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Journal Abstract Search

123 related items for PubMed ID: 1652737

  • 1. [Early myoclonic encephalopathy. Delimitation of the syndrome in view of genetic counseling].
    Voirin J, Bonté JB, Laloum D, Plessis G, Venezia R.
    Pediatrie; 1991; 46(4):323-7. PubMed ID: 1652737
    [Abstract] [Full Text] [Related]

  • 2. Benign myoclonus of early infancy or benign non-epileptic infantile spasms.
    Dravet C, Giraud N, Bureau M, Roger J, Gobbi G, Dalla Bernardina B.
    Neuropediatrics; 1986 Feb; 17(1):33-8. PubMed ID: 3960282
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  • 3. Relation of spasms and myoclonus to suppression-burst on EEG in epileptic encephalopathy in early infancy.
    Kobayashi K, Inoue T, Kikumoto K, Endoh F, Miya K, Oka M, Yoshinaga H, Ohtsuka Y.
    Neuropediatrics; 2007 Oct; 38(5):244-50. PubMed ID: 18330839
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  • 4. Malignant epileptic encephalopathies in children.
    Dulac OJ, Chiron C.
    Baillieres Clin Neurol; 1996 Dec; 5(4):765-81. PubMed ID: 9068880
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  • 5. Atypical glycine encephalopathy in an extremely low birth weight infant: description of a new mutation and clinical and electroencephalographic analysis.
    Pardal-Fernández JM, Carrascosa-Romero MC, de Cabo-de la Vega C, Iniesta-López I, Gil-Pons E, Martínez-Gutiérrez A.
    Epileptic Disord; 2009 Mar; 11(1):48-53. PubMed ID: 19299230
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  • 7. [Syndrome of Ohtahara].
    Yelin K, Alfonso I, Papazian O.
    Rev Neurol; 2009 Mar; 29(4):340-2. PubMed ID: 10797923
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  • 9. Early myoclonic encephalopathy and nonketotic hyperglycinemia.
    Rossi S, Daniele I, Bastrenta P, Mastrangelo M, Lista G.
    Pediatr Neurol; 2009 Nov; 41(5):371-4. PubMed ID: 19818941
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  • 11. [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
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  • 13. Benign myoclonus of early infancy.
    Pachatz C, Fusco L, Vigevano F.
    Epileptic Disord; 1999 Mar; 1(1):57-61. PubMed ID: 10937134
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  • 15. Early myoclonic encephalopathy.
    Kamate M, Mahantshetti N, Chetal V.
    Indian Pediatr; 2009 Sep; 46(9):804-6. PubMed ID: 19812426
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [Neonatal EEG trace of burst suppression. Etiological and evolutionary factors].
    Martínez-Bermejo A, Roche C, López-Martín V, Arcas J, Tendero A.
    Rev Neurol; 2016 Jan; 33(6):514-8. PubMed ID: 11727229
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  • 19. Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy.
    Gürsoy S, Erçal D.
    J Child Neurol; 2016 Mar; 31(4):523-32. PubMed ID: 26271793
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  • 20. High-frequency EEG activity in epileptic encephalopathy with suppression-burst.
    Toda Y, Kobayashi K, Hayashi Y, Inoue T, Oka M, Endo F, Yoshinaga H, Ohtsuka Y.
    Brain Dev; 2015 Feb; 37(2):230-6. PubMed ID: 24796721
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