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Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?
Pennisi A, Rötig A, Roux CJ, Lévy R, Henneke M, Gärtner J, Teke Kisa P, Sarioglu FC, Yiş U, Konczal LL, Burkardt DD, Wu S, Gaignard P, Besmond C, Hubert L, Rio M, Barcia G, Munnich A, Boddaert N, Schiff M. Pennisi A, et al. Among authors: teke kisa p. J Med Genet. 2022 Feb;59(2):204-208. doi: 10.1136/jmedgenet-2020-107367. Epub 2020 Nov 16. J Med Genet. 2022. PMID: 33199448
A challenging etiology of myopathy: The late-onset Pompe disease.
Yüce İnel T, Köken Avşar A, Teke Kısa P, Özer E, Sarı İ. Yüce İnel T, et al. Among authors: teke kisa p. Eur J Rheumatol. 2023 Jan;10(1):26-28. doi: 10.5152/eurjrheum.2022.21156. Eur J Rheumatol. 2023. PMID: 35943460 Free article.