UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 448

Sortiert nach

Newly diagnosed IgA nephropathy with gross haematuria following COVID-19 vaccination

QJM : An International Journal of Medicine, 2022-01, Vol.115 (1), p.28-29

2022

Volltextzugriff (PDF)

Erythropoietic Protoporphyria in a Japanese Population

Acta dermato-venereologica, 2019-06, Vol.99 (7), p.634-639

2019

Volltextzugriff (PDF)

Nagashima‐type palmoplantar keratoderma and malignant melanoma in Japanese patients

British journal of dermatology (1951), 2019-02, Vol.180 (2), p.415-416

2019

Volltextzugriff (PDF)

Endoplasmic reticulum stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e92-e93

2017

Volltextzugriff (PDF)

Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3‐48C polymorphism in the ferrochelatase gene

British journal of dermatology (1951), 2016-01, Vol.174 (1), p.172-175

2016

Volltextzugriff (PDF)

Treatment of acquired reactive perforating collagenosis with 308-nm excimer laser

Clinical and experimental dermatology, 2016-10, Vol.41 (7), p.820-821

2016

Volltextzugriff (PDF)

Usefulness of ultrasonography in the diagnosis of ischaemic fasciitis

Clinical and experimental dermatology, 2016-07, Vol.41 (5), p.502-505

2016

Volltextzugriff (PDF)

Atopic diathesis in hypohidrotic/anhidrotic ectodermal dysplasia

Acta dermato-venereologica, 2015-04, Vol.95 (4), p.476-479

2015

Volltextzugriff (PDF)

P241: Change of cerebral cortex excitability after electromyogram triggered electrical stimulation combined with mirror visual feedback in healthy elderly subjects

Clinical neurophysiology, 2014-06, Vol.125, p.S112-S112

2014

Volltextzugriff (PDF)

816 A novel COL7A1 mutation c.3570G>A resulted in relatively mild clinical phenotype of recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S140-S140

2023

Volltextzugriff (PDF)

302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S232-S232

2022

Volltextzugriff (PDF)

Hyper-IgE syndrome with a novel mutation of the STAT3 gene

Clinical and experimental dermatology, 2016-08, Vol.41 (6), p.687-689

2016

Volltextzugriff (PDF)

P4: Active inhibition for task-irrelevant sound in patients with attention deficits after traumatic brain injury: an fNIRS study

Clinical neurophysiology, 2014-06, Vol.125, p.S49-S50

2014

Volltextzugriff (PDF)

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.199-201

2011

Volltextzugriff (PDF)

The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis

Clinical and experimental dermatology, 2003-05, Vol.28 (3), p.235-240

2003

Volltextzugriff (PDF)

Partial anhidrosis demonstrated by Q-SART in a patient with a novel mutation in the EDARADD gene

Journal of the European Academy of Dermatology and Venereology, 2015-07, Vol.29 (7), p.1443-1444

2015

Volltextzugriff (PDF)

A reddish, pedunculated, granulomatous nodule on the nasal dorsum

Clinical and experimental dermatology, 2015-08, Vol.40 (6), p.703-705

2015

Volltextzugriff (PDF)

Q-switched ruby laser therapy and long-term follow-up evaluation of small to medium-sized congenital melanocytic naevi

Clinical and experimental dermatology, 2012-06, Vol.37 (4), p.438-440

2012

Volltextzugriff (PDF)

Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation

British journal of dermatology (1951), 2012-04, Vol.166 (4), p.900-903

2012

Volltextzugriff (PDF)

Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases

British journal of dermatology (1951), 2006-08, Vol.155 (2), p.313-317

2006

Volltextzugriff (PDF)

Leuprorelin acetate granulomas: case reports and review of the literature

British journal of dermatology (1951), 2005-05, Vol.152 (5), p.1045-1047

2005

Volltextzugriff (PDF)

Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation

British journal of dermatology (1951), 2011-12, Vol.165 (6), p.1290-1292

2011

Volltextzugriff (PDF)

Childhood epidermolysis bullosa acquisita with autoantibodies against the noncollagenous 1 and 2 domains of type VII collagen: case report and review of the literature

British journal of dermatology (1951), 2006-11, Vol.155 (5), p.1048-1052

2006

Volltextzugriff (PDF)

CD20+ primary cutaneous T-cell lymphoma presenting as a solitary extensive plaque

British journal of dermatology (1951), 2009-04, Vol.160 (4), p.894-896

2009

Volltextzugriff (PDF)

Cowden syndrome: a novel mutation and overlooked glycogenic acanthosis in gingiva

British journal of dermatology (1951), 2009-05, Vol.160 (5), p.1116-1118

2009

Volltextzugriff (PDF)

1 – 25 von 448

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(372)
Mit Volltextzugriff
(393)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(247)
Life Sciences & Biomedicine
(219)
Humans
(211)
Dermatology
(139)
Biological And Medical Sciences
(126)
Male
(120)
Female
(104)
Medical Sciences
(101)
Animals
(70)
Adult
(59)
Middle Aged
(53)
Aged
(42)
Mice
(33)
Mutation
(33)
Fundamental And Applied Biological Sciences. Psychology
(28)
Rats
(28)
Laser Technology & Holography
(26)
Molecular Sequence Data
(26)
Plasma Physics
(26)
Scientific Equipment & Techniques, Laboratory Equipment
(26)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Newly diagnosed IgA nephropathy with gross haematuria following COVID-19 vaccination

Erythropoietic Protoporphyria in a Japanese Population

Nagashima‐type palmoplantar keratoderma and malignant melanoma in Japanese patients

Endoplasmic reticulum stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa

Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3‐48C polymorphism in the ferrochelatase gene

Treatment of acquired reactive perforating collagenosis with 308-nm excimer laser

Usefulness of ultrasonography in the diagnosis of ischaemic fasciitis

Atopic diathesis in hypohidrotic/anhidrotic ectodermal dysplasia

P241: Change of cerebral cortex excitability after electromyogram triggered electrical stimulation combined with mirror visual feedback in healthy elderly subjects

816 A novel COL7A1 mutation c.3570G>A resulted in relatively mild clinical phenotype of recessive dystrophic epidermolysis bullosa

302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa

Hyper-IgE syndrome with a novel mutation of the STAT3 gene

P4: Active inhibition for task-irrelevant sound in patients with attention deficits after traumatic brain injury: an fNIRS study

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation

The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis

Partial anhidrosis demonstrated by Q-SART in a patient with a novel mutation in the EDARADD gene

A reddish, pedunculated, granulomatous nodule on the nasal dorsum

Q-switched ruby laser therapy and long-term follow-up evaluation of small to medium-sized congenital melanocytic naevi

Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation

Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases

Leuprorelin acetate granulomas: case reports and review of the literature

Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation

Childhood epidermolysis bullosa acquisita with autoantibodies against the noncollagenous 1 and 2 domains of type VII collagen: case report and review of the literature

CD20+ primary cutaneous T-cell lymphoma presenting as a solitary extensive plaque

Cowden syndrome: a novel mutation and overlooked glycogenic acanthosis in gingiva

Suchergebnisse filtern