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Research 421–450 of 1000+
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Isolated Linear Discoid Lupus Erythematosus of Scalp Following Lines of Blaschko
- Treatments for Dissecting Cellulitis of the Scalp: A Systematic Review and Treatment Algorithm
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- An Approach to Detect Alopecia Areata Hair Disease Using Deep Learning
- Use of Videodermatoscopy in Scalp Disorders
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- An overview of scalp dermatoses in a tertiary care institute
- Body to scalp: Evolving trends in body hair transplantation
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Myotonic Dystrophy—A Progeroid Disease?
- Altered FGF expression profile in human scalp-derived fibroblasts upon WNT activation: implication of their role to provide folliculogenetic microenvironment
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- An ancestral recipe of “Champigny Saumure” to be used tepid by topical way could be useful to combat Patton-Lynch’s Erosive pustular dermatosis of the scalp
- Profile of Female Hyperandrogenism at the Medical Clinic II: About 19 Cases
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Current Genetics in Hair Diseases
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Analogs of human genetic skin disease in domesticated animals
- The Carcinogenesis of the Human Scalp: An Immunometabolic-Centered View
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- 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