Episodic memory effects of gamma frequency precuneus transcranial magnetic stimulation in Alzheimer's disease: A randomized multiple baseline study.


Journal

Journal of neuropsychology
ISSN: 1748-6653
Titre abrégé: J Neuropsychol
Pays: England
ID NLM: 101468753

Informations de publication

Date de publication:
06 2023
Historique:
revised: 05 10 2022
received: 25 09 2020
accepted: 18 10 2022
medline: 9 6 2023
pubmed: 10 11 2022
entrez: 9 11 2022
Statut: ppublish

Résumé

Episodic memory decline is the prominent neuropsychological feature of typical Alzheimer's Disease (AD), for which current treatments have a limited clinical response. Recently, gamma entrainment therapy has been used as a non-invasive treatment in AD, providing evidence that it may have the potential to alleviate brain pathology and improve cognitive function in AD patients. At the same time, the precuneus (PC) has been recognized as a key area involved in AD related memory deficits and as a key node of the Default Mode Network. This study aimed to investigate the effectiveness of a 40 Hz Transcranial Magnetic Stimulation (TMS) intervention, delivered bilaterally to the precuneus for 10 days, in improving the patients' episodic memory performance. Secondary outcome variables investigated included general cognitive function, semantic and spatial memory, as well as attention and executive function. A concurrent multiple baseline design across five cases was employed. Four patients completed the study. Visual analysis combined with effect size indices were used to evaluate changes across phases. An increase in the average level of immediate recalled words was observed in three out of four patients. Effect size indices indicated significant improvement of attention skills in two patients. No treatment effect was observed for semantic and visual memory, or for executive function. An immediate treatment effect was observed in all patients' general cognitive function as assessed with the Alzheimer's Disease Assessment Scale (mean reduction of 5 points), which was maintained and improved further three months post-treatment. The neuropsychological evaluations indicated improved performance three months post-treatment in immediate and delayed recall, attention, phonological verbal fluency, anxiety, and neuropsychiatric symptoms. This study provides preliminary evidence for the efficacy of a novel non-pharmacological treatment using gamma-band TMS in addressing cognitive dysfunction in AD.

Identifiants

pubmed: 36351687
doi: 10.1111/jnp.12299
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

279-301

Informations de copyright

© 2022 The Authors. Journal of Neuropsychology published by John Wiley & Sons Ltd on behalf of The British Psychological Society.

