Cristina Has - Dissemin

Papers authored by Cristina Has

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2017 Y. He, J. Leppert, H. Steinke, C. Has

Homozygous Nonsense Mutation and Additional Deletion of an Amino Acid in BPAG1e Causing Mild Localized Epidermolysis Bullosa Simplex

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Agnes Schwieger-Briel

, Dimitra Kiritsi, Christoph Schempp, Cristina Has

, Hauke Schumann

Betulin-Based Oleogel to Improve Wound Healing in Dystrophic Epidermolysis Bullosa: A Prospective Controlled Proof-of-Concept Study

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C. Has

Mosaicism in the skin: lumping or splitting?

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Jouni Uitto, Cristina Has

, Hassan Vahidnezhad, Leila Youssefian, Leena Bruckner-Tuderman

Molecular pathology of the basement membrane zone in heritable blistering diseases:

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2016 Jasmin K. Kroeger, Silke C. Hofmann, Juna Leppert, Cristina Has

, Claus-Werner Franzke

Amino acid duplication in the coiled-coil structure of collagen XVII alters its maturation and trimerization causing mild junctional epidermolysis bullosa

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S. Dănescu, J. Leppert, R. Cosgarea, S. Zurac, S. Pop, A. Baican, C. Has

Compound heterozygosity for dominant and recessiveDSG1mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)

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Johanna Hammersen, Cristina Has

, Nora Naumann-Bartsch, Daniel Stachel, Dimitra Kiritsi, Stephan Söder, Mathilde Tardieu, Markus Metzler, Leena Bruckner-Tuderman, Holm Schneider

Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa

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Kristin Maier, Yinghong He, Ute Wölfle, Philipp R. Esser, Tilman Brummer, Christoph Schempp, Leena Bruckner-Tuderman, Cristina Has

UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome

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Özge Aşkın, Yalçın Tüzün, Iliana Tantcheva-Poór, Burhan Engin, Vinzenz Oji, Güllü Gencebay, Cristina Has

A multistep approach to the diagnosis of rare genodermatoses

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Dimitra Kiritsi, Manthoula Valari, Athanasios Michos

, Vaia Karakosta, Cristina Has

The mysteries of mosaicism: phenotypic variability in a family with incontinentia pigmenti

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B. Mayer, P. Silló, M. Mazán, D. Pintér, M. Medvecz, C. Has

, D. Castiglia, F. Petit, A. Charlesworth, Z.-S. Hatvani, H. Pamjav, S. Kárpáti

A uniqueLAMB3splice-site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries

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Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Kimia Ahmadizadeh, Cristina Has

, Jouni Uitto

Kindler syndrome, an orphan disease of cell/matrix adhesion in the skin – molecular genetics and therapeutic opportunities

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Cristina Has

, Yinghong He

Research Techniques Made Simple: Immunofluorescence Antigen Mapping in Epidermolysis Bullosa

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Yinghong He, Meena Balasubramanian, Nigel Humphreys, Catherine Waruiru, Martin Brauner, Juergen Kohlhase, Ruth O'Reilly, Cristina Has

Intronic ITGA3 mutation impacts splicing regulation and causes interstitial lung disease, nephrotic syndrome and epidermolysis bullosa

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Jouni Uitto, Leena Bruckner-Tuderman, Angela M. Christiano, John A. McGrath, Cristina Has

, Andrew P. South, Brett Kopelan, E. Clare Robinson, E. Clare Robinson

Progress toward Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015

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Cristina Has

, Kristin Technau-Hafsi

Palmoplantar keratodermas: clinical and genetic aspects

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K. Maier, Y. He, U. Wolfle, C. Schempp, L. Bruckner-Tuderman, C. Has

Kindlin-1 protects keratinocytes against UV-B: Prospects for antioxidant treatment in Kindler syndrome

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Y. He, K. Thriene, M. Boerries, H. Busch, J. Dengjel, C. Has

Loss of integrin alpha 3 impacts keratinocyte microenvironment

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M. Mobes, C. Has

, A. Fabian, K. Techanu-Hafsi, A. May, F. Meiss

Primary mucosally localized CD30-positive anaplastic large-cell T-cell Lymphoma

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Kristin Maier, Yinghong He, Philipp R. Esser, Kerstin Thriene, Daniela Sarca, Jürgen Kohlhase, Jörn Dengjel, Ludovic Martin, Cristina Has

Single amino acid deletion in kindlin-1 results in partial protein degradation which can be rescued by chaperone treatment

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Papers authored by Cristina Has