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Association of the C677T Polymorphism in the MTHFR Gene with Migraine: A Meta-Analysis

Cephalalgia, 2009-08, Vol.29 (8), p.818-825

2009

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A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations

European journal of neurology, 2010-04, Vol.17 (4), p.541-549

2010

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Association between the interleukin-1α gene and Alzheimer’s disease: a meta-analysis

Neurobiology of aging, 2004-11, Vol.25 (10), p.1293-1298

2004

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A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy

Journal of neurology, neurosurgery and psychiatry, 2009-02, Vol.80 (2), p.237-240

2009

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A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)

Human molecular genetics, 2015-06, Vol.24 (11), p.3143-3154

2015

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Incidence of ALS in Italy: evidence for a uniform frequency in Western countries

Neurology, 2001-01, Vol.56 (2), p.239-244

2001

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The 1246G→A polymorphism of the HCRTR2 gene is not associated with migraine

Cephalalgia, 2007-08, Vol.27 (8), p.945-949

2007

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Investigating the genetic role of aquaporin4 gene in migraine

Journal of headache and pain, 2009-04, Vol.10 (2), p.111-114

2009

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Mutations in the lamin B1 gene are not present in multiple sclerosis

European journal of neurology, 2009-04, Vol.16 (4), p.544-546

2009

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Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14

Nature genetics, 1992-12, Vol.2 (4), p.330-334

1992

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Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy

Journal of neurology, neurosurgery and psychiatry, 2007-12, Vol.78 (12), p.1349-1353

2007

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Guillain-Barré syndrome: a prospective, population-based incidence and outcome survey

Neurology, 2003-04, Vol.60 (7), p.1146-1150

2003

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Early symptom progression rate is related to ALS outcome: a prospective population-based study

Neurology, 2002-07, Vol.59 (1), p.99-103

2002

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Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene

Neurology, 1992-08, Vol.42 (8), p.1445-1445

1992

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Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis

Neuron (Cambridge, Mass.), 1994-09, Vol.13 (3), p.727-736

1994

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Two Italian Families with ITPR1 Gene Deletion Presenting a Broader Phenotype of SCA15

Cerebellum (London, England), 2010-03, Vol.9 (1), p.115-123

2010

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SOD1 missense mutation in an Italian family with ALS

Neurology, 1994-02, Vol.44 (2), p.347-347

1994

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Autosomal Dominant Late-Onset Leukoencephalopathy

European neurology, 1997, Vol.37 (1), p.53-61

1997

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MRI and CT in an autosomal-dominant, adult-onset leukodystrophy

Neuroradiology, 1997-06, Vol.39 (6), p.423-426

1997

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Risk of cancer in patients with Guillain-Barré syndrome (GBS): A population-based study

Journal of neurology, 2004-03, Vol.251 (3), p.321-326

2004

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Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease

Neurology, 1993-11, Vol.43 (11), p.2275-2275

1993

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The 1246 G/A polymorphism of the HCRTR2 gene is not associated with migraine

Cephalalgia, 2007-08, Vol.27 (8), p.945-949

2007

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The 1246G arrow right A polymorphism of the HCRTR2 gene is not associated with migraine

Cephalalgia, 2007-08, Vol.27 (8), p.945-949

2007

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An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene

Human molecular genetics, 1992-12, Vol.1 (9), p.781-781

1992

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Association between the interleukin-1alpha gene and Alzheimer's disease: a meta-analysis

Neurobiology of aging, 2004-11, Vol.25 (10), p.1293-1298

2004

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Association of the C677T Polymorphism in the MTHFR Gene with Migraine: A Meta-Analysis

A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations

Association between the interleukin-1α gene and Alzheimer’s disease: a meta-analysis

A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy

A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)

Incidence of ALS in Italy: evidence for a uniform frequency in Western countries

The 1246G→A polymorphism of the HCRTR2 gene is not associated with migraine

Investigating the genetic role of aquaporin4 gene in migraine

Mutations in the lamin B1 gene are not present in multiple sclerosis

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14

Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy

Guillain-Barré syndrome: a prospective, population-based incidence and outcome survey

Early symptom progression rate is related to ALS outcome: a prospective population-based study

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene

Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis

Two Italian Families with ITPR1 Gene Deletion Presenting a Broader Phenotype of SCA15

SOD1 missense mutation in an Italian family with ALS

Autosomal Dominant Late-Onset Leukoencephalopathy

MRI and CT in an autosomal-dominant, adult-onset leukodystrophy

Risk of cancer in patients with Guillain-Barré syndrome (GBS): A population-based study

Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease

The 1246 G/A polymorphism of the HCRTR2 gene is not associated with migraine

The 1246G arrow right A polymorphism of the HCRTR2 gene is not associated with migraine

An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene

Association between the interleukin-1alpha gene and Alzheimer's disease: a meta-analysis

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