• <em>De Novo</em> Mutation in <em>KRT1</em> Leads to Epidermolytic Palmoplantar Keratoderma: from Chinese Traditional Treatment to Prenatal Diagnosis Using Whole-Exome Sequencing-Plus
• "African" acral keratoderma: Further evidence for a single entity. A retrospective study of 42 patients
• A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma
• A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma
• A Japanese case of Vorner-type palmoplantar keratoderma caused by a novel KRT1 variant
• A novel heterozygous missense mutation of the desmoglein 1 gene in a Chinese family with diffuse nonepidermolytic palmoplantar keratoderma
• A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma
• A survey study with assessment of esophageal screening and genetic counseling in patients with Howel-Evans syndrome
• Acquired diffuse palmoplantar erythema with keratoderma in Chinese patients with pustular psoriasis: A predictor for IL36 receptor antagonist c.115+6T>C mutation?
• Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
• An in-frame 18 bp deletion in linker domain L1 of KRT9 identified in a Japanese patient with epidermolytic palmoplantar keratoderma
• An Uncommon Presentation of Darier-White Disease with Hystrix-like Palmoplantar Keratoderma
• Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
• Anatomical characterization and technological properties of Pterogyne nitens wood, a very interesting species of the Brazilian Caatinga biome
• Annular Epidermolytic Ichthyosis Mimicking Greither Disease: A Case Report and Literature Review
• Annular epidermolytic ichthyosis with palmoplantar keratosis: a unique phenotype associated with interfamilial phenotypic heterogeneity
• Atopic keratoconjunctivitis with corneal ulcer. Case report
• Atypical epidermolytic palmoplantar keratoderma is a minimal phenotypic variant of epidermolytic ichthyosis: A new insight from ultrastructural findings
• Bothnian Palmoplantar Keratoderma: Further Delineation of the Associated Phenotype
• Cleavage of the pseudoprotease iRhom2 by the signal peptidase complex reveals an ER-to-nucleus signaling pathway
• Clinical and biological perspectives on non-canonical esophageal squamous cell carcinoma in rare subtypes
• Clinical and Histopathological Findings in Palmoplantar Lichen Planus Presenting as Diffuse Keratoderma
• Coexistence of Lichen Planus Pemphigoides, Palmoplantar Keratoderma of Unna-Thost, and Atopic Dermatitis
• Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report
• De Novo Mutation in KRT1 Leads to Epidermolytic Palmoplantar Keratoderma: from Chinese Traditional Treatment to Prenatal Diagnosis Using Whole-Exome Sequencing-Plus
• Dermoscopic furrow ink test of the palmar lesion in loricrin keratoderma
• Diagnosis and Management of Inherited Palmoplantar Keratodermas
• Diffuse palmoplanta keratoderma: a pedigree with 23 cases
• Diffuse Palmoplantar Keratoderma, Onychodystrophy, universal Hypotrichosis and Cysts
• Diffuse palmoplantar keratotic papules and melanosis
• ECFS standards of care on CFTR-related disorders: Identification and care of the disorders
• Epidermolytic palmoplantar keratoderma of Vorner
• Esophageal Cancer: An Updated Review
• Esophageal Manifestations of Dermatological Diseases, Diagnosis and Management
• Evaluation and Management of Premalignant Conditions of the Esophagus: A Systematic Survey of International Guidelines
• Exome sequencing identifies a KRT9 pathogenic variant in a Chinese pedigree with epidermolytic palmoplantar keratoderma
• First Extensive Microscopic Study of Butternut Defense Mechanisms Following Inoculation with the Canker Pathogen Ophiognomonia clavigignenti-juglandacearum Reveals Compartmentalization of Tissue Damage
• Focal Palmoplantar Keratoderma and Gingival Keratosis Caused by a KRT16 Mutation
• Focal palmoplantar keratoderma in a patient with the KRT6B mutation
• Fossil evidence of tylosis formation in Late Devonian plants
• Generalized epidermolytic ichthyosis with palmoplantar hyperkeratosis
• Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma
• Genetic deletion of amphiregulin restores the normal skin phenotype in a mouse model of the human skin disease tylosis
• Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients
• Hereditary Palmoplantar Keratoderma: A Practical Approach to the Diagnosis
• Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing
• Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma
• Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome <em>via</em> Exome Sequencing and Low-Coverage Whole-Genome Sequencing
• Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing
• Increase in ring width, vessel number and δ18O in olive trees infected with Xylella fastidiosa
• Investigating iRHOM2-Associated Transcriptional Changes in Tylosis With Esophageal Cancer
• Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients
• iRHOM2: A Regulator of Palmoplantar Biology, Inflammation, and Viral Susceptibility
• Isolated hereditary diffuse palmoplantar keratoderma in Hong Kong Chinese patients: a case series
• Japanese case of Bothnian-type palmoplantar keratoderma with a novel missense mutation of p.Trp35Ser in extracellular loop A of aquaporin-5
• Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review
• Mal de Meleda
• Mechanics hands in patients with antisynthetase syndrome: 25 cases
• Mechanistic insight on the role of iRhom2-TNF-α-BAFF signaling pathway in various autoimmune disorders
• Molecular Modeling of Pathogenic Mutations in the Keratin 1B Domain
• Morpho-Anatomical Traits and Soluble Sugar Concentration Largely Explain the Responses of Three Deciduous Tree Species to Progressive Water Stress
• Mutations in the highly conserved 1A rod domain of keratin 9 responsible for epidermolytic palmoplantar keratoderma in four Chinese families
• Nagashima-Type Palmoplantar Keratosis with Compound Heterozygous Mutations in SERPINB7
• Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads
• Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma
• Novel KRT9 missense mutation in a Japanese case of epidermolytic palmoplantar keratoderma
• Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian family
• Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes
• Novel Splice-Site Mutation of KRT1 Underlies Diffuse Palmoplantar Keratoderma in a Large Chinese Pedigree
• Oral verruciform hyperkeratotic lesions indicating the presence of plantar or palmoplantar keratodermas
• Pain Hypersensitivity in SLURP1 and SLURP2 Knock-out Mouse Models of Hereditary Palmoplantar Keratoderma
• PAIN HYPERSENSITIVITY IN SLURP1 AND SLURP2 KNOCKOUT MOUSE MODELS OF HEREDITARY PALMOPLANTAR KERATODERMA
• Palmoplantar Hyperkeratosis and Strong Family History of Esophageal Cancer: Tylosis or Not?
• Palmoplantar keratoderma Bothnia type with acrokeratoelastoidosis-like features due to AQP5 mutations
• Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B
• Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia
• Palmoplantar keratoderma, pseudo-ainhum and knuckle pads in an African patient: A case report
• Pathogen-induced hydraulic decline limits photosynthesis and starch storage in grapevines (Vitis sp.)
• Pathological mutations reveal the key role of the cytosolic iRhom2 N-terminus for phosphorylation-independent 14-3-3 interaction and ADAM17 binding, stability, and activity
• Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma
• Physiological and developmental disturbances caused by Botryosphaeria dieback in the annual stems of grapevine
• Pityriasis Rubra Pilaris
• Pityriasis rubra pilaris post-infection due COVID-19: case report
• Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders
• RHBDF2-Regulated Growth Factor Signaling in a Rare Human Disease, Tylosis With Esophageal Cancer: What Can We Learn From Murine Models?
• Risk factors for esophageal cancer: emphasis on infectious agents
• Second-line antitubercular therapy with ethionamide and pyrazinamide causing pellagroid dermatitis presenting as diffuse palmoplantar keratoderma
• Spontaneous clinical remission of Nagashima-type palmoplantar keratoderma in a patient of Korean descent with a heterozygous SERPINB7 mutation
• Synchronized Efficacy and Mechanism of Alkaline Fertilizer and Biocontrol Fungi for <em>Fusarium</em><em>oxysporum</em> f. sp. <em>cubense</em> Tropical Race 4
• The Proteolytic Network in Palmoplantar Keratoderma: SERPINA12 Joins the Family
• Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma
• Tissue-specific role of RHBDF2 in cutaneous wound healing and hyperproliferative skin disease
• Two Italian Patients with <em>ELOVL4</em>-Related Neuro-Ichthyosis:  Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization
• Two novel mutations of SERPINB7 in eight cases of Nagashima-type palmoplantar keratosis in the Chinese population
• Two patients with Papillon-Lefèvre syndrome without periodontal involvement of the permanent dentition
• Tylosis associated with squamous cell carcinoma of the oesophagus (TOC): Report of an African family with a novel RHBDF2 variant
• Uncommon Endoscopic Findings in a Tylosis Patient: A Case Report
• Vohwinkel syndrome: ichthyosiform variant in a family
• Whole Exome Sequencing Identified a Novel Mutation of the RHBDF2 Gene in a Chinese Family of Tylosis with Esophageal Cancer
• Xylem Vessel Diameter Affects the Compartmentalization of the Vascular Pathogen <em>Phaeomoniella chlamydospora</em> in Grapevine