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- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Ichthyosis with confetti: clinics, molecular genetics and management
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Bad Hair Days: A Clinical and Trichoscopic Evaluation of Scalp Lesions
- Keratin disorders: from gene to therapy
- Secondary cicatricial and other permanent alopecias
- The Genetics of Human Skin Disease
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Ichthyosis
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Trichoscopy in genetic hair shaft abnormalities
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Oral retinoids-present status
- Group IID, IIE, IIF and III secreted phospholipase A2s