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Research 901–930 of 1000+
- Monilethrix in three generations
- Management of folliculitis decalvans: The EADV task force on hair diseases position statement
- Nilotinib-induced generalized keratosis pilaris: Report of a rare case
- A rare case of multiple keratoacanthomas treated with oral acitretin and intralesional methotrexate
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Eruptive vellus hair cysts: An underdiagnosed entity
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Cutaneous manifestations of endocrine diseases in children
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Enhancing Hair Regrowth in Pediatric Morphea en Coup de Sabre by Fractional CO<sub>2</sub> Laser‐Assisted Exosome Delivery
- Avian-Inspired Analogies in Dermatology
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Pruritus in Lichen Planopilaris and Frontal Fibrosing Alopecia—Clinical Characteristics and Dermoscopic Correlations
- Pruritic Trichostasis Spinulosa: A Rare Variant
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- Adnexotropic Variants of the Interface Dermatitides: A Review
- Monilethrix – Case report of a rare disease
- Frontal fibrosing alopecia
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Discreet monilethrix: De novo mutation on the example of polish families
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- The Use of Janus Kinase Inhibitors for Primary Neutrophilic Cicatricial Alopecias
- Exploring Acne Treatments: From Pathophysiological Mechanisms to Emerging Therapies
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Diagnostic utility of dermatoscopy in hydroquinone‐induced exogenous ochronosis