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Brain & Development|June 1, 1997
The effectiveness of clonazepam on the Rolandic dischargesA Mitsudome, M Ohfu, S Yasumoto, et al.Neurology|May 1, 1981
Electronmicroscopy of conjunctival biopsy in mannosidosisT Yamano, M Shimada, S Okada, et al.No to Shinkei = Brain and Nerve|November 22, 1997
[An operated case of intractable occipital lobe epilepsy associated with calcification in the occipital lobe]S Ohara, T Morioka, S Nishio, et al.Epilepsia|January 22, 2000
Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese familyM Ito, K Kobayashi, T Fujii, et al.Neurology|November 24, 1999
A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsyS Hirose, H Iwata, H Akiyoshi, et al.Human Genetics|March 10, 1999
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G-->A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiencyN Kanai, F Yanai, S Hirose, et al.Neuromuscular Disorders : NMD|September 1, 1995
A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophinE Arikawa-Hirasawa, R Koga, T Tsukahara, et al.No to Hattatsu = Brain and Development|June 8, 2001
[Interleukin-6 in the cerebrospinal fluid of two patients with herpes zoster meningitis]M Ohfu, M Masuzaki, S Inoue, et al.Neurologia Medico-Chirurgica|November 1, 1994
Symptomatic Chiari malformation and associated pathophysiology in pediatric and adult patients without myelodysplasiaT Fukushima, T Matsuda, H Tsuchimochi, et al.Neurology|August 29, 2001
Nav1.1 mutations cause febrile seizures associated with afebrile partial seizuresT Sugawara, E Mazaki-Miyazaki, M Ito, et al.Pageof 5