Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5250_Библиотеки_им_академика_М_И_Перельмана.pdf
X
- •Foreword
- •Preface
- •Contents
- •1.1.2.5 Priming (Guiding) Transcranial Magnetic Stimulation (pTMS)
- •1.1.2.6 Synchronized Transcranial Magnetic Stimulation (sTMS)
- •1.1.2.8 Magnetic Seizure Therapy (MST)
- •1.2.1 Treatment Procedures
- •1.2.2 TMS Treatment Precautions
- •1.2.2.1 Seizure Risk
- •1.2.2.3 Other Precautions
- •1.3.1.1 Membrane Potential Alterations
- •1.4 Effect Factors
- •1.4.1 Stimulation Frequency
- •About the Editors
- •1: Transcranial Magnetic Stimulation
- •1.1 Introduction
- •1.1.2.1 Repetitive Transcranial Magnetic Stimulation (rTMS)
- •1.1.2.2 Prolonged Intermittent Theta Burst Stimulation (piTBS)
- •1.1.2.4 Deep Transcranial Magnetic Stimulation (dTMS)
- •1.4.2 Stimulation Intensity
- •1.4.3 Pulse Duration
- •1.4.5 Interstimulus Interval
- •1.5 Conclusion
- •References
- •2: Transcranial Direct Current Stimulation
- •2.1 Introduction
- •2.3.3 Nonneuronal Mechanisms
- •2.3.4 Others
- •2.4 Effect Factors
- •2.4.1 Stimulus Polarity
- •2.4.2 Duration
- •2.4.3 Current Intensity
- •2.4.4 Others
- •2.5 Summary and Outlook
- •References
- •3: Major Depressive Disorder
- •3.1 Introduction
- •3.2 TMS
- •3.2.1 rTMS
- •3.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.2 Deep TMS
- •3.2.2.1 Efficacy
- •3.2.2.2 Safety
- •3.2.2.3 Treatment Regimen
- •3.2.2.4 Clinical Recommendations
- •3.2.3 Priming rTMS
- •3.2.3.1 Efficacy
- •3.2.3.2 Safety
- •3.2.3.3 Treatment Regimen
- •3.2.3.4 Clinical Recommendations
- •3.2.4 Synchronized rTMS
- •3.2.4.1 Efficacy
- •3.2.4.2 Safety
- •3.2.4.3 Treatment Regimen
- •3.2.4.4 Clinical Recommendations
- •3.2.5 TBS
- •3.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.3 Continuous TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.6 Magnetic Seizure Therapy (MST)
- •3.2.6.1 Efficacy
- •3.2.6.2 Safety
- •3.2.6.3 Treatment Regimen
- •3.2.6.4 Clinical Recommendations
- •3.3 tDCS
- •3.3.1 Conventional tDCS
- •3.3.1.1 Efficacy
- •3.3.1.3 Treatment Regimen
- •3.3.1.4 Clinical Recommendations
- •3.3.2 HD-tDCS
- •3.3.2.1 Efficacy
- •3.3.2.2 Safety
- •3.3.2.3 Treatment Regimen
- •3.3.2.4 Clinical Recommendations
- •3.4 TMS Vs. tDCS
- •3.4.1 Efficacy
- •3.4.2 Safety
- •3.5 Conclusion
- •References
- •3.3.1.2 Safety
- •4: Bipolar Disorder
- •4.1 Introduction
- •4.2 TMS
- •4.2.1 rTMS
- •4.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.2 Deep TMS
- •4.2.2.1 Efficacy
- •4.2.2.2 Safety
- •4.2.2.3 Treatment Regimen
- •4.2.2.4 Clinical Recommendations
- •4.2.3 Priming TMS
- •4.2.3.1 Efficacy
- •4.2.3.2 Safety
- •4.2.3.3 Treatment Regimen
- •4.2.3.4 Clinical Recommendations
- •4.2.4 Synchronized TMS
- •4.2.4.1 Efficacy
- •4.2.4.2 Safety
- •4.2.4.3 Treatment Regimen
- •4.2.4.4 Clinical Recommendations
- •4.2.5 TBS
- •4.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.3 Continuous TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.6 MST
- •4.2.6.1 Efficacy
- •4.2.6.2 Safety
- •4.2.6.3 Treatment Regimen
- •4.2.6.4 Clinical Recommendations
- •4.3 tDCS
- •4.3.1 Conventional tDCS
- •4.3.1.1 Efficacy
- •4.3.1.2 Safety
- •4.3.1.3 Treatment Regimen
- •4.3.1.4 Clinical Recommendations
- •4.3.2 HD-tDCS
- •4.3.2.1 Efficacy
- •4.3.2.2 Safety
- •4.3.2.3 Treatment Regimen
- •4.3.2.4 Clinical Recommendations
- •4.4 TMS vs. tDCS
- •4.4.1 Efficacy
- •4.4.2 Safety
- •4.5 Conclusion
- •References
- •5: Schizophrenia
- •5.1 Schizophrenia
- •5.2 TMS
- •5.2.1 rTMS
- •5.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.2 Deep TMS
- •5.2.2.1 Efficacy
- •5.2.2.2 Safety
- •5.2.2.3 Treatment Regimen
- •5.2.2.4 Clinical Recommendations
- •5.2.3 Priming TMS
- •5.2.3.1 Efficacy
- •5.2.3.2 Safety
- •5.2.3.3 Treatment Regimen
- •5.2.3.4 Clinical Recommendations
- •5.2.4 Synchronized TMS
- •5.2.4.1 Efficacy
- •5.2.4.2 Safety
- •5.2.4.3 Treatment Regimen
- •5.2.4.4 Clinical Recommendations
- •5.2.5 TBS
- •5.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.6 MST
- •5.2.6.1 Efficacy
- •5.2.6.2 Safety
- •5.2.6.3 Treatment Regimen
- •5.2.6.4 Clinical Recommendations
- •5.3 tDCS
- •5.3.1 Conventional tDCS
- •5.3.1.1 Efficacy
- •5.3.1.2 Safety
- •5.3.1.3 Treatment Regimen
- •5.3.1.4 Clinical Recommendations
- •5.3.2 HD-tDCS
- •5.3.2.1 Efficacy
- •5.3.2.2 Safety
- •5.3.2.3 Treatment Regimen
- •5.3.2.4 Clinical Recommendations
- •5.4 TMS vs. tDCS
- •5.4.1 Efficacy
- •5.4.2 Safety
- •5.5 Conclusion
- •References
- •6: Addictive Disorders
- •6.1 Addictive Disorders
- •6.2 TMS
- •6.2.1 rTMS
- •6.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •6.2.1.2 Bilateral rTMS
- •6.2.1.3 Accelerated rTMS
- •6.2.2 Deep TMS
- •6.2.3 Priming TMS
- •6.2.4 Synchronized TMS
- •6.2.5 TBS
- •6.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •6.2.5.2 Accelerated iTBS
- •6.2.5.3 Continuous TBS
- •6.2.5.4 Bilateral TBS
- •6.2.6 MST
- •6.3 tDCS
- •6.3.1 Conventional tDCS
- •6.3.1.1 Efficacy
- •6.3.1.2 Safety
- •6.3.1.3 Treatment Regimen
- •6.3.1.4 Clinical Recommendations
- •6.3.2 HD-tDCS
- •6.4 TMS vs. tDCS
- •6.4.1 Efficacy
- •6.4.2 Safety
- •6.5 Conclusion
- •References
- •7: Obsessive-Compulsive Disorder
- •7.1 Introduction
- •7.2 TMS
- •7.2.1 rTMS
- •7.2.1.1 Unilateral rTMS
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.2 Deep TMS
- •7.2.2.1 Efficacy
- •7.2.2.2 Safety
- •7.2.2.3 Treatment Regimen
- •7.2.2.4 Clinical Recommendations
- •7.2.3 Priming TMS
- •7.2.3.1 Efficacy
- •7.2.3.2 Safety
- •7.2.3.3 Treatment Regimen
- •7.2.3.4 Clinical Recommendations
- •7.2.4 Synchronized TMS
- •7.2.4.1 Efficacy
- •7.2.4.2 Safety
- •7.2.4.3 Treatment Regimen
- •7.2.4.4 Clinical Recommendations
- •7.2.5 TBS
- •7.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.6 MST
- •7.2.6.1 Safety
- •7.2.6.2 Treatment Regimen
- •7.2.6.3 Clinical Recommendations
- •7.3 tDCS
- •7.3.1 Conventional tDCS
- •7.3.1.1 Efficacy
- •7.3.1.2 Safety
- •7.3.1.3 Treatment Regimen
- •7.3.1.4 Clinical Recommendations
- •7.3.2 HD-tDCS
- •7.3.2.1 Efficacy
- •7.3.2.2 Safety
- •7.3.2.3 Treatment Regimen
- •7.3.2.4 Clinical Recommendations
- •7.4 TMS vs. tDCS
- •7.4.1 Efficacy
- •7.4.2 Safety
- •7.5 Conclusion
- •References
- •8: Attention Deficit Hyperactivity Disorder
- •8.1 ADHD
- •8.1.2 Therapeutic Method
- •8.2 TMS
- •8.2.1 Single-Pulse TMS (spTMS)
- •8.2.1.1 Efficacy
- •8.2.1.2 Safety
- •8.2.1.3 Treatment Regimen
- •8.2.1.4 Clinical Recommendations
- •8.2.2 Paired-Pulse TMS (ppTMS)
- •8.2.2.1 Efficacy
- •8.2.2.2 Safety
- •8.2.2.3 Treatment Regimen
- •8.2.2.4 Clinical Recommendations
- •8.2.3 rTMS
- •8.2.3.1 Low-Frequency rTMS (LF-rTMS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.3.2 High-Frequency rTMS (HF-rTMS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.4 TBS
- •8.2.4.1 Intermittent TBS (iTBS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.4.2 Continuous iTBS (cTBS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.3 tDCS
- •8.3.1 Conventional tDCS
- •8.3.1.1 Efficacy
- •8.3.1.2 Safety
- •8.3.1.3 Treatment Regimen
- •8.3.1.4 Clinical Recommendations
- •8.3.2.1 Efficacy
- •8.3.2.2 Safety
- •8.3.2.3 Treatment Regimen
- •8.3.2.4 Clinical Recommendations
- •8.4 TMS vs. tDCS
- •8.4.1 Efficacy
- •8.4.2 Safety
- •8.5 Conclusion
- •References
- •9: Autism Spectrum Disorder
- •9.1 Introduction
- •9.2 rTMS
- •9.2.1 Unilateral rTMS
- •9.2.1.1 Efficacy
- •9.2.1.2 Safety
- •9.2.1.3 Treatment Regimen
- •9.2.1.4 Clinical Recommendations
- •9.2.1.5 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.1.6 Accelerated rTMS
- •9.2.2 Deep TMS
- •9.2.2.1 Efficacy
- •9.2.2.2 Safety
- •9.2.2.3 Treatment Regimen
- •9.2.2.4 Clinical Recommendations
- •9.2.3 Priming TMS
- •9.2.4 Synchronized TMS
- •9.2.5 TBS
- •9.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.5.2 Accelerated iTBS
- •9.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.6 MST
- •9.3 tDCS
- •9.3.1 Conventional tDCS
- •9.3.1.1 Efficacy
- •9.3.1.2 Safety
- •9.3.1.3 Treatment Regimen
- •9.3.1.4 Clinical Recommendations
- •9.3.2 HD-tDCS
- •9.3.2.1 Efficacy
- •9.3.2.2 Safety
- •9.3.2.3 Treatment Regimen
- •9.3.2.4 Clinical Recommendations
- •9.4 TMS Vs. tDCS
- •9.4.1 Efficacy
- •9.4.1.1 Cognitive Effects
- •9.4.1.3 Biological Effects
- •9.4.2 Safety
- •9.5 Conclusion
- •References
- •10: Anxiety Disorder
- •10.1 Introduction
- •10.2 TMS
- •10.2.1 rTMS
- •10.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.2 Deep TMS
- •10.2.2.1 Efficacy
- •10.2.2.2 Safety
- •10.2.2.3 Treatment Regimen
- •10.2.2.4 Clinical Recommendations
- •10.2.3 Priming TMS
- •10.2.3.1 Efficacy
- •10.2.3.2 Safety
- •10.2.3.3 Treatment Regimen
- •10.2.3.4 Clinical Recommendations
- •10.2.4 Synchronized TMS
- •10.2.4.1 Efficacy
- •10.2.4.2 Safety
- •10.2.4.3 Treatment Regimen
- •10.2.4.4 Clinical Recommendations
- •10.2.5 TBS
- •10.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.6 Magnetic Seizure Therapy (MST)
- •10.3 tDCS
- •10.3.1 Conventional tDCS
- •10.3.1.1 Efficacy
- •10.3.1.2 Safety
- •10.3.1.3 Treatment Regimen
- •10.3.1.4 Clinical Recommendations
- •10.3.2 HD-tDCS
- •10.3.2.1 Efficacy
- •10.3.2.2 Safety
- •10.3.2.3 Clinical Recommendations
- •10.4 TMS versus tDCS
- •10.4.1 Efficacy
- •10.4.2 Safety
- •10.5 Conclusion
- •References
- •11: Post-traumatic Stress Disorder
- •11.1 Introduction
- •11.2 TMS
- •11.2.1 rTMS
- •11.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.2 Deep TMS
- •11.2.2.1 Efficacy
- •11.2.2.2 Safety
- •11.2.2.3 Treatment Regimen
- •11.2.2.4 Clinical Recommendations
- •11.2.3 Priming TMS
- •11.2.3.1 Efficacy
- •11.2.3.2 Safety
- •11.2.3.3 Treatment Regimen
- •11.2.3.4 Clinical Recommendations
- •11.2.4 Synchronized TMS
- •11.2.4.1 Efficacy
- •11.2.4.2 Safety
- •11.2.4.3 Treatment Regimen
- •11.2.4.4 Clinical Recommendations
- •11.2.5 TBS
- •11.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.5.3 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.6 MST
- •11.2.6.1 Efficacy
- •11.2.6.2 Safety
- •11.2.6.3 Treatment Regimen
- •11.2.6.4 Clinical Recommendations
- •11.3 tDCS
- •11.3.1 Conventional tDCS
- •11.3.1.1 Efficacy
- •11.3.1.2 Safety
- •11.3.1.3 Treatment Regimen
- •11.3.1.4 Clinical Recommendations
- •11.3.2 HD-tDCS
- •11.3.2.1 Efficacy
- •11.3.2.2 Safety
- •11.3.2.3 Treatment Regimen
- •11.3.2.4 Clinical Recommendations
- •11.4 TMS vs. tDCS
- •11.4.1 Efficacy
- •11.4.2 Safety
- •11.5 ECT
- •11.5.1 Efficacy
- •11.5.2 Safety
- •11.5.3 Treatment Regimen
- •11.5.4 Clinical Recommendations
- •11.6 Conclusion
- •References
- •12: Sleep Disorders
- •12.1 Introduction
- •12.2 TMS
- •12.2.1 rTMS
- •12.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.1.3 Accelerated rTMS
- •12.2.2 Deep TMS
- •12.2.3 Priming TMS
- •12.2.4 Synchronised TMS
- •12.2.5 TBS
- •12.2.5.1 iTBS
- •12.2.5.2 Accelerated iTBS
- •12.2.5.3 cTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.5.4 Bilateral TBS
- •12.2.6 MST
- •12.3 tDCS
- •12.3.1 Efficacy
- •12.3.2 Safety
- •12.3.3 Treatment Regimen
- •12.3.4 Clinical Recommendations
- •12.4 TMS Combined tDCS
- •12.4.1 Efficacy
- •12.4.2 Safety
- •12.5 Conclusion
- •References
- •13: Neurocognitive Disorders
- •13.1 Introduction
- •13.2 TMS
- •13.2.1 TMS
- •13.2.1.1 Conventional rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •13.2.1.2 Accelerated rTMS
- •13.2.2 Deep TMS
- •13.2.2.1 Efficacy
- •13.2.2.2 Safety
- •13.2.2.3 Treatment Regimen
- •13.2.2.4 Clinical Recommendations
- •13.2.3 Priming TMS
- •13.2.4 Synchronized TMS
- •13.2.5 iTBS
- •13.2.5.1 Efficacy
- •13.2.5.2 Safety
- •13.2.5.3 Treatment Regimen
- •13.2.5.4 Clinical Recommendations
- •13.2.6 Magnetic Seizure Therapy
- •13.3.1 Conventional tDCS
- •13.3.1.1 Efficacy
- •13.3.1.2 Safety
- •13.3.1.3 Treatment Regimen
- •13.3.1.4 Clinical Recommendations
- •13.3.2 HD-tDCS
- •13.3.2.1 Efficacy
- •13.3.2.2 Safety
- •13.3.2.3 Treatment Regimen
- •13.3.2.4 Clinical Recommendations
- •13.4 TMS vs. tDCS
- •13.4.1 Efficacy
- •13.4.2 Safety
- •13.5 Conclusion
- •References

13 Neurocognitive Disorders
357
conditions like MCI and AD, with no reports of serious adverse events, including
seizures or shock. Despite this, given the variability in patient characteristics and treatment parameters, vigilant monitoring for potential adverse reactions remains essential.
13.5 Conclusion
This study offers a comprehensive overview of recent advancements in TMS and
tDCS interventions for neurocognitive disorders. Despite the development of several new TMS paradigms, rTMS remains the dominant approach. Evidence suggests that rTMS signicantly enhances global cognitive function, as measured by
tools such as the MMSE, MoCA, and ADAS-Cog, when compared to sham stimulation. While improvements in specic cognitive domains, including memory, working memory, and executive function, have been observed, these may reect the
relatively limited number of studies focusing on these areas. Future research should
move beyond broad cognitive assessments and utilize more sensitive measures that
target specic cognitive domains. This approach could help identify the neuropsychological functions most responsive to improvement. Additionally, research may
reveal that TMS applied to specic brain regions can lead to more pronounced
effects in certain cognitive domains. For example, stimulation of the frontal regions
may enhance executive function and working memory more than new learning [15].
This would facilitate a more personalized approach, where TMS interventions are
tailored to address the individual cognitive impairments of each patient. The safety
and tolerability of TMS are well-established, particularly when appropriate safety
protocols are followed, even in older adults with depression [23]. Adherence to
contemporary safety guidelines [22], including thorough participant screening,
maintaining stimulation parameters within safety thresholds, and using qualied
technicians and clinicians, can signicantly mitigate the risk of seizures [25].
Extensive research suggests that tDCS may be a valuable tool for neuromodulating
cognitive function and may potentially support successful cognitive aging [81].
However, these ndings need replication and clinical application. Further studies are
necessary to enhance our understanding of the underlying mechanisms, therapeutic
outcomes, and inuencing factors, as well as to optimize stimulation parameters.
Future research should focus on determining the ideal stimulation parameters, including dosage, session duration, intersession intervals, optimal stimulation sites, and the
most effective combinations with pharmacological agents and other techniques that
may inuence disease progression. Despite the positive feedback from clinical trials,
tDCS remains an evolving technique, requiring further investigation to establish its
long-term safety. Additionally, healthcare professionals must receive adequate training in tDCS and adhere strictly to safety guidelines when implementing the technique.
Acknowledgments Acknowledgments are extended to all contributors who have facilitated the
completion of this academic manuscript. We thank Bullet Edits Limited for the linguistic editing
and proofreading of the manuscript. Special recognition is given to the geriatric team at Beijing
Anding Hospital for their substantial support and to Dr. Zheng Wei for his valuable input.

358
Disclosure/Conicts of Interest The authors declare no conicts of interest in conducting this
study or preparing the manuscript.
Financial Support This study was funded by the National Natural Science Foundation of China
(82401791); Capital’s Funds for Health Improvement and Research (CFH 2022-3-2124); HighLevel Public Health Technical Personnel Construction Training Program (Discipline
Backbone-02-38); Beijing Municipal Science and Technology Project (Z141107002514121). The
funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
C. Liu et al.
References
1. Sachdev PS, Blacker D, Blazer DG, et al. Classifying neurocognitive disorders: the DSM-5
approach. Nat Rev Neurol. 2014;10(11):634–42. https://doi.org/10.1038/nrneurol.2014.181.
2. Sachdev P, Andrews G, Hobbs MJ, et al. Neurocognitive disorders: cluster 1 of the proposed
meta-structure for DSM-V and ICD-11. Psychol Med. 2009;39(12):2001–12. https://doi.
org/10.1017/s0033291709990262.
3. American Psychological Association. Diagnostic and statistical manual of mental disorders.
5th ed. Washington, DC: American Psychiatric Pub; 2013.
4. Petersen RC, Lopez O, Armstrong MJ, et al. Practice guideline update summary: mild cognitive impairment: report of the guideline development, dissemination, and implementation subcommittee of the American Academy of Neurology. Neurology. 2018;90(3):126–35. https://
doi.org/10.1212/wnl.0000000000004826.
5. Esang M, Gupta M. Aducanumab as a novel treatment for Alzheimer’s disease: a decade
of hope, controversies, and the future. Cureus. 2021;13(8):e17591. https://doi.org/10.7759/
cureus.17591.
6. van Dyck CH, Swanson CJ, Aisen P, et al. Lecanemab in early Alzheimer’s disease. N Engl J
Med. 2023;388(1):9–21. https://doi.org/10.1056/NEJMoa2212948.
