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M G Marrosu

Showing results (81-90 of 115) with videos related to

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Journal of Affective Disorders|December 4, 2013
The risk of Bipolar Disorders in Multiple SclerosisM G Carta, M F Moro, L Lorefice, et al.
Multiple Sclerosis and Related Disorders|October 22, 2018
Assessing the burden of vascular risk factors on brain atrophy in multiple sclerosis: A case- control MRI studyL Lorefice, J Frau, G Coghe, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 22, 2015
A genetic study of the FMR1 gene in a Sardinian multiple sclerosis populationL Lorefice, S Tranquilli, G Fenu, et al.
Journal of the Neurological Sciences|August 3, 2015
A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: the TARDBP Ala382Thr mutation and C9orf72 expansionL Lorefice, M R Murru, G Fenu, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A genome screen for multiple sclerosis in Sardinian multiplex familiesF Coraddu, S Sawcer, S D'Alfonso, et al.
Multiple Sclerosis and Related Disorders|March 16, 2018
Adult brain volume in multiple sclerosis: The impact of paediatric onsetG Fenu, L Lorefice, L Loi, et al.
Human Molecular Genetics|December 15, 2000
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseasesR Lampis, L Morelli, M Congia, et al.
BMC Neurology|August 25, 2016
Combining HLA-DRB1-DQB1 and Mycobacterium Avium Subspecies Paratubercolosis (MAP) antibodies in Sardinian multiple sclerosis patients: associated or independent risk factors?J Frau, D Cossu, C Sardu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 12, 2006
A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalitiesM R Murru, A Vannelli, G Marrosu, et al.
Spinal Cord|January 1, 1997
Urinary tract dysfunction in multiple sclerosis: is there a relation with disease-related parameters?D Porru, G Campus, A Garau, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
Journal of Affective Disorders|December 4, 2013
The risk of Bipolar Disorders in Multiple SclerosisM G Carta, M F Moro, L Lorefice, et al.
Multiple Sclerosis and Related Disorders|October 22, 2018
Assessing the burden of vascular risk factors on brain atrophy in multiple sclerosis: A case- control MRI studyL Lorefice, J Frau, G Coghe, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 22, 2015
A genetic study of the FMR1 gene in a Sardinian multiple sclerosis populationL Lorefice, S Tranquilli, G Fenu, et al.
Journal of the Neurological Sciences|August 3, 2015
A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: the TARDBP Ala382Thr mutation and C9orf72 expansionL Lorefice, M R Murru, G Fenu, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A genome screen for multiple sclerosis in Sardinian multiplex familiesF Coraddu, S Sawcer, S D'Alfonso, et al.
Multiple Sclerosis and Related Disorders|March 16, 2018
Adult brain volume in multiple sclerosis: The impact of paediatric onsetG Fenu, L Lorefice, L Loi, et al.
Human Molecular Genetics|December 15, 2000
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseasesR Lampis, L Morelli, M Congia, et al.
BMC Neurology|August 25, 2016
Combining HLA-DRB1-DQB1 and Mycobacterium Avium Subspecies Paratubercolosis (MAP) antibodies in Sardinian multiple sclerosis patients: associated or independent risk factors?J Frau, D Cossu, C Sardu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 12, 2006
A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalitiesM R Murru, A Vannelli, G Marrosu, et al.
Spinal Cord|January 1, 1997
Urinary tract dysfunction in multiple sclerosis: is there a relation with disease-related parameters?D Porru, G Campus, A Garau, et al.
Pageof 12