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Brain & development

Showing results (111-120 of 5,161) with videos related to

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Brain & Development|June 15, 2011
Neuropathology of fetal stage Seckel syndrome: a case report providing a morphological correlate for the emerging molecular mechanismsBrendan Fitzgerald, Mark O'Driscoll, Karen Chong, et al.
Brain & Development|January 1, 1990
Developmental and aging changes in the expression patterns of beta-amyloid in the brains of normal and Down syndrome casesS Takashima, H Kuruta, T Mito, et al.
Brain & Development|March 26, 2011
Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomaliesAkihiko Ishiyama, Yoshiaki Saito, Kenji Sugai, et al.
Brain & Development|May 10, 2011
Repeated seizures induce prefrontal growth disturbance in frontal lobe epilepsyHideaki Kanemura, Fumikazu Sano, Tomoko Tando, et al.
Brain & Development|May 11, 2011
TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatmentCarmen Fons, Patrizia Rizzu, Angels Garcia-Cazorla, et al.
Brain & Development|May 3, 2011
Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse: lymphocyte markers as disease activityMakiko Oguma, Akira Morimoto, Akiko Takada, et al.
Brain & Development|March 2, 2011
Clinicogenetical features of a Japanese patient with giant axonal neuropathyMotohiro Akagi, Ikuko Mohri, Yoshiko Iwatani, et al.
Brain & Development|April 8, 2011
Klinefelter's syndrome complicated with West syndrome in a 4-month-old boyHirofumi Inoue, Tomoko Orita, Takeshi Matsushige, et al.
Brain & Development|October 26, 2011
The differences in epileptic characteristics in patients with porencephaly and schizencephalyMiki Shimizu, Tomoki Maeda, Tatsuro Izumi
Brain & Development|October 11, 2011
MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disordersStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Pageof 517

Showing results (111-120 of 5,161) with videos related to

Sort By:
Pageof 517
Brain & Development|June 15, 2011
Neuropathology of fetal stage Seckel syndrome: a case report providing a morphological correlate for the emerging molecular mechanismsBrendan Fitzgerald, Mark O'Driscoll, Karen Chong, et al.
Brain & Development|January 1, 1990
Developmental and aging changes in the expression patterns of beta-amyloid in the brains of normal and Down syndrome casesS Takashima, H Kuruta, T Mito, et al.
Brain & Development|March 26, 2011
Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomaliesAkihiko Ishiyama, Yoshiaki Saito, Kenji Sugai, et al.
Brain & Development|May 10, 2011
Repeated seizures induce prefrontal growth disturbance in frontal lobe epilepsyHideaki Kanemura, Fumikazu Sano, Tomoko Tando, et al.
Brain & Development|May 11, 2011
TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatmentCarmen Fons, Patrizia Rizzu, Angels Garcia-Cazorla, et al.
Brain & Development|May 3, 2011
Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse: lymphocyte markers as disease activityMakiko Oguma, Akira Morimoto, Akiko Takada, et al.
Brain & Development|March 2, 2011
Clinicogenetical features of a Japanese patient with giant axonal neuropathyMotohiro Akagi, Ikuko Mohri, Yoshiko Iwatani, et al.
Brain & Development|April 8, 2011
Klinefelter's syndrome complicated with West syndrome in a 4-month-old boyHirofumi Inoue, Tomoko Orita, Takeshi Matsushige, et al.
Brain & Development|October 26, 2011
The differences in epileptic characteristics in patients with porencephaly and schizencephalyMiki Shimizu, Tomoki Maeda, Tatsuro Izumi
Brain & Development|October 11, 2011
MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disordersStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Pageof 517