UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 381

Sortiert nach

The epidemiology of hand eczema in the general population - prevalence and main findings

Contact dermatitis, 2010-02, Vol.62 (2), p.75-87

2010

Volltextzugriff (PDF)

The transcriptome of hand eczema assessed by tape stripping

Contact dermatitis, 2022-02, Vol.86 (2), p.71-79

2022

Volltextzugriff (PDF)

Genetic analysis of a novel splice-site mutation in TMC8 reveals the in vivo importance of the transmembrane channel-like domain of TMC8

British journal of dermatology (1951), 2016-10, Vol.175 (4), p.803-806

2016

Volltextzugriff (PDF)

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

British journal of dermatology (1951), 2018-03, Vol.178 (3), p.e207-e209

2018

Volltextzugriff (PDF)

Predictive factors of self-reported hand eczema in adult Danes: a population-based cohort study with 5-year follow-up

British journal of dermatology (1951), 2016-08, Vol.175 (2), p.287-295

2016

Volltextzugriff (PDF)

A Polymorphism in the Cytidine Deaminase Promoter Predicts Severe Capecitabine-Induced Hand-Foot Syndrome

Clinical cancer research, 2011-04, Vol.17 (7), p.2006-2013

2011

Volltextzugriff (PDF)

Impact of systemic alitretinoin treatment on skin barrier gene and protein expression in patients with chronic hand eczema

British journal of dermatology (1951), 2016-12, Vol.175 (6), p.1243-1250

2016

Volltextzugriff (PDF)

Morphological and molecular characterization of actinic lentigos reveals alterations of the dermal extracellular matrix

British journal of dermatology (1951), 2017-12, Vol.177 (6), p.1619-1632

2017

Volltextzugriff (PDF)

Whole-exome sequencing solves diagnostic dilemma in a rare case of sporadic acrokeratosis verruciformis

Journal of the European Academy of Dermatology and Venereology, 2016-04, Vol.30 (4), p.695-697

2016

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Aquagenic wrinkling: A unique facial presentation

Journal of the American Academy of Dermatology, 2014-10, Vol.71 (4), p.e150-e152

2014

Volltextzugriff (PDF)

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British journal of dermatology (1951), 2015-02, Vol.172 (2), p.527-531

2015

Volltextzugriff (PDF)

Lack of association between mutation in IL36RN and palmoplantar pustular psoriasis in Chinese patients

Anais brasileiros de dermatología, 2019-11, Vol.94 (6), p.658-663

2019

Volltextzugriff (PDF)

Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma

Clinical and experimental dermatology, 2017-04, Vol.42 (3), p.316-319

2017

Volltextzugriff (PDF)

Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3

Clinical and experimental dermatology, 2014-06, Vol.39 (4), p.492-495

2014

Volltextzugriff (PDF)

Late‐onset cutaneous porphyria in a patient heterozygous for a uroporphyrinogen III synthase gene mutation

British journal of dermatology (1951), 2016-12, Vol.175 (6), p.1346-1350

2016

Volltextzugriff (PDF)

Inherited palmoplantar keratodermas: the heart of the matter

Clinical and experimental dermatology, 2018-03, Vol.43 (2), p.228-230

2018

Volltextzugriff (PDF)

Cover Image: Aquagenic wrinkling of the palms: a clue to underlying cystic fibrosis heterozygosity

British journal of dermatology (1951), 2017-02, Vol.176 (2), p.553-554

2017

Volltextzugriff (PDF)

Acral Peeling Skin Syndrome: A Case Report and Literature Review

Actas dermo-sifiliográficas (English ed.), 2016-10, Vol.107 (8), p.702-704

2016

Volltextzugriff (PDF)

Filaggrin loss-of-function mutations and atopic dermatitis as risk factors for hand eczema in apprentice nurses: part II of a prospective cohort study

Contact dermatitis, 2014-03, Vol.70 (3), p.139-150

2014

Volltextzugriff (PDF)

Hand eczema, atopic dermatitis and filaggrin mutations in adult Danes: a registry‐based study assessing risk of disability pension

Contact dermatitis, 2017-08, Vol.77 (2), p.95-105

2017

Volltextzugriff (PDF)

Aquagenic wrinkling of the palms

Canadian Medical Association journal (CMAJ), 2015-12, Vol.187 (18), p.E515

2015

Volltextzugriff (PDF)

Erythema palmare hereditarium (Lane's disease): Report of a paediatric case

Annales de dermatologie et de vénéréologie, 2016-01, Vol.143 (1), p.32-35

2016

Volltextzugriff (PDF)

A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient

Clinical and experimental dermatology, 2016-12, Vol.41 (8), p.933-934

2016

Volltextzugriff (PDF)

Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study

British journal of dermatology (1951), 2010-07, Vol.163 (1), p.115-120

2010

Volltextzugriff (PDF)

1 – 25 von 381

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(289)
Mit Volltextzugriff
(253)

Publikationsform

Artikel
(380)
magazinearticle
(1)

Sprache

6 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The epidemiology of hand eczema in the general population - prevalence and main findings

The transcriptome of hand eczema assessed by tape stripping

Genetic analysis of a novel splice-site mutation in TMC8 reveals the in vivo importance of the transmembrane channel-like domain of TMC8

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

Predictive factors of self-reported hand eczema in adult Danes: a population-based cohort study with 5-year follow-up

A Polymorphism in the Cytidine Deaminase Promoter Predicts Severe Capecitabine-Induced Hand-Foot Syndrome

Impact of systemic alitretinoin treatment on skin barrier gene and protein expression in patients with chronic hand eczema

Morphological and molecular characterization of actinic lentigos reveals alterations of the dermal extracellular matrix

Whole-exome sequencing solves diagnostic dilemma in a rare case of sporadic acrokeratosis verruciformis

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

Aquagenic wrinkling: A unique facial presentation

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

Lack of association between mutation in IL36RN and palmoplantar pustular psoriasis in Chinese patients

Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma

Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3

Late‐onset cutaneous porphyria in a patient heterozygous for a uroporphyrinogen III synthase gene mutation

Inherited palmoplantar keratodermas: the heart of the matter

Cover Image: Aquagenic wrinkling of the palms: a clue to underlying cystic fibrosis heterozygosity

Acral Peeling Skin Syndrome: A Case Report and Literature Review

Filaggrin loss-of-function mutations and atopic dermatitis as risk factors for hand eczema in apprentice nurses: part II of a prospective cohort study

Hand eczema, atopic dermatitis and filaggrin mutations in adult Danes: a registry‐based study assessing risk of disability pension

Aquagenic wrinkling of the palms

Erythema palmare hereditarium (Lane's disease): Report of a paediatric case

A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient

Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study

Suchergebnisse filtern