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Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Journal of the neurological sciences, 2012-08, Vol.319 (1), p.37-41

2012

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Spring and fall blood concentrations of adrenocorticotropic hormone, insulin, and thyroxine in healthy horses in Saskatchewan

Canadian veterinary journal, 2024-04, Vol.65 (4), p.335-342

2024

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3. Cutaneous innervation involvement in CADASIL

Clinical neurophysiology, 2013-11, Vol.124 (11), p.e189-e190

2013

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67. A case of sudden unexpected death in epilepsy (SUDEP) in a patient affected by septic shock

Clinical neurophysiology, 2013-11, Vol.124 (11), p.e204-e204

2013

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From Table to Stable: A Comparative Review of Selected Aspects of Human and Equine Metabolic Syndrome

Journal of equine veterinary science, 2019-08, Vol.79, p.131-138

2019

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Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease

Acta neurologica Scandinavica, 2009-02, Vol.119 (2), p.131-134

2009

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Investigation of a Yersinia enterocolitica outbreak in a commercial alpaca farm in Saskatchewan

Canadian veterinary journal, 2019-08, Vol.60 (8), p.877-882

2019

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cAMP and Vfr Control Exolysin Expression and Cytotoxicity of Pseudomonas aeruginosa Taxonomic Outliers

Journal of bacteriology, 2018-06, Vol.200 (12)

2018

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Morphometric, metabolic, and inflammatory markers across a cohort of client-owned horses and ponies on the insulin dysregulation spectrum

Journal of equine veterinary science, 2021-10, Vol.105, p.103715-103715, Article 103715

2021

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High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities

Journal of neurology, 2010-06, Vol.257 (6), p.1039-1042

2010

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Septic fibrinous pericarditis in 4 horses in Saskatchewan following an outbreak of forest tent caterpillars in 2017

Canadian veterinary journal, 2020-07, Vol.61 (7), p.724-730

2020

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The Italian multiple sclerosis register

Neurological sciences, 2019-01, Vol.40 (1), p.155-165

2019

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Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia

Journal of neurology, neurosurgery and psychiatry, 1999-01, Vol.66 (1), p.93-96

1999

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Prophylactic platelet transfusions

The New England journal of medicine, 2010-06, Vol.362 (22), p.2141; author reply 2141-2141; author reply 2142

2010

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Cognitive impairment and its relation with disease measures in mildly disabled patients with relapsing–remitting multiple sclerosis: baseline results from the Cognitive Impairment in Multiple Sclerosis (COGIMUS) study

Multiple sclerosis, 2009-07, Vol.15 (7), p.779-788

2009

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Bilateral paramedian thalamic syndrome: abnormal circadian wake-sleep and autonomic functions

Journal of neurology, neurosurgery and psychiatry, 2002-12, Vol.73 (6), p.772-774

2002

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Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene

Neurological sciences, 2006-09, Vol.27 (4), p.252-256

2006

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Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation

Neurological sciences, 2007-08, Vol.28 (4), p.181-184

2007

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Subcutaneous interferon β-1a may protect against cognitive impairment in patients with relapsing-remitting multiple sclerosis: 5-year follow-up of the COGIMUS study

PloS one, 2013-08, Vol.8 (8), p.e74111

2013

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Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family

Neurological sciences, 2005-06, Vol.26 (2), p.67-71

2005

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Patterns of motor control reorganization in a patient with mirror movements

Clinical neurophysiology, 2000-02, Vol.111 (2), p.318-325

2000

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Autosomal dominant cerebellar ataxia type I : multimodal electrophysiological study and comparison between SCA1 and SCA2 patients

Journal of the neurological sciences, 1996-10, Vol.142 (1-2), p.45-53

1996

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Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia

Neurology, 1997-12, Vol.49 (6), p.1617-1620

1997

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Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy

Neurology, 2001-01, Vol.56 (1), p.100-103

2001

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Basis for intracellular retention of a human mutant of the retinal rod channel alpha subunit

The Journal of membrane biology, 2002-01, Vol.185 (2), p.129

2002

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Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Spring and fall blood concentrations of adrenocorticotropic hormone, insulin, and thyroxine in healthy horses in Saskatchewan

3. Cutaneous innervation involvement in CADASIL

67. A case of sudden unexpected death in epilepsy (SUDEP) in a patient affected by septic shock

From Table to Stable: A Comparative Review of Selected Aspects of Human and Equine Metabolic Syndrome

Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease

Investigation of a Yersinia enterocolitica outbreak in a commercial alpaca farm in Saskatchewan

cAMP and Vfr Control Exolysin Expression and Cytotoxicity of Pseudomonas aeruginosa Taxonomic Outliers

Morphometric, metabolic, and inflammatory markers across a cohort of client-owned horses and ponies on the insulin dysregulation spectrum

High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities

Septic fibrinous pericarditis in 4 horses in Saskatchewan following an outbreak of forest tent caterpillars in 2017

The Italian multiple sclerosis register

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia

Prophylactic platelet transfusions

Cognitive impairment and its relation with disease measures in mildly disabled patients with relapsing–remitting multiple sclerosis: baseline results from the Cognitive Impairment in Multiple Sclerosis (COGIMUS) study

Bilateral paramedian thalamic syndrome: abnormal circadian wake-sleep and autonomic functions

Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation

Subcutaneous interferon β-1a may protect against cognitive impairment in patients with relapsing-remitting multiple sclerosis: 5-year follow-up of the COGIMUS study

Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family

Patterns of motor control reorganization in a patient with mirror movements

Autosomal dominant cerebellar ataxia type I : multimodal electrophysiological study and comparison between SCA1 and SCA2 patients

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy

Basis for intracellular retention of a human mutant of the retinal rod channel alpha subunit

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