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Brain Computer Interfaces and Emotional Involvement: Theory, Research, and Applications

Lucchiari, Claudio

2022

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Prevalence study of muscle channelopathies in Italy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S197-S197

2016

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Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease

Neuromuscular disorders : NMD, 2014-03, Vol.24 (3), p.272-276

2014

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Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2013-10, Vol.64 (5), p.669

2013

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Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.161-168

2009

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Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL

Human mutation, 2006-06, Vol.27 (6), p.600-601

2006

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P.10 Compound CACNA1S heterozygosity resulting in a novel phenotype of congenital myopathy and early onset periodic paralysis: report of two probands

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S47

2022

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Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion

Journal of the neurological sciences, 2008-12, Vol.275 (1), p.159-163

2008

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Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency

Acta myologica, 2007-07, Vol.26 (1), p.72-74

2007

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Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL

Human mutation, 2002-12, Vol.20 (6), p.480-480

2002

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Mutational analysis of the AGL gene: Five novel mutations in GSD III patients

Human mutation, 2003-10, Vol.22 (4), p.337-337

2003

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Mutational analysis of theAGL gene: Five novel mutations in GSD III patients

Human mutation, 2003-10, Vol.22 (4), p.337-337

2003

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Brain Stimulation and Behavioral Change

2019

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P.371 - Prevalence study of muscle channelopathies in Italy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S197-S197

2016

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β-enolase deficiency, a new metabolic myopathy of distal glycolysis

Annals of neurology, 2001-08, Vol.50 (2), p.202-207

2001

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Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa

Journal of inherited metabolic disease, 1999-08, Vol.22 (6), p.762-763

1999

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Optimized detection of DNA point mutations by double gradient denaturing gradient gel electrophoresis

Clinical chemistry and laboratory medicine, 1998-12, Vol.36 (12), p.959-961

1998

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Developmental and tissue-specific regulation of a novel dysferlin isoform

Muscle & nerve, 2004-09, Vol.30 (3), p.366-374

2004

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Hepatic and neuromuscular forms of glycogenosis type III: nine mutations inAGL

Human mutation, 2006-06, Vol.27 (6), p.600-601

2006

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Clinical and genetic variability of glycogen storage disease type IIIa: Seven novel AGL gene mutations in the mediterranean area

American journal of medical genetics, 2002-05, Vol.109 (3), p.183-190

2002

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Molecular characterisation of GSD III subjects and identification of six novel mutations inAGL

Human mutation, 2002-12, Vol.20 (6), p.480-480

2002

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Validation of double gradient denaturing gradient gel electrophoresis through multigenic retrospective analysis

Clinical chemistry (Baltimore, Md.), 1999, Vol.45 (1), p.35-40

1999

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The role of interleukin-6 (IL-6) in the proliferation and differentiation of human neural stem cells

Neuroscience research communications, 2001-07, Vol.29 (1), p.1-14

2001

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Cancer-Cell-Intrinsic cGAS Expression Mediates Tumor Immunogenicity

Cell reports (Cambridge), 2019-10, Vol.29 (5), p.1236-1248.e7

2019

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Promoting Creativity Through Transcranial Direct Current Stimulation (tDCS). A Critical Review

Frontiers in behavioral neuroscience, 2018-08, Vol.12, p.167-167

2018

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Brain Computer Interfaces and Emotional Involvement: Theory, Research, and Applications

Prevalence study of muscle channelopathies in Italy

Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease

Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient

Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene

Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL

P.10 Compound CACNA1S heterozygosity resulting in a novel phenotype of congenital myopathy and early onset periodic paralysis: report of two probands

Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion

Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency

Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL

Mutational analysis of the AGL gene: Five novel mutations in GSD III patients

Mutational analysis of theAGL gene: Five novel mutations in GSD III patients

Brain Stimulation and Behavioral Change

P.371 - Prevalence study of muscle channelopathies in Italy

β-enolase deficiency, a new metabolic myopathy of distal glycolysis

Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa

Optimized detection of DNA point mutations by double gradient denaturing gradient gel electrophoresis

Developmental and tissue-specific regulation of a novel dysferlin isoform

Hepatic and neuromuscular forms of glycogenosis type III: nine mutations inAGL

Clinical and genetic variability of glycogen storage disease type IIIa: Seven novel AGL gene mutations in the mediterranean area

Molecular characterisation of GSD III subjects and identification of six novel mutations inAGL

Validation of double gradient denaturing gradient gel electrophoresis through multigenic retrospective analysis

The role of interleukin-6 (IL-6) in the proliferation and differentiation of human neural stem cells

Cancer-Cell-Intrinsic cGAS Expression Mediates Tumor Immunogenicity

Promoting Creativity Through Transcranial Direct Current Stimulation (tDCS). A Critical Review

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