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Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort

Journal of the European Academy of Dermatology and Venereology, 2024-05

2024

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Histopathology‐guided mass spectrometry differentiates benign nevi from malignant melanoma

Journal of cutaneous pathology, 2020-03, Vol.47 (3), p.226-240

2020

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A multistep approach to the diagnosis of rare genodermatoses

Journal der Deutschen Dermatologischen Gesellschaft, 2016-10, Vol.14 (10), p.969-986

2016

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Generalized pustular psoriasis: A possible association with severe hypocalcaemia due to primary hypoparathyroidism

Journal of dermatology, 2017-12, Vol.44 (12), p.1416-1417

2017

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Cutaneous Vascular Malformations in a 53-Year-Old Woman With Neurologic Symptoms

JAMA dermatology (Chicago, Ill.), 2023-10, Vol.159 (10), p.1133

2023

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Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease

Frontiers in immunology, 2022-07, Vol.13, p.945176-945176

2022

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Primary cutaneous diffuse large B‐cell lymphoma, NOS and leg type: Clinical, morphologic and prognostic differences

Journal der Deutschen Dermatologischen Gesellschaft, 2019-03, Vol.17 (3), p.275-285

2019

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Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen

Journal der Deutschen Dermatologischen Gesellschaft, 2016-10, Vol.14 (10), p.969-987

2016

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Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis

Journal of dermatology, 2016-02, Vol.43 (2), p.225-226

2016

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Primär kutanes diffus‐großzelliges B‐Zell‐Lymphom, NOS oder leg type: klinische, morphologische und prognostische Unterschiede

Journal der Deutschen Dermatologischen Gesellschaft, 2019-03, Vol.17 (3), p.275-286

2019

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Inflammatory dermatoses in children and adolescents : Diagnosis and treatment of atopic dermatitis and psoriasis

Dermatologie (Heidelberg, Germany), 2024-04, Vol.75 (4), p.325-339

2024

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Linear Scars in a 4-Week-Old Girl

JAMA dermatology (Chicago, Ill.), 2016-02, Vol.152 (2), p.209

2016

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Phase II Trial of a Toll-Like Receptor 9–Activating Oligonucleotide in Patients With Metastatic Melanoma

Journal of clinical oncology, 2006-12, Vol.24 (36), p.5716-5724

2006

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P75 nerve growth factor receptor staining is superior to S100 in identifying spindle cell and desmoplastic melanoma

Journal of the American Academy of Dermatology, 2010-11, Vol.63 (5), p.852-858

2010

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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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Detection of the germline KIT S476I mutation in a kindred with familial mastocytosis associated with gastrointestinal stromal tumors

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2021-05, Vol.9 (5), p.2123-2125.e1

2021

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Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

Human genetics, 2012-11, Vol.131 (11), p.1761-1773

2012

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Viral exanthems in children

Hautarzt, 2022-06, Vol.73 (6), p.452-460

2022

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Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation

Dermatology (Basel), 2016-01, Vol.232 (1), p.30-37

2016

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The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome

Journal of investigative dermatology, 2014-03, Vol.134 (3), p.845-849

2014

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Primär kutanes diffus‐großzelliges B‐Zell‐Lymphom, NOS oder leg type: klinische, morphologische und prognostische Unterschiede

Journal der Deutschen Dermatologischen Gesellschaft, 2019-03, Vol.17 (3), p.275-286

2019

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Neonate female with blister formation shortly after birth : Preparation for the specialist examination: part 34

Hautarzt, 2019-04, Vol.70 (Suppl 1), p.31-33

2019

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Although Abundant in Tumor Tissue, Mast Cells Have No Effect on Immunological Micro-milieu or Growth of HPV-Induced or Transplanted Tumors

Cell reports (Cambridge), 2018-01, Vol.22 (1), p.27-35

2018

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Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations

EJD. European journal of dermatology, 2011-03, Vol.21 (2), p.170-172

2011

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Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort

Histopathology‐guided mass spectrometry differentiates benign nevi from malignant melanoma

A multistep approach to the diagnosis of rare genodermatoses

Generalized pustular psoriasis: A possible association with severe hypocalcaemia due to primary hypoparathyroidism

Cutaneous Vascular Malformations in a 53-Year-Old Woman With Neurologic Symptoms

Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease

Primary cutaneous diffuse large B‐cell lymphoma, NOS and leg type: Clinical, morphologic and prognostic differences

Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen

Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis

Primär kutanes diffus‐großzelliges B‐Zell‐Lymphom, NOS oder leg type: klinische, morphologische und prognostische Unterschiede

Inflammatory dermatoses in children and adolescents : Diagnosis and treatment of atopic dermatitis and psoriasis

Linear Scars in a 4-Week-Old Girl

Phase II Trial of a Toll-Like Receptor 9–Activating Oligonucleotide in Patients With Metastatic Melanoma

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

P75 nerve growth factor receptor staining is superior to S100 in identifying spindle cell and desmoplastic melanoma

Epidemiology of inherited epidermolysis bullosa in Germany

Detection of the germline KIT S476I mutation in a kindred with familial mastocytosis associated with gastrointestinal stromal tumors

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

Viral exanthems in children

Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation

The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome

Primär kutanes diffus‐großzelliges B‐Zell‐Lymphom, NOS oder leg type: klinische, morphologische und prognostische Unterschiede

Neonate female with blister formation shortly after birth : Preparation for the specialist examination: part 34

Although Abundant in Tumor Tissue, Mast Cells Have No Effect on Immunological Micro-milieu or Growth of HPV-Induced or Transplanted Tumors

Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations

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