De Falco Fa - Concepedia

Author

De Falco Fa

Ospedale Santa Maria di Loreto Nuovo ORCID

Also Known As

De Falco Fa, Domenico Consoli, F A De Falco, F A de Falco, F Falco, F a de Falco, F. A. De Falco, F. A. de Falco, F.A de Falco, F.A. De Falco

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Ospedale Santa Maria di Loreto Nuovo University of Naples Federico II Istituto Giannina Gaslini Federico II University Hospital Ente Ospedaliero Ospedali Galliera

About

De Falco Fa is an author at Ospedale Santa Maria di Loreto Nuovo specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	446
2	Public Health	2	2	30
3	Health Sciences	1	1	30
4	Social Sciences	1	1	19
5	Cell Biology	1	1	156

De Falco Fa

Publications

829

Citations

H-Index

Page 1

	Year	Citations
TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy Antonio Falace, Fabia Filipello, Veronica La Padula, The American Journal of Human Genetics Is MutatedArf6-interacting ProteinGenetic DisorderGeneticsDisease Gene Identification	2010	156
<i>TBC1D24</i> genotype–phenotype correlation Simona Balestrini, Mathieu Milh, Claudia Castiglioni, Neurology	2016	126
Benign adult familial myoclonic epilepsy De Falco Fa, Pasquale Striano, Arturo de Falco, Neurology	2003	73
The neurologist in the emergency department. An Italian nationwide epidemiological survey De Falco Fa, Roberto Sterzi, Vito Toso, Neurological Sciences NeuroepidemiologyPatient SafetyClinical NeurologyBrain InjuryNeurology	2008	57
Mapping of a Locus for a Familial Autosomal Recessive Idiopathic Myoclonic Epilepsy of Infancy to Chromosome 16p13 Federico Zara, Elena Di Gennaro, M Stabile, The American Journal of Human Genetics MedicineGeneticsNeurogeneticsGenetic Disorder	2000	48
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families Francesca Madia, Pasquale Striano, Carlo Di Bonaventura, Neurogenetics Mendelian DisorderGenetic DisorderGeneticsClinical GeneticsChromosome 2P11.1-q12.2	2008	41
Calcium Antagonist Nimodipine in Intractable Epilepsy De Falco Fa, U. Bartiromo, Luigi Majello, Epilepsia	1992	39
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without<i><scp>LGI</scp>1</i>mutations Roberto Michelucci, Elena Pasini, Sandro Malacrida, Epilepsia	2013	38
A Novel Loss-of-Function LGI1 Mutation Linked to Autosomal Dominant Lateral Temporal Epilepsy Pasquale Striano, Arturo de Falco, Erica Diani, Archives of Neurology	2008	37
Otoneurological Findings in Friedreich's Ataxia and Other Inherited Neuropathies Ettore Cassandro, F Mosca, Luigi Sequino, International Journal of Audiology Auditory ProcessingSpeech PerceptionOtoneurological FindingsNeurological DisorderClinical Neurology	1986	30

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