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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
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1993 5
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1997 4
1998 3
1999 2
2000 5
2001 8
2002 6
2003 5
2005 1
2006 5
2007 6
2008 8
2009 6
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Page 1
[Syndrome of Ohtahara].
Yelin K, Alfonso I, Papazian O. Yelin K, et al. Rev Neurol. 1999 Aug 16-31;29(4):340-2. Rev Neurol. 1999. PMID: 10797923 Review. Spanish.
INTRODUCTION: A literature review using the term Ohtahara syndrome and early infantile epileptic encephalopathy revealed 51 cases. ...ACTH was effective in a few cases and hemispherectomy was successful in one case. CONCLUSION: We believe that Ohtahara syn …
INTRODUCTION: A literature review using the term Ohtahara syndrome and early infantile epileptic encephalopathy revealed 51 ca …
Ohtahara syndrome with emphasis on recent genetic discovery.
Pavone P, Spalice A, Polizzi A, Parisi P, Ruggieri M. Pavone P, et al. Brain Dev. 2012 Jun;34(6):459-68. doi: 10.1016/j.braindev.2011.09.004. Epub 2011 Oct 2. Brain Dev. 2012. PMID: 21967765 Review.
Ohtahara syndrome or Early Infantile Epileptic Encephalopathy (EIEE) with Suppression-Burst, is the most severe and the earliest developing age-related epileptic encephalopathy. ...
Ohtahara syndrome or Early Infantile Epileptic Encephalopathy (EIEE) with Suppression-Burst, is the most severe and the earlie …
Haploinsufficiency of STXBP1 and Ohtahara syndrome.
Saitsu H, Kato M, Matsumoto N. Saitsu H, et al. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. PMID: 22787616 Free Books & Documents. Review.
Ohtahara syndrome (OS) is one of the most severe and earliest forms of epilepsy. ...
Ohtahara syndrome (OS) is one of the most severe and earliest forms of epilepsy. ...
Ohtahara syndrome: with special reference to its developmental aspects for differentiating from early myoclonic encephalopathy.
Ohtahara S, Yamatogi Y. Ohtahara S, et al. Epilepsy Res. 2006 Aug;70 Suppl 1:S58-67. doi: 10.1016/j.eplepsyres.2005.11.021. Epub 2006 Jul 10. Epilepsy Res. 2006. PMID: 16829045 Review.
Ohtahara syndrome (OS) is well known as a peculiar early onset epileptic syndrome with serious prognosis. ...
Ohtahara syndrome (OS) is well known as a peculiar early onset epileptic syndrome with serious prognosis. ...
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
Bayat A, Bayat M, Rubboli G, Møller RS. Bayat A, et al. Genes (Basel). 2021 Jul 8;12(7):1051. doi: 10.3390/genes12071051. Genes (Basel). 2021. PMID: 34356067 Free PMC article. Review.
At the same time, some genes such as SCN2A can be associated with a wide range of epilepsy syndromes ranging from self-limited familial neonatal epilepsy at the mild end to Ohtahara syndrome, EIFMS, West syndrome, Lennox-Gastaut syndrome, or unclassifiable DEEs at t …
At the same time, some genes such as SCN2A can be associated with a wide range of epilepsy syndromes ranging from self-limited familial neon …
Neonatal Seizures: An Overview of Genetic Causes and Treatment Options.
Spoto G, Saia MC, Amore G, Gitto E, Loddo G, Mainieri G, Nicotera AG, Di Rosa G. Spoto G, et al. Brain Sci. 2021 Sep 29;11(10):1295. doi: 10.3390/brainsci11101295. Brain Sci. 2021. PMID: 34679360 Free PMC article. Review.
To date, three main groups of neonatal epilepsies are recognised during the neonatal period: benign familial neonatal epilepsy (BFNE), early myoclonic encephalopathy (EME) and 'Ohtahara syndrome' (OS). Recent advances showed the role of several genes in the pathogen …
To date, three main groups of neonatal epilepsies are recognised during the neonatal period: benign familial neonatal epilepsy (BFNE), early …
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.
Stamberger H, Nikanorova M, Willemsen MH, Accorsi P, Angriman M, Baier H, Benkel-Herrenbrueck I, Benoit V, Budetta M, Caliebe A, Cantalupo G, Capovilla G, Casara G, Courage C, Deprez M, Destrée A, Dilena R, Erasmus CE, Fannemel M, Fjær R, Giordano L, Helbig KL, Heyne HO, Klepper J, Kluger GJ, Lederer D, Lodi M, Maier O, Merkenschlager A, Michelberger N, Minetti C, Muhle H, Phalin J, Ramsey K, Romeo A, Schallner J, Schanze I, Shinawi M, Sleegers K, Sterbova K, Syrbe S, Traverso M, Tzschach A, Uldall P, Van Coster R, Verhelst H, Viri M, Winter S, Wolff M, Zenker M, Zoccante L, De Jonghe P, Helbig I, Striano P, Lemke JR, Møller RS, Weckhuysen S. Stamberger H, et al. Neurology. 2016 Mar 8;86(10):954-62. doi: 10.1212/WNL.0000000000002457. Epub 2016 Feb 10. Neurology. 2016. PMID: 26865513 Free article. Review.
Ninety-five percent of patients have epilepsy. While one-third of patients presented with Ohtahara syndrome (21%) or West syndrome (9.5%), the majority has a nonsyndromic early-onset epilepsy and encephalopathy (53%) with epileptic spasms or tonic seizures as main s …
Ninety-five percent of patients have epilepsy. While one-third of patients presented with Ohtahara syndrome (21%) or West synd …
Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy.
Beal JC, Cherian K, Moshe SL. Beal JC, et al. Pediatr Neurol. 2012 Nov;47(5):317-23. doi: 10.1016/j.pediatrneurol.2012.06.002. Pediatr Neurol. 2012. PMID: 23044011 Free article. Review.
Ohtahara syndrome and early myoclonic encephalopathy are the earliest presenting of the epileptic encephalopathies. ...
Ohtahara syndrome and early myoclonic encephalopathy are the earliest presenting of the epileptic encephalopathies. ...
Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?
Djukic A, Lado FA, Shinnar S, Moshé SL. Djukic A, et al. Epilepsy Res. 2006 Aug;70 Suppl 1:S68-76. doi: 10.1016/j.eplepsyres.2005.11.022. Epub 2006 Jul 7. Epilepsy Res. 2006. PMID: 16829044 Review.
BACKGROUND: Early myoclonic encephalopathy (EME) and the Ohtahara syndrome are currently listed as two separate syndromes in the classification of epilepsies. ...Tonic seizures are considered a manifestation of brainstem dysfunction and it is possible that this is m …
BACKGROUND: Early myoclonic encephalopathy (EME) and the Ohtahara syndrome are currently listed as two separate syndromes in t …
410 results