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Alessandro Orsini

Showing results (11-20 of 110) with videos related to

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Genes|June 26, 2026
Expanding the Phenotypic Spectrum of Raynaud-Claes Syndrome: A Rett-like Presentation with Two New CasesRoberta Milone, Alessandro Orsini, Gemma Marinella, et al.
Minerva Pediatrica|July 29, 2016
A rare case of hypomelanosis of Ito presenting with generalized alopeciaAlessandro Orsini, Roberta Mazza, Ilaria Mantellassi, et al.
Minerva Stomatologica|March 18, 2020
Long-term dentoskeletal changes of class II growing patients' treatment with the propulseur universal light appliance. A prospective controlled studyMarco Migliorati, Sara Drago, Chiara Calzolari, et al.
Minerva Pediatrica|June 27, 2018
Should children over 12 years have an EEG after a single unprovoked epileptic seizure?Alessandro Orsini, Elizabeth Morris, Saumya Thomas, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Maternally derived 15q11.2-q13.1 duplication in a child with Lennox-Gastaut-type epilepsy and dysmorphic features: Clinical-genetic characterization of the family and review of the literatureAlice Bonuccelli, Angelo Valetto, Alessandro Orsini, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
A 6.5 mb deletion at 3q24q25.2 narrows Wisconsin syndrome critical region to a 750 kb interval: A potential role for MBNLIVeronica Bertini, Alessandro Orsini, Roberta Mazza, et al.
Journal of Clinical Medicine|September 28, 2023
Ataxia Telangiectasia Arising as Immunodeficiency: The Intriguing Differential DiagnosisFederica Cavone, Susanna Cappelli, Alice Bonuccelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 9, 2020
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patientsAlessandro Orsini, Martina Corsi, Andrea Santangelo, et al.
Cephalalgia : an International Journal of Headache|September 27, 2021
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literatureThomas Foiadelli, Alessandra Rossi, Chiara Trabatti, et al.
Frontiers in Pediatrics|April 6, 2017
A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?Veronica Bertini, Angelo Valetto, Alessia Azzarà, et al.
Pageof 11

Showing results (11-20 of 110) with videos related to

Sort By:
Pageof 11
Genes|June 26, 2026
Expanding the Phenotypic Spectrum of Raynaud-Claes Syndrome: A Rett-like Presentation with Two New CasesRoberta Milone, Alessandro Orsini, Gemma Marinella, et al.
Minerva Pediatrica|July 29, 2016
A rare case of hypomelanosis of Ito presenting with generalized alopeciaAlessandro Orsini, Roberta Mazza, Ilaria Mantellassi, et al.
Minerva Stomatologica|March 18, 2020
Long-term dentoskeletal changes of class II growing patients' treatment with the propulseur universal light appliance. A prospective controlled studyMarco Migliorati, Sara Drago, Chiara Calzolari, et al.
Minerva Pediatrica|June 27, 2018
Should children over 12 years have an EEG after a single unprovoked epileptic seizure?Alessandro Orsini, Elizabeth Morris, Saumya Thomas, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Maternally derived 15q11.2-q13.1 duplication in a child with Lennox-Gastaut-type epilepsy and dysmorphic features: Clinical-genetic characterization of the family and review of the literatureAlice Bonuccelli, Angelo Valetto, Alessandro Orsini, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
A 6.5 mb deletion at 3q24q25.2 narrows Wisconsin syndrome critical region to a 750 kb interval: A potential role for MBNLIVeronica Bertini, Alessandro Orsini, Roberta Mazza, et al.
Journal of Clinical Medicine|September 28, 2023
Ataxia Telangiectasia Arising as Immunodeficiency: The Intriguing Differential DiagnosisFederica Cavone, Susanna Cappelli, Alice Bonuccelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 9, 2020
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patientsAlessandro Orsini, Martina Corsi, Andrea Santangelo, et al.
Cephalalgia : an International Journal of Headache|September 27, 2021
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literatureThomas Foiadelli, Alessandra Rossi, Chiara Trabatti, et al.
Frontiers in Pediatrics|April 6, 2017
A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?Veronica Bertini, Angelo Valetto, Alessia Azzarà, et al.
Pageof 11