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Acta Paediatrica (Oslo, Norway : 1992)
|
January 6, 2009
Neuronal migration disorders: clinical, neuroradiologic and genetics aspects
Alberto Spalice, Pasquale Parisi, Francesco Nicita, et al.
Journal of Pediatric Neurosciences
|
June 4, 2014
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS
Giovanna Vitaliti, Rosario R Trifiletti, Raffaele Falsaperla, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
December 15, 2010
Tension-type headache in paediatric age
Pasquale Parisi, Laura Papetti, Alberto Spalice, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 24, 2006
Bilateral perysilvian polymicrogyria in Chiari I malformation
Alberto Spalice, Pasquale Parisi, Mario Mastrangelo, et al.
Brain Sciences
|
June 26, 2026
Neonatal Epilepsy: Beyond Seizures in a Developing Brain-A Narrative Review
Giovanni Boscarino, Eleonora Cresta, Lucia Leonardi, et al.
Archives of Disease in Childhood
|
February 2, 2012
Cow's milk allergy and rolandic epilepsy: a close relationship?
Sandra Lucarelli, Alberto Spalice, Ylenia D'Alfonso, et al.
Ophthalmic Genetics
|
December 5, 2012
Unilateral Lisch nodules in a 47-year-old woman without other stigmata of neurofibromatosis type I: an example of segmental neurofibromatosis?
Francesco Nicita, Ludovico Iannetti, Alberto Spalice, et al.
Frontiers in Neurology
|
March 13, 2023
Case report: A case of acute disseminated encephalomyelitis after SARS-CoV-2 infection in pediatric patients
Francesca Cautilli, Mariavittoria Feleppa, Massimiliano Valeriani, et al.
Annals of Human Genetics
|
March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1
Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2016
The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome
Laura Papetti, Livia Schettini, Giacomo Garone, et al.
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of 19
Search research articles
Search
Showing results (31-40 of 182) with videos related to
Sort By:
Page
of 19
Acta Paediatrica (Oslo, Norway : 1992)
|
January 6, 2009
Neuronal migration disorders: clinical, neuroradiologic and genetics aspects
Alberto Spalice, Pasquale Parisi, Francesco Nicita, et al.
Journal of Pediatric Neurosciences
|
June 4, 2014
A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS
Giovanna Vitaliti, Rosario R Trifiletti, Raffaele Falsaperla, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
December 15, 2010
Tension-type headache in paediatric age
Pasquale Parisi, Laura Papetti, Alberto Spalice, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 24, 2006
Bilateral perysilvian polymicrogyria in Chiari I malformation
Alberto Spalice, Pasquale Parisi, Mario Mastrangelo, et al.
Brain Sciences
|
June 26, 2026
Neonatal Epilepsy: Beyond Seizures in a Developing Brain-A Narrative Review
Giovanni Boscarino, Eleonora Cresta, Lucia Leonardi, et al.
Archives of Disease in Childhood
|
February 2, 2012
Cow's milk allergy and rolandic epilepsy: a close relationship?
Sandra Lucarelli, Alberto Spalice, Ylenia D'Alfonso, et al.
Ophthalmic Genetics
|
December 5, 2012
Unilateral Lisch nodules in a 47-year-old woman without other stigmata of neurofibromatosis type I: an example of segmental neurofibromatosis?
Francesco Nicita, Ludovico Iannetti, Alberto Spalice, et al.
Frontiers in Neurology
|
March 13, 2023
Case report: A case of acute disseminated encephalomyelitis after SARS-CoV-2 infection in pediatric patients
Francesca Cautilli, Mariavittoria Feleppa, Massimiliano Valeriani, et al.
Annals of Human Genetics
|
March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1
Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2016
The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome
Laura Papetti, Livia Schettini, Giacomo Garone, et al.
Page
of 19