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Research 31–60 of 43
- Immunopathogenesis of Primary Cicatricial Alopecia
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Lichen Planopilaris
- Diagnostic Value of DermoscopicFindings of Hair and Scalp in Cicatricial Alopecia
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Comorbidities and Treatment Options for Acne Keloidalis Nuchae
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- Keratosis Follicularis Spinulosa Decalvans
- Common causes of hair loss – clinical manifestations, trichoscopy and therapy
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- Keratosis follicularis spinulosa decalvans in a family
- Primary Cicatricial Alopecias
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Unilateral keratosis pilaris atrophicans faciei mimicking follicular mucinosis
- Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation.
- Primary cicatricial alopecias
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Cicatricial Alopecias
- Keratosis follicularis spinulosa decalvans in a female
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Substance P in keratosis follicularis spinulosa decalvans