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.
234 related articles for article (PubMed ID: 19659453)
21. [Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children]. Caietta E; Cano A; Halbert C; Hugonenq C; Mancini J; Milh M; Lépine A; Villeneuve N; Chaussenot A; Paquis-Flucklinger V; Chabrol B Arch Pediatr; 2012 Aug; 19(8):794-802. PubMed ID: 22789745 [TBL] [Abstract][Full Text] [Related]
22. SURF-1 gene mutation associated with leukoencephalopathy in a 2-year-old. Timothy J; Geller T J Child Neurol; 2009 Oct; 24(10):1296-301. PubMed ID: 19805825 [TBL] [Abstract][Full Text] [Related]
23. Alternating hemiplegia of childhood: metabolic studies in the largest European series of patients. Fons C; Campistol J; Panagiotakaki E; Giannotta M; Arzimanoglou A; Gobbi G; Neville B; Ebinger F; Nevšímalová S; Laan L; Casaer P; Spiel G; Ninan M; Sange G; Artuch R; Schyns T; Vavassori R; Poncelin D; Eur J Paediatr Neurol; 2012 Jan; 16(1):10-4. PubMed ID: 21945173 [TBL] [Abstract][Full Text] [Related]
24. [Mitochondrial respiratory chain deficiency may present as multiple sclerosis]. Iñiguez C; Arenas J; Montoya J; Mostacero E; López del Val J; Morales F Neurologia; 1998 Apr; 13(4):199-203. PubMed ID: 9608760 [TBL] [Abstract][Full Text] [Related]
25. Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patients. Garcia-Cazorla A; De Lonlay P; Rustin P; Chretien D; Touati G; Rabier D; Slama A; Saudubray JM J Pediatr; 2006 Sep; 149(3):401-405. PubMed ID: 16939756 [TBL] [Abstract][Full Text] [Related]
26. Magnetic resonance imaging and proton magnetic resonance spectroscopy of the brain in the diagnostic evaluation of developmental delay. Verbruggen KT; Meiners LC; Sijens PE; Lunsing RJ; van Spronsen FJ; Brouwer OF Eur J Paediatr Neurol; 2009 Mar; 13(2):181-90. PubMed ID: 18579422 [TBL] [Abstract][Full Text] [Related]
27. Sedation medication received and adverse events related to sedation for brain MRI in children with and without developmental disabilities. Kannikeswaran N; Mahajan PV; Sethuraman U; Groebe A; Chen X Paediatr Anaesth; 2009 Mar; 19(3):250-6. PubMed ID: 19143958 [TBL] [Abstract][Full Text] [Related]
28. Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein. Sparkes R; Patton D; Bernier F Cardiol Young; 2007 Apr; 17(2):215-7. PubMed ID: 17244376 [TBL] [Abstract][Full Text] [Related]
29. White matter involvement in mitochondrial diseases. Lerman-Sagie T; Leshinsky-Silver E; Watemberg N; Luckman Y; Lev D Mol Genet Metab; 2005 Feb; 84(2):127-36. PubMed ID: 15670718 [TBL] [Abstract][Full Text] [Related]
30. Mitochondrial respiratory complex I deficiency simulating spinal muscular atrophy. Lee JS; Hwang JS; Ryu KH; Lee EH; Kim SH Pediatr Neurol; 2007 Jan; 36(1):45-7. PubMed ID: 17162196 [TBL] [Abstract][Full Text] [Related]
31. New pattern of brain MRI lesions in isolated complex I deficiency. Wolf NI; Seitz A; Harting I; Smeitink JA; Trijbels F; van den Heuvel LP; Schlemmer H; Ebinger F; Evert W; Rating D Neuropediatrics; 2003 Jun; 34(3):156-9. PubMed ID: 12910441 [TBL] [Abstract][Full Text] [Related]
32. Neuroradiologic findings in children with mitochondrial disorder: correlation with mitochondrial respiratory chain defects. Kim J; Lee SK; Kim EY; Kim DI; Lee YM; Lee JS; Kim HD Eur Radiol; 2008 Aug; 18(8):1741-8. PubMed ID: 18389251 [TBL] [Abstract][Full Text] [Related]
33. Subclinical seizures in children diagnosed with localization-related epilepsy: clinical and EEG characteristics. Akman CI; Montenegro MA; Jacob S; Eck K; McBrian D; Chiriboga CA; Patterson MC Epilepsy Behav; 2009 Sep; 16(1):86-98. PubMed ID: 19632903 [TBL] [Abstract][Full Text] [Related]
34. Otolaryngologic manifestations of mitochondrial cytopathies. Jeyakumar A; Williamson ME; Brickman TM; Krakovitz P; Parikh S Am J Otolaryngol; 2009; 30(3):162-5. PubMed ID: 19410120 [TBL] [Abstract][Full Text] [Related]
35. Heterogeneity of magnetic resonance imaging in Leigh syndrome with SURF1 gene 604G-->C mutation. Xie S; Xiao JX; Qi ZY; Yang YL; Jiang XX Clin Imaging; 2009; 33(1):1-6. PubMed ID: 19135921 [TBL] [Abstract][Full Text] [Related]
36. Major depression in adolescent children consecutively diagnosed with mitochondrial disorder. Koene S; Kozicz TL; Rodenburg RJ; Verhaak CM; de Vries MC; Wortmann S; van de Heuvel L; Smeitink JA; Morava E J Affect Disord; 2009 Apr; 114(1-3):327-32. PubMed ID: 18692904 [TBL] [Abstract][Full Text] [Related]
37. Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India. Bindu PS; Arvinda H; Taly AB; Govindaraju C; Sonam K; Chiplunkar S; Kumar R; Gayathri N; Bharath Mm S; Nagappa M; Sinha S; Khan NA; Govindaraj P; Nunia V; Paramasivam A; Thangaraj K Mitochondrion; 2015 Nov; 25():6-16. PubMed ID: 26341968 [TBL] [Abstract][Full Text] [Related]
38. Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type. Van Maldergem L; Yuksel-Apak M; Kayserili H; Seemanova E; Giurgea S; Basel-Vanagaite L; Leao-Teles E; Vigneron J; Foulon M; Greally M; Jaeken J; Mundlos S; Dobyns WB Neurology; 2008 Nov; 71(20):1602-8. PubMed ID: 18716235 [TBL] [Abstract][Full Text] [Related]
39. Leigh syndrome: clinical and neuroimaging follow-up. Lee HF; Tsai CR; Chi CS; Lee HJ; Chen CC Pediatr Neurol; 2009 Feb; 40(2):88-93. PubMed ID: 19135620 [TBL] [Abstract][Full Text] [Related]
40. Clinical manifestations in children with mitochondrial diseases. Chi CS; Lee HF; Tsai CR; Lee HJ; Chen LH Pediatr Neurol; 2010 Sep; 43(3):183-9. PubMed ID: 20691940 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]