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142 related items for PubMed ID: 16010070
1. Repetitive EEG recordings are necessary for the diagnosis of early myoclonic encephalopathy. Ozyürek H, Turanli G, Aliefendioglu D, Coskun T. Neurol India; 2005 Jun; 53(2):235-7. PubMed ID: 16010070 [Abstract] [Full Text] [Related]
2. Early myoclonic encephalopathy. Kamate M, Mahantshetti N, Chetal V. Indian Pediatr; 2009 Sep; 46(9):804-6. PubMed ID: 19812426 [Abstract] [Full Text] [Related]
3. Early epileptic encephalopathy with suppression burst electroencephalographic pattern--an analysis of eight Taiwanese patients. Chen PT, Young C, Lee WT, Wang PJ, Peng SS, Shen YZ. Brain Dev; 2001 Nov; 23(7):715-20. PubMed ID: 11701284 [Abstract] [Full Text] [Related]
4. [The clinical and electroencephalographic characteristics of early myoclonic encephalopathy]. Liu CT, Yin F, Huang R, Li B. Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):899-902. PubMed ID: 23324144 [Abstract] [Full Text] [Related]
5. The controversy regarding diagnostic criteria for early myoclonic encephalopathy. Wang PJ, Lee WT, Hwu WL, Young C, Yau KI, Shen YZ. Brain Dev; 1998 Oct; 20(7):530-5. PubMed ID: 9840674 [Abstract] [Full Text] [Related]
6. Dextromethorphan in the treatment of early myoclonic encephalopathy evolving into migrating partial seizures in infancy. Chien YH, Lin MI, Weng WC, Du JC, Lee WT. J Formos Med Assoc; 2012 May; 111(5):290-4. PubMed ID: 22656400 [Abstract] [Full Text] [Related]
9. A case of early myoclonic encephalopathy with intractable seizures successfully treated with high-dose phenobarbital. Kosaka T, Ohta G, Kometani H, Kawatani M, Ohshima Y. Brain Dev; 2019 Sep; 41(8):717-720. PubMed ID: 31027651 [Abstract] [Full Text] [Related]
13. Ohtahara syndrome: with special reference to its developmental aspects for differentiating from early myoclonic encephalopathy. Ohtahara S, Yamatogi Y. Epilepsy Res; 2006 Aug; 70 Suppl 1():S58-67. PubMed ID: 16829045 [Abstract] [Full Text] [Related]
14. Myoclonic-astatic epilepsy of early childhood--clinical and EEG analysis of myoclonic-astatic seizures, and discussions on the nosology of the syndrome. Oguni H, Fukuyama Y, Tanaka T, Hayashi K, Funatsuka M, Sakauchi M, Shirakawa S, Osawa M. Brain Dev; 2001 Nov; 23(7):757-64. PubMed ID: 11701290 [Abstract] [Full Text] [Related]
15. Early myoclonic epileptic encephalopathy (E.M.E.E.). Dalla Bernardina B, Dulac O, Fejerman N, Dravet C, Capovilla G, Bondavalli S, Colamaria V, Roger J. Eur J Pediatr; 1983 Nov; 140(3):248-52. PubMed ID: 6414818 [Abstract] [Full Text] [Related]
17. A novel AMT gene mutation in a newborn with nonketotic hyperglycinemia and early myoclonic encephalopathy. Belcastro V, Barbarini M, Barca S, Mauro I. Eur J Paediatr Neurol; 2016 Jan; 20(1):192-5. PubMed ID: 26371980 [Abstract] [Full Text] [Related]
19. Early childhood myoclonic epilepsy: An independent genetic generalized epilepsy with myoclonic seizures as the main seizure type. Yang Z, Xue J, Li H, Qian P, Liu X, Jiang Y, Zhang Y. Clin Neurophysiol; 2017 Sep; 128(9):1656-1663. PubMed ID: 28738275 [Abstract] [Full Text] [Related]
20. Hidden focal EEG seizures during prolonged suppressions and high-amplitude bursts in early infantile epileptic encephalopathy. Al-Futaisi A, Banwell B, Ochi A, Hew J, Chu B, Oishi M, Otsubo H. Clin Neurophysiol; 2005 May; 116(5):1113-7. PubMed ID: 15826852 [Abstract] [Full Text] [Related] Page: [Next] [New Search]