Gaetano Tortorella
Messina, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.
Journal: European journal of medical genetics
Published: June 07, 2016
Effects of Maternal Iodine Nutrition and Thyroid Status on Cognitive Development in Offspring: A Pilot Study.
Journal: Thyroid : official journal of the American Thyroid Association
Published: November 21, 2015
Cognitive training modifies frequency EEG bands and neuropsychological measures in Rett syndrome.
Journal: Research in developmental disabilities
Published: April 13, 2015
Cognitive, adaptive, and behavioral features in Joubert syndrome.
Journal: American journal of medical genetics. Part A
Published: February 15, 2015
Long-term neuropsychiatric follow-up in hyperprolinemia type I.
Journal: Psychiatric genetics
Published: May 21, 2014
Role of plasma homocysteine levels and MTHFR polymorphisms on IQ scores in children and young adults with epilepsy treated with antiepileptic drugs.
Journal: Epilepsy & behavior : E&B
Published: July 23, 2013
Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 21, 2013
Acute cerebellar ataxia following meningococcal group C conjugate vaccination.
Journal: Journal of child neurology
Published: January 01, 2013
Cognitive decline in Dravet syndrome: is there a cerebellar role?
Journal: Epilepsy research
Published: November 17, 2012
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.
Journal: Neurology
Published: October 19, 2012
Pediatric Hashimoto's encephalopathy with peripheral nervous system involvement.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: October 06, 2012
Early-onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females.
Journal: Clinical genetics
Published: August 31, 2012
Last Updated: 09/26/2026