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Research 691–720 of 1000+
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- The aetiology and pathogenesis of alopecia areata
- COLOCOLIZATION OF VITILIGO AND ALOPECIA AREATA
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Association of epidemiological and biochemical factors with premature graying of hair: A case–control study
- Hair Coloration by Gene Regulation: Fact or Fiction?
- Central centrifugal cicatricial alopecia: possible familial aetiology in two African families from South Africa
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Azathioprine‐induced alopecia and leukopenia associated with NUDT15 polymorphisms
- The Role of Cytochrome P-450 in Dermatology
- What is behind the ‘swarm of bees’ in alopecia areata
- Retinoids Putting the “A” in Alopecia
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A study of patterns of androgenetic alopecia in men: an Indian perspective
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- Controversial Concepts
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Prunus mira Koehne in Sichuan, China: Recorded History as a Medicine and Food, Modern Applications, Distribution, and Ethnobotanical Investigations
- Emerging Topics in Cardiometabolic and Psychologic Sequelae, Pathogenesis, and Treatment of Polycystic Ovarian Syndrome: A Review
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless