Results 171 to 180 of about 50,269 (341)
Kyrle's disease. Hyperkeratosis follicularis et parafollicularis in cutem penetrans
R Pajarre, M. Alavaikko
openalex +2 more sources
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edwin Cuperus +7 more
wiley +1 more source
Genetic Susceptibility to Periodontitis
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
Nevoid hyperkeratosis of the nipple and areola mammae: ineffectiveness of etretinate therapy
Ortonne Jp, P. El Baze, L Juhlin
openalex +2 more sources
Nicotine replacement lozenges: abuse-related hyperkeratosis of the lateral border of the tongue. A case report [PDF]
Kurt Naudi, D H Felix
openalex +1 more source
Focal Acral Hyperkeratosis [PDF]
Ji Yeon Byun +4 more
openaire +3 more sources
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
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
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
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