Références

Adaikkan, C., Middleton, S. J., Marco, A., Pao, P. C., Mathys, H., Kim, D. N. W., Gao, F., Young, J. Z., Suk, H. J., Boyden, E. S., McHugh, T., & Tsai, L. H. (2019). Gamma entrainment binds higher-order brain regions and offers neuroprotection. Neuron, 102(5), 929-943.e8. https://doi.org/10.1016/j.neuron.2019.04.011
Ahmed, M. A., Darwish, E. S., Khedr, E. M., & Ali, A. M. (2012). Effects of low versus high frequencies of repetitive transcranial magnetic stimulation on cognitive function and cortical excitability in Alzheimer's dementia. Journal of Neurology, 259, 83-92. https://doi.org/10.1007/s00415-011-6128-4
Bäckman, L., Small, B. J., & Fratiglioni, L. (2001). Stability of the preclinical episodic memory deficit in Alzheimer's disease. Brain, 124(1), 96-102. https://doi.org/10.1093/brain/124.1.96
Beck, I. R., Gagneux-Zurbriggen, A., Berres, M., Taylor, K. I., & Monsch, A. U. (2012). Comparison of verbal episodic memory measures: Consortium to establish a registry for Alzheimer's disease-Neuropsychological Assessment Battery (CERAD-NAB) versus California Verbal Learning Test (CVLT). Archives of Clinical Neuropsychology, 27(5), 510-519. https://doi.org/10.1093/arclin/acs056
Benninger, D. H., Iseki, K., Kranick, S., Luckenbaugh, D. A., Houdayer, E., & Hallett, M. (2012). Controlled study of 50-Hz repetitive transcranial magnetic stimulation for the treatment of parkinson disease. Neurorehabilitation and Neural Repair, 26(9), 1096-1105. https://doi.org/10.1177/1545968312445636
Benussi, A., Cantoni, V., Cotelli, M. S., Cotelli, M., Brattini, C., Datta, A., Thomas, C., Santarnecchi, E., Pascual-Leone, A., & Borroni, B. (2021). Exposure to gamma tACS in Alzheimer's disease: A randomized, double- blind, sham-controlled, crossover, pilot study. Brain Stimulation., 14, 531-540. https://doi.org/10.1016/j.brs.2021.03.007
Bonnì, S., Veniero, D., Mastropasqua, C., Ponzo, V., Caltagirone, C., Bozzali, M., & Koch, G. (2015). TMS evidence for a selective role of the precuneus in source memory retrieval. Behavioural Brain Research, 282, 70-75. https://doi.org/10.1016/j.bbr.2014.12.032
Braak, H., Alafuzoff, I., Arzberger, T., Kretzschmar, H., & Del Tredici, K. (2006). Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry. Acta Neuropathologica, 112(4), 389-404. https://doi.org/10.1007/s00401-006-0127-z
Braak, H., Braak, E., & Bohl, J. (1993). Staging of Alzheimer-related cortical destruction. European Neurology, 33(6), 403-408. 389-404-403-408. 389-408. https://doi.org/10.1159/000116984
Buckner, R. L., Andrews-Hanna, J. R., & Schacter, D. L. (2008). The brain's default network: Anatomy, function, and relevance to disease. Annals of the New York Academy of Science, 1124, 1-38. https://doi.org/10.1196/annals.1440.011
Canter, R. G., Penney, J., & Tsai, L. H. (2016). The road to restoring neural circuits for the treatment of Alzheimer's disease. Nature, 539(7628), 187-196. https://doi.org/10.1038/nature20412
Caputi, N., Di Giacomo, D., Aloisio, F., & Passafiume, D. (2016). Deterioration of semantic associative relationships in mild cognitive impairment and Alzheimer Disease. Applied Neuropsychology: Adult, 23(3), 186-195. https://doi.org/10.1080/23279095.2015.1030020
Chan, D., Suk, H. J., Jackson, B., Milman, N. P., Stark, D., Klerman, E. B., Kitchener, E., Avalos, V. S. F., Banerjee, A., Beach, S. D., Blanchard, J., Stearns, C., Boes, A., Uitermarkt, B., Gander, P., Howard III, M., Sternberg, E. J., Nieto-Castanon, A., Anteraper, S., … Tsai, L. H. (2021). Gamma frequency sensory stimulation in probable mild Alzheimer's dementia patients: Results of a preliminary clinical trial. MedRxiv [preprint]. https://doi.org/10.1101/2021.03.01.21252717. May 17, 2021 (Accessed 15th March 2022).
