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High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm

Neurological sciences, 2006-11, Vol.27 (5), p.303-311

2006

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Clinical features and neurophysiological follow-up in a case of Brown-Vialetto-Van Laere syndrome

Neuromuscular disorders : NMD, 2005-08, Vol.15 (8), p.565-568

2005

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PP09.14 – 2843: Congenital absence of gluteal muscles without spina bifida occulta: The first case report

European journal of paediatric neurology, 2015-05, Vol.19, p.S68-S69

2015

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Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study

Brain (London, England : 1878), 2004-08, Vol.127 (8), p.1785-1795

2004

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Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S224-S225

2015

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Brain structural damage in spinocerebellar ataxia type 1: A VBM study

Journal of neurology, 2008-08, Vol.255 (8), p.1153-1158

2008

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P8-17 NIRS (near infrared spectroscopy): evaluation of oxygen consumption in neuropathic and myopathic patients

Clinical neurophysiology, 2010, Vol.121, p.S151-S151

2010

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Health risk assessment for exposure to low levels of dangerous chemicals mixtures in research laboratories

Toxicology letters, 2011-08, Vol.205, p.S212-S212

2011

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D.P.9 Whole exome sequencing filtered by novel candidate genes as tool for gene discovery in a recessive family with Parkinson and ataxia

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.810-810

2012

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Introducción. El suicidio en la literatura, el cine y el arte visual en España e Hispanoamérica

Revista canadiense de estudios hispánicos, 2018-01, Vol.42 (2), p.211-223

2018

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Two Italian patients with novel AAAS gene mutation expand allelic and phenotypic spectrum of triple A (Allgrove) syndrome

Clinical genetics, 2010-03, Vol.77 (3), p.298-301

2010

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Time and frequency domain analysis of surface myoelectric signals during electrically-elicited cramps

Neurophysiologie clinique, 2009-02, Vol.39 (1), p.15-25

2009

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P1.19 Whole genetic and protein characterisation in DMD symptomatic female carriers excludes correlation with X-inactivation and transcriptional DMD allele balancing

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.647-647

2011

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The therapeutic use of botulinum toxin

Expert opinion on investigational drugs, 1997-10, Vol.6 (10), p.1383-1394

1997

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Effect of fentanyl on heart rate variability during spontaneous and paced breathing in healthy volunteers

Acta anaesthesiologica Scandinavica, 2008-09, Vol.52 (8), p.1064-1070

2008

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Successful botulinum toxin treatment of dysphagia in oculopharyngeal muscular dystrophy

Gastroenterology (New York, N.Y. 1943), 2000-11, Vol.119 (5), p.1416-1416

2000

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Early MR imaging and spectroscopy appearance of eIF2B-related leukoencephalopathy

Neurology, 2006-08, Vol.67 (3), p.537

2006

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The variability in the clinical effect induced by botulinum toxin type A: The role of muscle activity in humans

Movement disorders, 1997-01, Vol.12 (1), p.89-94

1997

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Stiff person syndrome does not always occur with maternal passive transfer of GAD65 antibodies

Neurology, 2004-06, Vol.62 (11), p.2101

2004

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NeUroGastroenterology

Corazziari, Enrico

1, 2020

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Botulinum toxin treatment for slipping rib syndrome: a case report

The Clinical journal of pain, 2013-10, Vol.29 (10), p.e1-e3

2013

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72. A novel ATP7A-related phenotype with distal motor neuropathy and autonomic dysfunction: Case report of two sibs

Clinical neurophysiology, 2017-12, Vol.128 (12), p.e432-e432

2017

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G.P.18.09 Functional characterisation of a novel mutation causing episodic ataxia type 1 occurring in the KCNA1 gene

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.892-893

2007

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Visceral manifestations in spinal cord lesions

NeUroGastroenterology, 2020, p.283-288

2020

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The role of gustatory flushing in Frey's syndrome and its treatment with botulinum toxin type A

Clinical autonomic research, 2002-06, Vol.12 (3), p.174-178

2002

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High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm

Clinical features and neurophysiological follow-up in a case of Brown-Vialetto-Van Laere syndrome

PP09.14 – 2843: Congenital absence of gluteal muscles without spina bifida occulta: The first case report

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study

Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction

Brain structural damage in spinocerebellar ataxia type 1: A VBM study

P8-17 NIRS (near infrared spectroscopy): evaluation of oxygen consumption in neuropathic and myopathic patients

Health risk assessment for exposure to low levels of dangerous chemicals mixtures in research laboratories

D.P.9 Whole exome sequencing filtered by novel candidate genes as tool for gene discovery in a recessive family with Parkinson and ataxia

Introducción. El suicidio en la literatura, el cine y el arte visual en España e Hispanoamérica

Two Italian patients with novel AAAS gene mutation expand allelic and phenotypic spectrum of triple A (Allgrove) syndrome

Time and frequency domain analysis of surface myoelectric signals during electrically-elicited cramps

P1.19 Whole genetic and protein characterisation in DMD symptomatic female carriers excludes correlation with X-inactivation and transcriptional DMD allele balancing

The therapeutic use of botulinum toxin

Effect of fentanyl on heart rate variability during spontaneous and paced breathing in healthy volunteers

Successful botulinum toxin treatment of dysphagia in oculopharyngeal muscular dystrophy

Early MR imaging and spectroscopy appearance of eIF2B-related leukoencephalopathy

The variability in the clinical effect induced by botulinum toxin type A: The role of muscle activity in humans

Stiff person syndrome does not always occur with maternal passive transfer of GAD65 antibodies

NeUroGastroenterology

Botulinum toxin treatment for slipping rib syndrome: a case report

72. A novel ATP7A-related phenotype with distal motor neuropathy and autonomic dysfunction: Case report of two sibs

G.P.18.09 Functional characterisation of a novel mutation causing episodic ataxia type 1 occurring in the KCNA1 gene

Visceral manifestations in spinal cord lesions

The role of gustatory flushing in Frey's syndrome and its treatment with botulinum toxin type A

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