User profiles for "author:F M Boneschi"
Filippo Martinelli BoneschiUniversity of Milan; Ospedale Maggiore Policlinico of Milan Verified email at unimi.it Cited by 18470 |
Mitoxantrone for multiple sclerosis
FM Boneschi, L Vacchi, M Rovaris… - Cochrane Database …, 2013 - cochranelibrary.com
Mitoxantrone for multiple sclerosis - Martinelli Boneschi, F - 2013 | Cochrane Library Skip to
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Content Cookies Our site uses cookies to improve your experience. You can find out more …
Disease‐modifying therapies and coronavirus disease 2019 severity in multiple sclerosis
MP Sormani, N De Rossi, I Schiavetti… - Annals of …, 2021 - Wiley Online Library
Objective This study was undertaken to assess the impact of immunosuppressive and
immunomodulatory therapies on the severity of coronavirus disease 2019 (COVID‐19) in …
immunomodulatory therapies on the severity of coronavirus disease 2019 (COVID‐19) in …
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
S Kalachikov, O Evgrafov, B Ross, M Winawer… - Nature …, 2002 - nature.com
The epilepsies are a common, clinically heterogeneous group of disorders defined by
recurrent unprovoked seizures 1. Here we describe identification of the causative gene in …
recurrent unprovoked seizures 1. Here we describe identification of the causative gene in …
Role of hnRNP-A1 and miR-590-3p in Neuronal Death: Genetics and Expression Analysis in Patients with Alzheimer Disease and Frontotemporal Lobar …
C Villa, C Fenoglio, M De Riz, F Clerici… - Rejuvenation …, 2011 - liebertpub.com
An association study of heterogeneous nuclear ribonucleoprotein (hnRNP)-A1 was carried
out in a population of 274 patients with frontotemporal lobar degeneration (FTLD) and 287 …
out in a population of 274 patients with frontotemporal lobar degeneration (FTLD) and 287 …
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy
Background: Mental retardation is a clinical feature of Duchenne dystrophy (DD) and affects
about one-third of patients. No clear association has been found between DNA mutations …
about one-third of patients. No clear association has been found between DNA mutations …
Multimodal evoked potentials to assess the evolution of multiple sclerosis: a longitudinal study
L Leocani, M Rovaris, FM Boneschi… - Journal of Neurology …, 2006 - jnnp.bmj.com
Background: Evoked potentials are used in the functional assessment of sensory and motor
pathways. Their usefulness in monitoring the evolution of multiple sclerosis has not been …
pathways. Their usefulness in monitoring the evolution of multiple sclerosis has not been …
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
MT Bassi, N Bresolin, A Tonelli, K Nazos… - Journal of medical …, 2004 - jmg.bmj.com
Alternating hemiplegia of childhood (AHC, MIM 104290) is a rare syndrome, characterised
by early onset of episodic hemi-or quadriplegia lasting minutes to days. This disorder, first …
by early onset of episodic hemi-or quadriplegia lasting minutes to days. This disorder, first …
Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels
A Prelle, L Tancredi, M Sciacco, L Chiveri, GP Comi… - Journal of …, 2002 - Springer
A retrospective evaluation of asymptomatic subjects with persistent elevation of serum
creatine kinase (CK) levels (hyperCKemia) was made in order to verify the presence of …
creatine kinase (CK) levels (hyperCKemia) was made in order to verify the presence of …
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
MF George, FBS Briggs, X Shao… - Neurology …, 2016 - AAN Enterprises
Objective: We investigated the association between 52 risk variants identified through
genome-wide association studies and disease severity in multiple sclerosis (MS). Methods …
genome-wide association studies and disease severity in multiple sclerosis (MS). Methods …
The long pentraxin PTX3 as a correlate of cancer-related inflammation and prognosis of malignancy in gliomas
Inflammation is a component of glioma microenvironment. PTX3 is a component of the
humoral arm of innate immunity and a candidate marker of inflammation. In the present …
humoral arm of innate immunity and a candidate marker of inflammation. In the present …