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...

Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa

Journal of the American Academy of Dermatology, 2000-06, Vol.42 (6), p.1051-1066

2000

Volltextzugriff (PDF)

Human GLI2 and GLI1 are part of a positive feedback mechanism in basal cell carcinoma

Oncogene, 2002-08, Vol.21 (36), p.5529-5539

2002

Volltextzugriff (PDF)

Survival and Effectiveness of Tumour Necrosis Factor-alpha Inhibitors in the Treatment of Plaque Psoriasis under Daily Life Conditions: Report from the Psoriasis Registry Austria

Acta dermato-venereologica, 2016-02, Vol.96 (2), p.207-212

2016

Volltextzugriff (PDF)

A novel screening system improves genetic correction by internal exon replacement

Nucleic acids research, 2011-09, Vol.39 (16), p.e108-e108

2011

Volltextzugriff (PDF)

Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target

Microbiology (Society for General Microbiology), 2010-12, Vol.156 (Pt 12), p.3710-3721

2010

Volltextzugriff (PDF)

Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab

British journal of dermatology (1951), 2007-08, Vol.157 (2), p.417-419

2007

Volltextzugriff (PDF)

Prospective, Randomized, Multicenter, Double-Blind Placebo-Controlled Trial Comparing Adjuvant Interferon Alfa and Isotretinoin With Interferon Alfa Alone in Stage IIA and IIB Melanoma: European Cooperative Adjuvant Melanoma Treatment Study Group

Journal of clinical oncology, 2005-12, Vol.23 (34), p.8655-8663

2005

Volltextzugriff (PDF)

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

British journal of dermatology (1951), 2006-01, Vol.154 (1), p.185-187

2006

Volltextzugriff (PDF)

Pathogenesis of the Permeability Barrier Abnormality in Epidermolytic Hyperkeratosis

Journal of investigative dermatology, 2001-10, Vol.117 (4), p.837-847

2001

Volltextzugriff (PDF)

Human papillomavirus infection in Netherton's syndrome

British journal of dermatology (1951), 2001-05, Vol.144 (5), p.1044-1049

2001

Volltextzugriff (PDF)

Development of spliceosome-mediated RNA trans-splicing (SMaRT™) for the correction of inherited skin diseases

Experimental dermatology, 2003-02, Vol.12 (1), p.37-46

2003

Volltextzugriff (PDF)

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Journal of cutaneous pathology, 2003-10, Vol.30 (9), p.553-560

2003

Volltextzugriff (PDF)

Nephropathische Cystinose: Spätkomplikationen einer Multisystemerkrankung – Langzeitergebnisse der interdisziplinären Cystinose-Sprechstunde in Traunstein

Nieren- und Hockdruckkrankheiten, 2016-11, Vol.45 (11), p.432-438

2016

Volltextzugriff (PDF)

Intravenous immunoglobulin treatment in therapy-resistant epidermolysis bullosa acquisita

Journal of the American Academy of Dermatology, 1997-02, Vol.36 (2), p.331-335

1997

Volltextzugriff (PDF)

A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

The American journal of pathology, 2001-02, Vol.158 (2), p.617-625

2001

Volltextzugriff (PDF)

Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay

Laboratory investigation, 2004-10, Vol.84 (10), p.1279-1288

2004

Volltextzugriff (PDF)

Ocular involvement in IgA–epidermolysis bullosa acquisita

British journal of dermatology (1951), 1999-11, Vol.141 (5), p.887-892

1999

Volltextzugriff (PDF)

Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

Actas dermo-sifiliográficas (English ed.), 2010-10, Vol.101 (8), p.673-682

2010

Volltextzugriff (PDF)

Pathogenic mechanisms in epidermolysis bullosa naevi

Acta dermato-venereologica, 2003, Vol.83 (5), p.332-337

2003

Volltextzugriff (PDF)

Epidermolysis bullosa hereditaria

Monatsschrift Kinderheilkunde, 2008, Vol.156 (2), p.110-121

2008

Volltextzugriff (PDF)

A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner

Clinical and experimental dermatology, 2003-01, Vol.28 (1), p.77-79

2003

Volltextzugriff (PDF)

Mapeo por inmunofluorescencia para el diagnóstico de epidermólisis ampollosa congénita

Actas dermo-sifiliográficas, 2010, Vol.101 (8), p.673-682

2010

Volltextzugriff (PDF)

Gene symbol: Kind1. Disease: kindler syndrome

Human genetics, 2004-07, Vol.115 (2), p.175-175

2004

Volltextzugriff (PDF)

Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, Koebner

Human genetics, 2004-07, Vol.115 (2), p.171-171

2004

Volltextzugriff (PDF)

Ocular involvement in anti-epiligrin cicatricial pemphigoid

European journal of ophthalmology, 2006-11, Vol.16 (6), p.867-869

2006

Volltextzugriff (PDF)

1 – 25 von 91

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(64)
Mit Volltextzugriff
(64)

Publikationsform

Sprache

Englisch
(68)
Deutsch
(24)
Spanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa

Human GLI2 and GLI1 are part of a positive feedback mechanism in basal cell carcinoma

Survival and Effectiveness of Tumour Necrosis Factor-alpha Inhibitors in the Treatment of Plaque Psoriasis under Daily Life Conditions: Report from the Psoriasis Registry Austria

A novel screening system improves genetic correction by internal exon replacement

Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target

Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab

Prospective, Randomized, Multicenter, Double-Blind Placebo-Controlled Trial Comparing Adjuvant Interferon Alfa and Isotretinoin With Interferon Alfa Alone in Stage IIA and IIB Melanoma: European Cooperative Adjuvant Melanoma Treatment Study Group

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

Pathogenesis of the Permeability Barrier Abnormality in Epidermolytic Hyperkeratosis

Human papillomavirus infection in Netherton's syndrome

Development of spliceosome-mediated RNA trans-splicing (SMaRT™) for the correction of inherited skin diseases

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Nephropathische Cystinose: Spätkomplikationen einer Multisystemerkrankung – Langzeitergebnisse der interdisziplinären Cystinose-Sprechstunde in Traunstein

Intravenous immunoglobulin treatment in therapy-resistant epidermolysis bullosa acquisita

A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay

Ocular involvement in IgA–epidermolysis bullosa acquisita

Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

Pathogenic mechanisms in epidermolysis bullosa naevi

Epidermolysis bullosa hereditaria

A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner

Mapeo por inmunofluorescencia para el diagnóstico de epidermólisis ampollosa congénita

Gene symbol: Kind1. Disease: kindler syndrome

Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, Koebner

Ocular involvement in anti-epiligrin cicatricial pemphigoid

Suchergebnisse filtern