7. Arvanitakis Z, Shah RC, Bennett DA. Diagnosis and management of dementia: review.
JAMA. 2019;322(16):1589–99. https://doi.org/10.1001/jama.2019.4782.
8. Birba A, Ibáñez A, Sedeño L, et al. Non-invasive brain stimulation: a new strategy in
mild cognitive impairment? Front Aging Neurosci. 2017;9:16. https://doi.org/10.3389/
fnagi.2017.00016.
9. Cheng CPW, Wong CSM, Lee KK, et al. Effects of repetitive transcranial magnetic stimulation on improvement of cognition in elderly patients with cognitive impairment: a systematic
review and meta-analysis. Int J Geriatr Psychiatry. 2018;33(1):e1–e13. https://doi.org/10.1002/
gps.4726.
10. Dong X, Yan L, Huang L, et al. Repetitive transcranial magnetic stimulation for the treatment
of Alzheimer’s disease: a systematic review and meta-analysis of randomized controlled trials.
PLoS One. 2018;13(10):e0205704. https://doi.org/10.1371/journal.pone.0205704.
11. Fileccia E, Di Stasi V, Poda R, et al. Effects on cognition of 20-day anodal transcranial direct
current stimulation over the left dorsolateral prefrontal cortex in patients affected by mild
cognitive impairment: a case-control study. Neurol Sci. 2019;40(9):1865–72. https://doi.
org/10.1007/s10072-019-03903-6.
12. Ciullo V, Spalletta G, Caltagirone C, et al. Transcranial direct current stimulation and cognition in neuropsychiatric disorders: systematic review of the evidence and future directions.
Neuroscientist. 2021;27(3):285–309. https://doi.org/10.1177/1073858420936167.
13. Goette WF, Goette HE.A meta-analysis of the accuracy of embedded performance validity
indicators from the repeatable battery for the assessment of neuropsychological status. Clin
Neuropsychol. 2019;33(6):1044–68. https://doi.org/10.1080/13854046.2018.1538429.

13 Neurocognitive Disorders
14. Meinzer M, Lindenberg R, Phan MT, et al. Transcranial direct current stimulation in mild
cognitive impairment: behavioral effects and neural mechanisms. Alzheimers Dement.
2015;11(9):1032–40. https://doi.org/10.1016/j.jalz.2014.07.159.
15. Pagali SR, Kumar R, LeMahieu AM, et al. Efcacy and safety of transcranial magnetic stimulation on cognition in mild cognitive impairment, Alzheimer’s disease, Alzheimer’s diseaserelated dementias, and other cognitive disorders: a systematic review and meta-analysis. Int
Psychogeriatr. 2024:1–49. https://doi.org/10.1017/s1041610224000085.
16. Gy RR, Jv RL, Ricardo Garcell J, López Hidalgo M, Aguilar Fabré L, Trejo Cruz G, et al.
Effect of transcranial magnetic stimulation as an enhancer of cognitive stimulation sessions on
mild cognitive impairment: preliminary results. Psychiatry Res. 2021;304:114151. https://doi.
org/10.1016/j.psychres.2021.114151.
17. Dubreuil-Vall L, Chau P, Rufni G, et al. tDCS to the left DLPFC modulates cognitive and
physiological correlates of executive function in a state-dependent manner. Brain Stimul.
2019;12(6):1456–63. https://doi.org/10.1016/j.brs.2019.06.006.
18. Turriziani P, Smirni D, Zappalà G, et al. Enhancing memory performance with rTMS in healthy
subjects and individuals with mild cognitive impairment: the role of the right dorsolateral prefrontal cortex. Front Hum Neurosci. 2012;6:62. https://doi.org/10.3389/fnhum.2012.00062.
19. Cui H, Ren R, Lin G, et al. Repetitive transcranial magnetic stimulation induced hypoconnectivity within the default mode network yields cognitive improvements in amnestic mild
cognitive impairment: a randomized controlled study. J Alzheimers Dis. 2019;69(4):1137–51.
https://doi.org/10.3233/jad-181296.
20. Lin Y, Jiang WJ, Shan PY, et al. The role of repetitive transcranial magnetic stimulation
(rTMS) in the treatment of cognitive impairment in patients with Alzheimer’s disease: a systematic review and meta-analysis. J Neurol Sci. 2019;398:184–91. https://doi.org/10.1016/j.
jns.2019.01.038.
21. Teselink J, Bawa KK, Koo GK, et al. Efcacy of non-invasive brain stimulation on global
cognition and neuropsychiatric symptoms in Alzheimer’s disease and mild cognitive impairment: a meta-analysis and systematic review. Ageing Res Rev. 2021;72:101499. https://doi.
org/10.1016/j.arr.2021.101499.
22. Rossi S, Antal A, Bestmann S, et al. Safety and recommendations for TMS use in healthy
subjects and patient populations, with updates on training, ethical and regulatory issues:
expert guidelines. Clin Neurophysiol. 2021;132(1):269–306. https://doi.org/10.1016/j.
clinph.2020.10.003.
23. Iriarte IG, George MS.Transcranial magnetic stimulation (TMS) in the elderly. Curr Psychiatry
Rep. 2018;20(1):6. https://doi.org/10.1007/s11920-018-0866-2.
24. Pandis D, Scarmeas N. Seizures in Alzheimer disease: clinical and epidemiological data.
Epilepsy Curr. 2012;12(5):184–7. https://doi.org/10.5698/1535-7511-12.5.184.
