• A Case of Eczematoid Graft-Versus-Host Disease
• A Case of IFAP Syndrome with Severe Atopic Dermatitis
• A Cross-Sectional Study Comparing Application of Hanifin and Rajka Criteria in Indian Pediatric Atopic Dermatitis Patients to that of Other Countries
• A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis
• A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad
• A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia, and photophobia syndrome
• A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
• A Novel Mutation in the <em>MBTPS2</em> Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
• A Novel Mutation in the MBTPS2 Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
• A pilot trial of dermoscopy as a rapid assessment tool in pediatric dermatoses
• A Rare Case of KID Syndrome: The Use of Hydrosurgery and Strategies for Antiseptic Wound Care
• Allogeneic split-skin grafting in stem cell transplanted patients
• An intronic splice-site variant in MBTPS2 underlies ichthyosis follicularis with atrichia and photophobia syndrome
• Atrichia, ichthyosis, follicular hyperkeratosis, chronic candidiasis, keratitis, seizures, mental retardation and inguinal hernia: a severe manifestation of IFAP syndrome?
• Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome
• Bazex-Dupré-Christol syndrome: review of clinical and molecular aspects
• Cholesterol metabolsim defect associated with Conradi-Hunerman-Happle syndrome
• Chronic cutaneous graft-versus-host disease manifesting as calcinosis cutis universalis on a background of widespread sclerodermatoid changes
• Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
• Congenital Ichthyosis in 14 Great Dane Puppies With a New Presentation
• Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?
• Conradi-Hünermann-Happle syndrome (X-linked dominant chondrodysplasia punctata) confirmed by plasma sterol and mutation analysis
• Conradi-Hünermann-Happle syndrome: Clinical and trichoscopic findings
• De novo mutations in monilethrix
• Differentiation-associated localization of small proline-rich protein in normal and diseased human skin
• Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
• Dissecting cellulitis (Perifolliculitis Capitis Abscedens et Suffodiens): a comprehensive review focusing on new treatments and findings of the last decade with commentary comparing the therapies and causes of dissecting cellulitis to hidradenitis suppura
• Eccrine squamous metaplasia and periadnexal granulomas: new cutaneous histopathologic findings in cardiofaciocutaneous syndrome
• Epidermolytic hyperkeratosis within infundibular cysts
• Expanding the phenotype of IFAP/BRESECK syndrome: a new case with severe hypogammaglobulinemia
• Expression of trichohyalin in dermatological disorders: a comparative study with involucrin and filaggrin by immunohistochemical staining
• Extending the phenotypic spectrum of keratitis-ichthyosis-deafness syndrome: report of a patient with GJB2 (G12R) Connexin 26 mutation and unusual clinical findings
• Follicular Dowling Degos disease: a rare variant of an evolving dermatosis
• Follicular Graft Vs Host Reaction: A Rare Presentation
• Follicular toxic pustuloderma associated with allopurinol
• Genetic syndrome with ichthyosis: congenital ichthyosis, follicular atrophoderma, hypotrichosis, and woolly hair; second report
• Harlequin ichthyosis in a HanWoo calf
• Hereditary mucoepithelial dysplasia: clinical, ultrastructural and genetic study of eight patients and literature review
• Hidradenitis suppurrativa (acne inversa) as a systemic disease
• High-fat diet induces a predisposition to follicular hyperkeratosis and neutrophilic folliculitis in mice
• Histologic features of alopecias: part II: scarring alopecias
• Hodgkin Lymphoma in a Patient With IFAP Syndrome: A Case Report and Review of Literature
• Ichthyoses-A Clinical and Pathological Spectrum from Heterogeneous Cornification Disorders to Inflammation
• Ichthyosiform dermatosis in a Soft-Coated Wheaten Terrier
• Ichthyosiform mycosis fungoides
• Ichthyosiform mycosis fungoides: an atypical variant of cutaneous T-cell lymphoma
• Ichthyosis and keratotic follicular plugs containing dystrophic calcification in newborns: distinctive histopathologic features of x-linked dominant chondrodysplasia punctata (Conradi-Hunermann-Happle syndrome)
• Ichthyosis congenita type IV: a new case resembling diffuse cutaneous mastocytosis
