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Down Syndrome Biobank Consortium: A perspective.
Aldecoa I, Barroeta I, Carroll SL, Fortea J, Gilmore A, Ginsberg SD, Guzman SJ, Hamlett ED, Head E, Perez SE, Potter H, Molina-Porcel L, Raha-Chowdhury R, Wisniewski T, Yong WH, Zaman S, Ghosh S, Mufson EJ, Granholm AC. Aldecoa I, et al. Among authors: raha chowdhury r. Alzheimers Dement. 2024 Mar;20(3):2262-2272. doi: 10.1002/alz.13692. Epub 2024 Jan 25. Alzheimers Dement. 2024. PMID: 38270275 Free PMC article.
Interplay of Ferritin Accumulation and Ferroportin Loss in Ageing Brain: Implication for Protein Aggregation in Down Syndrome Dementia, Alzheimer's, and Parkinson's Diseases.
Raha AA, Biswas A, Henderson J, Chakraborty S, Holland A, Friedland RP, Mukaetova-Ladinska E, Zaman S, Raha-Chowdhury R. Raha AA, et al. Among authors: raha chowdhury r. Int J Mol Sci. 2022 Jan 19;23(3):1060. doi: 10.3390/ijms23031060. Int J Mol Sci. 2022. PMID: 35162984 Free PMC article.
Hepcidin Increases Cytokines in Alzheimer's Disease and Down's Syndrome Dementia: Implication of Impaired Iron Homeostasis in Neuroinflammation.
Raha AA, Ghaffari SD, Henderson J, Chakraborty S, Allinson K, Friedland RP, Holland A, Zaman SH, Mukaetova-Ladinska EB, Raha-Chowdhury R. Raha AA, et al. Among authors: raha chowdhury r. Front Aging Neurosci. 2021 Apr 30;13:653591. doi: 10.3389/fnagi.2021.653591. eCollection 2021. Front Aging Neurosci. 2021. PMID: 33994996 Free PMC article.
COVID-19 and neurocognitive disorders.
Mukaetova-Ladinska EB, Kronenberg G, Raha-Chowdhury R. Mukaetova-Ladinska EB, et al. Among authors: raha chowdhury r. Curr Opin Psychiatry. 2021 Mar 1;34(2):149-156. doi: 10.1097/YCO.0000000000000687. Curr Opin Psychiatry. 2021. PMID: 33395101 Free PMC article. Review.
Transplantation of Neural Precursors Derived from Induced Pluripotent Cells Preserve Perineuronal Nets and Stimulate Neural Plasticity in ALS Rats.
Forostyak S, Forostyak O, Kwok JCF, Romanyuk N, Rehorova M, Kriska J, Dayanithi G, Raha-Chowdhury R, Jendelova P, Anderova M, Fawcett JW, Sykova E. Forostyak S, et al. Among authors: raha chowdhury r. Int J Mol Sci. 2020 Dec 16;21(24):9593. doi: 10.3390/ijms21249593. Int J Mol Sci. 2020. PMID: 33339362 Free PMC article.
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.
Olsson KS, Wålinder O, Jansson U, Wilbe M, Bondeson ML, Stattin EL, Raha-Chowdhury R, Williams R. Olsson KS, et al. Among authors: raha chowdhury r. Hereditas. 2017 Dec 19;154:16. doi: 10.1186/s41065-017-0052-2. eCollection 2017. Hereditas. 2017. PMID: 29270100 Free PMC article.
42 results