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Research 121–150 of 822
- Disorders of Keratinization
- Hair Shaft Videodermoscopy in Netherton Syndrome
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Retinoids and Keratinization
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Off-Label Uses of Topical Vitamin D in Dermatology: A Systematic Review
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Sjogren-Larsson syndrome
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
- Sjogren-Larsson Syndrome
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Skin Manifestations of Hypothyroidism-A Clinical Study
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- Collodion baby case series: the success of oral retinoic acid
- [Netherton's syndrome in two sisters].
- The urine as a diagnostic key for a homozygous EGFR mutation
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- A STUDY ON CUTANEOUS MANIFESTATIONS OF HYPOTHYROIDISM IN A TERTIARY HOSPITAL IN SOUTH INDIA
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions