Showing results (31-40 of 64) with videos related to
Sort By:
Pageof 7
Developmental Medicine and Child Neurology|February 22, 2012
Early speech-language development in females with Rett syndrome: focusing on the preserved speech variantPeter B Marschik, Giorgio Pini, Katrin D Bartl-Pokorny, et al.American Journal of Medical Genetics. Part A|April 6, 2005
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q)Alfredo Orrico, Lucia Galli, Sabrina Buoni, et al.Frontiers in Neurology|April 15, 2022
Breathing Abnormalities During Sleep and Wakefulness in Rett Syndrome: Clinical Relevance and Paradoxical Relationship With Circulating Pro-oxidant MarkersSilvia Leoncini, Cinzia Signorini, Lidia Boasiako, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 6, 2005
Myoclonic encephalopathy in the CDKL5 gene mutationSabrina Buoni, Raffaella Zannolli, Vito Colamaria, et al.Human Mutation|July 9, 2004
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplicationFrancesca Ariani, Francesca Mari, Chiara Pescucci, et al.European Psychiatry : the Journal of the Association of European Psychiatrists|September 21, 2023
Economic analysis of early intervention for autistic children: findings from four case studies in England, Ireland, Italy, and SpainMichela Tinelli, Aine Roddy, Martin Knapp, et al.Research in Developmental Disabilities|June 16, 2012
Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndromePeter B Marschik, Walter E Kaufmann, Christa Einspieler, et al.Journal of Autism and Developmental Disorders|May 4, 2023
Economic Evaluation of anti-epileptic Medicines for Autistic Children with EpilepsyMichela Tinelli M, Aine Roddy, Martin Knapp, et al.American Journal of Medical Genetics|February 22, 2002
Analysis of ten candidate genes in autism by association and linkageAnne Philippe, Michel Guilloud-Bataille, Maria Martinez, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 16, 2010
EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndromeSabrina Buoni, Raffaella Zannolli, Claudio De Felice, et al.Pageof 7