125 related articles for article (PubMed ID: 30968306)
1. Magnetic resonance spectroscopy in Leigh-MELAS overlap syndrome.
Ko A; Lee YM
World J Pediatr; 2019 Jun; 15(3):306-308. PubMed ID: 30968306
[No Abstract] [Full Text] [Related]
2. Exclusive affection of the brain in m.4450G>A carriers rather suggests Leigh syndrome than MELAS.
Finsterer J
Brain Dev; 2019 Sep; 41(8):741. PubMed ID: 30952460
[No Abstract] [Full Text] [Related]
3. [MELAS-Leigh superposition syndrome: a case report].
Yang S; Sun C; Zhu WH
Zhonghua Nei Ke Za Zhi; 2020 Feb; 59(2):140-143. PubMed ID: 32074688
[TBL] [Abstract][Full Text] [Related]
4. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
Leng Y; Liu Y; Fang X; Li Y; Yu L; Yuan Y; Wang Z
Mitochondrial DNA; 2015 Apr; 26(2):208-12. PubMed ID: 24708134
[TBL] [Abstract][Full Text] [Related]
5. MELAS or Leigh syndrome, that's the question.
Finsterer J
Pediatr Endocrinol Diabetes Metab; 2021; 27(4):311-312. PubMed ID: 35114773
[TBL] [Abstract][Full Text] [Related]
6. [Neuroimaging of mitochondrial diseases].
Goto T; Momoi MY
Nihon Rinsho; 2002 Apr; 60 Suppl 4():236-9. PubMed ID: 12013855
[No Abstract] [Full Text] [Related]
7. A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.
Crimi M; Galbiati S; Moroni I; Bordoni A; Perini MP; Lamantea E; Sciacco M; Zeviani M; Biunno I; Moggio M; Scarlato G; Comi GP
Neurology; 2003 Jun; 60(11):1857-61. PubMed ID: 12796552
[TBL] [Abstract][Full Text] [Related]
8. [A case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode/Leigh overlap syndrome].
Matsui J; Takano T; Ryujin F; Anzai Y; Yoshioka S; Takeuchi Y; Goto Y
No To Hattatsu; 2014 Sep; 46(5):363-6. PubMed ID: 25403068
[TBL] [Abstract][Full Text] [Related]
9. Neurological mitochondrial cytopathies in children.
Mehndiratta MM; Aggarwal P
Indian Pediatr; 2000 Nov; 37(11):1175-9. PubMed ID: 11086298
[No Abstract] [Full Text] [Related]
10. [Rare MRI diagnosis of MELAS syndrome].
Niehues SM; Radtke A; Bohner G; Lemke AJ
Rofo; 2008 Apr; 180(4):346-8. PubMed ID: 18499912
[No Abstract] [Full Text] [Related]
11. Leigh disease presenting as Guillain-Barré syndrome.
Coker SB
Pediatr Neurol; 1993; 9(1):61-3. PubMed ID: 8452602
[TBL] [Abstract][Full Text] [Related]
12. Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum.
Grosso S; Carluccio MA; Cardaioli E; Cerase A; Malandrini A; Romano C; Federico A; Dotti MT
Brain Dev; 2017 Mar; 39(3):261-265. PubMed ID: 27742419
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial disorders.
Edmond JC
Int Ophthalmol Clin; 2009; 49(3):27-33. PubMed ID: 19584620
[No Abstract] [Full Text] [Related]
14. Antemortem diagnosis of Leigh's disease: role of magnetic resonance studies.
Ghosh D; Pradhan S
Indian J Pediatr; 1996; 63(5):683-9. PubMed ID: 10830040
[TBL] [Abstract][Full Text] [Related]
15. Answer to case of the month #110. Magnetic resonance imaging and spectroscopy in Leigh disease.
Tynan JR; Wiebe S; Robinson C; Harder S
Can Assoc Radiol J; 2006 Jun; 57(3):182-4. PubMed ID: 16881477
[No Abstract] [Full Text] [Related]
16. Magnetic resonance spectroscopy and diffusion-weighted imaging findings in a child with Leigh's disease.
Atalar MH; Egilmez H; Bulut S; Icagasioglu D
Pediatr Int; 2005 Oct; 47(5):601-3. PubMed ID: 16190976
[No Abstract] [Full Text] [Related]
17. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.
Chol M; Lebon S; Bénit P; Chretien D; de Lonlay P; Goldenberg A; Odent S; Hertz-Pannier L; Vincent-Delorme C; Cormier-Daire V; Rustin P; Rötig A; Munnich A
J Med Genet; 2003 Mar; 40(3):188-91. PubMed ID: 12624137
[TBL] [Abstract][Full Text] [Related]
18. Neuroimaging of mitochondrial disease.
Saneto RP; Friedman SD; Shaw DW
Mitochondrion; 2008 Dec; 8(5-6):396-413. PubMed ID: 18590986
[TBL] [Abstract][Full Text] [Related]
19. Neuroimaging in mitochondrial disease.
Distelmaier F; Klopstock T
Handb Clin Neurol; 2023; 194():173-185. PubMed ID: 36813312
[TBL] [Abstract][Full Text] [Related]
20. NDUFS4-related Leigh syndrome in Hutterites.
Finsterer J; Zarrouk-Mahjoub S
Am J Med Genet A; 2017 May; 173(5):1450-1451. PubMed ID: 28371352
[No Abstract] [Full Text] [Related]
[Next] [New Search]
