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Combustion efficiency and engine out emissions of a S.I. engine fueled with alcohol/gasoline blends

Applied energy, 2013-11, Vol.111, p.1162-1171

2013

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Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Neurology, 2009-07, Vol.73 (3), p.228-235

2009

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Numerical simulation and experimental test of dual fuel operated diesel engines

Applied thermal engineering, 2014-04, Vol.65 (1-2), p.403-417

2014

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In vivo microglia activation in very early dementia with Lewy bodies, comparison with Parkinson's disease

Parkinsonism & related disorders, 2013-01, Vol.19 (1), p.47-52

2013

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Outcome of noninvasive ventilation in children with neuromuscular disease

Neurology, 2007-01, Vol.68 (3), p.198-201

2007

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Motor neuron dysfunctions in the frontotemporal lobar degeneration spectrum: A clinical and neurophysiological study

Journal of the neurological sciences, 2015-04, Vol.351 (1), p.72-77

2015

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Functional Muscle Ischemia in Neuronal Nitric Oxide Synthase-Deficient Skeletal Muscle of Children with Duchenne Muscular Dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2000-12, Vol.97 (25), p.13818-13823

2000

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CFD study of a CI engine powered in the dual-fuel mode with syngas and waste vegetable oil

Journal of physics. Conference series, 2021-04, Vol.1868 (1), p.12014

2021

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Mechanics and spiral formation in the rat cornea

Biomechanics and modeling in mechanobiology, 2015-01, Vol.14 (1), p.107-122

2015

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Clinical course correlates poorly with muscle pathology in nemaline myopathy

Neurology, 2003-02, Vol.60 (4), p.665-673

2003

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Possible transport energy sources for the future

Transport policy, 2013-05, Vol.27, p.1-10

2013

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Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

American journal of human genetics, 1998-12, Vol.63 (6), p.1712-1723

1998

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P.7.14 Effects of a regular aquatic therapy program on one individual with Duchenne Muscular Dystrophy (DMD): A case study

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.777-778

2013

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Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Cell, 2001-05, Vol.105 (4), p.511-519

2001

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Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy

Neurology, 2005-06, Vol.64 (11), p.1931-1937

2005

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Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

Neurology, 2002-08, Vol.59 (4), p.613-617

2002

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G.P.312

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.915-915

2014

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Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy

Journal of neurology, neurosurgery and psychiatry, 2005-07, Vol.76 (7), p.1019-1021

2005

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Neuronal Nitric Oxide Synthase and Dystrophin-Deficient Muscular Dystrophy

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9142-9147

1996

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Rehabilitation of COVID-19 patients

Journal of rehabilitation medicine, 2020-04, Vol.52 (4), p.jrm00046-jrm00046

2020

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Nemaline myopathy: A clinical study of 143 cases

Annals of neurology, 2001-09, Vol.50 (3), p.312-320

2001

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Corrigendum to “ In vivo microglia activation in very early dementia with Lewy bodies, comparison with Parkinson's disease” [Parkinsonism Relat Disord 19 (2013) 47–52]

Parkinsonism & related disorders, 2013-10, Vol.19 (10), p.921-921

2013

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Andersen's syndrome: A distinct periodic paralysis

Annals of neurology, 1997-09, Vol.42 (3), p.305-312

1997

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G.O.18

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.920-920

2014

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Combustion efficiency and engine out emissions of a S.I. engine fueled with alcohol/gasoline blends

Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients

Numerical simulation and experimental test of dual fuel operated diesel engines

In vivo microglia activation in very early dementia with Lewy bodies, comparison with Parkinson's disease

Outcome of noninvasive ventilation in children with neuromuscular disease

Motor neuron dysfunctions in the frontotemporal lobar degeneration spectrum: A clinical and neurophysiological study

Functional Muscle Ischemia in Neuronal Nitric Oxide Synthase-Deficient Skeletal Muscle of Children with Duchenne Muscular Dystrophy

CFD study of a CI engine powered in the dual-fuel mode with syngas and waste vegetable oil

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Mechanics and spiral formation in the rat cornea

Clinical course correlates poorly with muscle pathology in nemaline myopathy

Possible transport energy sources for the future

Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

P.7.14 Effects of a regular aquatic therapy program on one individual with Duchenne Muscular Dystrophy (DMD): A case study

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy

Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

G.P.312

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy

Neuronal Nitric Oxide Synthase and Dystrophin-Deficient Muscular Dystrophy

Rehabilitation of COVID-19 patients

Nemaline myopathy: A clinical study of 143 cases

Corrigendum to “ In vivo microglia activation in very early dementia with Lewy bodies, comparison with Parkinson's disease” [Parkinsonism Relat Disord 19 (2013) 47–52]

Andersen's syndrome: A distinct periodic paralysis

G.O.18

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