Search Results - "MURRU, M. R"
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Mycobacterium avium subsp. paratuberculosis and multiple sclerosis in Sardinian patients: epidemiology and clinical features
Published in Multiple sclerosis (01-10-2013)“…Background: Mycobacterium avium subspecies paratuberculosis (MAP) is an infectious factor recently found in association with multiple sclerosis (MS) in…”
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2
HLA-DR, DQ and APOE genotypes and gender influence in Sardinian primary progressive MS
Published in Neurology (08-02-2005)“…The authors examined the influence of APOE and human leukocyte antigen-DRB1-DQB1 polymorphisms on the course of multiple sclerosis in 871 patients, 773 with…”
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3
Bias in parental transmission of the HLA-DR3 allele in sardinian multiple sclerosis
Published in Neurology (28-09-2004)“…The authors analyzed the female: male (F:M) ratio according to the HLA-DRB1-DQB1 genotype in a cohort of multiple sclerosis (MS) patients from Sardinia, where…”
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4
Long-term seismogenesis in Greece: Comparison of the evolving stress field and precursory scale increase approaches
Published in Journal of Geophysical Research - Solid Earth (01-05-2006)“…Recent strong (M ≥ 6.6) earthquakes in Greece are examined from the point of view of two current, but disparate, approaches to long‐term seismogenesis. These…”
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5
DRB1-DQA1-DQB1 Loci and Multiple Sclerosis Predisposition in the Sardinian Population
Published in Human molecular genetics (01-08-1998)“…Multiple sclerosis (MS) is a common neurological disease caused by genetic and environmental factors. Previous genetic analyses have suggested that the MHC/HLA…”
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6
Multiple Sclerosis in Sardinia Is Associated and in Linkage Disequilibrium with HLA-DR3 and -DR4 Alleles
Published in American journal of human genetics (01-08-1997)Get full text
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7
Interaction of loci within the HLA region influences multiple sclerosis course in the Sardinian population
Published in Journal of neurology (01-02-2006)“…We examined the influence of alleles at the HLA loci, previously found to be associated with multiple sclerosis (MS) in Sardinia, on the clinical course of the…”
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8
A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities
Published in Neurological sciences (01-04-2006)“…The objective of this study was to study genetic and phenotypic features of a family with X-linked Charcot-Marie-Tooth consisting of a healthy father, affected…”
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9
A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population
Published in Neurological sciences (01-12-2015)“…Multiple sclerosis (MS) is a complex autoimmune disease originated from the interplay between genetic and environmental factors. An overlap of clinical and…”
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10
Sardinian multiple sclerosis is associated with HLA-DR4: a serologic and molecular analysis
Published in Neurology (01-11-1988)“…HLA haplotypes in 45 unrelated Sardinian multiple sclerosis patients and in six multiplex families were defined, using both serologic and restriction fragment…”
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A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: The TARDBP Ala382Thr mutation and C9orf72 expansion
Published in Journal of the neurological sciences (15-10-2015)“…Abstract Multiple sclerosis (MS) is a chronic disease of the central nervous system characterized by inflammation and accompanied and followed by…”
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12
Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
Published in Human molecular genetics (01-12-2001)“…Several studies have indicated that multiple sclerosis (MS) is associated and linked to the major histocompatibility complex (MHC)/human leukocyte antigen…”
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13
HLA-DQA1 and -DQB1 associations with multiple sclerosis in Sardinia and French Canada : evidence for immunogenetically distinct patient groups
Published in Neurology (01-03-1993)“…We analyzed the association of HLA-DQA1 and -DQB1 alleles with multiple sclerosis (MS) in a collaborative study of 116 Sardinian and 75 French Canadian MS…”
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14
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
Published in Brain (London, England : 1878) (01-03-2012)“…A large hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72, a gene located on chromosome 9p21, has been recently reported to be…”
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15
A PvuII RFLP at D6S114E locus in the HLA region (RING4 locus)
Published in Nucleic acids research (25-12-1991)“…Images…”
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16
HLA-DQB1 genotype in Sardinian multiple sclerosis: evidence for a key role of DQB1 0201 and 0302 alleles
Published in Neurology (01-04-1992)“…We studied HLA-DQB1 haplotypes in 103 unrelated multiple sclerosis (UMS) patients and in 26 related (RMS) patients from 12 families from Sardinia, Italy, where…”
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17
Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot–Marie–Tooth and distal hereditary motor neuropathy
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2010)“…BackgroundHeat shock protein 27 (HSP27) mutations have been reported to cause both Charcot-Marie-Tooth disease (CMT) type 2F and distal hereditary motor…”
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A new allelic variant of HLA-DRB11101 (DRB111013) segregating in a Sardinian family
Published in Tissue antigens (01-11-1996)Get more information
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An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population
Published in Journal of neurovirology (01-05-2000)“…Subsequent to a genomic linkage study on Sardinian and Continental Italian families, we considered the possibility that some of the tested microsatellite…”
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Epithelial-like cells containing lymphocytes (nurse cells) in human adenoids and tonsils
Published in Thymus (1984)“…Epithelial cells filled with lymphocytes (nurse cells, NC), recently described in mouse, rat and human thymus, have been interpreted as mediators of direct…”
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