Chương 4: Bệnh Alzheimer xuất hiện như thế nào: Mồi lửa

1. Kumar, D. K., et al. Amyloid-beta peptide protects against microbial infection in mouse and worm models of Alzheimer’s disease. Science Translational Medicine 8: 340ra72, doi: 10.1126/scitranslmedaaf1059 (2016).

2. Kumar, D. K., W. A. Eimer, R. E. Tanzi, and R. D. Moir. Alzheimer’s disease: the potential therapeutic role of the natural antibiotic amyloid-beta peptide. Neurodegenerative Disease Management 6: 345–348, doi:10.2217/nmt-2016- 0035 (2016).

Chương 5: Tâm trạng bế tắc: Từ giường bệnh đến phòng thí nghiệm và ngược lại

1. https:// enwikipediaorg/ wiki/ Dependence_ receptor.

2. Lourenço, F. C., et al. Netrin-1 interacts with amyloid precursor protein and regulates amyloid-beta production. Cell Death and Differentiation 16: 655– 663, doi: cdd2008191 [pii]10.1038/ cdd.2008.191 (2009).

3. Galvan, V., et al. Reversal of Alzheimer’s-like pathology and behavior in human APP transgenic mice by mutation of Asp664. Proceedings of the National Academy of Science USA 103: 7130–7135, doi: 10.1073/ pnas.0509695103 (2006).

4. Spilman, P., et al. The multi-functional drug tropisetron binds APP and normalizes cognition in a murine Alzheimer’s model. Brain Research 1551: 25–44, doi: 10.1016/jbrainres.2013.12.029 (2014).

5. Ibid.

6. Clarkson, T. W., L. Magos, and G. J. Myers. The toxicology of mercury— current exposures and clinical manifestations. New England Journal of Medicine 349: 1731–1737, doi: 10.1056/ NEJMra022471 (2003).

Chương 6: Đoạn gen thần thánh và ba thể bệnh Alzheimer

1. Mutter, J., A. Curth, J. Naumann, R. Deth, and H. Walach. Does inorganic mercury play a role in Alzheimer’s disease? A systematic review and an integrated molecular mechanism. Journal of Alzheimer’s Disease 22: 357–374, doi:10.3233/JAD-2010-100705 (2010).

Chương 7: "Nội soi tầm soát nhận thức": Bạn đang đứng ở đâu?

1. den Heijer, T., et al. Homocysteine and brain atrophy on MRI of non- demented elderly. Brain 126 (Pt 1): 170–175 (2003).

2. Rocca, W. A., B. R. Grossardt, L. T. Shuster, and E. A. Stewart. Hysterectomy, oophorectomy, estrogen, and the risk of dementia. Neurodegenerative Diseases 10: 175–178, doi: 10.1159/ 000334764 (2012).

3. Brewer, G. J. Copper excess, zinc deficiency, and cognition loss in Alzheimer’s disease. Biofactors 38: 107–113, doi: 10.1002/ biof.1005 (2012).

4. Chausmer, A. B. Zinc, insulin and diabetes. Journal of the American College of Nutrition 17: 109–115 (1998).

5. Liu, G., J. G. Weinger, Z. L. Lu, F. Xue, and S. Sadeghpour. Efficacy and safety of MMFS-01, a synapse density enhancer, for treating cognitive impairment in older adults: a randomized, double-blind, placebo-controlled trial. Journal of Alzheimer’s Disease 49: 971–990, doi: 10.3233/JAD-150538 (2016).

6. Smorgon, C., et al. Trace elements and cognitive impairment: an elderly cohort study. Archives of Gerontology and Geriatrics Supplement 9: 393–402, doi: 10.1016/jarchger.2004.04.050 (2004).

7. Tyler, C. R., and A. M. Allan. The effects of arsenic exposure on neurological and cognitive dysfunction in human and rodent studies: a review. Current Environmental Health Reports 132–147, Report No.2196-5412 (Electronic) (2014).

8. Basha, M. R., et al. The fetal basis of amyloidogenesis: exposure to lead and latent overexpression of amyloid precursor protein and beta-amyloid in the aging brain. Journal of Neuroscience 25: 823–829, doi: 10.1523/ JNEUROSCI.4335-04.2005 (2005).

9. Bakulski, K. M., L. S. Rozek, D. C. Dolinoy, H. L. Paulson, and H. Hu. Alzheimer’s disease and environmental exposure to lead: the epidemiologic evidence and potential role of epigenetics. Current Alzheimer Research 9: 563–573 (2012).

10. Ashok A., N. K. Rai, S. Tripathi, and S. Bandyopadhyay. Exposure to As-, Cd-, and Pb-mixture induces Aβ, amyloidogenic APP processing and cognitive impairments via oxidative stress-dependent neuroinflammation in young rats. Toxicological Sciences 143: 64–80, doi: 10.1093/toxsci/ kfu208 (2015).

11. Dysken, M. W. et al. Effect of vitamin E and memantine on functional decline in Alzheimer disease: the TEAM-AD VA cooperative randomized trial. Journal of the American Medical Association 311: 33–44, doi: 10.1001/ jama.2013.282834 (2014).

12. Poole, S., S. K. Singhrao, L. Kesavalu, M. A. Curtis, and S. Crean. Determining the presence of periodontopathic virulence factors in short- term postmortem Alzheimer’s disease brain tissue. Journal of Alzheimer’s Disease 36: 665–677, doi: 10.3233/JAD-121918 (2013).

13. Descamps, O., Q. Zhang, V. John, and D. E. Bredesen. Induction of the C-terminal proteolytic cleavage of AβPP by statins. Journal of Alzheimer’s Disease 25: 51–57, doi: 10.3233/JAD-2011-101857 (2011).

14. Bredesen, D. E. Inhalational Alzheimer’s disease: an unrecognized—and treatable—epidemic. Aging (Albany NY) 8: 304–313 (2016).

Chương 8: ReCODE: Đảo ngược tiến trình suy giảm nhận thức

1. Heijer, T., et al. Association between blood pressure levels over time and brain atrophy in the elderly. Neurobiology of Aging 24: 307–313 (2003).

2. http://wwwhealthharvardedudiseases-and-conditionsglycemic-index- and-glycemic-load-for-100-foods.

3. Khan, A., M. Safdar, M. M. Ali Khan, K. N. Khattak, and R. A. Anderson. Cinnamon improves glucose and lipids of people with type 2 diabetes. Diabetes Care 26: 3215–3218 (2003).

4. http://articlesmercolacomsitesarticlesarchive/2014/09/21/hilary- boynton-mary-brackett-gaps-cookbook-interviewaspx.

5. https://draxecomscd-diet/

6. http://wwwdrperlmuttercomlearnresourcesprobiotics-five-core-species.

7. Thrasher, J. D., M. R. Gray, K. H. Kilburn, D. P. Dennis, and A. Yu. A water-damaged home and health of occupants: a case study. Journal of Environmental and Public Health 2012, doi: 10.1155/ 2012/ 312836 (2012).

8. http:// wwwsurvivingmoldcomshoemaker-protocolCertified- Physicians- Shoemaker-Protocol

9. https:// wwwfunctionalmedicineorg/ practitioner_ searchaspx? id= 117.

10. Shoemaker, R. C., MD. Surviving Mold: Life in the Era of Dangerous Buildings. Otter Bay Books, 2010.

Phụ Lục D

1. Galvan, V., et al. Reversal of Alzheimer’s-like pathology and behavior in human APP transgenic mice by mutation of Asp664. Proceedings of the National Academy of Science USA 103: 7130–7135, doi:10.1073/ pnas.0509695103 (2006).

2. Ibid.

3. Theendakara, V., et al. Neuroprotective sirtuin ratio reversed by ApoE4. Proceedings of the National Academy of Science USA 110: 18303–18308, doi: 10.1073/pnas.1314145110 (2013).

4. Lourenço, F. C., et al. Netrin-1 interacts with amyloid precursor protein and regulates amyloid-beta production. Cell Death and Differentiation 16: 655–663, doi: cdd2008191 [pii]10.1038/ cdd.2008.191 (2009).

5. Lu, D. C., et al. A second cytotoxic proteolytic peptide derived from amyloid-beta-protein precursor. Nature Medicine 6: 397–404, doi:10.1038/74656 (2000).

6. Spilman, P., B. Jagodzinska, D. E. Bredesen, and John Varghese. Enhancement of sAPPα as a therapeutic strategy for Alzheimer’s and other neurodegenerative diseases. HSOA Journal of Alzheimer’s & Neurodegenerative Diseases 1: 1–10 (2015).

7. Spilman, P. R., et al. Netrin-1 interrupts amyloid-beta amplification, increases sAβPPα in vitro and in vivo, and improves cognition in a mouse model of Alzheimer’s disease. Journal of Alzheimer’s Disease 52:223–242, doi: 10.3233/JAD-151046 (2016).

8. Julien, O., et al. Unraveling the mechanism of cell death induced by chemical fibrils. Nature Chemical Biology 10: 969–976, doi: 10.1038/nchembio.1639 (2014).

9. Matrone, C., et al. Activation of the amyloidogenic route by NGF deprivation induces apoptotic death in PC12 cells. Journal of Alzheimer’s Disease 13: 81–96 (2008).

10. Bredesen, D. E. Reversal of cognitive decline: A novel therapeutic program. Aging 6: 707–717, doi: 10.18632/ aging.100690 (2014).

11. Bredesen, D. E., et al. Reversal of cognitive decline in Alzheimer’s disease. Aging 8: 1250–1258, doi: 10.18632/ aging.100981 (2016).