de Falco FA - Search Results

1

Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance.

de Falco FA, Majello L, Santangelo R, Stabile M, Bricarelli FD, Zara F. de Falco FA, et al. Epilepsia. 2001 Dec;42(12):1541-8. doi: 10.1046/j.1528-1157.2001.26701.x. Epilepsia. 2001. PMID: 11879364 Free article.

2

Familial benign nonprogressive myoclonic epilepsies.

Striano P, de Falco FA, Minetti C, Zara F. Striano P, et al. Among authors: de falco fa. Epilepsia. 2009 May;50 Suppl 5:37-40. doi: 10.1111/j.1528-1167.2009.02118.x. Epilepsia. 2009. PMID: 19469844 Free article. Review.

3

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

Zara F, Gennaro E, Stabile M, Carbone I, Malacarne M, Majello L, Santangelo R, de Falco FA, Bricarelli FD. Zara F, et al. Among authors: de falco fa. Am J Hum Genet. 2000 May;66(5):1552-7. doi: 10.1086/302876. Epub 2000 Mar 30. Am J Hum Genet. 2000. PMID: 10741954 Free PMC article.

4

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME.

de Falco FA, Striano P, de Falco A, Striano S, Santangelo R, Perretti A, Balbi P, Cecconi M, Zara F. de Falco FA, et al. Among authors: de falco a. Neurology. 2003 Apr 22;60(8):1381-5. doi: 10.1212/01.wnl.0000055874.24000.4a. Neurology. 2003. PMID: 12707452

5

Autosomal recessive benign myoclonic epilepsy of infancy.

Zara F, De Falco FA. Zara F, et al. Among authors: de falco fa. Adv Neurol. 2005;95:139-45. Adv Neurol. 2005. PMID: 15508919 No abstract available.

6

Calcium antagonist nimodipine in intractable epilepsy.

de Falco FA, Bartiromo U, Majello L, Di Geronimo G, Mundo P. de Falco FA, et al. Epilepsia. 1992 Mar-Apr;33(2):343-5. doi: 10.1111/j.1528-1157.1992.tb02325.x. Epilepsia. 1992. PMID: 1547764

7

Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 years.

de Falco FA, Olivieri P, de Falco A, Concolino D, Battaglia F, Verardi R, Grande G, Stabile M. de Falco FA, et al. Among authors: de falco a. Seizure. 2006 Sep;15(6):449-53. doi: 10.1016/j.seizure.2006.03.004. Epub 2006 Jun 27. Seizure. 2006. PMID: 16806995 Free article.

8

Burden of acute stroke and hospital resources in the Campania region of Italy.

de Falco FA, Santangelo R, Majello L, Marasco G. de Falco FA, et al. Cerebrovasc Dis. 2002;14(2):116-21. doi: 10.1159/000064740. Cerebrovasc Dis. 2002. PMID: 12187016

9

Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters.

Boccella P, Striano P, Zara F, Barbieri F, Sarappa C, Vacca G, de Falco FA, Striano S. Boccella P, et al. Among authors: de falco fa. Clin Neurol Neurosurg. 2003 Dec;106(1):55-9. doi: 10.1016/j.clineuro.2003.07.003. Clin Neurol Neurosurg. 2003. PMID: 14643920

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: de falco a, de falco fa. 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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