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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2000 1
2001 1
2010 1
2011 1
2012 1
2017 1
2019 1
2020 1
2021 2
2022 2
2023 2
2024 0

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PubMed for id: 433158

10 results

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Page 1
Macrocytosis in Mitochondrial DNA Deletion Syndromes.
Almarzooqi F, Vallance H, Mezei M, Lehman A, Horvath G, Rakic B, Zypchen L, Mattman A. Almarzooqi F, et al. Acta Haematol. 2023;146(3):220-225. doi: 10.1159/000529311. Epub 2023 Feb 10. Acta Haematol. 2023. PMID: 36774923 Review.
Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes.
Jacoby E, Bar-Yosef O, Gruber N, Lahav E, Varda-Bloom N, Bolkier Y, Bar D, Blumkin MB, Barak S, Eisenstein E, Ahonniska-Assa J, Silberg T, Krasovsky T, Bar O, Erez N, Bielorai B, Golan H, Dekel B, Besser MJ, Pozner G, Khoury H, Jacobs A, Campbell J, Herskovitz E, Sher N, Yivgi-Ohana N, Anikster Y, Toren A. Jacoby E, et al. Sci Transl Med. 2022 Dec 21;14(676):eabo3724. doi: 10.1126/scitranslmed.abo3724. Epub 2022 Dec 21. Sci Transl Med. 2022. PMID: 36542693
Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalionienė K, Burnytė B, Balkelienė D, Ambrozaitytė L, Utkus A. Grigalionienė K, et al. Mol Genet Genomic Med. 2023 Jan;11(1):e2059. doi: 10.1002/mgg3.2059. Epub 2022 Oct 1. Mol Genet Genomic Med. 2023. PMID: 36181358 Free PMC article.
Primary Mitochondrial Disorders Overview.
Chinnery PF. Chinnery PF. 2000 Jun 8 [updated 2021 Jul 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Jun 8 [updated 2021 Jul 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301403 Free Books & Documents. Review.