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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations

British journal of dermatology (1951), 2017-04, Vol.176 (4), p.1068-1073

2017

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Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis

Journal of the European Academy of Dermatology and Venereology, 2022-04, Vol.36 (4), p.582-591

2022

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Update: advanced methods in three-dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders

British journal of dermatology (1951), 2014-12, Vol.171 (6), p.1289-1290

Eckl, K.M.

2014

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Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA

British journal of dermatology (1951), 2015-06, Vol.172 (6), p.1628-1632

2015

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Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen

Medizinische Genetik, 2009-12, Vol.21 (4)

2009

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Pharmacokinetics of temocapril and temocaprilat after 14 once daily oral doses of temocapril in hypertensive patients with varying degrees of renal impairment

British journal of clinical pharmacology, 1997-12, Vol.44 (6), p.531-536

1997

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Voglibose has no effect on the pharmacokinetics of hydrochlorothiazide

European journal of clinical pharmacology, 1998-05, Vol.54 (3), p.273-274

1998

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Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma

Journal of investigative dermatology, 2001-05, Vol.116 (5), p.825-827

2001

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Safety and immunogenicity of IMVAMUNE, a promising candidate as a third generation smallpox vaccine

Vaccine, 2006-03, Vol.24 (12), p.2065-2070

2006

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Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis

Human mutation, 2005-10, Vol.26 (4), p.351-361

2005

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Krankheitsspezifische Hautmodelle

Medizinische Genetik, 2009-11, Vol.21 (4), p.487-492

2009

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Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen

Medizinische Genetik, 2009-11, Vol.21 (4), p.487-492

2009

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The pharmacokinetics of paroxetine in patients with liver cirrhosis

Acta psychiatrica Scandinavica, 1989-01, Vol.80 (S350), p.91-92

1989

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Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome

American journal of human genetics, 2004-07, Vol.75 (1), p.138-145

2004

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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

Human genetics, 2003, Vol.112 (1), p.50-56

2003

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The effect of gepirone-er on steady state pharmacodynamics of warfarin

Clinical pharmacology and therapeutics, 2003-02, Vol.73 (2), p.P71-P71

2003

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Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies

Archives of Dermatological Research, 2005-06, Vol.296 (12), p.585-587

2005

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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations

The British journal of dermatology, 2017, Vol.176 (4), p.1068-1073

2017

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The reliability of QTc interval assessment

BMC news and views, 2003-04, Vol.3 (S1), Article p0002

2003

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Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma

The Journal of investigative dermatology, 2001, Vol.116 (5), p.825-827

2001

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Chemistry and biochemistry of lipid peroxidation products

Free radical research, 2010-10, Vol.44 (10), p.1098-1124

2010

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Highly sensitive ELISA‐based assay for quantification of allergen‐specific IgE antibody levels

Allergy (Copenhagen), 2020-10, Vol.75 (10), p.2668-2670

2020

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Maternal Adherence to the Mediterranean Diet during Pregnancy: A Review of Commonly Used a priori Indexes

Nutrients, 2021-02, Vol.13 (2), p.582

2021

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Basophils are not the key antigen-presenting cells in allergic patients

Allergy (Copenhagen), 2012-05, Vol.67 (5), p.601-608

2012

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Versatile 3D‐Printed Micro‐Reference Electrodes for Aqueous and Non‐Aqueous Solutions

Angewandte Chemie International Edition, 2021-10, Vol.60 (42), p.22783-22790

International ed. in English, 2021

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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations

Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis

Update: advanced methods in three-dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders

Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA

Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen

Pharmacokinetics of temocapril and temocaprilat after 14 once daily oral doses of temocapril in hypertensive patients with varying degrees of renal impairment

Voglibose has no effect on the pharmacokinetics of hydrochlorothiazide

Genetic and Clinical Heterogeneity in Transgressive Palmoplantar Keratoderma

Safety and immunogenicity of IMVAMUNE, a promising candidate as a third generation smallpox vaccine

Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis

Krankheitsspezifische Hautmodelle

Krankheitsspezifische Hautmodelle: In-vitro-Modelle für die Entwicklung von Therapien bei angeborenen Verhornungsstörungen am Beispiel der kongenitalen Ichthyosen

The pharmacokinetics of paroxetine in patients with liver cirrhosis

Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

The effect of gepirone-er on steady state pharmacodynamics of warfarin

Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies

Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations

The reliability of QTc interval assessment

Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma

Chemistry and biochemistry of lipid peroxidation products

Highly sensitive ELISA‐based assay for quantification of allergen‐specific IgE antibody levels

Maternal Adherence to the Mediterranean Diet during Pregnancy: A Review of Commonly Used a priori Indexes

Basophils are not the key antigen-presenting cells in allergic patients

Versatile 3D‐Printed Micro‐Reference Electrodes for Aqueous and Non‐Aqueous Solutions

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