Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Susan L. Fong"'
Autor:
Hisako, Fujiwara, Darren S, Kadis, Hansel M, Greiner, Katherine D, Holland, Ravindra, Arya, Gewalin, Aungaroon, Susan L, Fong, Todd M, Arthur, Kelly M, Kremer, Nan, Lin, Wei, Liu, Francesco T, Mangano, Jesse, Skoch, Paul S, Horn, Jeffrey R, Tenney
Publikováno v:
Clinical Neurophysiology. 142:199-208
To clinically validate the connectivity-based magnetoencephalography (MEG) analyses to identify seizure onset zone (SOZ) with comparing to equivalent current dipole (ECD).The ECD cluster was quantitatively analyzed by calculating the centroid of the
Further Characterization of SMC1A Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome
Autor:
Kristin W. Barañano, Amy Kimball, Susan L. Fong, Alena S. Egense, Catherine Hudon, Antonie D. Kline
Publikováno v:
Journal of Child Neurology. 37:390-396
Cornelia de Lange syndrome is a rare developmental malformation syndrome characterized by small stature, limb anomalies, distinctive facial features, developmental delays, and behavioral issues. The diagnosis of Cornelia de Lange syndrome is made cli
Autor:
Gewalin Aungaroon, Kishore Vedala, Anna W. Byars, Brian Ervin, Leonid Rozhkov, Paul S. Horn, S. K. Z. Ihnen, Katherine D. Holland, Jeffrey R. Tenney, Kelly Kremer, Susan L. Fong, Nan Lin, Wei Liu, Todd M. Arthur, Hisako Fujiwara, Jesse Skoch, James L. Leach, Francesco T. Mangano, Hansel M. Greiner, Ravindra Arya
Publikováno v:
Epilepsia.
Autor:
Kristin W, Barañano, Amy, Kimball, Susan L, Fong, Alena S, Egense, Catherine, Hudon, Antonie D, Kline
Publikováno v:
Journal of child neurology. 37(5)
Cornelia de Lange syndrome is a rare developmental malformation syndrome characterized by small stature, limb anomalies, distinctive facial features, developmental delays, and behavioral issues. The diagnosis of Cornelia de Lange syndrome is made cli