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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 17109792)

  • 1. Alpers syndrome: progressive neuronal degeneration of children with liver disease.
    Gordon N
    Dev Med Child Neurol; 2006 Dec; 48(12):1001-3. PubMed ID: 17109792
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases].
    Castro-Gago M; González-Conde V; Fernández-Seara MJ; Rodrigo-Sáez E; Fernández-Cebrián S; Alonso-Martín A; Campos Y; Arenas J; Eirís-Puñal J
    Rev Neurol; 1999 Nov 16-30; 29(10):912-7. PubMed ID: 10637838
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease).
    Simonati A; Filosto M; Savio C; Tomelleri G; Tonin P; Dalla Bernardina B; Rizzuto N
    Acta Neuropathol; 2003 Jul; 106(1):57-65. PubMed ID: 12721699
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progressive cerebral degeneration of childhood with liver disease (Alpers Huttenlocher disease) with cytochrome oxidase deficiency presenting with epilepsia partialis continua as the first clinical manifestation.
    Wörle H; Köhler B; Schlote W; Winkler P; Bastanier CK
    Clin Neuropathol; 1998; 17(2):63-8. PubMed ID: 9561326
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.
    Uusimaa J; Hinttala R; Rantala H; Päivärinta M; Herva R; Röyttä M; Soini H; Moilanen JS; Remes AM; Hassinen IE; Majamaa K
    Epilepsia; 2008 Jun; 49(6):1038-45. PubMed ID: 18294203
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Respiratory chain deficiency in Alpers syndrome.
    Gauthier-Villars M; Landrieu P; Cormier-Daire V; Jacquemin E; Chrétien D; Rötig A; Rustin P; Munnich A; de Lonlay P
    Neuropediatrics; 2001 Jun; 32(3):150-2. PubMed ID: 11521212
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Progressive myoclonic epilepsy as a sign of a late form of Alpers syndrome].
    Galván-Manso M; Tabuenca Y; Medrano P; Ruiz-Escusol S; Giménez-Mas JA; López-Pisón J
    Rev Neurol; 2000 Dec 1-15; 31(11):1036-9. PubMed ID: 11190870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alpers' syndrome presenting with seizures and multiple stroke-like episodes in a 17-year-old male.
    Montine TJ; Powers JM; Vogel FS; Radtke RA
    Clin Neuropathol; 1995; 14(6):322-6. PubMed ID: 8605737
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Alpers syndrome with mutations in POLG: clinical and investigative features.
    Hunter MF; Peters H; Salemi R; Thorburn D; Mackay MT
    Pediatr Neurol; 2011 Nov; 45(5):311-8. PubMed ID: 22000311
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular diagnosis of Alpers syndrome.
    Nguyen KV; Sharief FS; Chan SS; Copeland WC; Naviaux RK
    J Hepatol; 2006 Jul; 45(1):108-16. PubMed ID: 16545482
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features.
    Wolf NI; Rahman S; Schmitt B; Taanman JW; Duncan AJ; Harting I; Wohlrab G; Ebinger F; Rating D; Bast T
    Epilepsia; 2009 Jun; 50(6):1596-607. PubMed ID: 19054397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Valproate-induced liver failure in one of two siblings with Alpers disease.
    Schwabe MJ; Dobyns WB; Burke B; Armstrong DL
    Pediatr Neurol; 1997 May; 16(4):337-43. PubMed ID: 9258971
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence that Alpers-Huttenlocher syndrome could be a mitochondrial disease.
    Rasmussen M; Sanengen T; Skullerud K; Kvittingen EA; Skjeldal OH
    J Child Neurol; 2000 Jul; 15(7):473-7. PubMed ID: 10921519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA depletion in Alpers syndrome.
    Tesarova M; Mayr JA; Wenchich L; Hansikova H; Elleder M; Blahova K; Sperl W; Zeman J
    Neuropediatrics; 2004 Aug; 35(4):217-23. PubMed ID: 15328560
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alpers syndrome with prominent white matter changes.
    Bao X; Wu Y; Wong LJ; Zhang Y; Xiong H; Chou PC; Truong CK; Jiang Y; Qin J; Yuan Y; Lin Q; Wu X
    Brain Dev; 2008 Apr; 30(4):295-300. PubMed ID: 17923349
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure.
    Delarue A; Paut O; Guys JM; Montfort MF; Lethel V; Roquelaure B; Pellissier JF; Sarles J; Camboulives J
    Pediatr Transplant; 2000 Feb; 4(1):67-71. PubMed ID: 10731063
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma.
    Zsurka G; Baron M; Stewart JD; Kornblum C; Bös M; Sassen R; Taylor RW; Elger CE; Chinnery PF; Kunz WS
    J Neuropathol Exp Neurol; 2008 Sep; 67(9):857-66. PubMed ID: 18716558
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
    [TBL] [Abstract][Full Text] [Related]  

  • 19. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion.
    Naviaux RK; Nguyen KV
    Ann Neurol; 2004 May; 55(5):706-12. PubMed ID: 15122711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Juvenile Alpers disease.
    Wiltshire E; Davidzon G; DiMauro S; Akman HO; Sadleir L; Haas L; Zuccollo J; McEwen A; Thorburn DR
    Arch Neurol; 2008 Jan; 65(1):121-4. PubMed ID: 18195149
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.