PubMed for id: 443976

Year	Number of Results
1970	1
1976	1
1987	1
1988	1
1989	1
1990	1
1992	1
1993	8
1994	4
1995	2
1996	6
1997	5
1998	6
1999	3
2000	3
2001	4
2002	8
2003	3
2004	4
2005	3
2006	11
2007	10
2008	5
2009	15
2010	8
2012	10
2013	9
2014	9
2015	17
2016	16
2017	21
2018	31
2019	34
2020	41
2021	42
2022	51
2023	31

1

Intractable Epilepsy in Maternally Inherited Leigh Syndrome (MILS) Due to the Sporadic Variant m.8993T>G in MT-ATP6: A Case Report.

Finsterer J. Finsterer J. Cureus. 2022 Feb 28;14(2):e22716. doi: 10.7759/cureus.22716. eCollection 2022 Feb. Cureus. 2022. PMID: 35371783 Free PMC article.

2

Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome.

Debray FG, Lambert M, Allard P, Mitchell GA. Debray FG, et al. J Child Neurol. 2010 Aug;25(8):1000-2. doi: 10.1177/0883073809351983. Epub 2010 May 14. J Child Neurol. 2010. PMID: 20472868

3

Maternally inherited Leigh syndrome: an unusual cause of infantile apnea.

Shuk-kuen Chau C, Kwok KL, Ng DK, Lam CW, Tong SF, Chan YW, Siu WK, Yuen YP. Shuk-kuen Chau C, et al. Sleep Breath. 2010 Jun;14(2):161-5. doi: 10.1007/s11325-009-0288-9. Epub 2009 Aug 11. Sleep Breath. 2010. PMID: 19669818

4

Maternally inherited Leigh syndrome: T8993G mutation in a Tunisian family.

Mkaouar-Rebai E, Chaari W, Younes S, Bousoffara R, Sfar MT, Fakhfakh F. Mkaouar-Rebai E, et al. Pediatr Neurol. 2009 Jun;40(6):437-42. doi: 10.1016/j.pediatrneurol.2009.01.004. Pediatr Neurol. 2009. PMID: 19433277

5

Maternally-inherited Leigh syndrome-related mutations bolster mitochondrial-mediated apoptosis.

Carrozzo R, Rizza T, Stringaro A, Pierini R, Mormone E, Santorelli FM, Malorni W, Matarrese P. Carrozzo R, et al. J Neurochem. 2004 Jul;90(2):490-501. doi: 10.1111/j.1471-4159.2004.02505.x. J Neurochem. 2004. PMID: 15228605 Free article.

6

Maternally inherited Leigh syndrome.

Ciafaloni E, Santorelli FM, Shanske S, Deonna T, Roulet E, Janzer C, Pescia G, DiMauro S. Ciafaloni E, et al. J Pediatr. 1993 Mar;122(3):419-22. doi: 10.1016/s0022-3476(05)83431-6. J Pediatr. 1993. PMID: 8095070

7

Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations.

Henke MT, Zink A, Diecke S, Prigione A, Schuelke M. Henke MT, et al. Stem Cell Res. 2023 Mar;67:103030. doi: 10.1016/j.scr.2023.103030. Epub 2023 Jan 17. Stem Cell Res. 2023. PMID: 36669241 Free article.

8

Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome.

Na JH, Lee YM. Na JH, et al. Pediatr Neurol. 2023 Jan;138:27-32. doi: 10.1016/j.pediatrneurol.2022.09.006. Epub 2022 Oct 5. Pediatr Neurol. 2023. PMID: 36335839

9

Synthesis, modifications and applications of MILs Metal-organic frameworks for environmental remediation: The cutting-edge review.

Khan S, Guan Q, Liu Q, Qin Z, Rasheed B, Liang X, Yang X. Khan S, et al. Sci Total Environ. 2022 Mar 1;810:152279. doi: 10.1016/j.scitotenv.2021.152279. Epub 2021 Dec 10. Sci Total Environ. 2022. PMID: 34902423 Review.

10

Is minimally invasive liver surgery a reasonable option in recurrent HCC? A snapshot from the I Go MILS registry.

Levi Sandri GB, Colasanti M, Aldrighetti L, Guglielmi A, Cillo U, Mazzaferro V, Dalla Valle R, De Carlis L, Gruttadauria S, Di Benedetto F, Ferrero A, Ettorre GM; I Go MILS Group on HCC. Levi Sandri GB, et al. Updates Surg. 2022 Feb;74(1):87-96. doi: 10.1007/s13304-021-01161-w. Epub 2021 Oct 3. Updates Surg. 2022. PMID: 34601669 Free article.

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