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...

GNA14 Somatic Mutation Causes Congenital and Sporadic Vascular Tumors by MAPK Activation

American journal of human genetics, 2016-08, Vol.99 (2), p.443-450

2016

Volltextzugriff (PDF)

Second-Hit Somatic Mutations in Mevalonate Pathway Genes Underlie Porokeratosis

Journal of investigative dermatology, 2019-12, Vol.139 (12), p.2409-2411

2019

Volltextzugriff (PDF)

Associations between ichthyosis and mood disorders: A case-control study in the All of Us Research Program

Journal of the American Academy of Dermatology, 2024-02, Vol.90 (2), p.439-440

2024

Volltextzugriff (PDF)

Topical cholesterol/lovastatin for the treatment of porokeratosis: A pathogenesis-directed therapy

Journal of the American Academy of Dermatology, 2020-01, Vol.82 (1), p.123-131

2020

Volltextzugriff (PDF)

Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a Child

JAMA dermatology (Chicago, Ill.), 2019-02, Vol.155 (2), p.256

2019

Volltextzugriff (PDF)

Association of Somatic ATP2A2 Damaging Variants With Grover Disease

JAMA dermatology (Chicago, Ill.), 2023-07, Vol.159 (7), p.745

2023

Volltextzugriff (PDF)

CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

Journal of the American Academy of Dermatology, 2018-09, Vol.79 (3), p.487-494

2018

Volltextzugriff (PDF)

Second-Hit, Postzygotic PMVK and MVD Mutations in Linear Porokeratosis

JAMA dermatology (Chicago, Ill.), 2019-05, Vol.155 (5), p.548

2019

Volltextzugriff (PDF)

Somatic Mutations in NEK9 Cause Nevus Comedonicus

American journal of human genetics, 2016-05, Vol.98 (5), p.1030-1037

2016

Volltextzugriff (PDF)

Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia

American journal of human genetics, 2019-11, Vol.105 (5), p.1023-1029

2019

Volltextzugriff (PDF)

More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations

Journal of the American Academy of Dermatology, 2019-03, Vol.80 (3), p.617-625

2019

Volltextzugriff (PDF)

Somatic p.T771R KDR (VEGFR2) Mutation Arising in a Sporadic Angioma During Ramucirumab Therapy

JAMA dermatology (Chicago, Ill.), 2015-11, Vol.151 (11), p.1240

2015

Volltextzugriff (PDF)

Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia

Journal of investigative dermatology, 2015-06, Vol.135 (6), p.1540-1547

2015

Volltextzugriff (PDF)

Improving outcomes for harlequin ichthyosis

Journal of the American Academy of Dermatology, 2013-11, Vol.69 (5), p.808-809

2013

Volltextzugriff (PDF)

Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines

The American journal of pathology, 2018-06, Vol.188 (6), p.1419-1429

2018

Volltextzugriff (PDF)

Somatic V600E BRAF Mutation in Linear and Sporadic Syringocystadenoma Papilliferum

Journal of investigative dermatology, 2015-10, Vol.135 (10), p.2536-2538

2015

Volltextzugriff (PDF)

Intravenous immunoglobulin-induced eczematous dermatitis treated with dupilumab

JAAD Case Reports, 2024-07, Vol.49, p.102-105

2024

Volltextzugriff (PDF)

Recent advances in understanding ichthyosis pathogenesis [version 1; peer review: 2 approved]

F1000 research, 2016, Vol.5, p.1497

2016

Volltextzugriff (PDF)

Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis

Journal of investigative dermatology, 2015-12, Vol.135 (12), p.3041-3050

2015

Volltextzugriff (PDF)

Keratoacanthoma: Clinical and histopathologic features of regression

Journal of the American Academy of Dermatology, 2012-11, Vol.67 (5), p.1008-1012

2012

Volltextzugriff (PDF)

Cutaneous mosaicism: Special considerations for women

International journal of women's dermatology, 2021-12, Vol.7 (5), p.539-544

2021

Volltextzugriff (PDF)

How Efforts to Understand Somatic Mosaicism Will Impact Dermatology

Journal of investigative dermatology, 2024-03, Vol.144 (3), p.453-455

2024

Volltextzugriff (PDF)

Cutaneous and hepatic vascular lesions due to a recurrent somatic GJA4 mutation reveal a pathway for vascular malformation

HGG advances, 2021-04, Vol.2 (2), p.100028, Article 100028

2021

Volltextzugriff (PDF)

Mosaicism in genodermatoses

Clinics in dermatology, 2020-07, Vol.38 (4), p.408-420

2020

Volltextzugriff (PDF)

Palmoplantar Keratoderma in Costello Syndrome Responsive to Acitretin

Pediatric dermatology, 2017-03, Vol.34 (2), p.160-162

2017

Volltextzugriff (PDF)

1 – 25 von 175

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(154)
Mit Volltextzugriff
(148)

Publikationsform

Sprache

Englisch
(174)
Koreanisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

GNA14 Somatic Mutation Causes Congenital and Sporadic Vascular Tumors by MAPK Activation

Second-Hit Somatic Mutations in Mevalonate Pathway Genes Underlie Porokeratosis

Associations between ichthyosis and mood disorders: A case-control study in the All of Us Research Program

Topical cholesterol/lovastatin for the treatment of porokeratosis: A pathogenesis-directed therapy

Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a Child

Association of Somatic ATP2A2 Damaging Variants With Grover Disease

CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

Second-Hit, Postzygotic PMVK and MVD Mutations in Linear Porokeratosis

Somatic Mutations in NEK9 Cause Nevus Comedonicus

Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia

More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations

Somatic p.T771R KDR (VEGFR2) Mutation Arising in a Sporadic Angioma During Ramucirumab Therapy

Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia

Improving outcomes for harlequin ichthyosis

Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines

Somatic V600E BRAF Mutation in Linear and Sporadic Syringocystadenoma Papilliferum

Intravenous immunoglobulin-induced eczematous dermatitis treated with dupilumab

Recent advances in understanding ichthyosis pathogenesis [version 1; peer review: 2 approved]

Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis

Keratoacanthoma: Clinical and histopathologic features of regression

Cutaneous mosaicism: Special considerations for women

How Efforts to Understand Somatic Mosaicism Will Impact Dermatology

Cutaneous and hepatic vascular lesions due to a recurrent somatic GJA4 mutation reveal a pathway for vascular malformation

Mosaicism in genodermatoses

Palmoplantar Keratoderma in Costello Syndrome Responsive to Acitretin

Suchergebnisse filtern