25. Targa Dias Anastacio H, Matosin N, Ooi L.Neuronal hyperexcitability in Alzheimer’s disease: what are the drivers behind this aberrant phenotype? Transl Psychiatry. 2022;12(1):257.
https://doi.org/10.1038/s41398-022-02024-7.
26. Antal A, Luber B, Brem AK, et al. Non-invasive brain stimulation and neuroenhancement.
Clin Neurophysiol Pract. 2022;7:146–65. https://doi.org/10.1016/j.cnp.2022.05.002.
27. Fitzgerald PB, Chen L, Richardson K, et al. A pilot investigation of an intensive theta
burst stimulation protocol for patients with treatment resistant depression. Brain Stimul.
2020;13(1):137–44. https://doi.org/10.1016/j.brs.2019.08.013.
28. Cheng CM, Li CT, Tsai SJ. Current updates on newer forms of transcranial magnetic
stimulation in major depression. Adv Exp Med Biol. 2021;1305:333–49. https://doi.
org/10.1007/978-981-33-6044-0_18.
29. Zangen A, Roth Y, Voller B, et al. Transcranial magnetic stimulation of deep brain regions:
evidence for efcacy of the H-coil. Clin Neurophysiol. 2005;116(4):775–9. https://doi.
org/10.1016/j.clinph.2004.11.008.
359

360
30. Harel EV, Rabany L, Deutsch L, et al. H-coil repetitive transcranial magnetic stimulation for
treatment resistant major depressive disorder: an 18-week continuation safety and feasibility study. World J Biol Psychiatry. 2014;15(4):298–306. https://doi.org/10.3109/1562297
5.2011.639802.
31. Spagnolo F, Volonté MA, Fichera M, et al. Excitatory deep repetitive transcranial magnetic stimulation with H-coil as add-on treatment of motor symptoms in Parkinson’s disease: an open label, pilot study. Brain Stimul. 2014;7(2):297–300. https://doi.org/10.1016/j.
brs.2013.10.007.
32. Chieffo R, Ferrari F, Battista P, et al. Excitatory deep transcranial magnetic stimulation with H-coil over the right homologous Broca’s region improves naming in chronic
post-stroke aphasia. Neurorehabil Neural Repair. 2014;28(3):291–8. https://doi.
org/10.1177/1545968313508471.
33. Chieffo R, De Prezzo S, Houdayer E, et al. Deep repetitive transcranial magnetic stimulation
with H-coil on lower limb motor function in chronic stroke: a pilot study. Arch Phys Med
Rehabil. 2014;95(6):1141–7. https://doi.org/10.1016/j.apmr.2014.02.019.
34. Aghamoosa S, Lopez J, Rbeiz K, et al. A phase I trial of accelerated intermittent theta burst
rTMS for amnestic MCI.J Neurol Neurosurg Psychiatry. 2024;95(11):1036–45. https://doi.
org/10.1136/jnnp-2023-332680.
35. Wu X, Yan Y, Hu P, et al. Effects of a periodic intermittent theta burst stimulation in Alzheimer’s
disease. Gen Psychiatr. 2024;37(1):e101106. https://doi.org/10.1136/gpsych-2023-101106.
36. Avirame K, Stehberg J, Todder D. Benets of deep transcranial magnetic stimulation
in Alzheimer disease: case series. J ECT. 2016;32(2):127–33. https://doi.org/10.1097/
yct.0000000000000286.
37. Leocani L, Dalla Costa G, Coppi E, et al. Repetitive transcranial magnetic stimulation with
H-coil in Alzheimer’s disease: a double-blind, placebo-controlled pilot study. Front Neurol.
2020;11:614351. https://doi.org/10.3389/fneur.2020.614351.
38. Tzirini M, Roth Y, Harmelech T, et al. Detailed measurements and simulations of electric
eld distribution of two TMS coils cleared for obsessive compulsive disorder in the brain
and in specic regions associated with OCD.PLoS One. 2022;17(8):e0263145. https://doi.
org/10.1371/journal.pone.0263145.
39. Iyer MB, Schleper N, Wassermann EM.Priming stimulation enhances the depressant effect of
low-frequency repetitive transcranial magnetic stimulation. J Neurosci. 2003;23(34):10867–72.
https://doi.org/10.1523/jneurosci.23-34-10867.2003.
40. Fitzgerald PB, Hoy K, McQueen S, et al. Priming stimulation enhances the effectiveness of
low-frequency right prefrontal cortex transcranial magnetic stimulation in major depression. J
Clin Psychopharmacol. 2008;28(1):52–8. https://doi.org/10.1097/jcp.0b013e3181603f7c.
41. Leuchter AF, Cook IA, Feifel D, et al. Efcacy and safety of low-eld synchronized transcranial magnetic stimulation (sTMS) for treatment of major depression. Brain Stimul.
2015;8(4):787–94. https://doi.org/10.1016/j.brs.2015.05.005.
42. Fröhlich F.Endogenous and exogenous electric elds as modiers of brain activity: rational design of noninvasive brain stimulation with transcranial alternating current stimulation.
Dialogues Clin Neurosci. 2014;16(1):93–102. https://doi.org/10.31887/DCNS.2014.16.1/
ffroehlich.
43. Grahek I, Shenhav A, Musslick S, et al. Motivation and cognitive control in depression.
Neurosci Biobehav Rev. 2019;102:371–81. https://doi.org/10.1016/j.neubiorev.2019.04.011.