Chen, Y., Liu, Z., Zhang, J., Chen, K., Yao, L., Li, X., Gong, G., Wang, J., & Zhang, Z. (2017). Precuneus degeneration in nondemented elderly individuals with APOE ɛ4: Evidence from structural and functional MRI analyses. Human Brain Mapping, 38(1), 271-282. https://doi.org/10.1002/hbm.23359
Cotelli, M., Calabria, M., Manenti, R., Rosini, S., Zanetti, O., Cappa, S. F., & Miniussi, C. (2011). Improved language performance in Alzheimer disease following brain stimulation. Journal of Neurology, Neurosurgery & Psychiatry, 82(7), 794-797. https://doi.org/10.1136/jnnp.2009.197848
Fan, L., Mao, C., Hu, X., Zhang, S., Yang, Z., Hu, Z., Sun, H., Fan, Y., Dong, Y., Yang, J., Shi, C., & Xu, Y. (2020). New insights into the pathogenesis of Alzheimer's disease. Frontiers in Neurology, 10(1312). https://doi.org/10.3389/fneur.2019.01312
Fitzgerald, P. J., & Watson, B. O. (2018). Gamma oscillations as a biomarker for major depression: An emerging topic. Translational Psychiatry, 8(1), 1-7. https://doi.org/10.1038/s41398-018-0239-y
Fransson, P., & Marrelec, G. (2008). The precuneus/posterior cingulate cortex plays a pivotal role in the default mode network: Evidence from a partial correlation network analysis. NeuroImage, 42(2), 1178-1184. https://doi.org/10.1016/j.neuroimage.2008.05.059
Gallagher, M., & Koh, M. T. (2011). Episodic memory on the path to Alzheimer's disease. Current Opinion in Neurobiology, 21(6), 929-934. https://doi.org/10.1016/j.conb.2011.10.021
Gilboa, A., Winocur, G., Grady, C. L., Hevenor, S. J., & Moscovitch, M. (2004). Remembering our past: Functional neuroanatomy of recollection of recent and very remote personal events. Cerebral Cortex, 14(11), 1214-1225. https://doi.org/10.1093/cercor/bhh082
Goutagny, R., Gu, N., Cavanagh, C., Jackson, J., Chabot, J. G., Quirion, R., Krantic, S., & Williams, S. (2013). Alterations in hippocampal network oscillations and theta-gamma coupling arise before Aβ overproduction in a mouse model of Alzheimer's disease. European Journal of Neuroscience, 37(12), 1896-1902. https://doi.org/10.1111/ejn.12233
Hartmann, D. P., Barrios, B. A., & Wood, D. D. (2004). Principles of behavioral observation. In S. H. Haynes (Ed.), Comprehensive handbook of psychological assessment. Behavioral assessment (Vol. 3, pp. 108-127). Wiley.
Hayes, S. C., Barlow, D. H., & Nelson-Gray, R. O. (1999). The scientist practitioner: Research and accountability in the age of managed care (2nd ed.). Allyn & Bacon.
He, Q., Colon-Motas, K. M., Pybus, A. F., Piendel, L., Seppa, J. K., Walker, M. L., Manzanares, C. M., Qiu, D., Miocinovic, S., Wood, L. B., Levey, A. I., Lah, J. J., & Singer, A. C. (2021). A feasibility trial of gamma sensory flicker for patients with prodromal Alzheimer's disease. Alzheimer's & Dementia, 7, 1-11. https://doi.org/10.1002/trc2.12178
Hebscher, M., Ibrahim, C., & Gilboa, A. (2020). Precuneus stimulation alters the neural dynamics of autobiographical memory retrieval. NeuroImage, 210, 116575. https://doi.org/10.1016/j.neuroimage.2020.116575
Iaccarino, H. F., Singer, A. C., Martorell, A. J., Rudenko, A., Gao, F., Gillingham, T. Z., Mathys, H., Seo, J., Kritskiy, O., Abdurrob, F., Adaikkan, C., Canter, R. G., Rueda, R., Brown, E. N., Boyden, E. S., & Tsai, L. H. (2016). Gamma frequency entrainment attenuates amyloid load and modifies microglia. Nature, 540(7632), 230-235. https://doi.org/10.1038/nature20587
Kehler, L., Francisco, C. O., Uehara, M. A., & Moussavi, Z. (2020). The effect of transcranial alternating current stimulation (tACS) on cognitive function in older adults with dementia. IEEE Engineering in Medicine and Biology Society Annual International Conference, 2020, 3649-3653. https://doi.org/10.1109/EMBC44109.2020.9175903
Kim, J., Kim, Y. H., & Lee, J. H. (2013). Hippocampus-precuneus functional connectivity as an early sign of Alzheimer's disease: A preliminary study using structural and functional magnetic resonance imaging data. Brain Research, 1945, 18-29. https://doi.org/10.1016/j.brainres.2012.12.011
Koch, G., Bonnì, S., Pellicciari, M. C., Casula, E. P., Mancini, M., Esposito, R., Ponzo, V., Picazio, S., Di Lorenzo, F., Serra, L., Motta, C., Maiella, M., Marra, C., Cercignani, M., Martorana, A., Caltagirone, C., & Bozzali, M. (2018). Transcranial magnetic stimulation of the precuneus enhances memory and neural activity in prodromal Alzheimer's disease. NeuroImage, 169, 302-311. https://doi.org/10.1016/j.neuroimage.2017.12.048
Krasny-Pacini, A., & Evans, J. (2018). Single-case experimental designs to assess intervention effectiveness in rehabilitation: A practical guide. Annals of Physical and Rehabilitation Medicine, 61(3), 164-179. https://doi.org/10.1016/j.rehab.2017.12.002
Kratochwill, T. R., Hitchcock, J., Horner, R. H., Levin, J. R., Odom, S. L., Rindskopf, D. M., & Shadish, W. R. (2010). Single-case designs technical documentation. https://eric.ed.gov/?id=ED510743
Kratochwill, T. R., & Levin, J. R. (2014). Enhancing the scientific credibility of single-case intervention research: Randomization to the rescue. Psychological Methods, 15, 124-144. https://doi.org/10.1037/a0017736
Krause, B. J., Schmidt, D., Mottaghy, F. M., Taylor, J., Halsband, U., Herzog, H., Tellmann, L., & Müller-Gärtner, H. W. (1999). Episodic retrieval activates the precuneus irrespective of the imagery content of word pair associates: A PET study. Brain, 122(2), 255-263. https://doi.org/10.1093/brain/122.2.255
Kwok, S. C., Shallice, T., & Macaluso, E. (2012). Functional anatomy of temporal organisation and domain-specificity of episodic memory retrieval. Neuropsychologia, 50(12), 2943-2955. doi:10.1016/j.neuropsychologia.2012.07.025
Liu, C., Han, T., Xu, Z., Liu, J., Zhang, M., Du, J., Zhou, Q., Duan, Y., Li, Y., Wang, J., Cui, D., & Wang, Y. (2022). Modulating gamma oscillations promotes brain connectivity to improve cognitive impairment. Cerebral Cortex., 32(12), 2644-2656. https://doi.org/10.1093/cercor/bhab371
Lobo, M. A., Moeyaert, M., Cunha, A. B., & Babik, I. (2017). Single-case design, analysis, and quality assessment for intervention research. Journal of Neurologic Physical Therapy: JNPT, 41(3), 187-197. https://doi.org/10.1097/npt.0000000000000187
Lundstrom, B. N., Ingvar, M., & Petersson, K. M. (2005). The role of precuneus and left inferior frontal cortex during source memory episodic retrieval. NeuroImage, 27(4), 824-834. https://doi.org/10.1016/j.neuroimage.2005.05.008
Mancini, M., Mastropasqua, C., Bonnì, S., Ponzo, V., Cercignani, M., Conforto, S., Koch, G., & Bozzali, M. (2017). Theta burst stimulation of the precuneus modulates resting state connectivity in the left temporal pole. Brain Topography, 30(3), 312-319. https://doi.org/10.1007/s10548-017-0559-x
Martorell, A. J., Paulson, A. L., Suk, H. J., Abdurrob, F., Drummond, G. T., Guan, W., Young, J. Z., Kim, D. N. W., Kritskiy, O., Barker, S. J., Mangena, V., Prince, S. M., Brown, E. N., Chung, K., Boyden, E. S., Singer, A. C., & Tsai, L. H. (2019). Multi-sensory gamma stimulation ameliorates Alzheimer's-associated pathology and improves cognition. Cell, 177(2), 256-271. https://doi.org/10.1016/j.cell.2019.02.014
Mattsson, N., Insel, P. S., Donohue, M., Jögi, J., Ossenkoppele, R., Olsson, T., Scholl, M., Smith, R., & Hansson, O. (2019). Predicting diagnosis and cognition with 18F-AV-1451 tau PET and structural MRI in Alzheimer's disease. Alzheimer's & Dementia, 15(4), 570-580. https://doi.org/10.1016/j.jalz.2018.12.001
McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack Jr, C. R., Kawas, C. H., Klunk, W. E., Koroshetz, W. J., Manly, J. J., Mayeux, R., Mohs, R. C., Morris, J. C., Rossor, M. N., Scheltens, P., Carrillo, M. C., Thies, B., Weintraub, S., & Phelps, C. H. (2011). The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's & Dementia, 7(3), 263-269. https://doi.org/10.1016/j.jalz.2011.03.005
Mussigmann, T., Lefaucheur, J. P., & McGonigal, A. (2021). Gamma-band activities in the context of pain: A signal from brain or muscle? Neurophysiologie Clinique, 51, 287-289. https://doi.org/10.1016/j.neucli.2021.03.007
Nestor, P. J., Scheltens, P., & Hodges, J. R. (2004). Advances in the early detection of Alzheimer's disease. Nature Medicine, 10(7), S34-S41. https://doi.org/10.1038/nrn1433
Perdices, M., & Tate, R. L. (2009). Single-subject designs as a tool for evidence-based clinical practice: Are they unrecognised and undervalued? Neuropsychological Rehabilitation, 19(6), 904-927. https://doi.org/10.1002/jcad.12038
Petersen, R. C., Smith, G. E., Ivnik, R. J., Kokmen, E., & Tangalos, E. G. (1994). Memory function in very early Alzheimer's disease. Neurology, 44(5), 867. https://doi.org/10.1212/wnl.44.5.867
Price, J. L., Davis, P. B., Morris, J. C., & White, D. L. (1991). The distribution of tangles, plaques and related immunohistochemical markers in healthy aging and Alzheimer's disease. Neurobiology of Aging, 12(4), 295-312. https://doi.org/10.1016/0197-4580(91)90006-6
Rabey, J. M., Dobronevsky, E., Aichenbaum, S., Gonen, O., Marton, R. G., & Khaigrekht, M. (2013). Repetitive transcranial magnetic stimulation combined with cognitive training is a safe and effective modality for the treatment of Alzheimer's disease: A randomized, double-blind study. Journal of Neural Transmission, 120(5), 813-819. https://doi.org/10.1007/s00702-012-0902-z
Reitan, R. M. (1955). The relation of the trail making test to organic brain damage. Journal of Consulting Psychology, 19(5), 393-398. https://doi.org/10.1037/h0044509
Rose, N. S., LaRocque, J. J., Riggall, A. C., Gosseries, O., Starrett, M. J., Meyering, E. E., & Postle, B. R. (2016). Reactivation of latent working memories with transcranial magnetic stimulation. Science, 354(6316), 1136-1139. https://doi.org/10.1126/science.aah7011
Rugg, M. D., Otten, L. J., & Henson, R. N. (2002). The neural basis of episodic memory: Evidence from functional neuroimaging. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 1424(357), 1097-1110. https://doi.org/10.1098/rstb.2002.1102
Schmidt, D., Krause, B. J., Mottaghy, F. M., Halsband, U., Herzog, H., Tellmann, L., & Müller-Gärtner, H. W. (2002). Brain systems engaged in encoding and retrieval of word-pair associates independent of their imagery content or presentation modalities. Neuropsychologia, 40(4), 457-470. https://doi.org/10.1016/s0028-3932(01)00102-6
Schrag, A., Schott, J. M., & Initiative, A.'s. D. N. (2012). What is the clinically relevant change on the ADAS-Cog? Journal of Neurology, Neurosurgery, and Psychiatry, 83(2), 171-173. https://doi.org/10.1136/jnnp-2011-300881
Scruggs, T. E., & Mastropieri, M. A. (1998). Summarizing single-subject research: Issues and applications. Behavior Modification, 22(3), 221-242. https://doi.org/10.1177/01454455980223001
Shallice, T., Fletcher, P., Frith, C. D., Grasby, P., Frackowiak, R. S. J., & Dolan, R. J. (1994). Brain regions associated with acquisition and retrieval of verbal episodic memory. Nature, 6472(368), 633-635. https://doi.org/10.1038/368633a0
