Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 6, 2008
Late-onset childhood occipital epilepsy (Gastaut type): a family studySalvatore Grosso, Rossella Vivarelli, Giuseppe Gobbi, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|February 23, 2010
Quantitative ultrasound and dual-energy x-ray absorptiometry in children and adolescents with neurofibromatosis of type 1Carla Caffarelli, Stefano Gonnelli, Loredana Tanzilli, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Craniofacial dyssynostosis: case report and reviewSalvatore Grosso, Rossella Vivarelli, Maria Carmela Muraca, et al.
Journal of Child Neurology|June 26, 2003
Epilepsy in neurofibromatosis 1Rossella Vivarelli, Salvatore Grosso, Fulvia Calabrese, et al.
Journal of Neurology|January 16, 2003
GM2 gangliosidosis variant B1 neuroradiological findingsSalvatore Grosso, Maria Angela Farnetani, Rosario Berardi, et al.
American Journal of Medical Genetics. Part A|March 7, 2013
Evaluation of tibial osteopathy occurrence in neurofibromatosis type 1 Italian patientsGuido Morcaldi, Maurizio Clementi, Giuliana Lama, et al.
Neurogenetics|July 8, 2009
Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationCostanza Bacci, Roberta Sestini, Aldesia Provenzano, et al.
The Journal of General Virology|April 15, 2003
Nucleotide variation in Sabin type 2 poliovirus from an immunodeficient patient with poliomyelitisGabriele Buttinelli, Valentina Donati, Stefano Fiore, et al.
Brain & Development|September 25, 2014
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disabilityFrancesca Mari, Annabella Marozza, Maria Antonietta Mencarelli, et al.
Human Molecular Genetics|August 3, 2013
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodelingDagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, et al.
Pageof 1