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 *

246 related articles for article (PubMed ID: 21631236)

  • 1. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with intestinal bleeding in chronic renal failure.
    Mima A; Shiota F; Matsubara T; Iehara N; Akagi T; Abe H; Nagai K; Matsuura M; Murakami T; Kishi S; Araoka T; Kishi F; Kondo N; Shigeta R; Yoshikawa K; Kita T; Doi T; Fukatsu A
    Ren Fail; 2011; 33(6):622-5. PubMed ID: 21631236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A surviving case of mitochondrial cardiomyopathy diagnosed from the symptoms of multiple organ dysfunction syndrome.
    Tsujita Y; Kunitomo T; Fujii M; Furukawa S; Otsuki H; Fujino K; Hamamoto T; Tabata T; Matsumura K; Sasaki T; Saotome T; Kawai H; Matsumoto T; Maeda K; Horie M; Eguchi Y
    Int J Cardiol; 2008 Aug; 128(1):e43-5. PubMed ID: 17689757
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure.
    Yanagihara C; Oyama A; Tanaka M; Nakaji K; Nishimura Y
    Intern Med; 2001 Jul; 40(7):662-5. PubMed ID: 11506313
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Late-onset mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with bitemporal lesions.
    Kisanuki YY; Gruis KL; Smith TL; Brown DL
    Arch Neurol; 2006 Aug; 63(8):1200-1. PubMed ID: 16908753
    [No Abstract]   [Full Text] [Related]  

  • 7. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N; Babazono T; Tsuchiya K; Tomonaga O; Suzuki A; Togashi M; Ujihara N; Sakka Y; Yokokawa H; Ogata M; Nihei H; Iwamoto Y
    J Hum Genet; 2001; 46(6):330-4. PubMed ID: 11393536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS).
    Matsumoto J; Saver JL; Brennan KC; Ringman JM
    Rev Neurol Dis; 2005; 2(1):30-4. PubMed ID: 16400302
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes].
    Carmi E; Defossez C; Morin G; Fraitag S; Lok C; Westeel PF; Canaple S; Denoeux JP
    Ann Dermatol Venereol; 2001 Oct; 128(10 Pt 1):1031-5. PubMed ID: 11907964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. CMR gives clue to "ragged red fibers" in the heart in a patient with mitochondrial myopathy.
    Jose T; Gdynia HJ; Mahrholdt H; Vöhringer M; Klingel K; Kandolf R; Bornemann A; Yilmaz A
    Int J Cardiol; 2011 May; 149(1):e24-7. PubMed ID: 19344965
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.
    Van Hove JL; Shanske S; Ciacci F; Ballinger S; Shoffner JS; Wallace DC; Hanioka T; Folkers K; Bossen EH; Kussin PS
    Am J Med Genet; 1994 Jun; 51(2):114-20. PubMed ID: 8092186
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.
    Sproule DM; Kaufmann P
    Ann N Y Acad Sci; 2008 Oct; 1142():133-58. PubMed ID: 18990125
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W; Hayasaka K; Shoji Y; Takahashi T; Takada G; Saito M; Fukawa O; Wachi E
    Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy.
    Nicoll JA; Moss TH; Love S; Campbell MJ; Schutt WH
    Clin Neuropathol; 1993; 12(1):38-43. PubMed ID: 8382573
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolated cytochrome c oxidase deficiency as a cause of MELAS.
    Rossmanith W; Freilinger M; Roka J; Raffelsberger T; Moser-Thier K; Prayer D; Bernert G; Bittner RE
    J Med Genet; 2008 Feb; 45(2):117-21. PubMed ID: 18245391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Depressive episode with catatonic features in a case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Ju Seok Ryu ; Sook Joung Lee ; In Young Sung ; Tae Sung Ko ; Han Ik Yoo
    J Child Neurol; 2009 Oct; 24(10):1307-9. PubMed ID: 19451268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.