Sorg, C., Riedl, V., Mühlau, M., Calhoun, V. D., Eichele, T., Läer, L., Drzezga, A., Forstl, H., Kurz, A., Zimmer, C., & Wohlschläger, A. M. (2007). Selective changes of resting-state networks in individuals at risk for Alzheimer's disease. Proceedings of the National Academy of Sciences, 104(47), 18760-18765. https://doi.org/10.1073/pnas.0708803104
Traikapi, A., & Konstantinou, N. (2021). Gamma oscillations in Alzheimer's disease and their potential therapeutic role. Frontiers in Systems Neuroscience, 15. https://doi.org/10.3389/fnsys.2021.782399
Traikapi, A., Phylactou, P., & Konstantinou, N. (2022). Repetitive magnetic stimulation of the human motor cortex in the gamma band reduces cortical excitability. Neurophysiologie Clinique, 52(5), 407-409. https://doi.org/10.1016/j.neucli.2022.09.005
Uhlhaas, P. J., & Singer, W. (2006). Neural synchrony in brain disorders: Relevance for cognitive dysfunctions and pathophysiology. Neuron, 52(1), 155-168. https://doi.org/10.1016/j.neuron.2006.09.020
Vannest, K. J., & Ninci, J. (2015). Evaluating intervention effects in single-case research designs. Journal of Counseling & Development, 93(4), 403-411. https://doi.org/10.1002/jcad.12038
Vannest, K. J., Parker, R. I., Gonen, O., & Adiguzel, T. (2016). Single case research: Web based calculators for SCR analysis . (Version 2.0) [Web-based application]. Texas A&M University singlecaseresearch.org. [Accessed 27th Tuesday September 2022].
Ye, Q., Zou, F., Dayan, M., Lau, H., Hu, Y., & Kwok, S. C. (2019). Individual susceptibility to TMS affirms the precuneal role in meta-memory upon recollection. Brain Structure and Function, 224(7), 2407-2419. https://doi.org/10.1007/s00429-019-01909-6
Yue, W. U., Wenwei, X. U., Xiaowei, L. I. U., Qing, X. U., Li, T. A. N. G., & Shuyan, W. U. (2015). Adjunctive treatment with high frequency repetitive transcranial magnetic stimulation for the behavioral and psychological symptoms of patients with Alzheimer's disease: A randomized, double-blind, sham-controlled study. Shanghai Archives of Psychiatry, 27(5), 280-288. https://doi.org/10.11919/j.issn.1002-0829.215107
Zhao, J., Li, Z., Cong, Y., Zhang, J., Tan, M., Zhang, H., Geng, N., Li, M., Yu, W., & Shan, P. (2017). Repetitive transcranial magnetic stimulation improves cognitive function of Alzheimer's disease patients. Oncotarget, 8(20), 33864-33871. https://doi.org/10.18632/oncotarget.13060
Zhao, Q., Lv, Y., Zhou, Y., Hong, Z., & Guo, Q. (2012). Short-term delayed recall of auditory verbal learning test is equivalent to long-term delayed recall for identifying amnestic mild cognitive impairment. PLoS One, 7(12), e51157. https://doi.org/10.1371/journal.pone.0051157
Zhou, B., Yao, H., Wang, P., Zhang, Z., Zhan, Y., Ma, J., Xu, K., Wang, L., An, N., Liu, Y., & Zhang, X. (2015). Aberrant functional connectivity architecture in Alzheimer's disease and mild cognitive impairment: A whole-brain, data-driven analysis. BioMed Research International, 2015. https://doi.org/10.1155/2015/495375

Auteurs

Artemis Traikapi (A)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Ioanna Kalli (I)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Andrea Kyriakou (A)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Elena Stylianou (E)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Rafaella Tereza Symeou (RT)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Akrivi Kardama (A)

Rehabilitation Center Melathron Agoniston EOKA, Limassol, Cyprus.

Yiolanda Panayiota Christou (YP)

Acropoleos Medical Center, Nicosia, Cyprus.

Phivos Phylactou (P)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Nikos Konstantinou (N)

Department of Rehabilitation Sciences, Faculty of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH