Cristina Has - Dissemin

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Papers authored by Cristina Has

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2019 Jasmin Kroeger, Esther Hoppe, Célimène Galiger, Cristina Has

ORCID

, Claus-Werner Franzke

Amino acid substitution in the C-terminal domain of collagen XVII reduces laminin-332 interaction causing mild skin fragility with atrophic scarring

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C. Has

ORCID

Chronic tissue damage: a common pathomechanism of genodermatoses

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Kathrin Giehl, Henning Hamm, Cristina Has

ORCID

Rolle des Dermatologen bei der Syndromerkennung

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A. Reimer

ORCID

, C. Has

ORCID

Syndrome mit Hautfragilität

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Steffen Emmert, Sebastian Iben, Judith Fischer, Katalin Komlosi, Regina C. Betz, Jorge Frank J., Christina Has

ORCID

Ein neues Forum für seltene Hauterkrankungen

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C. Has

ORCID

, J. Küsel, R. Happle, H. Steinke, K. Technau‐Hafsi, J. Fischer

Extending the phenotypic spectrum associated with mosaicism for GJB2 mutations

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Cristina Has

ORCID

, Kyle T. Amber, Dedee F. Murrell, Philippe Musette, Ralf J. Ludwig

Editorial: Skin Blistering Diseases

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Damian J. Ralser, Hideyuki Takeuchi, Günter Fritz, F. Buket Basmanav, Maike Effern, Sugirthan Sivalingam, Laila El-Shabrawi-Caelen, Ece N. Degirmentepe, Emek Kocatürk, Manuraj Singh, Nina Booken, Natalia M. K. Spierings, Viktor Schnabel, Andre Heineke, Jana Knuever and 12 other authors

Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights into Disease Pathogenesis

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Velina S. Atanasova, Celine Pourreyron, Mehdi Farshchian, Michael Lawler, Christian A. Brown, Stephen A. Watt, Sheila Wright, Michael Warkala, Christina Guttmann-Gruber

ORCID

, Josefina Piñón Hofbauer

ORCID

, Ignacia Fuentes, Marco Prisco, Elham Rashidghamat, Cristina Has

ORCID

, Julio C. Salas-Alanis and 6 other authors

Identification of Rigosertib for the Treatment of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma

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Maria Gkaitatzi, Evangelia Kalloniati, Cristina Has

ORCID

, Dimitra Kiritsi, Theofanis Spiliopoulos, Sophia Georgiou

Kindler syndrome: a rare case report from Greece

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Irina Condrat, Yinghong He, Rodica Cosgarea, Cristina Has

ORCID

Junctional Epidermolysis Bullosa: Allelic Heterogeneity and Mutation Stratification for Precision Medicine

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R. Higgins, A. Jensen, J. Wachstein, L. Bruckner-Tuderman, R. Spiegel, H. Traber, J. Achermann, M. Schaller, B. Fehrenbacher, M. Röcken, D. Ignatova, Y. Chang, T. Fischer, A. Schwieger-Briel, L. French and 7 other authors

Uniparental Disomy of Chromosome 2 Unmasks New ITGA6 Recessive Mutation and Results in a Lethal Junctional Epidermolysis Bullosa in a Newborn

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Daniela Haiges, Judith Fischer, Steffen Hörer, Cristina Has

ORCID

, Christoph M. Schempp

Biologika-Therapie mit Anti-IL-17A-Antikörper verbessert kongenitale ichthyosiforme Verhornungsstörung

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Yinghong He, Cristina Has

ORCID

Isolation and Culture of Epidermolysis Bullosa Cells and Organotypic Skin Models

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J. Hoffmann, F. Casetti, A. Reimer

ORCID

, J. Leppert, G. Grüninger, C. Has

ORCID

A Silent COL17A1 Variant Alters Splicing and Causes Junctional Epidermolysis Bullosa

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2018 P. Yilmaz, M. Medvecz, J. Kohlhase, J. Küsel, J. Fischer, C. Has

ORCID

Alitretinoin in punctate palmoplantar keratoderma

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Leah Lalor

ORCID

, Matthias Titeux, Francis Palisson, Ignacia Fuentes, María J. Yubero, Kaisa Tasanen, Laura Huilaja, Cristina Has

ORCID

, Gianluca Tadini

ORCID

, Anita N. Haggstrom

ORCID

, Alain Hovnanian, Anne W. Lucky

ORCID

Epidermolysis bullosa simplex-generalized severe type due to keratin 5 p.Glu477Lys mutation: Genotype-phenotype correlation and in silico modeling analysis

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Cristina Has

ORCID

, Alexander Nyström

ORCID

, Amir Hossein Saeidian, Leena Bruckner-Tuderman, Jouni Uitto

Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone

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C. Has

ORCID

Multiple facets of desmoglein 1 mutations

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Raymond J. Cho

ORCID

, Nicoline Y. den Breems, Ludmil B. Alexandrov

ORCID

, Elizabeth Purdom

ORCID

, Velina S. Atanasova, Tran N. Nguyen, Mehdi Farshchian, Kimal Rajapakshe

ORCID

, Marco Prisco, Cristian Coarfa

ORCID

, Joya Sahu, Patrick Tassone

ORCID

, Evan J. Greenawalt, Wei Wu

ORCID

, Hui Yao and 29 other authors

APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa

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