Di Bonaventura C - Search Results

1

Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases.

Canafoglia L, Franceschetti S, Gambardella A, Striano P, Giallonardo AT, Tinuper P, Di Bonaventura C, Michelucci R, Ferlazzo E, Granata T, Magaudda A, Licchetta L, Filla A, La Neve A, Riguzzi P, Cantisani TA, Fanella M, Castellotti B, Gellera C, Bahlo M, Zara F, Courage C, Lehesjoki AE, Oliver KL, Berkovic SF. Canafoglia L, et al. Among authors: di bonaventura c. Neurol Genet. 2021 Nov 12;7(6):e641. doi: 10.1212/NXG.0000000000000641. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34786481 Free PMC article.

2

fMRI/EEG in paroxysmal activity elicited by elimination of central vision and fixation.

Iannetti GD, Di Bonaventura C, Pantano P, Giallonardo AT, Romanelli PL, Bozzao L, Manfredi M, Ricci GB. Iannetti GD, et al. Among authors: di bonaventura c. Neurology. 2002 Mar 26;58(6):976-9. doi: 10.1212/wnl.58.6.976. Neurology. 2002. PMID: 11914422

3

Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism.

Pizzuti A, Flex E, Di Bonaventura C, Dottorini T, Egeo G, Manfredi M, Dallapiccola B, Giallonardo AT. Pizzuti A, et al. Among authors: di bonaventura c. Ann Neurol. 2003 Mar;53(3):396-9. doi: 10.1002/ana.10492. Ann Neurol. 2003. PMID: 12601709

4

Symptoms in focal sensory seizures. Clinical and electroencephalographic features.

Di Bonaventura C, Giallonardo AT, Fattouch J, Manfredi M. Di Bonaventura C, et al. Seizure. 2005 Jan;14(1):1-9. doi: 10.1016/j.seizure.2004.02.002. Seizure. 2005. PMID: 15642493 Free article.

5

Metabolic alteration transients during paroxysmal activity in an epileptic patient with fixation-off sensitivity: a case study.

Giove F, Garreffa G, Peca S, Carní M, Macrì MA, Di Bonaventura C, Vaudano AE, Giallonardo AT, Prencipe M, Bozzao L, Pantano P, Colonnese C, Maraviglia B. Giove F, et al. Among authors: di bonaventura c. Magn Reson Imaging. 2006 May;24(4):373-9. doi: 10.1016/j.mri.2005.11.003. Epub 2006 Mar 20. Magn Reson Imaging. 2006. PMID: 16677943

6

Status epilepticus in a patient with fragile X syndrome: electro-clinical features and peri-ictal neuroimaging.

Di Bonaventura C, Mari F, Pierallini A, Mecarelli O, Randi F, Manfredi M, Prencipe M, Giallonardo AT. Di Bonaventura C, et al. Epileptic Disord. 2006 Sep;8(3):195-9. Epileptic Disord. 2006. PMID: 16987740 Free article.

7

EEG/fMRI study of ictal and interictal epileptic activity: methodological issues and future perspectives in clinical practice.

Di Bonaventura C, Vaudano AE, Carnì M, Pantano P, Nucciarelli V, Garreffa G, Maraviglia B, Prencipe M, Bozzao L, Manfredi M, Giallonardo AT. Di Bonaventura C, et al. Epilepsia. 2006;47 Suppl 5:52-8. doi: 10.1111/j.1528-1167.2006.00878.x. Epilepsia. 2006. PMID: 17239107 Free article.

8

Over-interpretation of electroclinical and neuroimaging findings in syncopes misdiagnosed as epileptic seizures.

Fattouch J, Di Bonaventura C, Strano S, Vanacore N, Manfredi M, Prencipe M, Giallonardo AT. Fattouch J, et al. Among authors: di bonaventura c. Epileptic Disord. 2007 Jun;9(2):170-3. doi: 10.1684/epd.2007.0099. Epileptic Disord. 2007. PMID: 17525028 Free article.

9

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.

Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R. Striano P, et al. Among authors: di bonaventura c. J Neurol. 2008 Jan;255(1):16-23. doi: 10.1007/s00415-007-0653-1. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004642

10

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.

Madia F, Striano P, Di Bonaventura C, de Falco A, de Falco FA, Manfredi M, Casari G, Striano S, Minetti C, Zara F. Madia F, et al. Among authors: di bonaventura c. Neurogenetics. 2008 May;9(2):139-42. doi: 10.1007/s10048-008-0118-4. Epub 2008 Jan 30. Neurogenetics. 2008. PMID: 18231815

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