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La parità di genere

Rivista trimestrale di diritto pubblico, 2021-01 (1), p.9

Simonati, Anna

2021

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The (Draft) European Charter of the Commons – Between Opportunities and Challenges

Central European public administration review (Online), 2018-11, Vol.16 (2), p.91-108

Simonati, Anna

2018

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Gendered Citizenship in Italian Administrative Law: A Work in Progress Toward a New Public Ethics

Public integrity, 2016-01, Vol.18 (1), p.59-82

Simonati, Anna

2016

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The Principles of Administrative Procedure and the EU Courts: an Evolution in Progress?

Review of European administrative law, 2011-06, Vol.4 (1), p.45-81

Simonati, Anna

2011

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The Sound of Silence in European Administrative Law

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The Multi-interpretable Nature of Lawfulness in a National Framework

Quality of Governance, p.131-156

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Transparency in Action in Italy: The Triple Right of Access and Its Complicated Life

The Laws of Transparency in Action, p.255-293

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Ethics Policy

Global Encyclopedia of Public Administration, Public Policy, and Governance, p.4451-4456

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Legal Versus Ethical

Global Encyclopedia of Public Administration, Public Policy, and Governance, p.7602-7607

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Legal Versus Ethical

Global Encyclopedia of Public Administration, Public Policy, and Governance, p.3758-3762

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Ethics Policy

Global Encyclopedia of Public Administration, Public Policy, and Governance, p.2034-2039

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Administrative Silence in Italy, Between (Desired) Simplification and (Practical) Complication

The Sound of Silence in European Administrative Law, p.213-240

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ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria

Brain (London, England : 1878), 2021-05, Vol.144 (5), p.1435-1450

2021

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Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review

Neurogenetics, 2018-05, Vol.19 (2), p.123-130

2018

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Long-term outcome of a cohort of Italian patients affected with alpha-Mannosidosis

Clinical dysmorphology, 2024-01, Vol.33 (1), p.1

2024

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Congenital myopathies: clinical phenotypes and new diagnostic tools

Italian journal of pediatrics, 2017-11, Vol.43 (1), p.101-101, Article 101

2017

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Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)

Neurology, 2016-08, Vol.87 (6), p.579

2016

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Protein glutathionylation in human central nervous system: Potential role in redox regulation of neuronal defense against free radicals

Journal of neuroscience research, 2006-02, Vol.83 (2), p.256-263

2006

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Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.36-36, Article 36

2011

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Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

Orphanet journal of rare diseases, 2013-05, Vol.8 (1), p.75-75, Article 75

2013

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RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders

Clinical genetics, 2008-08, Vol.74 (2), p.164-170

2008

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La parità di genere

The (Draft) European Charter of the Commons – Between Opportunities and Challenges

Gendered Citizenship in Italian Administrative Law: A Work in Progress Toward a New Public Ethics

The Principles of Administrative Procedure and the EU Courts: an Evolution in Progress?

The Sound of Silence in European Administrative Law

The Multi-interpretable Nature of Lawfulness in a National Framework

Transparency in Action in Italy: The Triple Right of Access and Its Complicated Life

Ethics Policy

Legal Versus Ethical

Legal Versus Ethical

Ethics Policy

Administrative Silence in Italy, Between (Desired) Simplification and (Practical) Complication

ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria

Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review

Long-term outcome of a cohort of Italian patients affected with alpha-Mannosidosis

Congenital myopathies: clinical phenotypes and new diagnostic tools

Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings

Protein glutathionylation in human central nervous system: Potential role in redox regulation of neuronal defense against free radicals

Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients

Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders

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