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For: von Kleist-retzow J, Cormier-daire V, Viot G, Goldenberg A, Mardach B, Amiel J, Saada P, Dumez Y, Brunelle F, Saudubray J, Chrétien D, Rötig A, Rustin P, Munnich A, De Lonlay P. Antenatal manifestations of mitochondrial respiratory chain deficiency. The Journal of Pediatrics 2003;143:208-12. [DOI: 10.1067/s0022-3476(03)00130-6] [Cited by in Crossref: 96] [Cited by in F6Publishing: 29] [Article Influence: 5.1] [Reference Citation Analysis]
Number Citing Articles
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3 Gopan A, Sarma MS. Mitochondrial hepatopathy: Respiratory chain disorders- ‘breathing in and out of the liver’. World J Hepatol 2021; 13(11): 1707-1726 [PMID: 34904040 DOI: 10.4254/wjh.v13.i11.1707] [Reference Citation Analysis]
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5 Chang YL, Chao AS, Peng HH, Chang SD, Su SY, Chen KJ, Wang TH. Effects of inter-twin vascular anastomoses of monochorionic twins with selective intrauterine growth restriction on the contents of placental mitochondria DNA. BMC Pregnancy Childbirth 2018;18:74. [PMID: 29573746 DOI: 10.1186/s12884-018-1702-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
6 Priliani L, Prado EL, Restuadi R, Waturangi DE, Shankar AH, Malik SG. Maternal Multiple Micronutrient Supplementation Stabilizes Mitochondrial DNA Copy Number in Pregnant Women in Lombok, Indonesia. J Nutr 2019;149:1309-16. [PMID: 31177276 DOI: 10.1093/jn/nxz064] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
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9 Solomon BD. VACTERL/VATER Association. Orphanet J Rare Dis 2011;6:56. [PMID: 21846383 DOI: 10.1186/1750-1172-6-56] [Cited by in Crossref: 213] [Cited by in F6Publishing: 143] [Article Influence: 19.4] [Reference Citation Analysis]
10 Prayer D, Brugger PC. Investigation of normal organ development with fetal MRI. Eur Radiol 2007;17:2458-71. [PMID: 17342486 DOI: 10.1007/s00330-007-0604-3] [Cited by in Crossref: 47] [Cited by in F6Publishing: 35] [Article Influence: 3.1] [Reference Citation Analysis]
11 Lee S, Baek MS, Lee YM. Lennox-Gastaut Syndrome in Mitochondrial Disease. Yonsei Med J 2019;60:106-14. [PMID: 30554497 DOI: 10.3349/ymj.2019.60.1.106] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
12 Rosario FJ, Gupta MB, Myatt L, Powell TL, Glenn JP, Cox L, Jansson T. Mechanistic Target of Rapamycin Complex 1 Promotes the Expression of Genes Encoding Electron Transport Chain Proteins and Stimulates Oxidative Phosphorylation in Primary Human Trophoblast Cells by Regulating Mitochondrial Biogenesis. Sci Rep 2019;9:246. [PMID: 30670706 DOI: 10.1038/s41598-018-36265-8] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 7.3] [Reference Citation Analysis]
13 Emma F, Bertini E, Salviati L, Montini G. Renal involvement in mitochondrial cytopathies. Pediatr Nephrol 2012;27:539-50. [PMID: 21656172 DOI: 10.1007/s00467-011-1926-6] [Cited by in Crossref: 74] [Cited by in F6Publishing: 60] [Article Influence: 6.7] [Reference Citation Analysis]
14 Suthammarak W, Yang YY, Morgan PG, Sedensky MM. Complex I function is defective in complex IV-deficient Caenorhabditis elegans. J Biol Chem 2009;284:6425-35. [PMID: 19074434 DOI: 10.1074/jbc.M805733200] [Cited by in Crossref: 58] [Cited by in F6Publishing: 31] [Article Influence: 4.1] [Reference Citation Analysis]
15 Wambach JA, Stettner GM, Haack TB, Writzl K, Škofljanec A, Maver A, Munell F, Ossowski S, Bosio M, Wegner DJ, Shinawi M, Baldridge D, Alhaddad B, Strom TM, Grange DK, Wilichowski E, Troxell R, Collins J, Warner BB, Schmidt RE, Pestronk A, Cole FS, Steinfeld R. Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN). Hum Mutat 2017;38:1477-84. [PMID: 28726266 DOI: 10.1002/humu.23297] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.8] [Reference Citation Analysis]
16 Venditti CP, Harris MC, Huff D, Peterside I, Munson D, Weber HS, Rome J, Kaye EM, Shanske S, Sacconi S, Tay S, DiMauro S, Berry GT. Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency. J Inherit Metab Dis 2004;27:735-9. [PMID: 15505378 DOI: 10.1023/B:BOLI.0000045711.89888.5e] [Cited by in Crossref: 17] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
17 Lee WS, Sokol RJ. Liver disease in mitochondrial disorders. Semin Liver Dis. 2007;27:259-273. [PMID: 17682973 DOI: 10.1055/s-2007-985071] [Cited by in Crossref: 62] [Cited by in F6Publishing: 46] [Article Influence: 4.1] [Reference Citation Analysis]
18 Chen Y, Liu Z, Chen J, Zuo Y, Liu S, Chen W, Liu G, Qiu G, Giampietro PF, Wu N, Wu Z. The genetic landscape and clinical implications of vertebral anomalies in VACTERL association. J Med Genet 2016;53:431-7. [PMID: 27084730 DOI: 10.1136/jmedgenet-2015-103554] [Cited by in Crossref: 29] [Cited by in F6Publishing: 18] [Article Influence: 4.8] [Reference Citation Analysis]
19 Landsverk ML, Zhang VW, Wong LC, Andersson HC. A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomalies. Mol Genet Metab Rep 2014;1:451-4. [PMID: 27896121 DOI: 10.1016/j.ymgmr.2014.09.007] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
20 Chiaratti MR, Malik S, Diot A, Rapa E, Macleod L, Morten K, Vatish M, Boyd R, Poulton J. Is Placental Mitochondrial Function a Regulator that Matches Fetal and Placental Growth to Maternal Nutrient Intake in the Mouse? PLoS One 2015;10:e0130631. [PMID: 26132581 DOI: 10.1371/journal.pone.0130631] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 2.1] [Reference Citation Analysis]
21 Boal RL, Ng YS, Pickett SJ, Schaefer AM, Feeney C, Bright A, Taylor RW, Turnbull DM, Gorman GS, Cheetham T, McFarland R. Height as a Clinical Biomarker of Disease Burden in Adult Mitochondrial Disease. J Clin Endocrinol Metab 2019;104:2057-66. [PMID: 30423112 DOI: 10.1210/jc.2018-00957] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
22 Enns GM. Inborn Errors of Metabolism Masquerading as Hypoxic-Ischemic Encephalopathy. NeoReviews 2005;6:e549-58. [DOI: 10.1542/neo.6-12-e549] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
23 Vianey-Saban C, Acquaviva C, Cheillan D, Collardeau-Frachon S, Guibaud L, Pagan C, Pettazzoni M, Piraud M, Lamazière A, Froissart R. Antenatal manifestations of inborn errors of metabolism: biological diagnosis. J Inherit Metab Dis 2016;39:611-24. [PMID: 27393412 DOI: 10.1007/s10545-016-9947-8] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 3.5] [Reference Citation Analysis]
24 Garcia-Dominguez X, Marco-Jiménez F, Peñaranda DS, Vicente JS. Long-Term Phenotypic and Proteomic Changes Following Vitrified Embryo Transfer in the Rabbit Model. Animals (Basel) 2020;10:E1043. [PMID: 32560425 DOI: 10.3390/ani10061043] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
25 Vedolin L, de Souza CF, Silveira RS, Lopes BC, Laybauer LS, Saraiva Pereira ML, Giugliani R. Conventional MRI and MR spectroscopy in nonclassical mitochondrial disease: report of three patients with mitochondrial DNA deletion. Childs Nerv Syst 2006;22:1355-9. [PMID: 16552564 DOI: 10.1007/s00381-006-0082-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
26 Wirtz S, Schuelke M. Region-specific expression of mitochondrial complex I genes during murine brain development. PLoS One 2011;6:e18897. [PMID: 21556144 DOI: 10.1371/journal.pone.0018897] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 1.8] [Reference Citation Analysis]
27 Bebbere D, Ulbrich SE, Giller K, Zakhartchenko V, Reichenbach HD, Reichenbach M, Verma PJ, Wolf E, Ledda S, Hiendleder S. Mitochondrial DNA Depletion in Granulosa Cell Derived Nuclear Transfer Tissues. Front Cell Dev Biol 2021;9:664099. [PMID: 34124044 DOI: 10.3389/fcell.2021.664099] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Siebel S, Solomon BD. Mitochondrial Factors and VACTERL Association-Related Congenital Malformations. Mol Syndromol 2013;4:63-73. [PMID: 23653577 DOI: 10.1159/000346301] [Cited by in Crossref: 17] [Cited by in F6Publishing: 11] [Article Influence: 1.9] [Reference Citation Analysis]
29 Bénit P, Goncalves S, Dassa EP, Brière JJ, Rustin P. The variability of the harlequin mouse phenotype resembles that of human mitochondrial-complex I-deficiency syndromes. PLoS One 2008;3:e3208. [PMID: 18791645 DOI: 10.1371/journal.pone.0003208] [Cited by in Crossref: 57] [Cited by in F6Publishing: 53] [Article Influence: 4.1] [Reference Citation Analysis]
30 Le Tanno P, Latypova X, Rendu J, Fauré J, Bourg V, Gauthier M, Billy-Lopez G, Jouk PS, Dieterich K. Diagnostic workup in children with arthrogryposis: description of practices from a single reference centre, comparison with literature and suggestion of recommendations. J Med Genet 2021:jmedgenet-2021-107823. [PMID: 34876503 DOI: 10.1136/jmedgenet-2021-107823] [Reference Citation Analysis]
31 Chandler RJ, Sloan J, Fu H, Tsai M, Stabler S, Allen R, Kaestner KH, Kazazian HH, Venditti CP. Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle. BMC Med Genet 2007;8:64. [PMID: 17937813 DOI: 10.1186/1471-2350-8-64] [Cited by in Crossref: 40] [Cited by in F6Publishing: 43] [Article Influence: 2.7] [Reference Citation Analysis]
32 Solomon BD, Pineda-Alvarez DE, Raam MS, Bous SM, Keaton AA, Vélez JI, Cummings DA. Analysis of component findings in 79 patients diagnosed with VACTERL association. Am J Med Genet A 2010;152A:2236-44. [PMID: 20683998 DOI: 10.1002/ajmg.a.33572] [Cited by in Crossref: 55] [Cited by in F6Publishing: 46] [Article Influence: 4.6] [Reference Citation Analysis]