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Electron spectroscopic analysis of the human lipid skin barrier: cold atmospheric plasma-induced changes in lipid composition

Experimental dermatology, 2012-12, Vol.21 (12), p.921-925

2012

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Lessons learned from DNA repair defective syndromes

Experimental dermatology, 2007-06, Vol.16 (6), p.532-544

2007

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Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations

Experimental dermatology, 2013-01, Vol.22 (1), p.24-29

2013

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Xeroderma pigmentosum: Diagnostic procedures, interdisciplinary patient care, and novel therapeutic approaches

Journal der Deutschen Dermatologischen Gesellschaft, 2014-10, Vol.12 (10), p.867-872

2014

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Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans

British journal of dermatology (1951), 2023-01, Vol.188 (1), p.94-99

2023

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Novel pathogenic frameshift mutation in the POLH gene contributes to xeroderma pigmentosum variant type in a 16‐year‐old girl

Australasian journal of dermatology, 2021-11, Vol.62 (4), p.e615-e617

2021

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Epidemiology of inherited epidermolysis bullosa in Germany

Journal of the European Academy of Dermatology and Venereology, 2023-02, Vol.37 (2), p.402-410

2023

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Real‐world outcomes using PD‐1 antibodies and BRAF + MEK inhibitors for adjuvant melanoma treatment from 39 skin cancer centers in Germany, Austria and Switzerland

Journal of the European Academy of Dermatology and Venereology, 2023-05, Vol.37 (5), p.894-906

2023

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Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease

Journal der Deutschen Dermatologischen Gesellschaft, 2014-09, Vol.12 (9), p.781-788

2014

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Immune checkpoint inhibition and targeted therapy for melanoma: A patient‐oriented cross‐sectional comparative multicentre study

Journal of the European Academy of Dermatology and Venereology, 2023-05, Vol.37 (5), p.884-893

2023

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Comparative study of presurgical skin infiltration depth measurements of melanocytic lesions with OCT and high frequency ultrasound

Journal of biophotonics, 2017-06, Vol.10 (6-7), p.854-861

2017

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Skin cancer in organ transplant recipients: effects of immunosuppressive medications on DNA repair

Experimental dermatology, 2012-01, Vol.21 (1), p.2-6

2012

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A unique chromosomal in-frame deletion identified among seven XP-C patients

Photodermatology, photoimmunology & photomedicine, 2016-09, Vol.32 (5-6), p.276-283

2016

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S1 guidelines for the diagnosis and treatment of ichthyoses – update

Journal der Deutschen Dermatologischen Gesellschaft, 2017-10, Vol.15 (10), p.1053-1065

2017

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Photosensitive form of trichothiodystrophy associated with a novel mutation in the XPD gene

Photodermatology, photoimmunology & photomedicine, 2016-03, Vol.32 (2), p.110-112

2016

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Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Human mutation, 2006-11, Vol.27 (11), p.1092-1103

2006

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Cyclosporin A, but not everolimus, inhibits DNA repair mediated by calcineurin: implications for tumorigenesis under immunosuppression

Experimental dermatology, 2011-03, Vol.20 (3), p.232-236

2011

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Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes

Experimental dermatology, 2013-07, Vol.22 (7), p.486-489

2013

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The novel PI3 kinase inhibitor, BAY 80-6946, impairs melanoma growth in vivo and in vitro

Experimental dermatology, 2014-08, Vol.23 (8), p.579-584

2014

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Doxorubicin-induced activation of NF-κB in melanoma cells is abrogated by inhibition of IKKβ, but not by a novel IKKα inhibitor

Experimental dermatology, 2012-04, Vol.21 (4), p.301-304

2012

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Assessment of melanoma histotypes and associated patient related factors: Basis for a predictive statistical model

Journal der Deutschen Dermatologischen Gesellschaft, 2015-01, Vol.13 (1), p.37-44

2015

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Successful Treatment of Severe Keratosis Pilaris Rubra with a 595‐nm Pulsed Dye Laser

Dermatologic surgery, 2009-10, Vol.35 (10), p.1592-1595

2009

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Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition

Experimental dermatology, 2011-10, Vol.20 (10), p.795-799

2011

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Nucleotide Excision Repair Proteins Rapidly Accumulate but Fail to Persist in Human XP-E (DDB2 Mutant) Cells

Photochemistry and photobiology, 2011-05, Vol.87 (3), p.729-733

2011

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Grouped vesicles with brown background pigmentation on the abdomen of a 9‐year‐old girl

Journal der Deutschen Dermatologischen Gesellschaft, 2014-04, Vol.12 (4), p.362-364

2014

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Electron spectroscopic analysis of the human lipid skin barrier: cold atmospheric plasma-induced changes in lipid composition

Lessons learned from DNA repair defective syndromes

Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations

Xeroderma pigmentosum: Diagnostic procedures, interdisciplinary patient care, and novel therapeutic approaches

Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans

Novel pathogenic frameshift mutation in the POLH gene contributes to xeroderma pigmentosum variant type in a 16‐year‐old girl

Epidemiology of inherited epidermolysis bullosa in Germany

Real‐world outcomes using PD‐1 antibodies and BRAF + MEK inhibitors for adjuvant melanoma treatment from 39 skin cancer centers in Germany, Austria and Switzerland

Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease

Immune checkpoint inhibition and targeted therapy for melanoma: A patient‐oriented cross‐sectional comparative multicentre study

Comparative study of presurgical skin infiltration depth measurements of melanocytic lesions with OCT and high frequency ultrasound

Skin cancer in organ transplant recipients: effects of immunosuppressive medications on DNA repair

A unique chromosomal in-frame deletion identified among seven XP-C patients

S1 guidelines for the diagnosis and treatment of ichthyoses – update

Photosensitive form of trichothiodystrophy associated with a novel mutation in the XPD gene

Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Cyclosporin A, but not everolimus, inhibits DNA repair mediated by calcineurin: implications for tumorigenesis under immunosuppression

Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes

The novel PI3 kinase inhibitor, BAY 80-6946, impairs melanoma growth in vivo and in vitro

Doxorubicin-induced activation of NF-κB in melanoma cells is abrogated by inhibition of IKKβ, but not by a novel IKKα inhibitor

Assessment of melanoma histotypes and associated patient related factors: Basis for a predictive statistical model

Successful Treatment of Severe Keratosis Pilaris Rubra with a 595‐nm Pulsed Dye Laser

Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition

Nucleotide Excision Repair Proteins Rapidly Accumulate but Fail to Persist in Human XP-E (DDB2 Mutant) Cells

Grouped vesicles with brown background pigmentation on the abdomen of a 9‐year‐old girl

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