Similar articles for PMID: 25772319

Year	Number of Results
1993	1
2000	1
2001	1
2002	1
2003	1
2007	1
2008	1
2009	2
2010	1
2011	3
2012	2
2013	7
2014	5
2015	10
2016	4
2017	10
2018	9
2019	7
2021	4
2024	0

1

Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature.

Ardissone A, Granata T, Legati A, Diodato D, Melchionda L, Lamantea E, Garavaglia B, Ghezzi D, Moroni I. Ardissone A, et al. JIMD Rep. 2015;22:115-20. doi: 10.1007/8904_2015_419. Epub 2015 Mar 13. JIMD Rep. 2015. PMID: 25772319 Free PMC article.

2

A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.

Melchionda L, Damseh NS, Abu Libdeh BY, Nasca A, Elpeleg O, Zanolini A, Ghezzi D. Melchionda L, et al. Front Genet. 2014 Nov 14;5:397. doi: 10.3389/fgene.2014.00397. eCollection 2014. Front Genet. 2014. PMID: 25452764 Free PMC article.

3

Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review.

Mordaunt DA, Jolley A, Balasubramaniam S, Thorburn DR, Mountford HS, Compton AG, Nicholl J, Manton N, Clark D, Bratkovic D, Friend K, Yu S. Mordaunt DA, et al. Am J Med Genet A. 2015 Jun;167(6):1330-6. doi: 10.1002/ajmg.a.36968. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25899669 Review.

4

Mutations in the Complex III Assembly Factor Tetratricopeptide 19 Gene TTC19 Are a Rare Cause of Leigh Syndrome.

Atwal PS. Atwal PS. JIMD Rep. 2014;14:43-5. doi: 10.1007/8904_2013_282. Epub 2013 Dec 25. JIMD Rep. 2014. PMID: 24368687 Free PMC article.

5

Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies.

Ghezzi D, Arzuffi P, Zordan M, Da Re C, Lamperti C, Benna C, D'Adamo P, Diodato D, Costa R, Mariotti C, Uziel G, Smiderle C, Zeviani M. Ghezzi D, et al. Nat Genet. 2011 Mar;43(3):259-63. doi: 10.1038/ng.761. Epub 2011 Jan 30. Nat Genet. 2011. PMID: 21278747

6

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment.

Habibzadeh P, Inaloo S, Silawi M, Dastsooz H, Farazi Fard MA, Sadeghipour F, Faghihi Z, Rezaeian M, Yavarian M, Böhm J, Faghihi MA. Habibzadeh P, et al. Front Neurol. 2019 Sep 4;10:944. doi: 10.3389/fneur.2019.00944. eCollection 2019. Front Neurol. 2019. PMID: 31551910 Free PMC article.

7

Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency.

Nogueira C, Barros J, Sá MJ, Azevedo L, Taipa R, Torraco A, Meschini MC, Verrigni D, Nesti C, Rizza T, Teixeira J, Carrozzo R, Pires MM, Vilarinho L, Santorelli FM. Nogueira C, et al. Neurogenetics. 2013 May;14(2):153-60. doi: 10.1007/s10048-013-0361-1. Epub 2013 Mar 28. Neurogenetics. 2013. PMID: 23532514

8

Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.

Koch J, Freisinger P, Feichtinger RG, Zimmermann FA, Rauscher C, Wagentristl HP, Konstantopoulou V, Seidl R, Haack TB, Prokisch H, Ahting U, Sperl W, Mayr JA, Maier EM. Koch J, et al. Orphanet J Rare Dis. 2015 Apr 2;10:40. doi: 10.1186/s13023-015-0254-5. Orphanet J Rare Dis. 2015. PMID: 25887401 Free PMC article.

9

A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.

Kunii M, Doi H, Higashiyama Y, Kugimoto C, Ueda N, Hirata J, Tomita-Katsumoto A, Kashikura-Kojima M, Kubota S, Taniguchi M, Murayama K, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N, Tanaka F. Kunii M, et al. J Hum Genet. 2015 Apr;60(4):187-91. doi: 10.1038/jhg.2015.7. Epub 2015 Feb 5. J Hum Genet. 2015. PMID: 25652355 Review.

10

Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient.

Morino H, Miyamoto R, Ohnishi S, Maruyama H, Kawakami H. Morino H, et al. BMC Neurol. 2014 Jan 7;14:5. doi: 10.1186/1471-2377-14-5. BMC Neurol. 2014. PMID: 24397319 Free PMC article.

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