Severe myoclonic epilepsy in infancy: Dravet syndrome

C Dravet, M Bureau, H Oguni, Y Fukuyama… - Adv Neurol, 2005 - books.google.com
… Sugama M, Oguni H, Fukuyama Y. Clinical and electroencephalographic study of severe
myoclonic epilepsy in infancy (Dravet). Jpn J Psychiat Neurol 1987; 41: 463465. …

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group

…, B Leiendecker, UR Monani, H Oguni… - Epilepsia …, 2020 - Wiley Online Library
Glut1 deficiency syndrome (Glut1DS) is a brain energy failure syndrome caused by impaired
glucose transport across brain tissue barriers. Glucose diffusion across tissue barriers is …

Dravet syndrome (severe myoclonic epilepsy in infancy)

C Dravet, H Oguni - Handbook of clinical neurology, 2013 - Elsevier
… Author links open overlay panel Charlotte Dravet 1 , Hirokazu Oguni 2 … of the convulsive
seizures and is largely used in Germany and Japan (Oguni et al., 1994, Doose et al., 1998). …

Mutations in EFHC1 cause juvenile myoclonic epilepsy

…, Y Inoue, M Osawa, S Kaneko, H Oguni… - Nature …, 2004 - nature.com
… We dissected out the brains, postfixed them for an additional 3 h at 4C and cryoprotected them
… After serial washes in PBST, we incubated the sections for 3 h at 40 C with the secondary …

Mutations of Neuronal Voltage‐gated Na+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

G Fukuma, H Oguni, Y Shirasaka, K Watanabe… - …, 2004 - Wiley Online Library
Purpose: Severe myoclonic epilepsy in infancy (SMEI) is a distinct epilepsy syndrome. Patients
with borderline SMEI (SMEB) are a subgroup with clinical features similar to those of core …

Panayiotopoulos syndrome: a consensus view

…, M Koutroumanidis, Z Martinovic, H Oguni… - … medicine and child …, 2006 - cambridge.org
The aim of this paper is to promote the correct classification of, and provide guidelines on,
the diagnosis and management of Panayiotopoulos syndrome (PS). An international …

Treatment and long-term prognosis of myoclonic-astatic epilepsy of early childhood

H Oguni, T Tanaka, K Hayashi, M Funatsuka… - …, 2002 - thieme-connect.com
Purpose We retrospectively studied patients with myoclonic-astatic epilepsy of early
childhood (MAE) to investigate the most effective treatment and long-term seizure and …

Severe myoclonic epilepsy in infants–a review based on the Tokyo Women's Medical University series of 84 cases

H Oguni, K Hayashi, Y Awaya, Y Fukuyama… - Brain and …, 2001 - Elsevier
Severe myoclonic epilepsy in infants (SME) is one of the most malignant epileptic syndromes
recognized in the latest classification of epileptic syndromes. The clinical details and …

Anterior callosotomy in the treatment of medically intractable epilepsies: a study of 43 patients with a mean follow‐up of 39 months

H Oguni, A Olivier, F Andermann… - Annals of Neurology …, 1991 - Wiley Online Library
Oguni et at: Anterior Callosotomy for Epilepsy 363 … Ohvier A, Andermann F, Oguni H. Anterior
callosotomy in the treatment of intractable epilepsies. In: Canger R, Colicchio G, Fusco L, et …

STXBP1 mutations cause not only Ohtahara syndrome but also West syndrome—Result of Japanese cohort study

M Otsuka, H Oguni, JS Liang, H Ikeda, K Imai… - …, 2010 - Wiley Online Library
We performed STXBP1 mutation analyses in 86 patients with various types of epilepsies,
including 10 patients with OS, 43 with West syndrome, 2 with Lennox‐Gastaut syndrome, 12 …