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There are 1654884 results for: content related to: Dr. S hunsuke O htahara (1930–2013) remembered

  1. You have free access to this content
    Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers

    Epilepsia

    Volume 54, Issue 5, May 2013, Pages: e74–e80, Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, Anna C. Jansen, Daniele Hasaerts, Charlotte Dielman, Julitta de Bellescize, Nadia Boutry-Kryza, Gaetan Lesca, Sarah Von Spiczak, Ingo Helbig, Deepak Gill, Simone Yendle, Rikke S. Møller, Laura Klitten, Christian Korff, Catherine Godfraind, Kenou Van Rijckevorsel, Peter De Jonghe, Helle Hjalgrim, Ingrid E. Scheffer and Arvid Suls

    Version of Record online : 14 FEB 2013, DOI: 10.1111/epi.12124

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    Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation

    Epilepsia

    Volume 54, Issue 7, July 2013, Pages: 1282–1287, Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Hiroshi Arai, Sumimasa Yamashita, Taku Nakagawa, Takanari FujII, Kenji Sugai, Kaoru Imai, Tami Uster, David Chitayat, Shelly Weiss, Hirofumi Kashii, Ryosuke Kusano, Ayumi Matsumoto, Kazuyuki Nakamura, Yoshinobu Oyazato, Mari Maeno, Kiyomi Nishiyama, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Kayoko Saito, Kiyoshi Hayasaka, Naomichi Matsumoto and Hirotomo Saitsu

    Version of Record online : 26 APR 2013, DOI: 10.1111/epi.12200

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    Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations

    Epilepsia

    Volume 52, Issue 10, October 2011, Pages: 1828–1834, Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane, Anna Kaminska, Cécile Laroche, Marie Anne Barthez, Cyril Gitiaux, Céline Bartoli, Ana Borges-Correia, Pierre Cacciagli, Cécile Mignon-Ravix, Hélène Cuberos, Brigitte Chabrol and Laurent Villard

    Version of Record online : 19 JUL 2011, DOI: 10.1111/j.1528-1167.2011.03181.x

  4. Prenatal Etiologies of West Syndrome

    Epilepsia

    Volume 34, Issue 4, July 1993, Pages: 716–722, Shunsuke Ohtahara, Yoko Ohtsuka, Yasuko Yamatogi, Eiji Oka, Harumi Yoshinaga and Masahiro Sato

    Version of Record online : 3 AUG 2005, DOI: 10.1111/j.1528-1157.1993.tb00451.x

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    Frameshift mutations of the ARX gene in familial Ohtahara syndrome

    Epilepsia

    Volume 51, Issue 9, September 2010, Pages: 1679–1684, Mitushiro Kato, Norihisa Koyama, Masayasu Ohta, Kiyokuni Miura and Kiyoshi Hayasaka

    Version of Record online : 2 APR 2010, DOI: 10.1111/j.1528-1167.2010.02559.x

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    A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females

    Epilepsia

    Volume 52, Issue 5, May 2011, Pages: 984–992, Yaman Z. Ekşioğlu, Amanda W. Pong and Masanori Takeoka

    Version of Record online : 22 MAR 2011, DOI: 10.1111/j.1528-1167.2011.02980.x

  7. Surgical Treatment of an Early Epileptic Encephalopathy with Suppression-Bursts and Focal Cortical Dysplasia

    Epilepsia

    Volume 36, Issue 1, January 1995, Pages: 37–40, J. M. Pedespan, H. Loiseau, A. Vital, C. Marchal, D. Fontan and A. Rougier

    Version of Record online : 3 AUG 2005, DOI: 10.1111/j.1528-1157.1995.tb01662.x

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    Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion

    Epilepsia

    Volume 57, Issue 1, January 2016, Pages: e12–e17, Nicholas M. Allen, Judith Conroy, Amre Shahwan, Bryan Lynch, Raony G. Correa, Sergio D. J. Pena, Dara McCreary, Tiago R. Magalhães, Sean Ennis, Sally A. Lynch and Mary D. King

    Version of Record online : 9 DEC 2015, DOI: 10.1111/epi.13250

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    West Syndrome and its Related Epileptic Syndromes

    Epilepsia

    Volume 39, Issue S5, May 1998, Pages: 30–37, Yoko Ohtsuka

    Version of Record online : 5 NOV 2007, DOI: 10.1111/j.1528-1157.1998.tb05147.x

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    Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

    Epilepsia

    Volume 56, Issue 12, December 2015, Pages: 1931–1940, Chloé Di Meglio, Gaetan Lesca, Nathalie Villeneuve, Caroline Lacoste, Affef Abidi, Pierre Cacciagli, Cécilia Altuzarra, Agathe Roubertie, Alexandra Afenjar, Florence Renaldo-Robin, Bertrand Isidor, Agnes Gautier, Marie Husson, Claude Cances, Julia Metreau, Cécile Laroche, Mondher Chouchane, Dorothée Ville, Stéphanie Marignier, Christelle Rougeot, Marine Lebrun, Anne de Saint Martin, Alexandra Perez, Audrey Riquet, Catherine Badens, Chantal Missirian, Nicole Philip, Brigitte Chabrol, Laurent Villard and Mathieu Milh

    Version of Record online : 29 OCT 2015, DOI: 10.1111/epi.13214

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    Sunday, December 3, 2006 Poster Session II 7:30 a.m.–4:30 p.m.

