Search
for
Sort by
Research 121–150 of 1000+
- MULTIPLE DEFECTS OF THE HAIR SHAFT IN NETHERTON'S DISEASE.
- The keratins and their disorders
- Oral Retinoids in Dermatology
- Skin diseases in the alpaca (<i>Vicugna pacos</i>): a literature review and retrospective analysis of 68 cases (Cornell University 1997–2006)
- 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
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Sarcoidosis: Are there differences in your skin of color patients?
- 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
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- A STABILITY-INDICATING HPLC METHOD TO DETERMINE FINASTERIDE IN A TABLET FORMULATION
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Sjogren-Larsson syndrome
- 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
- Inherited Disorders of Corneocyte Proteins
- 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
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Sjogren-Larsson Syndrome
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention