357 related articles for article (PubMed ID: 9822126)
1. 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]
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. Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency.
Müller-Höcker J; Hübner G; Bise K; Förster C; Hauck S; Paetzke I; Pongratz D; Kadenbach B
Arch Pathol Lab Med; 1993 Feb; 117(2):202-10. PubMed ID: 8381271
[TBL] [Abstract][Full Text] [Related]
4. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
Melone MA; Tessa A; Petrini S; Lus G; Sampaolo S; di Fede G; Santorelli FM; Cotrufo R
Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
[TBL] [Abstract][Full Text] [Related]
6. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Tokunaga M; Mita S; Murakami T; Kumamoto T; Uchino M; Nonaka I; Ando M
Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
[TBL] [Abstract][Full Text] [Related]
7. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
Kawakami Y; Sakuta R; Hashimoto K; Fujino O; Fujita T; Hida M; Horai S; Goto Y; Nonaka I
Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
[TBL] [Abstract][Full Text] [Related]
9. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
Stratilová L; Zeman J; Hansíková H; Houstĕk J; Hermanská J; Dudková Z; Konrádová V; Hůlková H; Elleder M
Cas Lek Cesk; 1998 Jul; 137(14):430-3. PubMed ID: 9748738
[TBL] [Abstract][Full Text] [Related]
10. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
Horváth R; Reilmann R; Holinski-Feder E; Ringelstein EB; Klopstock T
Neuromuscul Disord; 2008 Jul; 18(7):553-6. PubMed ID: 18590963
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Mitochondrial DNA and RNA processing in MELAS.
Kaufmann P; Koga Y; Shanske S; Hirano M; DiMauro S; King MP; Schon EA
Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
Degoul F; Diry M; Pou-Serradell A; Lloreta J; Marsac C
Ann Neurol; 1994 Mar; 35(3):365-70. PubMed ID: 8122891
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [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]
[Next] [New Search]
