M Scarcella - Concepedia

Author

M Scarcella

University of Campania "Luigi Vanvitelli"

Also Known As

M SCARCELLA, M Scarcella, M. G. Scarcella, M. Scarcella, Maria Scarcella

Publications

236

Citations

H-Index

Concepts

All Affiliations

University of Campania "Luigi Vanvitelli"Università di Camerino Ospedali Riuniti di Ancona Federico II University Hospital

About

M Scarcella is an author at University of Campania "Luigi Vanvitelli" specializing in medicine, neuropathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	130
2	Natural Sciences	1	1	18
3	Social Sciences	1	1	47
4	Biology	1	1	18
5	Molecular Biology	1	1	18

M Scarcella

Publications

221

Citations

H-Index

Page 1

	Year	Citations
Parkinsonism is a Late, Not Rare, Feature of CADASIL Michele Ragno, A. Berbellini, Gabriella Cacchiò, Stroke	2013	48
Motor cortex cholinergic dysfunction in CADASIL: A transcranial magnetic demonstration Fiore Manganelli, Michele Ragno, Gabriella Cacchiò, Clinical Neurophysiology Transcranial Magnetic DemonstrationNeurophysiologyNeuroanatomyMedicineMotor System	2007	47
Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease M. Ragno, M Scarcella, Gabriella Cacchiò, Acta Neurologica Scandinavica	2008	32
“CADASIL coma” in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation Michele Ragno, Luigi Pianese, Manrico Morroni, Neurological Sciences Age-matched Heterozygous PatientsPathologyMri FindingsNeurologyNeuropathology	2013	31
Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene M. Ragno, Gian Maria Fabrizi, Gabriella Cacchiò, Neurological Sciences BiologyCentral ItalyNatural SciencesGeneticsMolecular Biology	2006	18
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family M. Ragno, A. Perretti, Imma Castaldo, Neurological Sciences Follow-up StudyNeurological DisorderMedicineMotor DisorderNeuroscience	2005	18
High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Alessia Cappelli, Michele Ragno, Gabriella Cacchiò, Neuroscience Letters MedicineR1006c Notch3 MutationCentral Italian PatientsNeurologyHigh Recurrence	2009	16
Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL) Michele Ragno, Luigi Pianese, Michele Pinelli, Neurogenetics	2011	11

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