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Autosomal‐dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation

Clinical genetics, 2018-05, Vol.93 (5), p.982-991

2018

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Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle

Journal of muscle research and cell motility, 2009-06, Vol.30 (3-4), p.139-144

2009

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Photoacoustic Measurement of Ethane with Near-Infrared DFB Diode Laser

Journal of Spectroscopy, 2018-01, Vol.2018 (2018), p.1-5

2018

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Autonomic neuropathy in mixed cryoglobulinemia

Journal of neurology, 2007-02, Vol.254 (2), p.215-219

2007

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G.P.14.09 Successful flecainide therapy in paramyotonia congenita

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.646-646

2009

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Clinical and 3D instrumental assessment of the short-term effect of Sativex on patients with multiple sclerosis

Gait & posture, 2019-09, Vol.74, p.12-12

2019

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New model of marker placement to assess sagittal spine and lower limb during sit to stand: Typical kinematic pattern in LOPD

Gait & posture, 2018-10, Vol.66, p.S13-S13

2018

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G.P.9.07 Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.787-788

2008

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Primary cerebral toxoplasmosis: a rare case of ventriculitis and hydrocephalus in AIDS

Clinical neuropathology, 2005-05, Vol.24 (3), p.106

2005

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Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia

Reumatismo, 2011-09, Vol.53 (1), p.26

2011

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Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son

Journal of medical genetics, 2003-11, Vol.40 (11), p.858-863

2003

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Chordomas: a histological and immunohistochemical study of cases with and without recurrent tumors

Clinical neuropathology, 2004-11, Vol.23 (6), p.277

2004

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P.223 - Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S162-S163

2017

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Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S162-S163

2017

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C.P.1.01 Congenital fiber type disproportion and noncompaction cardiomyopathy in a patient

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.834-834

2007

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P.215 - Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S160-S161

2017

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Calreticulin mutation in a case of myopathy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S229-S230

2017

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P.445 - Calreticulin mutation in a case of myopathy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S229-S230

2017

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Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S160-S161

2017

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Migrant health in Italy: a better health status difficult to maintain-country of origin and assimilation effects studied from the Italian risk factor surveillance data

Population health metrics, 2019-11, Vol.17 (1), p.14-11, Article 14

2019

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Peripheral nervous system involvement in Klippel-Trenaunay syndrome

Clinical neuropathology, 2005-01, Vol.24 (1), p.42

2005

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Prevalence and cardiovascular risk profile of chronic kidney disease in Italy: results of the 2008-12 National Health Examination Survey

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (5), p.806-814

2015

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Musculoskeletal impairment and functional limitations in a patient affected by mutation in the laminin a-5 gene

Functional neurology, 2018-04, Vol.33 (2), p.117

2018

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Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

Neuropsychiatric disease and treatment, 2016-01, Vol.12, p.2497-2502

2016

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Autosomal‐dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation

Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle

Photoacoustic Measurement of Ethane with Near-Infrared DFB Diode Laser

Autonomic neuropathy in mixed cryoglobulinemia

G.P.14.09 Successful flecainide therapy in paramyotonia congenita

Clinical and 3D instrumental assessment of the short-term effect of Sativex on patients with multiple sclerosis

New model of marker placement to assess sagittal spine and lower limb during sit to stand: Typical kinematic pattern in LOPD

G.P.9.07 Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance

Primary cerebral toxoplasmosis: a rare case of ventriculitis and hydrocephalus in AIDS

Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia

Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son

Chordomas: a histological and immunohistochemical study of cases with and without recurrent tumors

P.223 - Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

C.P.1.01 Congenital fiber type disproportion and noncompaction cardiomyopathy in a patient

Surge of Mpox cases in Lombardy region, Italy, October 2023 - January 2024

P.215 - Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Calreticulin mutation in a case of myopathy

P.445 - Calreticulin mutation in a case of myopathy

Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Migrant health in Italy: a better health status difficult to maintain-country of origin and assimilation effects studied from the Italian risk factor surveillance data

Peripheral nervous system involvement in Klippel-Trenaunay syndrome

Prevalence and cardiovascular risk profile of chronic kidney disease in Italy: results of the 2008-12 National Health Examination Survey

Musculoskeletal impairment and functional limitations in a patient affected by mutation in the laminin a-5 gene

Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

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