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Performance of Distributed Optical Fiber Sensors (DOFS) and Digital Image Correlation (DIC) in the monitoring of RC structures

IOP conference series. Materials Science and Engineering, 2019-10, Vol.615 (1), p.12101

2019

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Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)

Neurology, 2004-09, Vol.63 (6), p.1053-1058

2004

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Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

Nature genetics, 1998-04, Vol.18 (4), p.365-368

1998

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Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia

Neurology, 2000-03, Vol.54 (6), p.1373

2000

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A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect

Journal of neurology, neurosurgery and psychiatry, 2004-10, Vol.75 (10), p.1495-1498

2004

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Long‐term survival in Stuve‐Wiedemann syndrome: A neuro‐myo‐skeletal disorder with manifestations of dysautonomia

American journal of medical genetics, 2003-05, Vol.118A (4), p.362-368

2003

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Congenital hypomyelination due to myelin protein zero Q215X mutation

Annals of neurology, 1999-05, Vol.45 (5), p.676-678

1999

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Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency

Neurology, 1996-05, Vol.46 (5), p.1354-1354

1996

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Self-perception of oral health in the elderly associated with health literacy and related factors

European journal of public health, 2020-09, Vol.30 (Supplement_5)

2020

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Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria

Neurology, 1998-01, Vol.50 (1), p.296-298

1998

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What details are needed for wireless simulations? - A study of a site-specific indoor wireless model

2012 Proceedings IEEE INFOCOM, 2012, p.289-297

2012

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Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency

The American journal of pathology, 2002, Vol.160 (1), p.265-270

2002

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Forearm Semi-ischemic Exercise Test in Pediatric Patients

Journal of child neurology, 1998-06, Vol.13 (6), p.288-290

1998

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Disorganization of dystrophin costameric lattice in Becker muscular dystrophy

Muscle & nerve, 1998-02, Vol.21 (2), p.211-216

1998

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A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy

Neuromuscular disorders : NMD, 1999-10, Vol.9 (6), p.403-407

1999

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Altered aquaporin‐4 expression in human muscular dystrophies: a common feature?

The FASEB journal, 2002-07, Vol.16 (9), p.1120-1122

2002

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Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion

Clinical genetics, 2002-06, Vol.61 (6), p.465-467

2002

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Nicotine exerts a permissive role on NMDA receptor function in hippocampal noradrenergic terminals

Neuropharmacology, 2004-07, Vol.47 (1), p.65-71

2004

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Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria

Neuromuscular disorders : NMD, 1998-02, Vol.8 (1), p.3-6

1998

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Primary adrenal insufficiency in a child with a mitochondrial DNA deletion

Journal of inherited metabolic disease, 1998-04, Vol.21 (2), p.155-161

1998

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Increased Number of Caveolae and Caveolin-3 Overexpression in Duchenne Muscular Dystrophy

Biochemical and biophysical research communications, 1999-08, Vol.261 (3), p.547-550

1999

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Accuracy-preserving measurement collection for realistic wireless simulations

2012 IEEE Symposium on Computers and Communications (ISCC), 2012, p.000625-000630

2012

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Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene

Muscle & nerve, 2003-10, Vol.28 (4), p.508-511

2003

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Auriculo-condylar syndrome or new syndrome?

Clinical dysmorphology, 2002-04, Vol.11 (2), p.143-144

2002

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Embedded distributed optical fiber sensors for health monitoring of concrete bridges

Bridge Maintenance, Safety, Management, Life-Cycle Sustainability and Innovations, 2021, p.956-962

1, 2021

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Performance of Distributed Optical Fiber Sensors (DOFS) and Digital Image Correlation (DIC) in the monitoring of RC structures

Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia

A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect

Long‐term survival in Stuve‐Wiedemann syndrome: A neuro‐myo‐skeletal disorder with manifestations of dysautonomia

Congenital hypomyelination due to myelin protein zero Q215X mutation

Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency

Self-perception of oral health in the elderly associated with health literacy and related factors

Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria

What details are needed for wireless simulations? - A study of a site-specific indoor wireless model

Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency

Forearm Semi-ischemic Exercise Test in Pediatric Patients

Disorganization of dystrophin costameric lattice in Becker muscular dystrophy

A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy

Altered aquaporin‐4 expression in human muscular dystrophies: a common feature?

Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion

Nicotine exerts a permissive role on NMDA receptor function in hippocampal noradrenergic terminals

Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria

Primary adrenal insufficiency in a child with a mitochondrial DNA deletion

Increased Number of Caveolae and Caveolin-3 Overexpression in Duchenne Muscular Dystrophy

Accuracy-preserving measurement collection for realistic wireless simulations

Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene

Auriculo-condylar syndrome or new syndrome?

Embedded distributed optical fiber sensors for health monitoring of concrete bridges

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