UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Acquired dermal melanocytosis of the ear

International journal of dermatology, 2023-01, Vol.62 (1), p.e42-e44

2023

Volltextzugriff (PDF)

Real-world efficacy of biological agents in moderate-to-severe plaque psoriasis: An analysis of 75 patients in Taiwan

PloS one, 2020-12, Vol.15 (12), p.e0244620

2020

Volltextzugriff (PDF)

Evanescent and Persistent Pruritic Eruptions of Adult-Onset Still Disease: A Clinical and Pathologic Study of 36 Patients

Seminars in arthritis and rheumatism, 2012-12, Vol.42 (3), p.317-326

2012

Volltextzugriff (PDF)

A de novo, novel frameshift deletion in Conradi-Hünermann-Happle syndrome with ten-year follow-up from birth

Indian journal of dermatology, 2022-09, Vol.67 (5), p.606-607

2022

Volltextzugriff (PDF)

Sorafenib-Induced Eruptive Melanocytic Lesions

Indian journal of dermatology, 2021-11, Vol.66 (6), p.709-709

2021

Volltextzugriff (PDF)

Novel compound heterozygous indel ZMPSTE24 mutations in a Taiwanese male infant with restrictive dermopathy

Journal of dermatology, 2022-08, Vol.49 (8), p.e280-e282

2022

Volltextzugriff (PDF)

Tinea nigra due to Hortaea werneckii in Taiwan

Journal of microbiology, immunology and infection, 2022-06, Vol.55 (3), p.558-560

2022

Volltextzugriff (PDF)

Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients

Orphanet journal of rare diseases, 2022-12, Vol.17 (1), p.451-451, Article 451

2022

Volltextzugriff (PDF)

Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex

Acta dermato-venereologica, 2020-08, Vol.100 (15), p.adv00242-adv00242

2020

Volltextzugriff (PDF)

Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

Journal of dermatology, 2018-04, Vol.45 (4), p.475-478

2018

Volltextzugriff (PDF)

Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: a case report

BMC ophthalmology, 2019-07, Vol.19 (1), p.144-144, Article 144

2019

Volltextzugriff (PDF)

Histopathological differential diagnosis of keloid and hypertrophic scar

The American journal of dermatopathology, 2004-10, Vol.26 (5), p.379-384

2004

Volltextzugriff (PDF)

Cutaneous alternariosis in a renal transplant recipient: A case report and literature review

Asian journal of surgery, 2015-01, Vol.38 (1), p.47-57

2015

Volltextzugriff (PDF)

Eosinophilic pustular folliculitis associated with Demodex overgrowth or demodicosis on the face - A report of five cases

Dermatologica Sinica, 2021-07, Vol.39 (3), p.132-136

2021

Volltextzugriff (PDF)

Keratitis-ichthyosis-deafness syndrome with GJB2 mutation manifesting generalized erythematous plaques of porokeratotic eccrine ostial and dermal duct nevus

Dermatologica Sinica, 2019-04, Vol.37 (2), p.103-105

2019

Volltextzugriff (PDF)

Herpes zoster-associated severity and duration of pain, health-related quality of life, and healthcare utilization in Taiwan: a prospective observational study

International journal of dermatology, 2015-05, Vol.54 (5), p.529-536

2015

Volltextzugriff (PDF)

Cerebrotendinous xanthomatosis-a case report with novel compound heterozygous mutation of CYP27A1 gene

Zhonghua pi fu ke yi xue za zhi, 2018-12, Vol.36 (4), p.200-202

2018

Volltextzugriff (PDF)

Exertional plantar blistering as an easily overlooked clue for epidermolysis bullosa simplex

Dermatologica Sinica, 2019-07, Vol.37 (3), p.170-171

2019

Volltextzugriff (PDF)

Bowen's disease with features resembling myrmecia wart

Journal of dermatology, 2015-01, Vol.42 (1), p.90-93

2015

Volltextzugriff (PDF)

Arsenic methylation and skin cancer risk in southwestern Taiwan

Journal of occupational and environmental medicine, 2003-03, Vol.45 (3), p.241-248

