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Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

British journal of dermatology (1951), 2019-06, Vol.180 (6), p.1459-1467

2019

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Burden of itch in ichthyosis: a multicentre study in 94 patients

Journal of the European Academy of Dermatology and Venereology, 2019-11, Vol.33 (11), p.2095-2100

2019

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Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss

British journal of dermatology (1951), 2012-06, Vol.166 (6), p.1314-1318

2012

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Secreted ProNGF Is a Pathophysiological Death-Inducing Ligand after Adult CNS Injury

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.6226-6230

2004

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Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage

Journal of the European Academy of Dermatology and Venereology, 2021-06, Vol.35 (6), p.1386-1392

2021

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Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata

British journal of dermatology (1951), 2012-12, Vol.167 (6), p.1360-1365

2012

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Diminished protein‐bound ω‐hydroxylated ceramides in the skin of patients with ichthyosis with 12R‐lipoxygenase (LOX) or eLOX‐3 deficiency

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e119-e121

2017

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A retrospective study on the liver toxicity of oral retinoids in Chanarin–Dorfman syndrome

Journal of the European Academy of Dermatology and Venereology, 2023-10, Vol.37 (10), p.e1237-e1241

2023

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Chanarin–Dorfman syndrome with rare renal involvement

British journal of dermatology (1951), 2017-02, Vol.176 (2), p.545-548

2017

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Oncogenic Ras in tumour progression and metastasis

Biological chemistry, 2005-03, Vol.386 (3), p.193-205

Giehl, Klaudia

2005

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Characterization and expression analysis of the hair keratin associated protein KAP26.1

British journal of dermatology (1951), 2008-09, Vol.159 (3), p.725-729

2008

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Posttraumatic GABAA-Mediated [Ca2+]i Increase Is Essential for the Induction of Brain-Derived Neurotrophic Factor-Dependent Survival of Mature Central Neurons

The Journal of neuroscience, 2008-07, Vol.28 (27), p.6996-7005

2008

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The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients

British journal of dermatology (1951), 2014-04, Vol.170 (4), p.982-985

2014

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Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability

Acta dermato-venereologica, 2016-01, Vol.96 (4), p.468-472

2016

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Diminished protein-bound [omega]-hydroxylated ceramides in the skin of patients with ichthyosis with 12R-lipoxygenase (LOX) or eLOX-3 deficiency

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e119

2017

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Protein expression of melanocyte growth factors (bFGF, SCF) and their receptors (FGFR-1, c-kit) in nevi and melanoma

Journal of cutaneous pathology, 2007-01, Vol.34 (1), p.7-14

2007

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The proline‐rich focal adhesion and microfilament protein VASP is a ligand for profilins

The EMBO journal, 1995-04, Vol.14 (8), p.1583-1589

1995

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Non-invasive diagnosis of sweat gland dysplasia using optical coherence tomography and reflectance confocal microscopy in a family with anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome)

Journal of the European Academy of Dermatology and Venereology, 2016-04, Vol.30 (4), p.677-682

2016

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The TRAF1/C5 locus confers risk for familial and severe alopecia areata

British journal of dermatology (1951), 2010-04, Vol.162 (4), p.866-869

2010

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Palmoplantar dermatoses in children

Hautarzt, 2021-03, Vol.72 (3), p.215-224

2021

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Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss

British journal of dermatology (1951), 2011-09, Vol.165 (3), p.703-705

2011

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CUTL1 promotes tumor cell migration by decreasing proteasome-mediated Src degradation

Oncogene, 2007-08, Vol.26 (40), p.5939-5949

2007

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Identification and characterization of 20 immunocompetent patients with simultaneous varicella zoster and herpes simplex virus infection

Journal of the European Academy of Dermatology and Venereology, 2008-06, Vol.22 (6), p.722-728

2008

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Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysis

British journal of dermatology (1951), 2009-03, Vol.160 (3), p.527-533

2009

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Seltene Ursache einer Hämoptyse: Fünfzehnjährige Patientin mit eosinophiler Granulomatose mit Polyangiitis

Monatsschrift Kinderheilkunde, 2019-03, Vol.167 (3), p.234-240

2019

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Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

Burden of itch in ichthyosis: a multicentre study in 94 patients

Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss

Secreted ProNGF Is a Pathophysiological Death-Inducing Ligand after Adult CNS Injury

Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage

Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata

Diminished protein‐bound ω‐hydroxylated ceramides in the skin of patients with ichthyosis with 12R‐lipoxygenase (LOX) or eLOX‐3 deficiency

A retrospective study on the liver toxicity of oral retinoids in Chanarin–Dorfman syndrome

Chanarin–Dorfman syndrome with rare renal involvement

Oncogenic Ras in tumour progression and metastasis

Characterization and expression analysis of the hair keratin associated protein KAP26.1

Posttraumatic GABAA-Mediated [Ca2+]i Increase Is Essential for the Induction of Brain-Derived Neurotrophic Factor-Dependent Survival of Mature Central Neurons

The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients

Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability

Diminished protein-bound [omega]-hydroxylated ceramides in the skin of patients with ichthyosis with 12R-lipoxygenase (LOX) or eLOX-3 deficiency

Protein expression of melanocyte growth factors (bFGF, SCF) and their receptors (FGFR-1, c-kit) in nevi and melanoma

The proline‐rich focal adhesion and microfilament protein VASP is a ligand for profilins

Non-invasive diagnosis of sweat gland dysplasia using optical coherence tomography and reflectance confocal microscopy in a family with anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome)

The TRAF1/C5 locus confers risk for familial and severe alopecia areata

Palmoplantar dermatoses in children

Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss

CUTL1 promotes tumor cell migration by decreasing proteasome-mediated Src degradation

Identification and characterization of 20 immunocompetent patients with simultaneous varicella zoster and herpes simplex virus infection

Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysis

Seltene Ursache einer Hämoptyse: Fünfzehnjährige Patientin mit eosinophiler Granulomatose mit Polyangiitis

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