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1
Energy storage optimization strategies for smart grids

von Codemo, Claudio G. ; Erseghe, Tomaso ; Zanella, Andrea

2013 IEEE International Conference on Communications (ICC) Communications (ICC), 2013 IEEE International Conference on. :4089-4093 Jun, 2013
- Zum Volltext in IEEE Xplore
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2
Markov Decision Processes with Threshold Based Piecewise Linear Optimal Policies

von Erseghe, Tomaso ; Zanella, Andrea ; Codemo, Claudio G.

IEEE Wireless Communications Letters IEEE Wireless Commun. Lett. Wireless Communications Letters, IEEE. 2(4):459-462 Aug, 2013
- Zum Volltext in IEEE Xplore
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3
Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort

von Catteruccia, Michela ; Fattori, Fabiana ; Codemo, Valentina ; et al.

In Neuromuscular Disorders March 2013 23(3):229-238
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4
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

von Fusto, A. ; Cassandrini, D. ; Fiorillo, Claudio ; et al.

Schlagworte: Central core disease; Genotype–phenotype correlations; Multi-minicore disease; Neuromuscular disorder; Protein modelling; RYR1-related myopathies; Settore MED/26 - NEUROLOGIA; info:eu-repo/semantics/article
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5
The final version of this manuscript will appear in IEEE Wireless Communication Letters

von Tomaso Erseghe ; Andrea Zanella ; Claudio G Codemo ; et al.

http://www.dei.unipd.it/%7Ezanella/PAPER/CR_2013/WCL2013_CR.pdf.
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6
Optimal and compact control policies for energy storage units with single and multiple batteries

von ERSEGHE, TOMASO ; ZANELLA, ANDREA ; Claudio G. Codemo ; et al.

Schlagworte: Dynamic programming; energy storage; multiple batteries optimization; smart grid; threshold algorithm
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7
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

von Fattori, F ; Maggi, L ; Bruno, C ; et al.

Schlagworte: Algorithm; Centronuclear; Congenital myopathy; DNM2; RYR1; Adolescent; Adult; Age of Onset; Aged; Child; Child, Preschool; Cohort Studie; Connectin; Dynamin II; Female; Genetic Association Studie; Genetic Predisposition to Disease; Human; Infant; Infant, Newborn; Italy; Male; Middle Aged; Muscle, Skeletal; Mutation; Myopathies, Structural, Congenital; Phenotype; Protein Tyrosine Phosphatases, Non-Receptor; Ryanodine Receptor Calcium Release Channel; Young Adult; info:eu-repo/semantics/article
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8
An APOE haplotype Associated with Decreased epsilon4 Expression Increases the Risk of Late Onset Alzheimer's Disease.

von LESCAI, FRANCESCO ; PIRAZZINI, CHIARA ; SANTORO, AURELIA ; et al.

Schlagworte: ALZHEIMER DISEASE; Apolipoprotein E; GENETICS; POLYMORPHISM; Single Nucleotide
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9
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

von Fattori, Francesco ; Maggi, L. ; Bruno, C. ; et al.

Schlagworte: Algorithm; Centronuclear; Congenital myopathy; DNM2; RYR1; Settore MED/39 - NEUROPSICHIATRIA INFANTILE; Settore MED/33 - MALATTIE APPARATO LOCOMOTORE; info:eu-repo/semantics/article
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10
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohort

von Catteruccia, M ; Fattori, F ; Codemo, V ; et al.

Schlagworte: Centronuclear myopathy; DNM2; Muscle MRI; Somatic mosaicism; ‘Necklace’ fiber; 'Necklace' fiber; Adolescent; Adult; Child; Child, Preschool; Dynamin II; Female; Human; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Mosaicism; Muscle, Skeletal; Myopathies, Structural, Congenital; Phenotype; Mutation; info:eu-repo/semantics/article
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11
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

von Fattori, Fabiana ; Maggi, Lorenzo ; Bruno, Claudio ; et al.

Schlagworte: Algorithm; Centronuclear; Congenital myopathy; DNM2; RYR1; Adolescent; Adult; Age of Onset; Aged; Child; Preschool; Cohort Studie; Connectin; Dynamin II; Female; Genetic Association Studie; Genetic Predisposition to Disease; Human; Infant; Newborn; Italy; Male; Middle Aged; Muscle; Skeletal; Mutation; Myopathies; Structural; Congenital; Phenotype
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12
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

von Fiorillo C. ; D'Amico A. ; Pane M. ; et al.

Schlagworte: Central core disease; Genotype–phenotype correlations; Multi-minicore disease; Neuromuscular disorder; Protein modelling; RYR1-related myopathies; Settore MED/26 - NEUROLOGIA
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13
Correction to: Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.

von Cappellari M ; Bonetti B ; Baracchini C ; et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2023 Oct; Vol. 44 (10), pp. 3769.
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- Zur Referenz in PubMed
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14
Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.

von Cappellari M ; Bonetti B ; Baracchini C ; et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2023 Jun; Vol. 44 (6), pp. 2033-2039. Date of Electronic Publication: 2023 Feb 08.
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- Zur Referenz in PubMed
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15
An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease.

von Lescai F ; Chiamenti AM ; Codemo A ; et al.

Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2011; Vol. 24 (2), pp. 235-45.
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- Zur Referenz in PubMed
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