BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Lee WS, Sokol RJ. Mitochondrial hepatopathies: advances in genetics and pathogenesis. Hepatology. 2007;45:1555-1565. [PMID: 17538929 DOI: 10.1002/hep.21710] [Cited by in Crossref: 80] [Cited by in F6Publishing: 59] [Article Influence: 5.3] [Reference Citation Analysis]
Number Citing Articles
1 Brett A, Pinto C, Carvalho L, Garcia P, Diogo L, Gonçalves I. Acute liver failure in under two year-olds - are there markers of metabolic disease on admission? Annals of Hepatology 2013;12:791-6. [DOI: 10.1016/s1665-2681(19)31321-3] [Cited by in Crossref: 12] [Article Influence: 1.3] [Reference Citation Analysis]
2 Medeiros DM. Assessing mitochondria biogenesis. Methods 2008;46:288-94. [DOI: 10.1016/j.ymeth.2008.09.026] [Cited by in Crossref: 89] [Cited by in F6Publishing: 82] [Article Influence: 6.4] [Reference Citation Analysis]
3 Heissat S, Collardeau-frachon S, Baruteau J, Dubruc E, Bouvier R, Fabre M, Cordier MP, Broué P, Guigonis V, Debray D. Neonatal Hemochromatosis: Diagnostic Work-Up Based on a Series of 56 Cases of Fetal Death and Neonatal Liver Failure. The Journal of Pediatrics 2015;166:66-73. [DOI: 10.1016/j.jpeds.2014.09.030] [Cited by in Crossref: 26] [Cited by in F6Publishing: 17] [Article Influence: 3.7] [Reference Citation Analysis]
4 Collardeau-Frachon S, Heissat S, Bouvier R, Fabre M, Baruteau J, Broue P, Cordier MP, Debray D, Debiec H, Ronco P, Guigonis V. French retrospective multicentric study of neonatal hemochromatosis: importance of autopsy and autoimmune maternal manifestations. Pediatr Dev Pathol 2012;15:450-70. [PMID: 22901025 DOI: 10.2350/12-02-1155-OA.1] [Cited by in Crossref: 24] [Cited by in F6Publishing: 5] [Article Influence: 2.4] [Reference Citation Analysis]
5 Haber B, Ferreira CT, Aw M, Bezerra J, Sturm E, Thompson R, D'agostino D, Mckiernan P. Cholestasis: Current Issues and Plan for the Future. Journal of Pediatric Gastroenterology & Nutrition 2008;47:220-4. [DOI: 10.1097/mpg.0b013e318181b038] [Cited by in Crossref: 7] [Article Influence: 0.5] [Reference Citation Analysis]
6 Quaglia A, Portmann B. Histopathological basis of syndrome. Critical Care in Acute Liver Failure. Unitec House: Future Medicine Ltd; 2013. pp. 18-30. [DOI: 10.2217/ebo.12.382] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
7 Hadžić N. Challenging the dogmas; the NAC tie. Hepatology 2013;57:1297-300. [PMID: 22941945 DOI: 10.1002/hep.26044] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
8 Jestin M, Kapnick SM, Tarasenko TN, Burke CT, Zerfas PM, Diaz F, Vernon H, Singh LN, Sokol RJ, McGuire PJ. Mitochondrial disease disrupts hepatic allostasis and lowers the threshold for immune-mediated liver toxicity. Mol Metab 2020;37:100981. [PMID: 32283081 DOI: 10.1016/j.molmet.2020.100981] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 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]
10 Golden AS, Law YM, Shurtleff H, Warner M, Saneto RP. Mitochondrial electron transport chain deficiency, cardiomyopathy, and long-term cardiac transplant outcome: Mitochondrial cardiomyopathy and transplant. Pediatric Transplantation 2012;16:265-8. [DOI: 10.1111/j.1399-3046.2011.01635.x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
11 Larter CZ, Chitturi S, Heydet D, Farrell GC. A fresh look at NASH pathogenesis. Part 1: The metabolic movers. Journal of Gastroenterology and Hepatology 2010;25:672-90. [DOI: 10.1111/j.1440-1746.2010.06253.x] [Cited by in Crossref: 124] [Cited by in F6Publishing: 113] [Article Influence: 10.3] [Reference Citation Analysis]
12 Mazariegos G, Shneider B, Burton B, Fox IJ, Hadzic N, Kishnani P, Morton DH, McIntire S, Sokol RJ, Summar M, White D, Chavanon V, Vockley J. Liver transplantation for pediatric metabolic disease. Mol Genet Metab 2014;111:418-27. [PMID: 24495602 DOI: 10.1016/j.ymgme.2014.01.006] [Cited by in Crossref: 65] [Cited by in F6Publishing: 49] [Article Influence: 8.1] [Reference Citation Analysis]
13 Lefkowitch JH. Hepatobiliary pathology. Curr Opin Gastroenterol 2008;24:269-77. [PMID: 18408454 DOI: 10.1097/MOG.0b013e3282f8e28f] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
14 El-hattab AW, Li F, Schmitt E, Zhang S, Craigen WJ, Wong LC. MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations. Molecular Genetics and Metabolism 2010;99:300-8. [DOI: 10.1016/j.ymgme.2009.10.003] [Cited by in Crossref: 61] [Cited by in F6Publishing: 56] [Article Influence: 5.1] [Reference Citation Analysis]
15 Oliver D, Reddy PH. Dynamics of Dynamin-Related Protein 1 in Alzheimer's Disease and Other Neurodegenerative Diseases. Cells 2019;8:E961. [PMID: 31450774 DOI: 10.3390/cells8090961] [Cited by in Crossref: 43] [Cited by in F6Publishing: 42] [Article Influence: 14.3] [Reference Citation Analysis]
16 Di Giorgio A, Bartolini E, Calvo PL, Cananzi M, Cirillo F, Della Corte C, Dionisi-Vici C, Indolfi G, Iorio R, Maggiore G, Mandato C, Nebbia G, Nicastro E, Pinon M, Ranucci G, Sciveres M, Vajro P, D'Antiga L. Diagnostic Approach to Acute Liver Failure in Children: A Position Paper by the SIGENP Liver Disease Working Group. Dig Liver Dis 2021;53:545-57. [PMID: 33775575 DOI: 10.1016/j.dld.2021.03.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
17 Kaji S, Murayama K, Nagata I, Nagasaka H, Takayanagi M, Ohtake A, Iwasa H, Nishiyama M, Okazaki Y, Harashima H, Eitoku T, Yamamoto M, Matsushita H, Kitamoto K, Sakata S, Katayama T, Sugimoto S, Fujimoto Y, Murakami J, Kanzaki S, Shiraki K. Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II. Molecular Genetics and Metabolism 2009;97:292-6. [DOI: 10.1016/j.ymgme.2009.04.014] [Cited by in Crossref: 33] [Cited by in F6Publishing: 28] [Article Influence: 2.5] [Reference Citation Analysis]
18 Peeters A, Fraisl P, van den Berg S, Ver Loren van Themaat E, Van Kampen A, Rider MH, Takemori H, van Dijk KW, Van Veldhoven PP, Carmeliet P, Baes M. Carbohydrate metabolism is perturbed in peroxisome-deficient hepatocytes due to mitochondrial dysfunction, AMP-activated protein kinase (AMPK) activation, and peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) suppression. J Biol Chem 2011;286:42162-79. [PMID: 22002056 DOI: 10.1074/jbc.M111.299727] [Cited by in Crossref: 30] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
19 Levéen P, Kotarsky H, Mörgelin M, Karikoski R, Elmér E, Fellman V. The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy. Hepatology 2011;53:437-47. [PMID: 21274865 DOI: 10.1002/hep.24031] [Cited by in Crossref: 42] [Cited by in F6Publishing: 40] [Article Influence: 3.5] [Reference Citation Analysis]
20 Hazard FK, Ficicioglu CH, Ganesh J, Ruchelli ED. Liver pathology in infantile mitochondrial DNA depletion syndrome. Pediatr Dev Pathol 2013;16:415-24. [PMID: 24050659 DOI: 10.2350/12-07-1229-OA.1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
21 Krasnov GS, Oparina NIu, Khankin SL, Mashkova TD, Ershov AN, Zatsepina OG, Karpov VL, Beresten' SF. [Colorectal cancer 2D-proteomics: identification of altered protein expression]. Mol Biol (Mosk) 2009;43:348-56. [PMID: 19425502 DOI: 10.1134/s0026893309020186] [Cited by in Crossref: 4] [Cited by in F6Publishing: 10] [Article Influence: 0.3] [Reference Citation Analysis]
22 Molleston JP, Sokol RJ, Karnsakul W, Miethke A, Horslen S, Magee JC, Romero R, Squires RH, Van Hove JL. Evaluation of the child with suspected mitochondrial liver disease. J Pediatr Gastroenterol Nutr. 2013;57:269-276. [PMID: 23783016 DOI: 10.1097/mpg.0b013e31829ef67a] [Cited by in Crossref: 29] [Cited by in F6Publishing: 8] [Article Influence: 3.6] [Reference Citation Analysis]
23 Grabhorn E, Tsiakas K, Herden U, Fischer L, Freisinger P, Marquardt T, Ganschow R, Briem-Richter A, Santer R. Long-term outcomes after liver transplantation for deoxyguanosine kinase deficiency: a single-center experience and a review of the literature. Liver Transpl 2014;20:464-72. [PMID: 24478274 DOI: 10.1002/lt.23830] [Cited by in Crossref: 28] [Cited by in F6Publishing: 22] [Article Influence: 3.5] [Reference Citation Analysis]
24 Squires RH, Ng V, Romero R, Ekong U, Hardikar W, Emre S, Mazariegos GV. Evaluation of the pediatric patient for liver transplantation: 2014 practice guideline by the American Association for the Study of Liver Diseases, American Society of Transplantation and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Hepatology. 2014;60:362-398. [PMID: 24782219 DOI: 10.1002/hep.27191] [Cited by in Crossref: 101] [Cited by in F6Publishing: 77] [Article Influence: 12.6] [Reference Citation Analysis]
25 Takei S, Homma Y, Matsuyama R, Endo I. Hepatectomy for liver metastasis from rectal cancer in a patient with mitochondrial disease. BMJ Case Rep 2021;14:e238653. [PMID: 33547122 DOI: 10.1136/bcr-2020-238653] [Reference Citation Analysis]
26 Park KH, Gooz M, Ye ZW, Zhang J, Beeson GC, Rockey DC, Kim SH. Flavin Adenine Dinucleotide Depletion Caused by electron transfer flavoprotein subunit alpha Haploinsufficiency Leads to Hepatic Steatosis and Injury in Zebrafish. Hepatol Commun 2021;5:976-91. [PMID: 34141984 DOI: 10.1002/hep4.1691] [Reference Citation Analysis]
27 Lee WS, Sokol RJ. Mitochondrial hepatopathies: advances in genetics, therapeutic approaches, and outcomes. J Pediatr 2013;163:942-8. [PMID: 23810725 DOI: 10.1016/j.jpeds.2013.05.036] [Cited by in Crossref: 35] [Cited by in F6Publishing: 20] [Article Influence: 3.9] [Reference Citation Analysis]
28 Ebihara T, Nagatomo T, Sugiyama Y, Tsuruoka T, Osone Y, Shimura M, Tajika M, Matsuhashi T, Ichimoto K, Matsunaga A, Akiyama N, Ogawa-Tominaga M, Yatsuka Y, Nitta KR, Kishita Y, Fushimi T, Imai-Okazaki A, Ohtake A, Okazaki Y, Murayama K. Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis. Arch Dis Child Fetal Neonatal Ed 2021:fetalneonatal-2021-321633. [PMID: 34625524 DOI: 10.1136/archdischild-2021-321633] [Reference Citation Analysis]
29 Pronicka E, Weglewska-Jurkiewicz A, Pronicki M, Sykut-Cegielska J, Kowalski P, Pajdowska M, Jankowska I, Kotulska K, Kalicinski P, Jakobkiewicz-Banecka J, Wegrzyn G. Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene. Med Sci Monit 2011;17:CR203-9. [PMID: 21455106 DOI: 10.12659/msm.881716] [Cited by in Crossref: 25] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
30 Dimmock DP, Dunn JK, Feigenbaum A, Rupar A, Horvath R, Freisinger P, Mousson de Camaret B, Wong L, Scaglia F. Abnormal neurological features predict poor survival and should preclude liver transplantation in patients with deoxyguanosine kinase deficiency: Predictors of Survival in DGUOK Deficiency. Liver Transpl 2008;14:1480-5. [DOI: 10.1002/lt.21556] [Cited by in Crossref: 52] [Cited by in F6Publishing: 46] [Article Influence: 3.7] [Reference Citation Analysis]
31 Duff RM, Shearwood AM, Ermer J, Rossetti G, Gooding R, Richman TR, Balasubramaniam S, Thorburn DR, Rackham O, Lamont PJ, Filipovska A. A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome. Mitochondrion 2015;25:113-9. [PMID: 26524491 DOI: 10.1016/j.mito.2015.10.008] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
32 Bacman SR, Williams SL, Garcia S, Moraes CT. Organ-specific shifts in mtDNA heteroplasmy following systemic delivery of a mitochondria-targeted restriction endonuclease. Gene Ther 2010;17:713-20. [PMID: 20220783 DOI: 10.1038/gt.2010.25] [Cited by in Crossref: 68] [Cited by in F6Publishing: 59] [Article Influence: 5.7] [Reference Citation Analysis]
33 Di Donato S. Multisystem manifestations of mitochondrial disorders. J Neurol 2009;256:693-710. [DOI: 10.1007/s00415-009-5028-3] [Cited by in Crossref: 72] [Cited by in F6Publishing: 57] [Article Influence: 5.5] [Reference Citation Analysis]
34 Jankowska I, Czubkowski P, Rokicki D, Lipiński P, Piekutowska-Abramczuk D, Ciara E, Płoski R, Kaliciński P, Szymczak M, Pawłowska J, Socha P. Acute liver failure due to DGUOK deficiency-is liver transplantation justified? Clin Res Hepatol Gastroenterol 2021;45:101408. [PMID: 32278775 DOI: 10.1016/j.clinre.2020.02.018] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
35 Low E, Crushell EB, Harty SB, Ryan SP, Treacy EP. Reversible multiorgan system involvement in a neonate with complex IV deficiency. Pediatr Neurol 2008;39:368-70. [PMID: 18940565 DOI: 10.1016/j.pediatrneurol.2008.07.023] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
36 Qin Z, Yang Q, Yi S, Huang L, Shen Y, Luo J. Whole-exome sequencing identified novel compound heterozygous variants in a Chinese neonate with liver failure and review of literature. Mol Genet Genomic Med 2020;8:e1515. [PMID: 33205917 DOI: 10.1002/mgg3.1515] [Reference Citation Analysis]
37 Lefkowitch JH. Steatosis, Steatohepatitis and Related Conditions. Scheuer's Liver Biopsy Interpretation. Elsevier; 2010. pp. 93-114. [DOI: 10.1016/b978-0-7020-3410-7.00013-7] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
38 Basel-Vanagaite L, Zevit N, Har Zahav A, Guo L, Parathath S, Pasmanik-Chor M, McIntyre AD, Wang J, Albin-Kaplanski A, Hartman C, Marom D, Zeharia A, Badir A, Shoerman O, Simon AJ, Rechavi G, Shohat M, Hegele RA, Fisher EA, Shamir R. Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1. Am J Hum Genet 2012;90:49-60. [PMID: 22226083 DOI: 10.1016/j.ajhg.2011.11.028] [Cited by in Crossref: 53] [Cited by in F6Publishing: 47] [Article Influence: 5.3] [Reference Citation Analysis]
39 Devictor D, Tissieres P, Afanetti M, Debray D. Acute liver failure in children. Clin Res Hepatol Gastroenterol. 2011;35:430-437. [PMID: 21531191 DOI: 10.1016/j.clinre.2011.03.005] [Cited by in Crossref: 35] [Cited by in F6Publishing: 24] [Article Influence: 3.2] [Reference Citation Analysis]
40 DiMauro S, Hirano M. Pathogenesis and treatment of mitochondrial disorders. Adv Exp Med Biol 2009;652:139-70. [PMID: 20225024 DOI: 10.1007/978-90-481-2813-6_10] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 2.2] [Reference Citation Analysis]
41 Devictor D, Tissieres P, Durand P, Chevret L, Debray D. Acute liver failure in neonates, infants and children. Expert Review of Gastroenterology & Hepatology 2014;5:717-29. [DOI: 10.1586/egh.11.57] [Cited by in Crossref: 35] [Cited by in F6Publishing: 24] [Article Influence: 4.4] [Reference Citation Analysis]
42 Darwish AA, Mckiernan P, Chardot C. Paediatric liver transplantation for metabolic disorders. Part 2: Metabolic disorders with liver lesions. Clinics and Research in Hepatology and Gastroenterology 2011;35:271-80. [DOI: 10.1016/j.clinre.2011.01.008] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.6] [Reference Citation Analysis]
43 Kass GE, Price SC. Role of mitochondria in drug-induced cholestatic injury. Clin Liver Dis 2008;12:27-51, vii. [PMID: 18242496 DOI: 10.1016/j.cld.2007.11.005] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 0.9] [Reference Citation Analysis]
44 Fellman V, Kotarsky H. Mitochondrial hepatopathies in the newborn period. Semin Fetal Neonatal Med 2011;16:222-8. [PMID: 21680270 DOI: 10.1016/j.siny.2011.05.002] [Cited by in Crossref: 47] [Cited by in F6Publishing: 36] [Article Influence: 4.3] [Reference Citation Analysis]
45 Pirola CJ, Garaycoechea M, Flichman D, Castaño GO, Sookoian S. Liver mitochondrial DNA damage and genetic variability of Cytochrome b - a key component of the respirasome - drive the severity of fatty liver disease. J Intern Med 2021;289:84-96. [PMID: 32634278 DOI: 10.1111/joim.13147] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
46 Xu SC, Chen YB, Lin H, Pi HF, Zhang NX, Zhao CC, Shuai L, Zhong M, Yu ZP, Zhou Z, Bie P. Damage to mtDNA in liver injury of patients with extrahepatic cholestasis: the protective effects of mitochondrial transcription factor A. Free Radic Biol Med 2012;52:1543-51. [PMID: 22306509 DOI: 10.1016/j.freeradbiomed.2012.01.007] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 2.1] [Reference Citation Analysis]
47 Li S, Guo J, Ying Z, Chen S, Yang L, Chen K, Long Q, Qin D, Pei D, Liu X. Valproic acid-induced hepatotoxicity in alpers syndrome is associated with mitochondrial permeability transition pore opening-dependent apoptotic sensitivity in an induced pluripotent stem cell model: HEPATOLOGY, Vol. XX, No. X, 2015. Hepatology 2015;61:1730-9. [DOI: 10.1002/hep.27712] [Cited by in Crossref: 60] [Cited by in F6Publishing: 46] [Article Influence: 8.6] [Reference Citation Analysis]
48 Rahman S. Gastrointestinal and hepatic manifestations of mitochondrial disorders. J Inherit Metab Dis. 2013;36:659-673. [PMID: 23674168 DOI: 10.1007/s10545-013-9614-2] [Cited by in Crossref: 36] [Cited by in F6Publishing: 24] [Article Influence: 4.0] [Reference Citation Analysis]
49 Menon J, Vij M, Sachan D, Rammohan A, Shanmugam N, Kaliamoorthy I, Rela M. Pediatric metabolic liver diseases: Evolving role of liver transplantation. World J Transplant 2021; 11(6): 161-179 [PMID: 34164292 DOI: 10.5500/wjt.v11.i6.161] [Cited by in CrossRef: 1] [Article Influence: 1.0] [Reference Citation Analysis]
50 Bianchi M, Rizza T, Verrigni D, Martinelli D, Tozzi G, Torraco A, Piemonte F, Dionisi-Vici C, Nobili V, Francalanci P, Boldrini R, Callea F, Santorelli FM, Bertini E, Carrozzo R. Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy. Biochem Biophys Res Commun 2011;415:300-4. [PMID: 22027147 DOI: 10.1016/j.bbrc.2011.10.049] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
51 Richman TR, Ermer JA, Davies SM, Perks KL, Viola HM, Shearwood AM, Hool LC, Rackham O, Filipovska A. Mutation in MRPS34 compromises protein synthesis and causes mitochondrial dysfunction. PLoS Genet 2015;11:e1005089. [PMID: 25816300 DOI: 10.1371/journal.pgen.1005089] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 3.3] [Reference Citation Analysis]
52 Hynynen J, Komulainen T, Tukiainen E, Nordin A, Arola J, Kälviäinen R, Jutila L, Röyttä M, Hinttala R, Majamaa K, Mäkisalo H, Uusimaa J. Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation. Liver Transpl 2014;20:1402-12. [PMID: 25065347 DOI: 10.1002/lt.23965] [Cited by in Crossref: 45] [Cited by in F6Publishing: 31] [Article Influence: 5.6] [Reference Citation Analysis]
53 Shawky RM, Abdel-gaffar TY, Eladawy MS, El-etriby MA, Elmoneiri MS, Elhefnawy NG, Elsherif R, Nour El-din SM. Mitochondrial alterations in children with chronic liver disease. Egyptian Journal of Medical Human Genetics 2010;11:143-51. [DOI: 10.1016/j.ejmhg.2010.10.006] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
54 Enkai S, Koinuma S, Ito R, Igaki J, Hasegawa Y, Murayama K, Ohtake A. Case of an infant with hepatic cirrhosis caused by mitochondrial respiratory chain disorder. Pediatr Int 2013;55:e103-6. [PMID: 23910810 DOI: 10.1111/ped.12098] [Reference Citation Analysis]
55 Arduini A, Serviddio G, Escobar J, Tormos AM, Bellanti F, Viña J, Monsalve M, Sastre J. Mitochondrial biogenesis fails in secondary biliary cirrhosis in rats leading to mitochondrial DNA depletion and deletions. American Journal of Physiology-Gastrointestinal and Liver Physiology 2011;301:G119-27. [DOI: 10.1152/ajpgi.00253.2010] [Cited by in Crossref: 36] [Cited by in F6Publishing: 33] [Article Influence: 3.3] [Reference Citation Analysis]
56 Mindikoglu AL, King D, Magder LS, Ozolek JA, Mazariegos GV, Shneider BL. Valproic acid-associated acute liver failure in children: case report and analysis of liver transplantation outcomes in the United States. J Pediatr 2011;158:802-7. [PMID: 21167499 DOI: 10.1016/j.jpeds.2010.10.033] [Cited by in Crossref: 26] [Cited by in F6Publishing: 14] [Article Influence: 2.2] [Reference Citation Analysis]
57 Broué P, Baruteau J. Conduite à tenir devant une insuffisance hépatique d’origine métabolique. Archives de Pédiatrie 2009;16:640-2. [DOI: 10.1016/s0929-693x(09)74096-5] [Cited by in Crossref: 2] [Article Influence: 0.2] [Reference Citation Analysis]
58 Reddy PH, Oliver DM. Amyloid Beta and Phosphorylated Tau-Induced Defective Autophagy and Mitophagy in Alzheimer's Disease. Cells 2019;8:E488. [PMID: 31121890 DOI: 10.3390/cells8050488] [Cited by in Crossref: 83] [Cited by in F6Publishing: 87] [Article Influence: 27.7] [Reference Citation Analysis]
59 Sciard C, Collardeau-Frachon S, Atallah A, Combourieu D, Massardier J, Heissat S, Gaucherand P, Guibaud L, Massoud M. Prenatal imaging features suggestive of liver gestational allo immune disease. J Gynecol Obstet Hum Reprod 2019;48:61-4. [PMID: 30465890 DOI: 10.1016/j.jogoh.2018.11.005] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
60 Engelmann G, Meyburg J, Shahbek N, Al-Ali M, Hairetis MH, Baker AJ, Rodenburg RJ, Wenning D, Flechtenmacher C, Ellard S, Smeitink JA, Hoffmann GF, Buchanan CR. Recurrent acute liver failure and mitochondriopathy in a case of Wolcott-Rallison syndrome. J Inherit Metab Dis 2008;31:540-6. [PMID: 18704764 DOI: 10.1007/s10545-008-0867-0] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 1.4] [Reference Citation Analysis]