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Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene

Journal of the neurological sciences, 2008-08, Vol.271 (1), p.207-210

2008

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US study of gliding in nondependent lung regions: the dark side of the moon

Critical care (London, England), 2014-03, Vol.18 (S1), p.P274-P274, Article P274

2014

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Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency

American journal of human genetics, 1994-05, Vol.54 (5), p.812-819

1994

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A rare association of early-onset inclusion body myositis, rheumatoid arthritis and autoimmune thyroiditis: a case report and literature review

Functional neurology, 2013-04, Vol.28 (2), p.127-132

2013

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Respiratory and metabolic responses during exercise and skeletal muscle morphology in obesity

Sport sciences for health, 2004-12, Vol.1 (1), p.47-54

2004

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Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy

Neuromuscular disorders : NMD, 1994-03, Vol.4 (2), p.143-146

1994

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Assessment of ventilation during the performance of elective endoscopic-guided percutaneous tracheostomy: Clinical evaluation of a new method

Chest, 2004-07, Vol.126 (1), p.159-164

2004

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Biological markers of oxidative stress in mitochondrial myopathies with progressive external ophthalmoplegia

Journal of the neurological sciences, 1991-09, Vol.105 (1), p.57-60

1991

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Non-invasive ventilation in trauma patients: is there a role?

Critical care (London, England), 2006, Vol.10 Suppl 1 (Suppl 1), p.P49-P49

2006

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Monitoring of lactate and base deficit: what is their role in the predictive outcome of severe trauma?

Critical care (London, England), 2006, Vol.10 Suppl 1 (Suppl 1), p.P314-P314

2006

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Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation

Journal of the neurological sciences, 2005-01, Vol.228 (1), p.93-97

2005

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Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers

Journal of neurology, neurosurgery and psychiatry, 1996-10, Vol.61 (4), p.424-425

1996

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Multimodal evoked potentials in progressive external ophthalmoplegia with mitochondrial myopathy

Acta neurologica Scandinavica, 1991-08, Vol.84 (2), p.107-110

1991

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Multiple sclerosis: disability and mortality in a cohort of clinically diagnosed patients

Neuroepidemiology, 1989-01, Vol.8 (5), p.249-253

1989

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Cardiomyology: an attempt to link structural cardiac and skeletal muscle damage in patients with dilated cardiomyopathy

European heart journal supplements, 2004-11, Vol.6 (suppl-F), p.F40-F53

2004

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Clinical Correlations in 16 Patients With Total or Partial Laminin α2 Deficiency Characterized Using Antibodies Against 2 Fragments of the Protein

Archives of neurology (Chicago), 1999-02, Vol.56 (2), p.209

1999

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Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

Brain & development (Tokyo. 1979), 1996-05, Vol.18 (3), p.207-211

1996

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Somatosensory evoked potentials by tibial nerve stimulation in the rabbit

Bollettino della Societa italiana di biologia sperimentale, 1989-02, Vol.65 (2), p.171

1989

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Somatosensory evoked potentials by median nerve stimulation in rabbits. I. Source localization by cortical and stereotaxic recordings

Bollettino della Societa italiana di biologia sperimentale, 1988-01, Vol.64 (1), p.47

1988

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Sleep apnea in a patient with Becker muscular dystrophy

Italian journal of neurological sciences, 1997, Vol.18 (1), p.59-60

1997

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Hypokalemic myopathy. Our experience at an intensive care unit

Minerva anestesiologica, 1992-01, Vol.58 (1-2), p.19

1992

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Selectivity and interaction of D-1 and D-2 antagonists. Neurophysiological and behavioural study

Pharmacological research communications, 1987, Vol.19 (12), p.943-944

1987

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Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the protein

Archives of neurology (Chicago), 1999-02, Vol.56 (2), p.209

1999

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A new family with periventricular nodular heterotopia and peculiar dysmorphic features. A probable X-linked dominant trait

Archives of neurology (Chicago), 1997-01, Vol.54 (1), p.61

1997

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Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers

Journal of neurology, neurosurgery, and psychiatry, 1996, Vol.61 (4), p.424-425

1996

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Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene

US study of gliding in nondependent lung regions: the dark side of the moon

Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency

A rare association of early-onset inclusion body myositis, rheumatoid arthritis and autoimmune thyroiditis: a case report and literature review

Respiratory and metabolic responses during exercise and skeletal muscle morphology in obesity

Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy

Assessment of ventilation during the performance of elective endoscopic-guided percutaneous tracheostomy: Clinical evaluation of a new method

Biological markers of oxidative stress in mitochondrial myopathies with progressive external ophthalmoplegia

Non-invasive ventilation in trauma patients: is there a role?

Monitoring of lactate and base deficit: what is their role in the predictive outcome of severe trauma?

Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation

Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers

Multimodal evoked potentials in progressive external ophthalmoplegia with mitochondrial myopathy

Multiple sclerosis: disability and mortality in a cohort of clinically diagnosed patients

Cardiomyology: an attempt to link structural cardiac and skeletal muscle damage in patients with dilated cardiomyopathy

Clinical Correlations in 16 Patients With Total or Partial Laminin α2 Deficiency Characterized Using Antibodies Against 2 Fragments of the Protein

Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

Somatosensory evoked potentials by tibial nerve stimulation in the rabbit

Somatosensory evoked potentials by median nerve stimulation in rabbits. I. Source localization by cortical and stereotaxic recordings

Sleep apnea in a patient with Becker muscular dystrophy

Hypokalemic myopathy. Our experience at an intensive care unit

Selectivity and interaction of D-1 and D-2 antagonists. Neurophysiological and behavioural study

Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the protein

A new family with periventricular nodular heterotopia and peculiar dysmorphic features. A probable X-linked dominant trait

Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers

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