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Journal Abstract Search

154 related items for PubMed ID: 9700831

  • 21. Electrographic Features of Epilepsy With Eyelid Myoclonia With Photoparoxysmal Responses.
    Zawar I, Shreshtha B, Benech D, Burgess RC, Bulacio J, Knight EMP.
    J Clin Neurophysiol; 2024 Jan 01; 41(1):83-92. PubMed ID: 35394968
    [Abstract] [Full Text] [Related]

  • 22. Nonconvulsive status epilepticus in eyelid myoclonia with absences--evidence of provocation unrelated to photosensitivity.
    Wakamoto H, Nagao H, Manabe K, Kobayashi H, Hayashi M.
    Neuropediatrics; 1999 Jun 01; 30(3):149-50. PubMed ID: 10480211
    [Abstract] [Full Text] [Related]

  • 23. Eyelid myoclonia with absences in adults: a clinical and video-EEG study.
    Giannakodimos S, Panayiotopoulos CP.
    Epilepsia; 1996 Jan 01; 37(1):36-44. PubMed ID: 8603622
    [Abstract] [Full Text] [Related]

  • 24. Eyelid myoclonia with absences: an overlooked epileptic syndrome?
    Striano S, Striano P, Nocerino C, Boccella P, Bilo L, Meo R, Ruosi P.
    Neurophysiol Clin; 2002 Nov 01; 32(5):287-96. PubMed ID: 12490326
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  • 25. Epilepsy with Eyelid myoclonias - A diagnosis concealed in other genetic generalized epilepsies with photoparoxysmal response.
    Zawar I, Toribio MGG, Xu X, Alnakhli RS, Benech D, Valappil AMN, Wyllie E, Burgess R, Kotagal P, Lachhwani D, Gupta A, Knight EP.
    Epilepsy Res; 2022 Mar 01; 181():106886. PubMed ID: 35180638
    [Abstract] [Full Text] [Related]

  • 26. An Overview of the Electroencephalographic (EEG) Features of Epilepsy with Eyelid Myoclonia (Jeavons Syndrome).
    Zawar I, Pestana Knight EM.
    Neurodiagn J; 2020 Jun 01; 60(2):113-127. PubMed ID: 32369428
    [Abstract] [Full Text] [Related]

  • 27. [Eyelid myoclonus with absence].
    Petrukhin AS, Mukhin KIu, Kolpakchi AM, Shprekher BL.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997 Jun 01; 97(12):58-61. PubMed ID: 9591068
    [No Abstract] [Full Text] [Related]

  • 28. Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsy.
    Incorpora G, Sofia V, Pavone P, Biondi R, Barone B, Parano E.
    Eur J Pediatr; 2002 Mar 01; 161(3):175-7. PubMed ID: 11998921
    [Abstract] [Full Text] [Related]

  • 29. Unmasking the entity of 'drug-resistant' perioral myoclonia with absences: the twitches, darts and domes!
    Rudrabhatla PK, Er S, Radhakrishnan A, Menon RN.
    Epileptic Disord; 2021 Apr 01; 23(2):313-324. PubMed ID: 33851919
    [Abstract] [Full Text] [Related]

  • 30. [Eyelid myoclonia with absences (EMA)].
    Adachi M, Tsuneishi S, Nakamura H.
    Ryoikibetsu Shokogun Shirizu; 2002 Apr 01; (37 Pt 6):341-5. PubMed ID: 12483897
    [No Abstract] [Full Text] [Related]

  • 31. [Two siblings with eyelid myoclonia with absences].
    Yagi S, Matsuzawa J, Hongou K, Yamatani M, Miyawaki T, Konishi T.
    No To Hattatsu; 2001 Nov 01; 33(6):517-22. PubMed ID: 11725520
    [Abstract] [Full Text] [Related]

  • 32. Family studies of individuals with eyelid myoclonia with absences.
    Sadleir LG, Vears D, Regan B, Redshaw N, Bleasel A, Scheffer IE.
    Epilepsia; 2012 Dec 01; 53(12):2141-8. PubMed ID: 23205932
    [Abstract] [Full Text] [Related]

  • 33. [Clinical and electroencephalographic characteristics of Jeavons syndrome].
    Yang ZX, Liu XY, Qin J, Zhang YH.
    Zhonghua Er Ke Za Zhi; 2012 Jun 01; 50(6):445-9. PubMed ID: 22931943
    [Abstract] [Full Text] [Related]

  • 34. A comprehensive narrative review of epilepsy with eyelid myoclonia.
    Smith KM, Wirrell EC, Andrade DM, Choi H, Trenité DK, Knupp KG, Nordli DR, Riva A, Stern JM, Striano P, Thiele EA, Zawar I.
    Epilepsy Res; 2023 Jul 01; 193():107147. PubMed ID: 37121024
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  • 38. Neck myoclonia with absence seizures: report of 3 cases.
    Yang Z, Liu X, Qin J, Jiang Y.
    J Child Neurol; 2009 Aug 01; 24(8):1026-9. PubMed ID: 19666886
    [Abstract] [Full Text] [Related]

  • 39. Blinking and eyelid myoclonia: Characteristics and correlations of eyelid movements.
    da Conceição PO, Guaranha MS, Uchida CG, Carvalho K, Guilhoto LM, De Araújo-Filho GM, Júnior HC, Wolf P, Yacubian EM.
    Seizure; 2015 Jan 01; 24():12-6. PubMed ID: 25564313
    [Abstract] [Full Text] [Related]

  • 40. Eyelid myoclonia with absences, intellectual disability and attention deficit hyperactivity disorder: a clinical phenotype of the RORB gene mutation.
    Morea A, Boero G, Demaio V, Francavilla T, La Neve A.
    Neurol Sci; 2021 May 01; 42(5):2059-2062. PubMed ID: 33387058
    [Abstract] [Full Text] [Related]

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