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Serenella Servidei

Showing results (1-10 of 106) with videos related to

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Current Neurology and Neuroscience Reports|May 5, 2021
Sleep Disorders in Mitochondrial DiseasesValerio Brunetti, Giacomo Della Marca, Serenella Servidei, et al.
Cephalalgia : an International Journal of Headache|August 2, 2017
Migraine in mitochondrial disorders: Prevalence and characteristicsCatello Vollono, Guido Primiano, Giacomo Della Marca, et al.
Neuromuscular Disorders : NMD|April 9, 2021
Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patientAntonio Petrucci, Guido Primiano, Marco Savarese, et al.
Neurorehabilitation and Neural Repair|February 24, 2011
Nerve growth factor eye drop administration improves visual function in a patient with optic gliomaAntonio Chiaretti, Benedetto Falsini, Serenella Servidei, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 13, 2022
Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature reviewGuido Primiano, Eleonora Rollo, Marina Romozzi, et al.
International Journal of Molecular Sciences|January 8, 2023
Vitamin D in Neurological DiseasesDomenico Plantone, Guido Primiano, Carlo Manco, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 18, 2008
Acute auditory agnosia as the presenting hearing disorder in MELASGabriele Miceli, Guido Conti, Alessandro Cianfoni, et al.
International Journal of Molecular Sciences|October 16, 2024
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic ApproachMichela Cicchinelli, Guido Primiano, Serenella Servidei, et al.
Seizure|April 29, 2020
Focal status epilepticus as unique clinical feature of COVID-19: A case reportCatello Vollono, Eleonora Rollo, Marina Romozzi, et al.
The Journal of Headache and Pain|July 29, 2021
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family reportMarina Romozzi, Guido Primiano, Eleonora Rollo, et al.
Pageof 11

Showing results (1-10 of 106) with videos related to

Sort By:
Pageof 11
Current Neurology and Neuroscience Reports|May 5, 2021
Sleep Disorders in Mitochondrial DiseasesValerio Brunetti, Giacomo Della Marca, Serenella Servidei, et al.
Cephalalgia : an International Journal of Headache|August 2, 2017
Migraine in mitochondrial disorders: Prevalence and characteristicsCatello Vollono, Guido Primiano, Giacomo Della Marca, et al.
Neuromuscular Disorders : NMD|April 9, 2021
Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patientAntonio Petrucci, Guido Primiano, Marco Savarese, et al.
Neurorehabilitation and Neural Repair|February 24, 2011
Nerve growth factor eye drop administration improves visual function in a patient with optic gliomaAntonio Chiaretti, Benedetto Falsini, Serenella Servidei, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 13, 2022
Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature reviewGuido Primiano, Eleonora Rollo, Marina Romozzi, et al.
International Journal of Molecular Sciences|January 8, 2023
Vitamin D in Neurological DiseasesDomenico Plantone, Guido Primiano, Carlo Manco, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 18, 2008
Acute auditory agnosia as the presenting hearing disorder in MELASGabriele Miceli, Guido Conti, Alessandro Cianfoni, et al.
International Journal of Molecular Sciences|October 16, 2024
Resolving Phenotypic Variability in Mitochondrial Diseases: Preliminary Findings of a Proteomic ApproachMichela Cicchinelli, Guido Primiano, Serenella Servidei, et al.
Seizure|April 29, 2020
Focal status epilepticus as unique clinical feature of COVID-19: A case reportCatello Vollono, Eleonora Rollo, Marina Romozzi, et al.
The Journal of Headache and Pain|July 29, 2021
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family reportMarina Romozzi, Guido Primiano, Eleonora Rollo, et al.
Pageof 11