BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 9266144)

  • 1. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Di Trapani G; Gregori B; Servidei S; Ricci E; Sabatelli M; Tonali P
    Clin Neuropathol; 1997; 16(4):195-200. PubMed ID: 9266144
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y; Guo Z; Chen L; Zhang J; Wang W; Liu X; Ren H; Gao S
    Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Chen JC; Tsai TC; Liu CS; Lu CT
    Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].
    Ihara M; Tanaka H; Yashiro M; Nishimura Y
    Rinsho Shinkeigaku; 1996 Sep; 36(9):1069-73. PubMed ID: 8976130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics].
    Damian MS; Reichmann H; Seibel P; Bachmann G; Schachenmayr W; Dorndorf W
    Nervenarzt; 1994 Apr; 65(4):258-63. PubMed ID: 8015633
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial angiopathy in the cerebral blood vessels of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes)].
    Ohama E; Ohara S; Ikuta F; Tanaka K; Nishizawa M; Miyatake T
    No To Shinkei; 1988 Feb; 40(2):109-18. PubMed ID: 3370163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A case of MELAS presenting juvenile-onset hyperglycemic chorea-ballism].
    Nakagaki H; Furuya J; Santa Y; Nagano S; Araki E; Yamada T
    Rinsho Shinkeigaku; 2005 Jul; 45(7):502-5. PubMed ID: 16119832
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA; Wang N
    Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MELAS syndrome: peripheral neuropathy and cytochrome C-oxidase deficiency: a case report and review of the literature.
    Barak Y; Arnon S; Wolach B; Raz Y; Ashkenasi A; Glick B; Shapira Y
    Isr J Med Sci; 1995 Apr; 31(4):224-9. PubMed ID: 7721560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnosis and management of MELAS.
    Thambisetty M; Newman NJ
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A case of mitochondrial encephalomyopathy (MELAS)].
    Suzuki T; Fujino T; Sugiyama M; Ishida M
    Nihon Jinzo Gakkai Shi; 1996 Feb; 38(2):109-14. PubMed ID: 8717314
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assessment of the distribution of mitochondrial ribosomal RNA in melas and in thrombotic cerebral infarcts by in situ hybridization.
    Love S; Hilton DA
    J Pathol; 1996 Feb; 178(2):182-9. PubMed ID: 8683387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiac involvement in adults with m.3243A>G MELAS gene mutation.
    Vydt TC; de Coo RF; Soliman OI; Ten Cate FJ; van Geuns RJ; Vletter WB; Schoonderwoerd K; van den Bosch BJ; Smeets HJ; Geleijnse ML
    Am J Cardiol; 2007 Jan; 99(2):264-9. PubMed ID: 17223431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R; Zárate-Moysen A; Monsalvo-Reyes A; Herrero MD; Ruiz-Pesini E; López-Pérez M; Montoya J; Montiel-Sosa JF
    Rev Neurol; 2007 Jan 1-15; 44(1):18-22. PubMed ID: 17199225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Stroke due to mitochondrial disorders in Saudi children.
    Salih MA; Abdel-Gader AG; Zahraa JN; Al-Rayess MM; Alorainy IA; Hassan HH; Ruitenbeek W; Zeviani M
    Saudi Med J; 2006 Mar; 27 Suppl 1():S81-90. PubMed ID: 16532135
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Follow-up studies and disorders of endocrinologic function in MELAS syndrome].
    Robeck S; Stefan H; Engelhardt A; Neundörfer B
    Nervenarzt; 1996 Jun; 67(6):465-70. PubMed ID: 8767201
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Donegal kindred--clinical features and molecular genetic analysis.
    McEntagart M; Droogan O; Burke M; Brett F; Murphy S; Farrell M
    Ir Med J; 1997; 90(4):144-5. PubMed ID: 9267093
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [MELAS syndrome as a differential diagnosis of ischemic stroke].
    Finsterer J
    Fortschr Neurol Psychiatr; 2009 Jan; 77(1):25-31. PubMed ID: 19012224
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deep white matter pathologic features in watershed regions: a novel pattern of central nervous system involvement in MELAS.
    Apostolova LG; White M; Moore SA; Davis PH
    Arch Neurol; 2005 Jul; 62(7):1154-6. PubMed ID: 16009776
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.