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 *

115 related articles for article (PubMed ID: 615502)

  • 1. [Alpers' infantile cerebral poliodystrophy. A case with abnormal hepatic pyruvate carboxylase].
    Tommasi M; Jouvet-Telinge A; Kopp N; Pialat J; Gilly J
    Ann Anat Pathol (Paris); 1977; 22(4):337-42. PubMed ID: 615502
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase].
    David M; Baltassat P; Dinjon B; Lauras B; De Villard R; Tommasi M; Gilly J
    Arch Fr Pediatr; 1975; 32(6):580. PubMed ID: 1180638
    [No Abstract]   [Full Text] [Related]  

  • 3. Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.
    Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Willems JL; Janssen AJ; Slooff JL; Geelen JA; de Jager JP
    Neuropediatrics; 1982 May; 13(2):108-11. PubMed ID: 6813759
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progressive cerebral poliodystrophy--Alpers' disease. Disorganized giant neuronal mitochondria on electron microscopy.
    Sandbank U; Lerman P
    J Neurol Neurosurg Psychiatry; 1972 Dec; 35(6):749-55. PubMed ID: 4647849
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study.
    Hayhurst H; Anagnostou ME; Bogle HJ; Grady JP; Taylor RW; Bindoff LA; McFarland R; Turnbull DM; Lax NZ
    Brain Pathol; 2019 Jan; 29(1):97-113. PubMed ID: 30021052
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome.
    Frydman M; Jager-Roman E; de Vries L; Stoltenburg-Didinger G; Nussinovitch M; Sirota L
    Am J Med Genet; 1993 Aug; 47(1):31-6. PubMed ID: 8368248
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver.
    Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Sengers RC; Slooff JL
    Arch Neurol; 1981 Dec; 38(12):767-72. PubMed ID: 7316843
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI.
    Brunetti-Pierri N; Selby K; O'Sullivan M; Hendson G; Truong C; Waters PJ; Wong LJ
    Neuropediatrics; 2008 Jun; 39(3):179-83. PubMed ID: 18991199
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Phenotypic and genotypic variability in Alpers syndrome.
    Sofou K; Moslemi AR; Kollberg G; Bjarnadóttir I; Oldfors A; Nennesmo I; Holme E; Tulinius M; Darin N
    Eur J Paediatr Neurol; 2012 Jul; 16(4):379-89. PubMed ID: 22237560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Alpers disease(progressive infantile poliodystrophy)].
    Sakuta R
    Ryoikibetsu Shokogun Shirizu; 2001; (36):176-7. PubMed ID: 11596362
    [No Abstract]   [Full Text] [Related]  

  • 15. [Unilateral Alpers syndrome (Poliodystrophia progressiva corticalis)].
    Kammerer I
    Fortschr Neurol Psychiatr Grenzgeb; 1971 Aug; 39(8):439-56. PubMed ID: 5208421
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. POLG mutations in Alpers syndrome.
    Nguyen KV; Østergaard E; Ravn SH; Balslev T; Danielsen ER; Vardag A; McKiernan PJ; Gray G; Naviaux RK
    Neurology; 2005 Nov; 65(9):1493-5. PubMed ID: 16177225
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
    Ferrari G; Lamantea E; Donati A; Filosto M; Briem E; Carrara F; Parini R; Simonati A; Santer R; Zeviani M
    Brain; 2005 Apr; 128(Pt 4):723-31. PubMed ID: 15689359
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Alpers syndrome: the natural history of a case highlighting neuroimaging, neuropathology, and fat metabolism.
    Khan A; Trevenen C; Wei XC; Sarnat HB; Payne E; Kirton A
    J Child Neurol; 2012 May; 27(5):636-40. PubMed ID: 22114215
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.