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Jun Tohyama

Showing results (11-20 of 102) with videos related to

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Pediatric Neurology|March 14, 2007
Magnetoencephalographic findings of Panayiotopoulos syndrome with frontal epileptic dischargesNaka Saitoh, Osamu Kanazawa, Jun Tohyama, et al.
Pediatric Neurology|August 10, 2011
Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutationSawako Yamazaki, Kanju Ikeno, Tokinari Abe, et al.
Brain & Development|May 27, 2014
Gómez-López-Hernández syndrome in a Japanese patient: a case reportYu Kobayashi, Hideshi Kawashima, Shinichi Magara, et al.
Pediatric Neurology|August 7, 2007
Megalencephaly and polymicrogyria with polydactyly syndromeJun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
Human Genome Variation|February 23, 2017
A 7q31.33q32.1 microdeletion including <i>LRRC4</i> and <i>GRM8</i> is associated with severe intellectual disability and characteristics of autismNoriko Sangu, Keiko Shimojima, Yuya Takahashi, et al.
No to Hattatsu = Brain and Development|July 18, 2007
[An infant with multiple cavernous angiomas presenting with frequent epileptic seizures - detection of epileptic focus by magnetoencephalography]Jun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
Journal of the Neurological Sciences|October 12, 2007
Roles of matrix metalloproteinase-9 and tissue inhibitors of metalloproteinases 1 in acute encephalopathy following prolonged febrile seizuresNaoko Suenaga, Takashi Ichiyama, Masaya Kubota, et al.
Pediatric Neurology|August 7, 2013
Refractory infantile spasms associated with mosaic variegated aneuploidy syndromeNoriyuki Akasaka, Jun Tohyama, Atsushi Ogawa, et al.
Journal of Human Genetics|August 9, 2024
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia, and seizuresTakeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama, et al.
Brain & Development|December 7, 2014
Rub epilepsy in an infant with Turner syndromeShin-Ichi Magara, Hideshi Kawashima, Yu Kobayashi, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Pediatric Neurology|March 14, 2007
Magnetoencephalographic findings of Panayiotopoulos syndrome with frontal epileptic dischargesNaka Saitoh, Osamu Kanazawa, Jun Tohyama, et al.
Pediatric Neurology|August 10, 2011
Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutationSawako Yamazaki, Kanju Ikeno, Tokinari Abe, et al.
Brain & Development|May 27, 2014
Gómez-López-Hernández syndrome in a Japanese patient: a case reportYu Kobayashi, Hideshi Kawashima, Shinichi Magara, et al.
Pediatric Neurology|August 7, 2007
Megalencephaly and polymicrogyria with polydactyly syndromeJun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
Human Genome Variation|February 23, 2017
A 7q31.33q32.1 microdeletion including <i>LRRC4</i> and <i>GRM8</i> is associated with severe intellectual disability and characteristics of autismNoriko Sangu, Keiko Shimojima, Yuya Takahashi, et al.
No to Hattatsu = Brain and Development|July 18, 2007
[An infant with multiple cavernous angiomas presenting with frequent epileptic seizures - detection of epileptic focus by magnetoencephalography]Jun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
Journal of the Neurological Sciences|October 12, 2007
Roles of matrix metalloproteinase-9 and tissue inhibitors of metalloproteinases 1 in acute encephalopathy following prolonged febrile seizuresNaoko Suenaga, Takashi Ichiyama, Masaya Kubota, et al.
Pediatric Neurology|August 7, 2013
Refractory infantile spasms associated with mosaic variegated aneuploidy syndromeNoriyuki Akasaka, Jun Tohyama, Atsushi Ogawa, et al.
Journal of Human Genetics|August 9, 2024
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia, and seizuresTakeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama, et al.
Brain & Development|December 7, 2014
Rub epilepsy in an infant with Turner syndromeShin-Ichi Magara, Hideshi Kawashima, Yu Kobayashi, et al.
Pageof 11