Cristina Has
0000-0001-6066-507X
University of Freiburg
216 papers found
Refreshing results…
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa—an underestimated complication?
High rate of self‐improving phenotypes in children with non‐syndromic congenital ichthyosis: case series from south‐western Germany
Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease
Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort study
Molecular Therapeutics in Development for Epidermolysis Bullosa: Update 2020
An unusual type of telangiectatic naevus with underlying and surrounding dilated veins: report of four cases
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study
Flightless I, a contributing factor to skin blistering in Kindler syndrome patients?
A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out”
Withdrawn: Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self‐improving epidermolytic ichthyosis
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4
Combined anti‐inflammatory and low‐dose antiproliferative therapy for squamous cell carcinomas in recessive dystrophic epidermolysis bullosa
Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa
Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients
Postzygotic HRAS mutation in heterochromia of straight scalp hair
Amino acid substitution in the C-terminal domain of collagen XVII reduces laminin-332 interaction causing mild skin fragility with atrophic scarring
Chronic tissue damage: a common pathomechanism of genodermatoses
Rolle des Dermatologen bei der Syndromerkennung
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