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Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

British journal of dermatology (1951), 2015-11, Vol.173 (5), p.1291-1294

2015

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Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British journal of dermatology (1951), 2015-02, Vol.172 (2), p.527-531

2015

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Prosthetic foot design optimisation based on roll-over shape and ground reaction force characteristics

Proceedings of the Institution of Mechanical Engineers. Part C, Journal of mechanical engineering science, 2017-09, Vol.231 (17), p.3093-3103

2017

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Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family

British journal of dermatology (1951), 2015-05, Vol.172 (5), p.1407-1411

2015

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Mutations in EXPH5 result in autosomal recessive inherited skin fragility

British journal of dermatology (1951), 2014-01, Vol.170 (1), p.196-199

2014

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515 Mutations in KLHL24 add to the molecular heterogeneity of epidermolysis bullosa simplex

Journal of investigative dermatology, 2017-05, Vol.137 (5), p.S88-S88

2017

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Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

British journal of dermatology (1951), 2015-05, Vol.172 (5), p.1407-1411

2015

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Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British journal of dermatology (1951), 2015-02, Vol.172 (2), p.527-531

2015

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Crime Fiction and the Law

1, 2017

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Management of vitreous floaters: an international survey the European VitreoRetinal Society Floaters study report

Eye (London), 2020-05, Vol.34 (5), p.825-834

2020

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P-6. Ultrastructural abnormalities in muscle biopsies of patients with dysferlin deficiency

Acta myologica, 2009-07, Vol.28 (1), p.46-46

2009

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narrative and law

The New Oxford Companion to Law, 2008

Maria Aristodemou

1, 2008

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storytelling and law

The New Oxford Companion to Law, 2008

Maria Aristodemou

1, 2008

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French television crime fi ctions: The case of Spiral ( Engrenages) – coming out of the confusion

Crime Fiction and the Law, 2017, p.53-64

2017

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The rise of crime fi ction and the fading of law’s empire: Chronicle of a swap foretold

Crime Fiction and the Law, 2017, p.37-52

2017

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Critique, crime fi ction and the no right answer thesis

Crime Fiction and the Law, 2017, p.25-36

2017

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Locating justice in Wallander: Trading TV stories, local jurisdictions and global injustice in the Swedish and UK Wallanders

Crime Fiction and the Law, 2017, p.65-80

2017

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Necessary deceptions: Kafka and the mystery of law

Crime Fiction and the Law, 2017, p.97-114

2017

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Suspending democracy: Vigilante justice and the rule of law in Christopher Nolan’s Dark Knight trilogy

Crime Fiction and the Law, 2017, p.115-133

2017

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Attainable utopias

Crime Fiction and the Law, 2017, p.81-96

2017

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Lawless

Crime Fiction and the Law, 2017, p.134-149

2017

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The introduction didn’t do it

Crime Fiction and the Law, 2017, p.11-24

2017

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Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

British Journal of Dermatology, 2015, Vol.172 (5), p.1407-1411

2015

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Mutations in EXPH5 result in autosomal recessive inherited skin fragility

British Journal of Dermatology, 2014, Vol.170 (1), p.196-199

2014

Volltextzugriff (PDF)

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British Journal of Dermatology, 2015, Vol.172 (2), p.527-531

2015

Volltextzugriff (PDF)

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Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

Prosthetic foot design optimisation based on roll-over shape and ground reaction force characteristics

Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family

Mutations in EXPH5 result in autosomal recessive inherited skin fragility

515 Mutations in KLHL24 add to the molecular heterogeneity of epidermolysis bullosa simplex

Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

Crime Fiction and the Law

Management of vitreous floaters: an international survey the European VitreoRetinal Society Floaters study report

P-6. Ultrastructural abnormalities in muscle biopsies of patients with dysferlin deficiency

narrative and law

storytelling and law

French television crime fi ctions: The case of Spiral ( Engrenages) – coming out of the confusion

The rise of crime fi ction and the fading of law’s empire: Chronicle of a swap foretold

Critique, crime fi ction and the no right answer thesis

Locating justice in Wallander: Trading TV stories, local jurisdictions and global injustice in the Swedish and UK Wallanders

Necessary deceptions: Kafka and the mystery of law

Suspending democracy: Vigilante justice and the rule of law in Christopher Nolan’s Dark Knight trilogy

Attainable utopias

Lawless

The introduction didn’t do it

Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

Mutations in EXPH5 result in autosomal recessive inherited skin fragility

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

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