B. Burger

发表

Epidermodysplasia Verruciformis: Inborn Errors of Immunity to Human Beta-Papillomaviruses

J. Casanova, P. Itin, J. Uitto, 2018, Front. Microbiol..

A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Eli Sprecher, O. Sarig, P. Itin, 2011, American journal of human genetics.

Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation

P. Itin, C. Has, B. Burger, 2012, The British journal of dermatology.

The immigration delay disease: adermatoglyphia-inherited absence of epidermal ridges.

P. Itin, E. Sprecher, B. Burger, 2011, Journal of the American Academy of Dermatology.

MicroRNA expression differs in cutaneous squamous cell carcinomas and healthy skin of immunocompetent individuals

P. Itin, B. Burger, W. Kempf, 2013, Experimental dermatology.

HIV-positive child with epidermodysplasia verruciformis-like lesions and homozygous mutation in TMC6.

M. Battegay, P. Itin, A. Rütten, 2010, AIDS.

The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3 ′ End of KRT 10 FromDisease to a Syndrome

P. Itin, J. Fischer, B. Burger, 2015 .

The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome.

P. Itin, J. Fischer, B. Burger, 2015, JAMA dermatology.

Mosaic manifestations of monogenic skin diseases

P. Itin, B. Burger, 2009, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Novel TMC8 splice site mutation in epidermodysplasia verruciformis and review of HPV infections in patients with the disease

P. Itin, S. Tyring, P. Rady, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris

O. Sarig, P. Itin, J. Uitto, 2014, The British journal of dermatology.

The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

J. Casanova, E. Fuchs, J. Franco, 2018, The Journal of experimental medicine.

Detection of Merkel Cell Polyomavirus in Epidermodysplasia-Verruciformis-Associated Skin Neoplasms

K. Mertz, M. Pfaltz, P. Itin, 2010, Dermatology.

Spontaneous Fading of Reticular Pigmentation in Naegeli-Franceschetti-Jadassohn Syndrome

P. Itin, B. Burger, 2010, Dermatology.

Gene expression is stable in a complete CIB1 knockout keratinocyte model

S. Cichon, P. Itin, P. Hoffmann, 2020, Scientific Reports.

Homozygosity for the c.917A → T (p.N306l) Polymorphism in the EVER2/TMC8 Gene of Two Sisters with Epidermodysplasia Verruciformis Lewandowsky-Lutz Originally Described by Wilhelm Lutz

P. Itin, P. Häusermann, S. Tyring, 2010, Dermatology.

Number of tables and figures : 2 tables and 0 figures

P. Itin, J. Steiger, S. Schaub, 2018 .

Risk of Cutaneous Squamous Cell Carcinoma Development in Renal Transplant Recipients Is Independent of TMC/EVER Alterations

P. Itin, J. Steiger, S. Schaub, 2015, Dermatology.

Arginine‐ but not alanine‐rich carboxy‐termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti

P. Itin, J. Reichelt, E. Imahorn, 2019, Journal of cellular and molecular medicine.

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation‐associated genes

O. Sarig, P. Itin, E. Sprecher, 2014, The British journal of dermatology.

Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2023, NeuroImage.

Key Words Muir-Torre syndrome Familial cancer Fibrous papules

P. Itin, B. Burger, 2016 .

Muir-Torre Syndrome

P. Itin, B. Burger, 2008, Dermatology.

Mild Clinical Phenotype of Kindler Syndrome Associated with Late Diagnosis and Skin Cancer

P. Itin, C. Has, L. Bruckner-Tuderman, 2010, Dermatology.

SDHA gain-of-function engages inflammatory mitochondrial retrograde signaling via KEAP1–Nrf2

E. Ma, Russell G. Jones, C. Hess, 2019, Nature Immunology.

Multidimensional analysis of matched primary and recurrent glioblastoma identifies Fcγ receptors upregulation on microglia as a contributor of tumor recurrence

G. Hutter, B. Burger, M. Matter, 2023, bioRxiv.

Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression.

P. Itin, M. Indelman, E. Sprecher, 2010, EJD. European journal of dermatology.

Discovery of heterozygous KRT10 alterations in MAUIE cases underlines the importance of regular skin cancer screening in ichthyosis with confetti

P. Itin, C. Ng, S. Piscuoglio, 2020, The British journal of dermatology.

Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?

P. Itin, K. Heinimann, B. Burger, 2011, The oncologist.

Precalcaneal congenital fibrolipomatous hamartomas: is there a pathogenetic relationship with Gardner Syndrome?

P. Itin, K. Heinimann, B. Burger, 2010, European journal of dermatology : EJD.

Naegeli–Franceschetti–Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant

P. Itin, T. Leeb, E. Imahorn, 2019, British Journal of Dermatology.

Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Mohamed Chahine, Olivier Thériault, M. Boutjdir, 2017, The Canadian journal of cardiology.

A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy

B. Burger, M. Chahine, A. Mercier, 2018, Scientific Reports.