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Stefano D'Arrigo

Showing results (11-20 of 99) with videos related to

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Journal of Child Neurology|December 13, 2006
De novo duplication of chromosome 13(q32-q34) in a child with developmental delayDonatella Milani, Stefano D'Arrigo, Silvana Guerneri, et al.
Journal of Child Neurology|August 24, 2007
Craniodigital syndrome of Scott: clinical and neuroradiological features of a new caseDonatella Milani, Stefano D'Arrigo, Alessandra Erbetta, et al.
Frontiers in Neurology|August 7, 2023
Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmusSara Hafdaoui, Claudia Ciaccio, Barbara Castellotti, et al.
Neuropediatrics|December 1, 2019
A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic AspectsStefano D'Arrigo, Valeria Tessarollo, Franco Taroni, et al.
American Journal of Medical Genetics. Part A|March 28, 2017
ZC4H2 deletions can cause severe phenotype in female carriersCristina Zanzottera, Donatella Milani, Enrico Alfei, et al.
Epilepsy & Behavior : E&B|February 3, 2007
Intellectual and language findings and their relationship to EEG characteristics in benign childhood epilepsy with centrotemporal spikesDaria Riva, Chiara Vago, Silvana Franceschetti, et al.
Epilepsy Research|February 26, 2008
Verbal dichotic listening performance and its relationship with EEG features in benign childhood epilepsy with centrotemporal spikesSara Bulgheroni, Silvana Franceschetti, Chiara Vago, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 14, 2015
Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrumFederica Natacci, Enrico Alfei, Lucia Tararà, et al.
Journal of Child Neurology|April 12, 2008
Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosisStefano D'Arrigo, Daria Riva, Sara Bulgheroni, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Oligoyric microcephaly in a child with Williams syndromeFrancesca Faravelli, Stefano D'Arrigo, Irene Bagnasco, et al.
Pageof 10

Showing results (11-20 of 99) with videos related to

Sort By:
Pageof 10
Journal of Child Neurology|December 13, 2006
De novo duplication of chromosome 13(q32-q34) in a child with developmental delayDonatella Milani, Stefano D'Arrigo, Silvana Guerneri, et al.
Journal of Child Neurology|August 24, 2007
Craniodigital syndrome of Scott: clinical and neuroradiological features of a new caseDonatella Milani, Stefano D'Arrigo, Alessandra Erbetta, et al.
Frontiers in Neurology|August 7, 2023
Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmusSara Hafdaoui, Claudia Ciaccio, Barbara Castellotti, et al.
Neuropediatrics|December 1, 2019
A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic AspectsStefano D'Arrigo, Valeria Tessarollo, Franco Taroni, et al.
American Journal of Medical Genetics. Part A|March 28, 2017
ZC4H2 deletions can cause severe phenotype in female carriersCristina Zanzottera, Donatella Milani, Enrico Alfei, et al.
Epilepsy & Behavior : E&B|February 3, 2007
Intellectual and language findings and their relationship to EEG characteristics in benign childhood epilepsy with centrotemporal spikesDaria Riva, Chiara Vago, Silvana Franceschetti, et al.
Epilepsy Research|February 26, 2008
Verbal dichotic listening performance and its relationship with EEG features in benign childhood epilepsy with centrotemporal spikesSara Bulgheroni, Silvana Franceschetti, Chiara Vago, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 14, 2015
Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrumFederica Natacci, Enrico Alfei, Lucia Tararà, et al.
Journal of Child Neurology|April 12, 2008
Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosisStefano D'Arrigo, Daria Riva, Sara Bulgheroni, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Oligoyric microcephaly in a child with Williams syndromeFrancesca Faravelli, Stefano D'Arrigo, Irene Bagnasco, et al.
Pageof 10