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For: Finsterer J. Inherited mitochondrial neuropathies. J Neurol Sci 2011;304:9-16. [PMID: 21402391 DOI: 10.1016/j.jns.2011.02.012] [Cited by in Crossref: 34] [Cited by in F6Publishing: 33] [Article Influence: 3.1] [Reference Citation Analysis]
Number Citing Articles
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2 Luigetti M, Primiano G, Cuccagna C, Bernardo D, Sauchelli D, Vollono C, Servidei S. Small fibre neuropathy in mitochondrial diseases explored with sudoscan. Clinical Neurophysiology 2018;129:1618-23. [DOI: 10.1016/j.clinph.2018.04.755] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Luigetti M, Sauchelli D, Primiano G, Cuccagna C, Bernardo D, Lo Monaco M, Servidei S. Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experience. Eur J Neurol 2016;23:1020-7. [DOI: 10.1111/ene.12954] [Cited by in Crossref: 24] [Cited by in F6Publishing: 20] [Article Influence: 4.0] [Reference Citation Analysis]
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6 Slabbaert JR, Kuenen S, Swerts J, Maes I, Uytterhoeven V, Kasprowicz J, Fernandes AC, Blust R, Verstreken P. Shawn, the Drosophila Homolog of SLC25A39/40, Is a Mitochondrial Carrier That Promotes Neuronal Survival. J Neurosci 2016;36:1914-29. [PMID: 26865615 DOI: 10.1523/JNEUROSCI.3432-15.2016] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
7 Finsterer J, Zarrouk-mahjoub S. Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both. Neuromuscular Disorders 2016;26:548-9. [DOI: 10.1016/j.nmd.2016.06.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
8 Michaud M, Stojkovic T, Maisonobe T, Behin A, Rucheton B, Léonard-louis S, Eymard B, Laforêt P. Ganglionopathies Associated with MERRF Syndrome: An Original Report. JND 2020;7:419-23. [DOI: 10.3233/jnd-200513] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Mathis S, Duval F, Soulages A, Solé G, Le Masson G. The ataxic neuropathies. J Neurol 2021;268:3675-89. [DOI: 10.1007/s00415-020-09994-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Echaniz-Laguna A, Ghezzi D, Chassagne M, Mayençon M, Padet S, Melchionda L, Rouvet I, Lannes B, Bozon D, Latour P, Zeviani M, Mousson de Camaret B. SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease. Neurology 2013;81:1523-30. [PMID: 24027061 DOI: 10.1212/WNL.0b013e3182a4a518] [Cited by in Crossref: 41] [Cited by in F6Publishing: 11] [Article Influence: 4.6] [Reference Citation Analysis]
11 Samuelsson K, Kostulas K, Vrethem M, Rolfs A, Press R. Idiopathic small fiber neuropathy: phenotype, etiologies, and the search for fabry disease. J Clin Neurol 2014;10:108-18. [PMID: 24829596 DOI: 10.3988/jcn.2014.10.2.108] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 3.4] [Reference Citation Analysis]
12 Kornmann B. Quality control in mitochondria: use it, break it, fix it, trash it. F1000Prime Rep 2014;6:15. [PMID: 24669296 DOI: 10.12703/P6-15] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 2.3] [Reference Citation Analysis]
13 Maurer LL, Meyer JN. A systematic review of evidence for silver nanoparticle-induced mitochondrial toxicity. Environ Sci : Nano 2016;3:311-22. [DOI: 10.1039/c5en00187k] [Cited by in Crossref: 57] [Cited by in F6Publishing: 1] [Article Influence: 9.5] [Reference Citation Analysis]
14 Kappler L, Li J, Häring HU, Weigert C, Lehmann R, Xu G, Hoene M. Purity matters: A workflow for the valid high-resolution lipid profiling of mitochondria from cell culture samples. Sci Rep 2016;6:21107. [PMID: 26892142 DOI: 10.1038/srep21107] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 3.7] [Reference Citation Analysis]
15 Samuelsson K, Mariosa D, Fang F, Press R. Comorbidity of mitochondrial disease and dementia in patients with idiopathic polyneuropathy. Eur J Neurol 2018;25:882-7. [DOI: 10.1111/ene.13612] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
16 Jones RE, Lee J, Ali MM. Renal artery aneurysm associated with Leber hereditary optic neuropathy. J Vasc Surg Cases Innov Tech 2018;4:5-7. [PMID: 29725659 DOI: 10.1016/j.jvscit.2017.10.001] [Reference Citation Analysis]
17 Menezes MP, Ouvrier RA. Peripheral neuropathy associated with mitochondrial disease in children. Dev Med Child Neurol 2012;54:407-14. [PMID: 22435634 DOI: 10.1111/j.1469-8749.2012.04271.x] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 2.6] [Reference Citation Analysis]
18 Chou SJ, Tseng WL, Chen CT, Lai YF, Chien CS, Chang YL, Lee HC, Wei YH, Chiou SH. Impaired ROS Scavenging System in Human Induced Pluripotent Stem Cells Generated from Patients with MERRF Syndrome. Sci Rep. 2016;6:23661. [PMID: 27025901 DOI: 10.1038/srep23661] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 3.2] [Reference Citation Analysis]
19 Finsterer J. POLG1-related phenotypes are heterogeneous and progressive due to secondary mtDNA maintenance defects. Int J Neurosci 2020;130:1282-3. [PMID: 32065548 DOI: 10.1080/00207454.2020.1731506] [Reference Citation Analysis]
20 Towbin JA, Jefferies JL. Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism. Circ Res 2017;121:838-54. [PMID: 28912186 DOI: 10.1161/CIRCRESAHA.117.310987] [Cited by in Crossref: 56] [Cited by in F6Publishing: 23] [Article Influence: 11.2] [Reference Citation Analysis]
21 Vital A, Vital C. Mitochondria and peripheral neuropathies. J Neuropathol Exp Neurol 2012;71:1036-46. [PMID: 23147504 DOI: 10.1097/NEN.0b013e3182764d47] [Cited by in Crossref: 30] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
22 Breuer M, Koopman W, Koene S, Nooteboom M, Rodenburg R, Willems P, Smeitink J. The role of mitochondrial OXPHOS dysfunction in the development of neurologic diseases. Neurobiology of Disease 2013;51:27-34. [DOI: 10.1016/j.nbd.2012.03.007] [Cited by in Crossref: 53] [Cited by in F6Publishing: 50] [Article Influence: 5.9] [Reference Citation Analysis]
23 Demers-Lamarche J, Guillebaud G, Tlili M, Todkar K, Bélanger N, Grondin M, Nguyen AP, Michel J, Germain M. Loss of Mitochondrial Function Impairs Lysosomes. J Biol Chem 2016;291:10263-76. [PMID: 26987902 DOI: 10.1074/jbc.M115.695825] [Cited by in Crossref: 106] [Cited by in F6Publishing: 75] [Article Influence: 17.7] [Reference Citation Analysis]
24 Finsterer J. Auditory and Vestibular Dysfunction in M.3243A>G Carriers. Otol Neurotol 2019;40:1260. [PMID: 31469803 DOI: 10.1097/MAO.0000000000002411] [Reference Citation Analysis]
25 Rinwa P, Calvo-Enrique L, Zhang MD, Nyengaard JR, Karlsson P, Ernfors P. Demise of nociceptive Schwann cells causes nerve retraction and pain hyperalgesia. Pain 2021;162:1816-27. [PMID: 33979318 DOI: 10.1097/j.pain.0000000000002169] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
26 Bruhn H, Samuelsson K, Schober FA, Engvall M, Lesko N, Wibom R, Nennesmo I, Calvo-Garrido J, Press R, Stranneheim H, Freyer C, Wedell A, Wredenberg A. Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy. Neurol Genet 2021;7:e566. [PMID: 33732874 DOI: 10.1212/NXG.0000000000000566] [Reference Citation Analysis]
27 Lang-orsini M, Gonzalez-perez P. Neuropathic Pain as Main Manifestation of POLG-Related Disease: A Case Report. Front Neurol 2022;13:846110. [DOI: 10.3389/fneur.2022.846110] [Reference Citation Analysis]
28 Ge M, Bai X, Liu A, Liu L, Tian J, Lu T. An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway. Genes Dis 2021;8:545-54. [PMID: 34179316 DOI: 10.1016/j.gendis.2020.02.003] [Reference Citation Analysis]
29 Kabala AM, Lasserre JP, Ackerman SH, di Rago JP, Kucharczyk R. Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C. Biochimie 2014;100:200-6. [PMID: 24316278 DOI: 10.1016/j.biochi.2013.11.024] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.8] [Reference Citation Analysis]
30 Shin J, Kim D. Genetics of Mitochondrial Myopathies. J Genet Med 2013;10:20-6. [DOI: 10.5734/jgm.2013.10.1.20] [Cited by in Crossref: 3] [Article Influence: 0.3] [Reference Citation Analysis]
31 Pareyson D, Piscosquito G, Moroni I, Salsano E, Zeviani M. Peripheral neuropathy in mitochondrial disorders. Lancet Neurol 2013;12:1011-24. [PMID: 24050734 DOI: 10.1016/S1474-4422(13)70158-3] [Cited by in Crossref: 59] [Cited by in F6Publishing: 22] [Article Influence: 6.6] [Reference Citation Analysis]
32 El-Hattab AW, Scaglia F. Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options. Neurotherapeutics 2013;10:186-98. [PMID: 23385875 DOI: 10.1007/s13311-013-0177-6] [Cited by in Crossref: 163] [Cited by in F6Publishing: 142] [Article Influence: 18.1] [Reference Citation Analysis]
33 Yu JY, Pearl PL. Metabolic causes of epileptic encephalopathy. Epilepsy Res Treat 2013;2013:124934. [PMID: 23762547 DOI: 10.1155/2013/124934] [Cited by in Crossref: 7] [Cited by in F6Publishing: 14] [Article Influence: 0.8] [Reference Citation Analysis]
34 Bisceglia M, Crociani P, Fogli D, Centola A, Galliani CA, Pasquinelli G. Selected case from the Arkadi M. Rywlin International Pathology Slide Series: Mitochondrial myopathy presenting with chronic progressive external ophthalmoplegia (CPEO): a case report. Adv Anat Pathol 2014;21:461-8. [PMID: 25299315 DOI: 10.1097/PAP.0000000000000045] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
35 Guo H, Li S, Dai L, Huang X, Yu T, Yin Z, Bai Y. Genetic analysis in a cohort of patients with hereditary optic neuropathies in Southwest of China. Mitochondrion 2019;46:327-33. [PMID: 30201499 DOI: 10.1016/j.mito.2018.09.002] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
36 Lovan A, Ihtsham ul Haq, Balakrishnan N. Diagnostic challenges in movement disorders: Sensory Ataxia Neuropathy Dysarthria and Ophthalmoplegia (SANDO) syndrome. BMJ Case Rep 2013;2013:bcr2013010343. [PMID: 23997076 DOI: 10.1136/bcr-2013-010343] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]