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β-Hairpin mimics containing a piperidine-pyrrolidine scaffold modulate the β-amyloid aggregation process preserving the monomer species

Chemical science (Cambridge), 2017, Vol.8 (2), p.1295-1302

2017

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β-Hairpin mimics containing a piperidine-pyrrolidine scaffold modulate the β-amyloid aggregation process preserving the monomer speciesElectronic supplementary information (ESI) available: Computational methods and additional figures and tables. NMR additional data. Description of synthetic procedures and characterization of compounds. Experimental procedure for fluorescence-detected ThT binding assay; representative curves of ThT fluorescence assays. Experimental procedure for TEM studies, CE,

2017-01

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β-Hairpin mimics containing a piperidine–pyrrolidine scaffold modulate the β-amyloid aggregation process preserving the monomer species† †Electronic supplementary information (ESI) available: Computational methods and additional figures and tables. NMR additional data. Description of synthetic procedures and characterization of compounds. Experimental procedure for fluorescence-detected ThT binding assay; representative curves of ThT fluorescence assays. Experimental procedure for TEM studies, C

Chemical science (Cambridge), 2016-10, Vol.8 (2), p.1295-1302

2016

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Introduction of polar groups on the naphthalene scaffold of molecular tongs inhibiting wild-type and mutated HIV-1 protease dimerizationElectronic supplementary information (ESI) available: Experimental part with the synthesis procedures and characterisation of all the new compounds; characteristic 1H, 13C and 2D NMR spectra of a few molecular tongs; HPLC chromatograms of molecular tongs 3 and 8 and evolution with time of the concentration of molecular tongs 3 and 8 incubated at 37 °C in RPMI cu

2014-05

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Introduction of polar groups on the naphthalene scaffold of molecular tongs inhibiting wild-type and mutated HIV-1 protease dimerization

MedChemComm, 2014, Vol.5 (6), p.719-727

2014

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Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia

Journal of the neurological sciences, 2010-04, Vol.291 (1), p.89-91

2010

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Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden

Arteriosclerosis, thrombosis, and vascular biology, 1999-07, Vol.19 (7), p.1751

1999

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Occurrence and characterization of Pain in immune-mediated neuropathies: a multicentre prospective study

European journal of neurology, 2011-01, Vol.18 (1), p.177-183

2011

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Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype

Annals of neurology, 1999-06, Vol.45 (6), p.751-757

1999

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Natural history of CMT1A including QoL: A 2-year prospective study

Neuromuscular disorders : NMD, 2008-03, Vol.18 (3), p.199-203

2008

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Natural history of Charcot–Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life

Neurological sciences, 2010-04, Vol.31 (2), p.175-178

2010

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Influence of cholinergic circuitries in generation of high-frequency somatosensory evoked potentials

Clinical neurophysiology, 2003-08, Vol.114 (8), p.1538-1548

2003

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Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study

Neurological sciences, 2006-12, Vol.27 (6), p.417-423

2006

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Quality of life and disability assessment in neuropathy: a multicentre study

Journal of the peripheral nervous system, 2005-03, Vol.10 (1), p.3-10

2005

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Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings

Neurological sciences, 2008-06, Vol.29 (3), p.193-194

2008

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Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenstroem's macroglobulinaemia

Journal of the neurological sciences, 2010-04, Vol.291 (1-2), p.89-91

2010

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Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies

European journal of neurology, 2007-01, Vol.14 (1), p.e45-e46

2007

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The prognosis and main prognostic indicators of Guillain-Barré syndrome A multicentre prospective study of 297 patients

Brain (London, England : 1878), 1996-12, Vol.119 (6), p.2053-2061

The Italian Guillain--Barre Study Group

1996

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Non-DYT1 dystonia in a large Italian family

Journal of neurology, neurosurgery and psychiatry, 1997-04, Vol.62 (4), p.357-360

1997

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P13.3 Quality of life and disability in CMT patients: Italian multicenter study

Clinical neurophysiology, 2006-09, Vol.117, p.186-187

2006

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TP2.2 Charcot–Marie–Tooth type 1a: Correlation between neurophysiological pattern and quality of life

Clinical neurophysiology, 2006-09, Vol.117, p.1-2

2006

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Inhibitory effect of capsaicin evoked trigeminal pain on warmth sensation and warmth evoked potentials

International Congress series, 2005-03, Vol.1278, p.389-392

2005

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Neurophysiological abnormalities in adrenoleukodystrophy carriers : Evidence of different degrees of central nervous system involvement

Brain (London, England : 1878), 1997-07, Vol.120 (7), p.1139-1148

1997

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Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication

Muscle & nerve, 1995-06, Vol.18 (6), p.628-635

1995

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Reliability of the El Escorial Diagnostic Criteria for Amyotrophic Lateral Sclerosis

Neuroepidemiology, 2002-11, Vol.21 (6), p.265-270

2002

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β-Hairpin mimics containing a piperidine-pyrrolidine scaffold modulate the β-amyloid aggregation process preserving the monomer species

Introduction of polar groups on the naphthalene scaffold of molecular tongs inhibiting wild-type and mutated HIV-1 protease dimerization

Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia

Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden

Occurrence and characterization of Pain in immune-mediated neuropathies: a multicentre prospective study

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype

Natural history of CMT1A including QoL: A 2-year prospective study

Natural history of Charcot–Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life

Influence of cholinergic circuitries in generation of high-frequency somatosensory evoked potentials

Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study

Quality of life and disability assessment in neuropathy: a multicentre study

Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings

Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenstroem's macroglobulinaemia

Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies

The prognosis and main prognostic indicators of Guillain-Barré syndrome A multicentre prospective study of 297 patients

Non-DYT1 dystonia in a large Italian family

P13.3 Quality of life and disability in CMT patients: Italian multicenter study

TP2.2 Charcot–Marie–Tooth type 1a: Correlation between neurophysiological pattern and quality of life

Inhibitory effect of capsaicin evoked trigeminal pain on warmth sensation and warmth evoked potentials

Neurophysiological abnormalities in adrenoleukodystrophy carriers : Evidence of different degrees of central nervous system involvement

Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication

Reliability of the El Escorial Diagnostic Criteria for Amyotrophic Lateral Sclerosis

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