44. Liu C, Li L, Pan W, et al. Executive function decits in patients with the rst episode of latelife depression before and after SSRI treatment: a pilot fMRI study. Int J Geriatr Psychiatry.
2024;39(5):e6095. https://doi.org/10.1002/gps.6095.
45. Cauleld KA, Fleischmann HH, George MS, et al. A transdiagnostic review of safety, efcacy, and parameter space in accelerated transcranial magnetic stimulation. J Psychiatr Res.
2022;152:384–96. https://doi.org/10.1016/j.jpsychires.2022.06.038.
C. Liu et al.

13 Neurocognitive Disorders
46. Hoy KE, Emonson MRL, Bailey NW, et al. Gamma connectivity predicts response to intermittent theta burst stimulation in Alzheimer’s disease: a randomized controlled trial. Neurobiol
Aging. 2023;132:13–23. https://doi.org/10.1016/j.neurobiolaging.2023.08.006.
47. Wu X, Ji GJ, Geng Z, et al. Accelerated intermittent theta-burst stimulation broadly ameliorates symptoms and cognition in Alzheimer’s disease: a randomized controlled trial. Brain
Stimul. 2022;15(1):35–45. https://doi.org/10.1016/j.brs.2021.11.007.
48. Xiao G, Wu Y, Yan Y, et al. Optimized magnetic stimulation induced hypoconnectivity within
the executive control network yields cognition improvements in Alzheimer’s patients. Front
Aging Neurosci. 2022;14:847223. https://doi.org/10.3389/fnagi.2022.847223.
49. Lisanby SH.Update on magnetic seizure therapy: a novel form of convulsive therapy. J ect.
2002;18(4):182–8. https://doi.org/10.1097/00124509-200212000-00003.
50. Mutz J, Vipulananthan V, Carter B, et al. Comparative efcacy and acceptability of non-surgical brain stimulation for the acute treatment of major depressive episodes in adults: systematic
review and network meta-analysis. BMJ. 2019;364:l1079. https://doi.org/10.1136/bmj.l1079.
51. Benussi A, Dell’Era V, Cosseddu M, et al. Transcranial stimulation in frontotemporal
dementia: a randomized, double-blind, sham-controlled trial. Alzheimers Dement (N Y).
2020;6(1):e12033. https://doi.org/10.1002/trc2.12033.
52. Saxena V, Pal A. Role of transcranial direct current stimulation in the management of
Alzheimer’s disease: a meta-analysis of effects, adherence and adverse effects. Clin
Psychopharmacol Neurosci. 2021;19(4):589–99. https://doi.org/10.9758/cpn.2021.19.4.589.
53. Cespón J, Rodella C, Miniussi C, et al. Behavioural and electrophysiological modulations
induced by transcranial direct current stimulation in healthy elderly and Alzheimer’s disease
patients: a pilot study. Clin Neurophysiol. 2019;130(11):2038–52. https://doi.org/10.1016/j.
clinph.2019.08.016.
54. Gangemi A, Colombo B, Fabio RA. Effects of short- and long-term neurostimulation
(tDCS) on Alzheimer’s disease patients: two randomized studies. Aging Clin Exp Res.
2021;33(2):383–90. https://doi.org/10.1007/s40520-020-01546-8.
55. Khedr EM, Salama RH, Abdel Hameed M, et al. therapeutic role of transcranial direct current stimulation in Alzheimer disease patients: double-blind, placebo-controlled clinical trial.
Neurorehabil Neural Repair. 2019;33(5):384–94. https://doi.org/10.1177/1545968319840285.
56. Liu C, Pan W, Jia L, et al. Efcacy and safety of repetitive transcranial magnetic stimulation
for peripartum depression: a meta-analysis of randomized controlled trials. Psychiatry Res.
2020;294:113543. https://doi.org/10.1016/j.psychres.2020.113543.
57. Das S, Holland P, Frens MA, et al. Impact of transcranial direct current stimulation (tDCS) on
neuronal functions. Front Neurosci. 2016;10:550. https://doi.org/10.3389/fnins.2016.00550.
58. Qi S, Cao L, Wang Q, et al. The physiological mechanisms of transcranial direct current stimulation to enhance motor performance: a narrative review. Biology (Basel). 2024;13(10). https://
doi.org/10.3390/biology13100790.
59. Rroji O, van Kuyck K, Nuttin B, et al. Anodal tDCS over the primary motor cortex facilitates long-term memory formation reecting use-dependent plasticity. PLoS One.
2015;10(5):e0127270. https://doi.org/10.1371/journal.pone.0127270.
60. Majdi A, van Boekholdt L, Sadigh-Eteghad S, et al. A systematic review and meta-analysis of
transcranial direct-current stimulation effects on cognitive function in patients with Alzheimer’s
disease. Mol Psychiatry. 2022;27(4):2000–9. https://doi.org/10.1038/s41380-022-01444-7.
61. Cheng CP, Chan SS, Mak AD, et al. Would transcranial direct current stimulation (tDCS)
enhance the effects of working memory training in older adults with mild neurocognitive
disorder due to Alzheimer’s disease: study protocol for a randomized controlled trial. Trials.
2015;16:479. https://doi.org/10.1186/s13063-015-0999-0.
62. Fernandes SM, Mendes AJ, Rodrigues PFS, et al. Efcacy and safety of repetitive transcranial
magnetic stimulation and transcranial direct current stimulation in memory decits in patients
with Alzheimer’s disease: meta-analysis and systematic review. Int J Clin Health Psychol.
2024;24(2):100452. https://doi.org/10.1016/j.ijchp.2024.100452.
361

362
63. Galli G, Vadillo MA, Sirota M, et al. A systematic review and meta-analysis of the effects
of transcranial direct current stimulation (tDCS) on episodic memory. Brain Stimul.
2019;12(2):231–41. https://doi.org/10.1016/j.brs.2018.11.008.
64. Godinho MM, Junqueira DR, Castro ML, et al. Safety of transcranial direct current stimulation: evidence based update 2016. Brain Stimul. 2017;10(5):983–5. https://doi.org/10.1016/j.
brs.2017.07.001.
65. Rossi S, Hallett M, Rossini PM, et al. Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin
Neurophysiol. 2009;120(12):2008–39. https://doi.org/10.1016/j.clinph.2009.08.016.
66. Brunoni AR, Amadera J, Berbel B, et al. A systematic review on reporting and assessment of adverse effects associated with transcranial direct current stimulation. Int J
Neuropsychopharmacol. 2011;14(8):1133–45. https://doi.org/10.1017/s1461145710001690.
67. Im JJ, Jeong H, Bikson M, et al. Effects of 6-month at-home transcranial direct current stimulation on cognition and cerebral glucose metabolism in Alzheimer’s disease. Brain Stimul.
2019;12(5):1222–8. https://doi.org/10.1016/j.brs.2019.06.003.
68. Bystad M, Grønli O, Rasmussen ID, et al. Transcranial direct current stimulation as a memory enhancer in patients with Alzheimer’s disease: a randomized, placebo-controlled trial.
Alzheimers Res Ther. 2016;8(1):13. https://doi.org/10.1186/s13195-016-0180-3.
69. Fregni F, El-Hagrassy MM, Pacheco-Barrios K, et al. Evidence-based guidelines and secondary meta-analysis for the use of transcranial direct current stimulation in neurological and psychiatric disorders. Int J Neuropsychopharmacol. 2021;24(4):256–313. https://doi.org/10.1093/
ijnp/pyaa051.
70. Lefaucheur JP, Antal A, Ayache SS, et al. Evidence-based guidelines on the therapeutic use of
transcranial direct current stimulation (tDCS). Clin Neurophysiol. 2017;128(1):56–92. https://
doi.org/10.1016/j.clinph.2016.10.087.
71. Woods AJ, Antal A, Bikson M, et al. A technical guide to tDCS, and related non-invasive
brain stimulation tools. Clin Neurophysiol. 2016;127(2):1031–48. https://doi.org/10.1016/j.
clinph.2015.11.012.
72. Bikson M, Esmaeilpour Z, Adair D, et al. Transcranial electrical stimulation nomenclature.
Brain Stimul. 2019;12(6):1349–66. https://doi.org/10.1016/j.brs.2019.07.010.
73. He F, Li Y, Li C, et al. Repeated anodal high-denition transcranial direct current stimulation
over the left dorsolateral prefrontal cortex in mild cognitive impairment patients increased
regional homogeneity in multiple brain regions. PLoS One. 2021;16(8):e0256100. https://doi.
org/10.1371/journal.pone.0256100.
74. Iordan AD, Ryan S, Tyszkowski T, et al. High-denition transcranial direct current stimulation
enhances network segregation during spatial navigation in mild cognitive impairment. Cereb
Cortex. 2022;32(22):5230–41. https://doi.org/10.1093/cercor/bhac010.
75. Rasmussen ID, Boayue NM, Mittner M, et al. High-denition transcranial direct current
stimulation improves delayed memory in Alzheimer’s disease patients: a pilot study using
computational modeling to optimize electrode position. J Alzheimers Dis. 2021;83(2):753–69.
https://doi.org/10.3233/jad-210378.
76. Lang N, Siebner HR, Ward NS, et al. How does transcranial DC stimulation of the primary motor cortex alter regional neuronal activity in the human brain? Eur J Neurosci.
2005;22(2):495–504. https://doi.org/10.1111/j.1460-9568.2005.04233.x.
77. Kuo HI, Bikson M, Datta A, et al. Comparing cortical plasticity induced by conventional and
high-denition 4 × 1 ring tDCS: a neurophysiological study. Brain Stimul. 2013;6(4):644–8.
https://doi.org/10.1016/j.brs.2012.09.010.
78. Boayue NM, Csifcsák G, Kreis IV, et al. The interplay between executive control, behavioural
variability and mind wandering: Insights from a high-denition transcranial direct-current
stimulation study. Eur J Neurosci. 2021;53(5):1498–516. https://doi.org/10.1111/ejn.15049.
C. Liu et al.

13 Neurocognitive Disorders
79. Palimariciuc M, Oprea DC, Cristofor AC, et al. The effects of transcranial direct current stimulation in patients with mild cognitive impairment. Neurol Int. 2023;15(4):1423–42. https://doi.
org/10.3390/neurolint15040092.
80. Begemann MJ, Brand BA, Ćurčić-Blake B, et al. Efcacy of non-invasive brain stimulation on
cognitive functioning in brain disorders: a meta-analysis. Psychol Med. 2020;50(15):2465–86.
https://doi.org/10.1017/s0033291720003670.
81. Pezzoli S, Giorgio J, Martersteck A, et al. Successful cognitive aging is associated with thicker
anterior cingulate cortex and lower tau deposition compared to typical aging. Alzheimers
Dement. 2024;20(1):341–55. https://doi.org/10.1002/alz.13438.
363
Соседние файлы в папке Библиотека им академика М.И. Перельмана
