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Research 931–960 of 1000+
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Cutaneous extramedullary haematopoiesis: Implications in human disease and treatment
- Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- The Multiple Consequences of Obesity
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- Keratosis Pilaris and Scarring Alopecia
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- (16) The Graham-Little syndrome Follicular keratosis with cicatricial alopecia
- Follicular Keratosis of the Chin Treated with 1.24R‐Dihydroxyvitamin D3 Ointment
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Optical coherence tomography-assisted diagnosis of follicular keratosis of the chin
- <i>Malassezia</i> Display a Hyphae-like “Spaghetti-and-Meatballs” Configuration in Keratotic Plugs
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- Follicular keratotic diseases: a retrospective study of 50 cases in a tertiary care center of rural South India with dermoscopy and histopathology evaluation
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratosis follicularis spinulosa decalvans and acne keloidalis nuchae
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Keratosis follicularis spinulosa decalvans in a family
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications