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Francesco Nicita

Showing results (11-20 of 120) with videos related to

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Brain & Development|February 29, 2012
Complex malformation (Ruggieri-Happle) phenotype with "cutis tricolor" in a 10-year-old girlFrancesco Nicita, Alberto Spalice, Mario Roggini, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
Medical Hypotheses|May 14, 2011
Bilateral middle cerebral artery thromboembolic occlusion. Could maternal hyperthermia be a detrimental factor?Alberto Spalice, Francesca Del Balzo, Laura Papetti, et al.
Medical Hypotheses|November 29, 2019
Dilated Virchow-Robin spaces in children with seizures. A possible correlation?Alberto Spalice, Cristiana Alessia Guido, Francesco Nicita, et al.
European Journal of Pediatrics|May 23, 2013
Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associationsFiorenza Ulgiati, Francesco Nicita, Laura Papetti, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Eating and Weight Disorders : EWD|August 28, 2016
Beverage consumption and paediatric NAFLDAntonella Mosca, Claudia Della Corte, Maria Rita Sartorelli, et al.
Medical Hypotheses|March 11, 2011
Pediatric cerebellar stroke associated with elevated titer of antibodies to β2-glycoproteinAlberto Spalice, Francesca Del Balzo, Francesco Massimo Perla, et al.
Brain Sciences|January 16, 2021
Expanding the Clinical and Mutational Spectrum of the <i>PLP1</i>-Related Hypomyelination of Early Myelinated Structures (HEMS)Francesco Nicita, Chiara Aiello, Gessica Vasco, et al.
Italian Journal of Pediatrics|February 13, 2013
Four-year follow-up study in a NF1 boy with a focal pontine hamartomaPasquale Parisi, Severino Persechino, Maria Chiara Paolino, et al.
Pageof 12

Showing results (11-20 of 120) with videos related to

Sort By:
Pageof 12
Brain & Development|February 29, 2012
Complex malformation (Ruggieri-Happle) phenotype with "cutis tricolor" in a 10-year-old girlFrancesco Nicita, Alberto Spalice, Mario Roggini, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
Medical Hypotheses|May 14, 2011
Bilateral middle cerebral artery thromboembolic occlusion. Could maternal hyperthermia be a detrimental factor?Alberto Spalice, Francesca Del Balzo, Laura Papetti, et al.
Medical Hypotheses|November 29, 2019
Dilated Virchow-Robin spaces in children with seizures. A possible correlation?Alberto Spalice, Cristiana Alessia Guido, Francesco Nicita, et al.
European Journal of Pediatrics|May 23, 2013
Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associationsFiorenza Ulgiati, Francesco Nicita, Laura Papetti, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Eating and Weight Disorders : EWD|August 28, 2016
Beverage consumption and paediatric NAFLDAntonella Mosca, Claudia Della Corte, Maria Rita Sartorelli, et al.
Medical Hypotheses|March 11, 2011
Pediatric cerebellar stroke associated with elevated titer of antibodies to β2-glycoproteinAlberto Spalice, Francesca Del Balzo, Francesco Massimo Perla, et al.
Brain Sciences|January 16, 2021
Expanding the Clinical and Mutational Spectrum of the <i>PLP1</i>-Related Hypomyelination of Early Myelinated Structures (HEMS)Francesco Nicita, Chiara Aiello, Gessica Vasco, et al.
Italian Journal of Pediatrics|February 13, 2013
Four-year follow-up study in a NF1 boy with a focal pontine hamartomaPasquale Parisi, Severino Persechino, Maria Chiara Paolino, et al.
Pageof 12