• Ichthyosis fetalis in a cross-bred lamb
• Ichthyosis fetalis in Polled Hereford and Shorthorn calves
• Ichthyosis follicularis syndromes in patients with mutations in GJB2
• Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
• Ichthyosis follicularis with alopecia and photophobia syndrome (IFAP): A Case Report
• Ichthyosis Follicularis with Alopecia and Photophobia Syndrome with Coexisting Palmoplantar Keratoderma Treated with Acitretin
• Ichthyosis follicularis, alopecia and photophobia syndrome (IFAP): report of the first case with ocular and cutaneous manifestations in Brazil with a favorable response to treatment
• Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
• Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India
• Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
• Ichthyosis follicularis, alopecia, and photophobia syndrome: a case report and a pathological insight into pilosebaceous anomaly
• Ichthyosis follicularis, atrichia and photophobia (IFAP) and hereditary mucoepithelial dysplasia: Two syndromes that share a common clinical spectrum
• Ichthyosis follicularis: a case report and review of the literature
• Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing
• Increased Hemichannel Activity Displayed by a Connexin43 Mutation Causing a Familial Connexinopathy Exhibiting Hypotrichosis with Follicular Keratosis and Hyperostosis
• Inherited ichthyoses: a review of the histology of the skin
• Keratitis-ichthyosis-deafness (KID) syndrome
• Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa
• Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triad
• Keratosis follicularis spinulosa decalvans in a female
• Keratosis Pilaris
• Keratosis Pilaris
• Keratosis pilaris revisited: is it more than just a follicular keratosis?
• Keratosis pilaris: a common follicular hyperkeratosis
• Keratosis pilaris: an update and approach to management
• KID Syndrome and Hidradenitis Suppurativa: A Rare Association Responding to Surgical Treatment
• Kid Syndrome or Keratitis Ichthyosis-Deafness-syndrome: report of a case
• Late-Onset Nevus Comedonicus With Follicular Epidermolytic Hyperkeratosis-Case Report and Review of the Literature
• Linear lesions reflecting lyonization in women heterozygous for IFAP syndrome (ichthyosis follicularis with atrichia and photophobia)
• Linear nevus comedonicus with epidermolytic hyperkeratosis
• Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients
• Matriptase regulates proliferation and early, but not terminal, differentiation of human keratinocytes
• MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans
• Multiple functions of the SNARE protein Snap29 in autophagy, endocytic, and exocytic trafficking during epithelial formation in Drosophila
• Novel MBTPS2 missense mutation causes a keratosis follicularis spinulosa decalvans phenotype: mutation update and review of the literature
• Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families
• Novel p.Glu519Gln missense mutation in ST14 in a patient with ichthyosis, follicular atrophoderma and hypotrichosis and review of the literature
• Pathophysiology of acne
• Pityriasis rubra pilaris
• Primary cutaneous follicle center lymphoma mimicking folliculitis
• Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation
• Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency
• Skin diseases in the alpaca (Vicugna pacos): a literature review and retrospective analysis of 68 cases (Cornell University 1997-2006)
• Surgical therapy in a patient with Keratosis-Ichthyosis-Deafness (KID) syndrome associated with follicular occlusion triad
• Syndrome of short stature, mental deficiency, microcephaly, ectodermal dysplasia, and multiple skeletal anomalies
• Trichothiodystrophy: ultrastructural studies of two patients
• Ulerythema ophryogenes and keratosis pilaris in a child with monosomy 18p
• Ultrastructural and molecular confirmation of the trichodysplasia spinulosa-associated polyomavirus in biopsies of patients with trichodysplasia spinulosa
• Viral-associated trichodysplasia secondary to antineoplastic treatment in a patient with lymphoblastic leukemia
• Waxy papules, infiltrated alopecic plaques, and shin ichthyosis
• Whorled follicular keratosis, scarring alopecia in ichthyosis follicularis atrichia with photophobia syndrome
• X-linked dominant chondrodysplasia punctata (Happle syndrome) with uncommon symmetrical shortening of the tubular bones