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Research 421–450 of 1000+
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Monilethrix in three generations
- Immunologic findings in central centrifugal cicatricial alopecia
- Bachmann–Bupp syndrome and treatment
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Monilethrix – Case report of a rare disease
- Cure of alopecia areata after eradication of Helicobacter pylori: a new association?
- Erosive Pustular Dermatosis of the Scalp: A Clinicopathologic Study of Fifty Cases
- Treatment of Frontal Fibrosing Alopecia and Lichen Planopilaris
- Perifolliculitis Capitis Abscedens et Suffodiens in an 18-Year-Old Aboriginal Canadian Patient: Case Report and Review of the Literature
- (16) The Graham-Little syndrome Follicular keratosis with cicatricial alopecia
- Follicular Keratosis of the Chin Treated with 1.24R‐Dihydroxyvitamin D3 Ointment
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- KERATOSIS FOLLICULARIS WITH UNUSUAL INVOLVEMENT OF THE SCALP
- Optical coherence tomography-assisted diagnosis of follicular keratosis of the chin
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- 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
- [Electrophoretic studies of acid mucopolysaccharides in skin, prekeratin of hair follicles and in keratoses of wool].
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Mechanical and biological properties of keratose biomaterials
- 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
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- Keratolysis in a patient with pemphigus vulgaris
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome