These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
151 related articles for article (PubMed ID: 39055132)
1. Liver transplantation for mitochondrial DNA depletion syndrome caused by Wei LY; Chen XQ; Huang L; Shan QW; Tang Q Front Surg; 2024; 11():1348806. PubMed ID: 39055132 [TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular basis of hepatocerebral mitochondrial DNA depletion syndrome in Japan: evaluation of outcomes after liver transplantation. Shimura M; Kuranobu N; Ogawa-Tominaga M; Akiyama N; Sugiyama Y; Ebihara T; Fushimi T; Ichimoto K; Matsunaga A; Tsuruoka T; Kishita Y; Umetsu S; Inui A; Fujisawa T; Tanikawa K; Ito R; Fukuda A; Murakami J; Kaji S; Kasahara M; Shiraki K; Ohtake A; Okazaki Y; Murayama K Orphanet J Rare Dis; 2020 Jul; 15(1):169. PubMed ID: 32703289 [TBL] [Abstract][Full Text] [Related]
3. MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations. El-Hattab AW; Li FY; Schmitt E; Zhang S; Craigen WJ; Wong LJ Mol Genet Metab; 2010 Mar; 99(3):300-8. PubMed ID: 20074988 [TBL] [Abstract][Full Text] [Related]
4. [Analysis of 6 cases with hepatocerebral mitochondrial DNA depletion syndrome and literature review]. Zhao MX; Wang JS; Gong JY Zhonghua Er Ke Za Zhi; 2022 May; 60(5):457-461. PubMed ID: 35488641 [No Abstract] [Full Text] [Related]
5. Outcomes after liver transplantation in MPV17 deficiency (Navajo neurohepatopathy): A single-center case series. Huang AC; Ebel NH; Romero D; Martin B; Jhun I; Brown M; Enns GM; Esquivel C; Bonham C Pediatr Transplant; 2022 Aug; 26(5):e14274. PubMed ID: 35466509 [TBL] [Abstract][Full Text] [Related]
6. MPV17-related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects. El-Hattab AW; Wang J; Dai H; Almannai M; Staufner C; Alfadhel M; Gambello MJ; Prasun P; Raza S; Lyons HJ; Afqi M; Saleh MAM; Faqeih EA; Alzaidan HI; Alshenqiti A; Flore LA; Hertecant J; Sacharow S; Barbouth DS; Murayama K; Shah AA; Lin HC; Wong LC Hum Mutat; 2018 Apr; 39(4):461-470. PubMed ID: 29282788 [TBL] [Abstract][Full Text] [Related]
7. MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome. Kim J; Kang E; Kim Y; Kim JM; Lee BH; Murayama K; Kim GH; Choi IH; Kim KM; Yoo HW Mol Genet Metab Rep; 2016 Sep; 8():74-6. PubMed ID: 27536553 [TBL] [Abstract][Full Text] [Related]
8. Hong KT; Lim BC; Moon JS; Ko JS Korean J Gastroenterol; 2021 May; 77(5):248-252. PubMed ID: 34035203 [TBL] [Abstract][Full Text] [Related]
9. Hepatic presentations of mitochondrial DNA depletion syndrome in children: A single tertiary liver centre experience. Vara R; Pinon M; Fratter C; Hegarty R; Hadzic N J Inherit Metab Dis; 2023 Jul; 46(4):634-648. PubMed ID: 37204315 [TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series. Mahjoub G; Habibzadeh P; Dastsooz H; Mirzaei M; Kavosi A; Jamali L; Javanmardi H; Katibeh P; Faghihi MA; Dastgheib SA BMC Med Genet; 2019 Oct; 20(1):167. PubMed ID: 31664948 [TBL] [Abstract][Full Text] [Related]
11. [Genetic testing and prenatal diagnosis for a Chinese pedigree affected with mitochondrial DNA depletion syndrome due to variant of MPV17 gene]. Zhao G; Zhao X; Zhao X; Liu L; Wang C; Kong X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Oct; 39(10):1085-1088. PubMed ID: 36184088 [TBL] [Abstract][Full Text] [Related]
12. The zebrafish orthologue of the human hepatocerebral disease gene Martorano L; Peron M; Laquatra C; Lidron E; Facchinello N; Meneghetti G; Tiso N; Rasola A; Ghezzi D; Argenton F Dis Model Mech; 2019 Mar; 12(3):. PubMed ID: 30833296 [TBL] [Abstract][Full Text] [Related]
13. Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene. Uusimaa J; Evans J; Smith C; Butterworth A; Craig K; Ashley N; Liao C; Carver J; Diot A; Macleod L; Hargreaves I; Al-Hussaini A; Faqeih E; Asery A; Al Balwi M; Eyaid W; Al-Sunaid A; Kelly D; van Mourik I; Ball S; Jarvis J; Mulay A; Hadzic N; Samyn M; Baker A; Rahman S; Stewart H; Morris AA; Seller A; Fratter C; Taylor RW; Poulton J Eur J Hum Genet; 2014 Feb; 22(2):184-91. PubMed ID: 23714749 [TBL] [Abstract][Full Text] [Related]
14. Fulminant Neonatal Liver Failure in MPV 17-Related Mitochondrial DNA Depletion Syndrome. Abduljalil R; Ben Turkia H; Fakhroo A; Skrypnyk C Case Reports Hepatol; 2023; 2023():4514552. PubMed ID: 37384111 [TBL] [Abstract][Full Text] [Related]
15. Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations. Spinazzola A; Santer R; Akman OH; Tsiakas K; Schaefer H; Ding X; Karadimas CL; Shanske S; Ganesh J; Di Mauro S; Zeviani M Arch Neurol; 2008 Aug; 65(8):1108-13. PubMed ID: 18695062 [TBL] [Abstract][Full Text] [Related]
16. MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report. Pyal A; Paramasivam A; Meena AK; Bhavana VB; Thangaraj K Mitochondrion; 2017 Nov; 37():41-45. PubMed ID: 28673863 [TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure. Al-Hussaini A; Faqeih E; El-Hattab AW; Alfadhel M; Asery A; Alsaleem B; Bakhsh E; Ali A; Alasmari A; Lone K; Nahari A; Eyaid W; Al Balwi M; Craig K; Butterworth A; He L; Taylor RW J Pediatr; 2014 Mar; 164(3):553-9.e1-2. PubMed ID: 24321534 [TBL] [Abstract][Full Text] [Related]