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Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko|March 23, 2019
[Secondary spondylogenic epidural abscess]A Yu Bazarov, K S Sergeev, V M Osintsev, et al.Biomeditsinskaia Khimiia|May 16, 2015
[The possibility of using PlasmaDeepDive™ MRM panel in clinical diagnostics]Iu V Miroshnichenko, N A Petushkova, N E Moskaleva, et al.Voprosy Onkologii|May 29, 2015
[Complications and effectiveness of treatment of patients with locally advanced prostate cancer after combined radiotherapy and radical prostatectomy with postoperative radiotherapy]V A Solodky, A Yu Pavlov, G A Panshin, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 9, 2025
[The effect of psychopharmacological load on various aspects of the condition in patients with depressive syndrome during remission]M A Morozova, E Yu Nikonova, G Ch Ashurova, et al.Bulletin of Experimental Biology and Medicine|September 15, 2012
Assessment of intramural blood flow and neurogenic control in intact and hypertrophic urinary bladder with harmonic analysis of bioimpedance in ratsV I Kirpatovsky, I S Mudraya, S V Revenko, et al.Voprosy Pitaniia|August 14, 2020
[Evaluating the efficacy of diet therapy with protein component modification at Wilson disease]A Yu Baranovsky, A S Belodedova, T F Fedorova, et al.Vestnik Oftalmologii|April 21, 2021
[Change of transcription level of photoreceptor-specific CRX gene in the peripheral blood of the participants of an arctic world oceanic international flight]S G Gorokhova, O Yu Atkov, A Yu Gorbachev, et al.Bulletin of Experimental Biology and Medicine|July 19, 2025
Analysis of Lysyl Oxidase Expression and Vascular Bed in Human Uveal MelanomaA Yu Shatruk, N P Bgatova, N V Kononova, et al.Bulletin of Experimental Biology and Medicine|July 3, 2024
Correlation between the Colony Phenotype and Amino Acid Sequence of the Variable Vaa Antigen in Clinical Isolates of Mycoplasma hominisM A Galyamina, K V Sikamov, D R Urazaeva, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 29, 2024
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation]G E Rudenskaya, D M Guseva, O L Shatokhina, et al.Pageof 275