    Epilepsia

    Volume 47, Issue s4, October 2006, Pages: 119–204,

    Version of Record online : 30 OCT 2006, DOI: 10.1111/j.1528-1167.2006.00001_6.x

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    A Case of Ohtahara Syndrome with Olivary–dentate Dysplasia and Agenesis of Mamillary Bodies

    Epilepsia

    Volume 42, Issue 7, July 2001, Pages: 950–953, E. Trinka, C. Rauscher, M. Nagler, T. Moroder, G. Ladurner, E. Irnberger, W. Sperl and P. Pilz

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1528-1157.2001.042007950.x

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    Mislocalization of syntaxin-1 and impaired neurite growth observed in a human iPSC model for STXBP1-related epileptic encephalopathy

    Epilepsia

    Volume 57, Issue 4, April 2016, Pages: e81–e86, Satoshi Yamashita, Tomohiro Chiyonobu, Michiko Yoshida, Hiroshi Maeda, Masashi Zuiki, Satoshi Kidowaki, Kenichi Isoda, Masafumi Morimoto, Mitsuhiro Kato, Hirotomo Saitsu, Naomichi Matsumoto, Tatsutoshi Nakahata, Megumu K. Saito and Hajime Hosoi

    Version of Record online : 25 FEB 2016, DOI: 10.1111/epi.13338

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    Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings

    Epilepsia

    Volume 54, Issue 5, May 2013, Pages: e81–e85, Marlin Touma, Mugdha Joshi, Meghan C. Connolly, P. Ellen Grant, Anne R. Hansen, Omar Khwaja, Gerard T. Berry, Hannah C. Kinney, Annapurna Poduri and Pankaj B. Agrawal

    Version of Record online : 28 MAR 2013, DOI: 10.1111/epi.12137

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    GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders

    Epilepsia

    Volume 56, Issue 6, June 2015, Pages: 841–848, Chihiro Ohba, Masaaki Shiina, Jun Tohyama, Kazuhiro Haginoya, Tally Lerman-Sagie, Nobuhiko Okamoto, Lubov Blumkin, Dorit Lev, Souichi Mukaida, Fumihito Nozaki, Mitsugu Uematsu, Akira Onuma, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Fumiaki Tanaka, Mitsuhiro Kato, Kazuhiro Ogata, Hirotomo Saitsu and Naomichi Matsumoto

    Version of Record online : 10 APR 2015, DOI: 10.1111/epi.12987

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    CASK aberrations in male patients with Ohtahara syndrome and cerebellar hypoplasia

    Epilepsia

    Volume 53, Issue 8, August 2012, Pages: 1441–1449, Hirotomo Saitsu, Mitsuhiro Kato, Hitoshi Osaka, Nobuko Moriyama, Hideki Horita, Kiyomi Nishiyama, Yuriko Yoneda, Yukiko Kondo, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kiyoshi Hayasaka and Naomichi Matsumoto

    Version of Record online : 18 JUN 2012, DOI: 10.1111/j.1528-1167.2012.03548.x

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    De novo GABRA1 mutations in Ohtahara and West syndromes

    Epilepsia

    Volume 57, Issue 4, April 2016, Pages: 566–573, Hirofumi Kodera, Chihiro Ohba, Mitsuhiro Kato, Toshiyuki Maeda, Kaoru Araki, Daisuke Tajima, Muneaki Matsuo, Naomi Hino-Fukuyo, Kosuke Kohashi, Akihiko Ishiyama, Saoko Takeshita, Hirotaka Motoi, Taro Kitamura, Atsuo Kikuchi, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Masayuki Sasaki, Shigeo Kure, Kazuhiro Haginoya, Hirotomo Saitsu and Naomichi Matsumoto

    Version of Record online : 25 FEB 2016, DOI: 10.1111/epi.13344

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    Epileptic encephalopathies (including severe epilepsy syndromes)

    Epilepsia

    Volume 53, Issue s4, September 2012, Pages: 114–126, Athanasios Covanis

    Version of Record online : 4 SEP 2012, DOI: 10.1111/j.1528-1167.2012.03621.x

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    Monday, December 4, 2006 Poster Session IV 7:30 a.m. – 4:30 p.m.

    Epilepsia

    Volume 47, Issue s4, October 2006, Pages: 289–373,

    Version of Record online : 30 OCT 2006, DOI: 10.1111/j.1528-1167.2006.00001_8.x

  20. The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 2)

    Epileptic Disorders

    Volume 19, Issue 4, December 2017, Pages: 385–437, Michalis Koutroumanidis, Alexis Arzimanoglou, Roberto Caraballo, Sushma Goyal, Anna Kaminska, Pramote Laoprasert, Hirokazu Oguni, Guido Rubboli, William Tatum, Pierre Thomas, Eugen Trinka, Luca Vignatelli and Solomon L. Moshé

    Version of Record online : 26 JAN 2018, DOI: 10.1684/epd.2017.0952