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Seizure|March 3, 2018
Ehlers-Danlos syndromes and epilepsy: An updated reviewFrancesca Cortini, Chiara Villa
Seizure|July 25, 2018
Epileptic seizures in autosomal dominant forms of Alzheimer's diseaseFrancesca Cortini, Claudia Cantoni, Chiara Villa
Ageing Research Reviews|January 6, 2019
Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's diseaseFrancesca Cortini, Francesca Roma, Chiara Villa
Dermatology Online Journal|September 29, 2018
Ehlers-Danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: an Italian family without cardiovascular eventsFrancesca Cortini, Barbara Marinelli, Manuela Seia, et al.
Dermatology Online Journal|January 26, 2019
RETRACTED: Ehlers-Danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: an Italian family without cardiovascular eventsFrancesca Cortini, Barbara Marinelli, Manuela Seia, et al.
Archives of Dermatological Research|March 4, 2019
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencingFrancesca Cortini, Chiara Villa, Barbara Marinelli, et al.
Pediatric Neurosurgery|April 26, 2018
A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid BifurcationMaurizio Domanin, Silvia Lanfranconi, Silvia Romagnoli, et al.
Journal of Medical Case Reports|November 2, 2016
Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case reportFrancesca Cortini, Barbara Marinelli, Manuela Seia, et al.
Leukemia Research|April 20, 2006
Usefulness of JAK2V617F mutation in distinguishing idiopathic erythrocytosis from polycythemia veraDavide Rossi, Francesca Cortini, Clara Deambrogi, et al.
Vascular and Endovascular Surgery|February 11, 2017
A New COL3A1 Mutation in Ehlers-Danlos Syndrome Vascular Type With Different Phenotypes in the Same FamilyFrancesca Cortini, Barbara Marinelli, Silvia Romi, et al.
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