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...

Erythema nodosum leprosum post‐COVID‐19 vaccination: endemic while pandemic

Journal of the European Academy of Dermatology and Venereology, 2022-07, Vol.36 (7), p.e505-e506

2022

Volltextzugriff (PDF)

Preservatives in cosmetics in the Israeli market conform well to the EU legislation

Journal of the European Academy of Dermatology and Venereology, 2015-04, Vol.29 (4), p.761-766

2015

Volltextzugriff (PDF)

Pyoderma gangrenosum along superficial vein thrombosis during pregnancy

Clinical and experimental dermatology, 2016-01, Vol.41 (1), p.112-113

2016

Volltextzugriff (PDF)

Squamous cell carcinoma in situ in association with HPV 11 in Netherton's syndrome patient: a case report

Journal of the European Academy of Dermatology and Venereology, 2016-12, Vol.30 (12), p.e232-e234

2016

Volltextzugriff (PDF)

Noninvasive in vivo confocal laser scanning microscopy is effective in differentiating allergic from nonallergic equivocal patch test reactions

Lasers in medical science, 2015-04, Vol.30 (3), p.1081-1087

2015

Volltextzugriff (PDF)

CYLD mutations in familial skin appendage tumours

Journal of medical genetics, 2008-05, Vol.45 (5), p.298-302

2008

Volltextzugriff (PDF)

A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance

British journal of dermatology (1951), 2012-06, Vol.166 (s2), p.20-26

2012

Volltextzugriff (PDF)

A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis

Journal of the European Academy of Dermatology and Venereology, 2010-07, Vol.24 (7), p.858

2010

Volltextzugriff (PDF)

Kerion celsi of the vulva: An unusual location

Journal de mycologie médicale, 2014-12, Vol.24 (4), p.359-360

2014

Volltextzugriff (PDF)

A novel deletion mutation in P2RY5/LPA6 gene cause autosomal recessive woolly hair with hypotrichosis

Journal of the European Academy of Dermatology and Venereology, 2010-07, Vol.24 (7), p.858-859

2010

Volltextzugriff (PDF)

Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex

British journal of dermatology (1951), 2011-05, Vol.164 (5), p.1113-1116

2011

Volltextzugriff (PDF)

A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma

Journal of the European Academy of Dermatology and Venereology, 2010-11, Vol.24 (11), p.1349-1353

2010

Volltextzugriff (PDF)

Exacerbation of Hailey-Hailey Disease Following SARS-CoV-2 Vaccination

Acta dermato-venereologica, 2021-09, Vol.101 (9), p.adv00554-adv00554

2021

Volltextzugriff (PDF)

Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24

Journal of medical genetics, 2003-12, Vol.40 (12), p.872-878

2003

Volltextzugriff (PDF)

Monilethrix: a keratin hHb6 mutation is co-dominant with variable expression

Experimental dermatology, 1998-10, Vol.7 (5), p.268-272

1998

Volltextzugriff (PDF)

Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6

Human heredity, 2000-09, Vol.50 (5), p.325-330

2000

Volltextzugriff (PDF)

A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance: Novel mutation in coil 2A of KRT86 causing monilethrix

British journal of dermatology (1951), 2012-06, Vol.166, p.20-26

2012

Volltextzugriff (PDF)

Novel and Recurrent FERMT1 Gene Mutations in Kindler Syndrome

Acta dermato-venereologica, 2011-05, Vol.91 (3), p.267-270

2011

Volltextzugriff (PDF)

Prevalence of alexithymia in patients with psoriasis and its association with disease burden: a multicentre observational study

British journal of dermatology (1951), 2017-05, Vol.176 (5), p.1195-1203

2017

Volltextzugriff (PDF)

A novel deletion mutation in P2RY5/LPA 6 gene cause autosomal recessive woolly hair with hypotrichosis

Journal of the European Academy of Dermatology and Venereology, 2010-07, Vol.24 (7), p.858-859

2010

Volltextzugriff (PDF)

Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex: Correspondence

British journal of dermatology (1951), 2011-05, Vol.164 (5), p.1113-1116

2011

Volltextzugriff (PDF)

Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata

Journal of investigative dermatology, 2003-10, Vol.121 (4), p.741-744

2003

Volltextzugriff (PDF)

South American cutaneous leishmaniasis: report of ten cases in Israeli travelers

Journal of the European Academy of Dermatology and Venereology, 1998-07, Vol.11 (1), p.32-36

1998

Volltextzugriff (PDF)

Investigation of the threshold for allergic reactivity to chromium

Contact dermatitis, 2001-02, Vol.44 (2), p.70-74

2001

Volltextzugriff (PDF)

Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency

Clinical and experimental dermatology, 2003-01, Vol.28 (1), p.80-84

2003

Volltextzugriff (PDF)

1 – 25 von 123

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(113)
Mit Volltextzugriff
(109)

Publikationsform

Artikel
(119)
Berichte
(4)

Sprache

Englisch
(122)
Ukrainisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(96)
Life Sciences & Biomedicine
(95)
Humans
(84)
Male
(65)
Female
(63)
Biological And Medical Sciences
(54)
Medical Sciences
(53)
Child
(37)
Adult
(29)
Radiology, Nuclear Medicine & Medical Imaging
(28)
Dermatology
(23)
Adolescent
(22)
Pediatrics
(22)
Child, Preschool
(21)
Magnetic Resonance Imaging
(20)
Middle Aged
(18)
Infant
(17)
Neurosciences & Neurology
(15)
Aged
(14)
Clinical Neurology
(14)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Erythema nodosum leprosum post‐COVID‐19 vaccination: endemic while pandemic

Preservatives in cosmetics in the Israeli market conform well to the EU legislation

Pyoderma gangrenosum along superficial vein thrombosis during pregnancy

Squamous cell carcinoma in situ in association with HPV 11 in Netherton's syndrome patient: a case report

Noninvasive in vivo confocal laser scanning microscopy is effective in differentiating allergic from nonallergic equivocal patch test reactions

CYLD mutations in familial skin appendage tumours

A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance

A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis

Kerion celsi of the vulva: An unusual location

A novel deletion mutation in P2RY5/LPA6 gene cause autosomal recessive woolly hair with hypotrichosis

Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex

A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma

Exacerbation of Hailey-Hailey Disease Following SARS-CoV-2 Vaccination

Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24

Monilethrix: a keratin hHb6 mutation is co-dominant with variable expression

Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6

A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance: Novel mutation in coil 2A of KRT86 causing monilethrix

Novel and Recurrent FERMT1 Gene Mutations in Kindler Syndrome

Prevalence of alexithymia in patients with psoriasis and its association with disease burden: a multicentre observational study

A novel deletion mutation in P2RY5/LPA 6 gene cause autosomal recessive woolly hair with hypotrichosis

Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex: Correspondence

Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata

South American cutaneous leishmaniasis: report of ten cases in Israeli travelers

Investigation of the threshold for allergic reactivity to chromium

Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency

Suchergebnisse filtern