2003

Volltextzugriff (PDF)

Factors Related to Missed Diagnosis of Incidental Scabies Infestations in Patients Admitted Through the Emergency Department to Inpatient Services

Academic emergency medicine, 2010-09, Vol.17 (9), p.958-964

2010

Volltextzugriff (PDF)

A novel mutation of the RNA-specific adenosine deaminase 1 gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria and Becker's nevus-like lesion

Zhonghua pi fu ke yi xue za zhi, 2016-06, Vol.34 (2), p.110-111

2016

Volltextzugriff (PDF)

Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes

Human genetics, 2002-01, Vol.110 (1), p.41-51

2002

Volltextzugriff (PDF)

A novel splice mutation in the ATP2C1 gene in a woman with concomitant psoriasis vulgaris and disseminated Hailey-Hailey disease

International journal of dermatology, 2012-08, Vol.51 (8), p.947-951

2012

Volltextzugriff (PDF)

Early intervention with high-dose steroid pulse therapy prolongs disease-free interval of severe alopecia areata: a retrospective study

Annals of Dermatology, 2013, 25(4), , pp.471-474

2013

Volltextzugriff (PDF)

1 – 25 von 119

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(111)
Mit Volltextzugriff
(75)

Publikationsform

Artikel
(113)
Berichte
(6)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(81)
Life Sciences & Biomedicine
(80)
Humans
(60)
Dermatology
(51)
Male
(42)
Female
(39)
Adult
(30)
Biological And Medical Sciences
(26)
Medical Sciences
(26)
Middle Aged
(22)
Taiwan
(21)
Aged
(17)
Mutation
(15)
General & Internal Medicine
(14)
Medicine, General & Internal
(14)
Child
(12)
Skin - Pathology
(10)
Skin Involvement In Other Diseases. Miscellaneous. General Aspects
(10)
Dna Mutational Analysis
(9)
Mutation Analysis
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Acquired dermal melanocytosis of the ear

Real-world efficacy of biological agents in moderate-to-severe plaque psoriasis: An analysis of 75 patients in Taiwan

Evanescent and Persistent Pruritic Eruptions of Adult-Onset Still Disease: A Clinical and Pathologic Study of 36 Patients

A de novo, novel frameshift deletion in Conradi-Hünermann-Happle syndrome with ten-year follow-up from birth

Sorafenib-Induced Eruptive Melanocytic Lesions

Novel compound heterozygous indel ZMPSTE24 mutations in a Taiwanese male infant with restrictive dermopathy

Tinea nigra due to Hortaea werneckii in Taiwan

Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients

Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex

Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: a case report

Histopathological differential diagnosis of keloid and hypertrophic scar

Cutaneous alternariosis in a renal transplant recipient: A case report and literature review

Eosinophilic pustular folliculitis associated with Demodex overgrowth or demodicosis on the face - A report of five cases

Keratitis-ichthyosis-deafness syndrome with GJB2 mutation manifesting generalized erythematous plaques of porokeratotic eccrine ostial and dermal duct nevus

Herpes zoster-associated severity and duration of pain, health-related quality of life, and healthcare utilization in Taiwan: a prospective observational study

Cerebrotendinous xanthomatosis-a case report with novel compound heterozygous mutation of CYP27A1 gene

Exertional plantar blistering as an easily overlooked clue for epidermolysis bullosa simplex

Bowen's disease with features resembling myrmecia wart

Arsenic methylation and skin cancer risk in southwestern Taiwan

Factors Related to Missed Diagnosis of Incidental Scabies Infestations in Patients Admitted Through the Emergency Department to Inpatient Services

A novel mutation of the RNA-specific adenosine deaminase 1 gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria and Becker's nevus-like lesion

Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes

A novel splice mutation in the ATP2C1 gene in a woman with concomitant psoriasis vulgaris and disseminated Hailey-Hailey disease

Early intervention with high-dose steroid pulse therapy prolongs disease-free interval of severe alopecia areata: a retrospective study

Suchergebnisse filtern