206 related articles for article (PubMed ID: 7603510)
21. Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation.
Bataillard M; Chatzoglou E; Rumbach L; Sternberg D; Tournade A; Laforêt P; Jardel C; Maisonobe T; Lombès A
Neurology; 2001 Feb; 56(3):405-7. PubMed ID: 11171912
[TBL] [Abstract][Full Text] [Related]
22. Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes).
Bakker A; Barthélémy C; Frachon P; Chateau D; Sternberg D; Mazat JP; Lombès A
Pediatr Res; 2000 Aug; 48(2):143-50. PubMed ID: 10926287
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.
Miyahara H; Matsumoto S; Mokuno K; Dei R; Akagi A; Mimuro M; Iwasaki Y; Yoshida M
Neuropathology; 2019 Jun; 39(3):212-217. PubMed ID: 30972844
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutation.
Brackmann F; Abicht A; Ahting U; Schröder R; Trollmann R
Eur J Pediatr; 2012 May; 171(5):859-62. PubMed ID: 22270878
[TBL] [Abstract][Full Text] [Related]
28. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
Mongini T; Doriguzzi C; Chiadò-Piat L; Silvestri G; Servidei S; Palmucci L
Clin Neuropathol; 2002; 21(2):72-6. PubMed ID: 12005255
[TBL] [Abstract][Full Text] [Related]
29. Detection and quantification of point mutations in mitochondrial DNA by PCR.
Yoneda M; Tanno Y; Tsuji S; Attardi G
Methods Enzymol; 1996; 264():432-41. PubMed ID: 8965716
[No Abstract] [Full Text] [Related]
30. 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]
31. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
Campos Y; Garcia-Silva T; Barrionuevo CR; Cabello A; Muley R; Arenas J
Pediatr Neurol; 1995 Jul; 13(1):69-72. PubMed ID: 7575854
[TBL] [Abstract][Full Text] [Related]
32. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts.
Hirano M; Pavlakis SG
J Child Neurol; 1994 Jan; 9(1):4-13. PubMed ID: 8151079
[TBL] [Abstract][Full Text] [Related]
33. mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girl.
Topaloğlu H; Seyrantepe V; Kandemir N; Akçören Z; Ozgüç M
Pediatr Neurol; 1998 May; 18(5):429-31. PubMed ID: 9650685
[TBL] [Abstract][Full Text] [Related]
34. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.
Campos Y; Lorenzo G; Martín MA; Torregrosa A; del Hoyo P; Rubio JC; García A; Arenas J
Neuromuscul Disord; 2000 Oct; 10(7):493-6. PubMed ID: 10996780
[TBL] [Abstract][Full Text] [Related]
35. Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
Morgan-Hughes JA; Sweeney MG; Cooper JM; Hammans SR; Brockington M; Schapira AH; Harding AE; Clark JB
Biochim Biophys Acta; 1995 May; 1271(1):135-40. PubMed ID: 7599199
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.
Taylor RW; Chinnery PF; Haldane F; Morris AA; Bindoff LA; Wilson J; Turnbull DM
Ann Neurol; 1996 Sep; 40(3):459-62. PubMed ID: 8797538
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [MERRF/MELAS overlap syndrome].
Goto Y
Nihon Rinsho; 2002 Apr; 60 Suppl 4():296-7. PubMed ID: 12013869
[No Abstract] [Full Text] [Related]
40. [MERRF/MELAS overlap syndrome].
Goto Y
Ryoikibetsu Shokogun Shirizu; 2001; (36):159. PubMed ID: 11596353
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]