 2004
[A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain]M Raspall-Chaure, A Solano, E Vázquez, et al.
Journal of Helminthology|December 22, 2025
Cylicospirura wishkai sp. nov. (Spiruroidea: Spirocercidae), a new nematode species in the neotropical felid jaguarundi, Herpailurus yagouaroundi (Carnivora: Felidae)A Rojas, L M Romero-Vega, A Conejo-Chacón, et al.
European Journal of Biochemistry|September 24, 1998
An adrenocorticotropin-regulated phosphoprotein intermediary in steroid synthesis is similar to an acyl-CoA thioesterase enzymeC Finkielstein, P Maloberti, C F Mendez, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 2, 2021
Nitrous oxide versus lidocaine versus no analgesic for in-office hysteroscopy: a randomised clinical trialJ A Solano Calvo, C Del Valle Rubido, A Rodríguez-Miguel, et al.
Psicothema|October 21, 2022
Development and Validation of SERR Scale for Detecting Extremism and Religious RadicalismRodolfo Ramos-Álvarez, Maili Kapp, Amanda Clinton, et al.
Molecules (Basel, Switzerland)|May 20, 2020
Synthesis of Chitosan Beads Incorporating Graphene Oxide/Titanium Dioxide Nanoparticles for In Vivo StudiesCarlos David Grande Tovar, Jorge Iván Castro, Carlos Humberto Valencia, et al.
Journal of Medical Genetics|January 7, 2009
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated proteinE López-Gallardo, A Solano, M D Herrero-Martín, et al.
Revista De Neurologia|June 18, 2004
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin]M Pineda, A Playán-Ariso, M J Alcaine-Villarroya, et al.
Revista De Neurologia|December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]L Coelho-Miranda, A Playan, R Artuch, et al.
Pageof 42