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Virulence factors and clinical patterns of multiple-clone hypermucoviscous KPC-2 producing K. pneumoniae

Heliyon, 2019-06, Vol.5 (6), p.e01829, Article e01829

2019

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Ultrasound elastography is useful to distinguish acute and chronic deep vein thrombosis

Journal of thrombosis and haemostasis, 2018-12, Vol.16 (12), p.2482-2491

2018

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A genetic association study of dopamine metabolism-related genes and chronic headache with drug abuse

European journal of neurology, 2006-09, Vol.13 (9), p.1009-1013

2006

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Investigation of the T3111C CLOCK gene polymorphism in cluster headache

Journal of neurology, 2008-02, Vol.255 (2), p.299-300

2008

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A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes

Neurological sciences, 2003-02, Vol.23 (6), p.301-305

2003

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Pharmacogenetics of headache treatment

Neurological sciences, 2005-05, Vol.26 Suppl 2 (S2), p.s143-s147

2005

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The genetics of chronic headaches

Neurological sciences, 2003-05, Vol.24 Suppl 2 (S2), p.S51-s56

2003

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Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family

Neurological sciences, 2002-04, Vol.23 (1), p.7-10

2002

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Abnormal Platelet Mitochondrial Function in Patients Affected by Migraine With and Without Aura

Cephalalgia, 1994-02, Vol.14 (1), p.21-23

1994

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Testing Models for Genetic Determination in Migraine

Cephalalgia, 1993-12, Vol.13 (6), p.389-394

1993

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Searching for migraine genes: exclusion of 290 cM out of the whole human genome

Italian journal of neurological sciences, 1997-10, Vol.18 (5), p.277-282

1997

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Inverse problem for a class of two-dimensional diffusion equations with piecewise constant coefficients

Journal of optimization theory and applications, 1999, Vol.100 (1), p.29-57

1999

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Cloud fraction within GOME footprint using a refined cloud clearing algorithm

Advances in space research, 2000, Vol.25 (5), p.993-996

2000

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Prevalence of depression and cognitive deficit in a geriatric population

Archives of gerontology and geriatrics, 2001, Vol.33, p.351-355

2001

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Lipemia retinalis in an infant treated for retinopathy of prematurity

Journal of AAPOS, 2017-06, Vol.21 (3), p.254-257

2017

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Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

The New England journal of medicine, 1992-02, Vol.326 (7), p.444-449

1992

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Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura

Journal of the neurological sciences, 2003-09, Vol.213 (1), p.7-10

2003

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A null allele for the Afm175xg3 marker at locus D17S795 caused by a primer binding failure

International journal of legal medicine, 1996, Vol.109 (2), p.104-106

1996

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Dopamine transporter gene polymorphism, spect imaging, and levodopa response in patients with Parkinson disease

Clinical neuropharmacology, 2004-05, Vol.27 (3), p.111-115

2004

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Arylsulphatase A (ASA) activity in parkinsonism and symptomatic essential tremor

Acta neurologica Scandinavica, 1994-03, Vol.89 (3), p.171-174

1994

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Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family

Italian journal of neurological sciences, 1998-02, Vol.19 (1), p.41-44

1998

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Familial spasmodic dysphonia with low arylsulphatase A (ASA) level

Acta neurologica Scandinavica, 1995-03, Vol.91 (3), p.196-199

1995

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Bleed-Through Removal from Degraded Documents Using a Color Decorrelation Method

Document Analysis Systems VI, 2004, p.229-240

2004

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Blind Source Separation Techniques for Detecting Hidden Texts and Textures in Document Images

Image Analysis and Recognition, p.241-248

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Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsy

Italian journal of neurological sciences, 1997-06, Vol.18 (3), p.183-183

1997

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Virulence factors and clinical patterns of multiple-clone hypermucoviscous KPC-2 producing K. pneumoniae

Ultrasound elastography is useful to distinguish acute and chronic deep vein thrombosis

A genetic association study of dopamine metabolism-related genes and chronic headache with drug abuse

Investigation of the T3111C CLOCK gene polymorphism in cluster headache

A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes

Pharmacogenetics of headache treatment

The genetics of chronic headaches

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family

Abnormal Platelet Mitochondrial Function in Patients Affected by Migraine With and Without Aura

Testing Models for Genetic Determination in Migraine

Searching for migraine genes: exclusion of 290 cM out of the whole human genome

Inverse problem for a class of two-dimensional diffusion equations with piecewise constant coefficients

Cloud fraction within GOME footprint using a refined cloud clearing algorithm

Prevalence of depression and cognitive deficit in a geriatric population

Lipemia retinalis in an infant treated for retinopathy of prematurity

Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura

A null allele for the Afm175xg3 marker at locus D17S795 caused by a primer binding failure

Dopamine transporter gene polymorphism, spect imaging, and levodopa response in patients with Parkinson disease

Arylsulphatase A (ASA) activity in parkinsonism and symptomatic essential tremor

Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family

Familial spasmodic dysphonia with low arylsulphatase A (ASA) level

Bleed-Through Removal from Degraded Documents Using a Color Decorrelation Method

Blind Source Separation Techniques for Detecting Hidden Texts and Textures in Document Images

Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsy

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