Antonio Di Muzio - Concepedia

Author

Antonio Di Muzio

Also Known As

A DI MUZIO, A Di Muzio, A Muzio, A. Di Muzio, A. Muzio, A. di Muzio, Anna Di Muzio, Anna Elisa Muzio, Antonino Di Muzio, Antonio Di Muzio

172

Publications

3.3K

Citations

H-Index

125

Concepts

All Affiliations

University of Chieti-Pescara Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico University of Pisa University of Verona University of Messina

About

Antonio Di Muzio is an author at University of Chieti-Pescara specializing in medicine, neuropathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	37	1.8K
2	Health Sciences	7	7	163
3	Social Sciences	7	7	405
4	Public Health	4	4	177
5	Anatomy	1	1	11

Antonio Di Muzio

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial Ivo N. van Schaik, Vera Bril, Nan van Geloven, The Lancet Neurology Subcutaneous ImmunoglobulinAutoimmune DiseaseChronic InflammatoryMaintenance TreatmentImmunotherapy	2017	258
Phase II study of pemetrexed in combination with carboplatin in patients with malignant pleural mesothelioma (MPM) B. Castagneto, Mario Botta, Enrico Aitini, Annals of Oncology Malignant Pleural MesotheliomaMedicinePhase Ii StudyPathologyPleural Disease	2007	138
Large-Scale Population Analysis Challenges the Current Criteria for the Molecular Diagnosis of Fascioscapulohumeral Muscular Dystrophy Isabella Scionti, Francesca Gabriella Greco, Giulia Ricci, The American Journal of Human Genetics Genetic AnalysisMolecular DiagnosisMendelian DisorderMedicineGenetic Epidemiology	2012	123
Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy Giulia Ricci, Isabella Scionti, Francesco Sera, Brain	2013	119
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA) Valentina Gatta, Oronzo Scarciolla, Anna Rita Gaspari, Human Genetics Carrier FemalesMendelian DisorderDmd GeneGenetic DisorderGenetics	2005	113
Both Laminin and Schwann Cell Dystroglycan Are Necessary for Proper Clustering of Sodium Channels at Nodes of Ranvier Simona Occhi, Desirée Zambroni, Ubaldo Del Carro, Journal of Neuroscience Synaptic TransmissionMolecular BiologyPeripheral NervePeripheral NervesCellular Neurobiology	2005	113
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes Giulia Ricci, Lucia Ruggiero, Liliana Vercelli, Journal of Neurology	2016	95
Physiological basis of voluntary activity inhibition induced by transcranial cortical stimulation Antonino Uncini, M. Treviso, Antonio Di Muzio, Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section Stimulation DeviceNeurophysiologyNeuroanatomyVoluntary Activity InhibitionMedicine	1993	91
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine Antonino Uncini, Raffaele Lodi, Antonio Di Muzio, Journal of the Neurological Sciences Cluster HeadacheNeurophysiologyNeurological DisorderMuscle Energy MetabolismNeuroscience	1995	84
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry Ana Nikolić, Giulia Ricci, Francesco Sera, BMJ Open	2016	76

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