Results 171 to 180 of about 50,269 (341)

A novel MBTPS2 missense variant identifying keratosis follicularis spinulosa decalvans in a case of neonatal erythroderma

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edwin Cuperus   +7 more
wiley   +1 more source

Genetic Susceptibility to Periodontitis

open access: yesJournal of Periodontal Research, EarlyView.
Aim: The aim of this narrative review was to identify genes carrying risk alleles associated with an increased risk of periodontitis and to place them in a biological context. Methods: The literature was reviewed based on predefined criteria. Results: The identified genes largely fall into functions linking immune response with tissue repair. The genes
Gesa M. Richter, Arne S. Schaefer
wiley   +1 more source

Focal Acral Hyperkeratosis [PDF]

open access: yesThe Ewha Medical Journal, 2021
Ji Yeon Byun   +4 more
openaire   +3 more sources

Cranial osteomyelitis in a patient with KID syndrome: Importance of thorough investigation in chronic wounds

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Michael Wolfgang Höner   +2 more
wiley   +1 more source

Comparative Analysis of the Tumour Mutational Burden in Erosive and Reticular Oral Lichen Planus

open access: yesOral Diseases, EarlyView.
ABSTRACT Objective Oral lichen planus (OLP) is a chronic inflammatory disease classified as an oral potentially malignant lesion. The erosive and reticular forms of OLP have the potential for malignant transformation, with no consistent data indicating that one form is more likely to undergo malignant transformation than the other.
Priscila Laiza Rubim Leão   +10 more
wiley   +1 more source

Bimekizumab plus topical photochemotherapy effective in palmoplantar pustulosis in a patient with hidradenitis suppurativa

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Neda Cramer   +3 more
wiley   +1 more source

Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the NIPAL4 Gene

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT We report on a novel pathogenic genetic variant in compound heterozygosis of the NIPAL4 gene c.396C>Gp.(Ile132Met); additionally, we comment on key clinical findings that contribute to the expansion of the EKVP phenotype in childhood.
Luis Fernando Sánchez‐Espino   +5 more
wiley   +1 more source

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