Federico Melani - Concepedia

Author

Federico Melani

Meyer Children's Hospital

Also Known As

F MELANI, F Melani, F. Melani, FEDERICO MELANI, Federico Melani

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Meyer Children's Hospital University of Florence University of Siena Fondazione Stella Maris Istituti di Ricovero e Cura a Carattere Scientifico

About

Federico Melani is an author at Meyer Children's Hospital specializing in medicine, neuroscience, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	216
2	Neuroscience	4	4	220
3	Social Sciences	3	3	178
4	Neurology	3	3	174
5	Psychiatry	1	1	16

Federico Melani

Publications

681

Citations

H-Index

Page 1

	Year	Citations
<i>HCN1</i>mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond Carla Marini, Alessandro Porro, Agnès Rastetter, Brain	2018	134
Occurrence of scalp-fast oscillations among patients with different spiking rate and their role as epileptogenicity marker Federico Melani, Rina Zelmann, François Dubeau, Epilepsy Research NeurodynamicsNeurophysiologyComputational NeuroscienceNeuroanatomyNeurological Function	2013	86
<i>CDKL5</i> gene‐related epileptic encephalopathy: electroclinical findings in the first year of life Federico Melani, Davide Mei, Tiziana Pisano, Developmental Medicine & Child Neurology	2011	73
Continuous High Frequency Activity: A peculiar SEEG pattern related to specific brain regions Federico Melani, Rina Zelmann, Francesco Mari, Clinical Neurophysiology Peculiar Seeg PatternBrain CircuitryNeurophysiologyNeuroanatomyMedicine	2013	72
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD Margherita Nosadini, Michael Eyre, Thea Giacomini, Neurology Neuroimmunology & Neuroinflammation	2022	64
Next-generation sequencing approach to hyperCKemia Anna Rubegni, Alessandro Malandrini, Claudia Dosi, Neurology Genetics	2019	45
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease Daniel G. Calame, Tianyu Guo, Chen Wang, The American Journal of Human Genetics Neurodegenerative DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderMonoallelic Variation	2023	42
Expanding the genetic and phenotypic spectrum of <scp><i>CHD2</i></scp>‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy Beatrice De Maria, Simona Balestrini, Davide Mei, American Journal of Medical Genetics Part A	2021	28
Epileptic scalp ripples are associated with corticothalamic <scp>BOLD</scp> changes Firas Fahoum, Federico Melani, Luciana P. A. Andrade‐Valença, Epilepsia	2014	22
Deep Brain Stimulation of the Anterior Limb of the Internal Capsule May Be Efficacious for Explosive Aggressive Behaviour Flavio Giordano, Michele Alessandro Cavallo, Barbara Spacca, Stereotactic and Functional Neurosurgery	2016	21

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