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Research 241–270 of 1000+
- Scanning electron microscopic features of the ovine interdigital sinus
- Circumscribed alopecia areata incognita
- Atypical folliculitis caused by Malassezia spp. in immunosuppressed patients
- Integrative Homeopathic and Exosome-Assisted Management of Chronic Androgenetic Alopecia After Failure of Conventional Approaches
- A CASE STUDY OF LEECH THERAPY (JALAUKAVCHARAN) IN KHALITYA W. S. R. ALOPECIA AREATA
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Some progress in global existence of solutions to a higher-dimensional chemotaxis system modelling Alopecia Areata
- HAIR REJUVENATION THROUGH AYURVEDA: A REVIEW
- Isotretinoin-unresponsive acne as a sign of a congenital disorder: a case of 21-hydroxylase deficiency
- Attention Balanced Multi-Dimension Multi-Task Deep Learning for Alopecia Recognition
- Author response: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Concept and Management of Diffuse Hair Loss (Intithār al-Sha‘r) in the light of Unani medicine: A Review
- Steroidogenesis of the testis – new genes and pathways
- Established risk factors for coronary heart disease are unrelated to androgen-induced baldness in female-to-male transsexuals
- Telogen Effluvium after SARS-CoV-2 Infection: A Series of Cases and Possible Pathogenetic Mechanisms
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Frontal Fibrosing Alopecia Involving the Limbs Shows Inflammatory Pattern on Histology: A Review of 13 Cases
- Late onset nevus comedonicus of scalp: a rare site for an uncommon condition
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- DIVERSE CLINICAL PRESENTATIONS AND PATTERNS OF THYROID DISORDERS: A HOSPITAL-BASED CROSS-SECTIONAL STUDY
- 50832 Confetti variant of Alopecia Areata: A Single Center Retrospective Study to Describe a Novel Entity
- Scalp capillarectasia as a trichoscopic sign of COVID‐19‐associated telogen effluvium
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- The Genetics of Human Skin Disease
- Determinação de minoxidil em formulações farmacêuticas usando permanganometria
- Molecular histology in skin appendage morphogenesis
- Determinação de minoxidil em formulações farmacêuticas usando permanganometria
- Gelatin nanoparticles & nanocrystals for dermal delivery
- The Case of Paris and Helen Through Time, Society, and Anti-Aging Medicine
- A Rare Case Report of Congenital Adrenal Hyperplasia: 46XX at Tertiary Care Centre, Visnagar, North Gujarat.