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Research 901–930 of 1000+
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- A Comprehensive Review of Acne Vulgaris
- Dermatological problems of the puberty
- The Role of Diet as an Adjuvant Treatment in Scarring and Nonscarring Alopecia
- A Randomized Double-Blind, Placebo-Controlled Study to Evaluate the Anti-Skin-Aging Effect of LactoSporin – The Extracellular Metabolite from Bacillus coagulans (Weizmannia coagulans) MTCC 5856 in Healthy Female Volunteers
- Demographic Characteristics and Association of Serum Vitamin B12, Ferritin and Thyroid Function with Premature Canities in Indian Patients from an Urban Skin Clinic of North India: A Retrospective Analysis of 71 Cases.
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Anatomy and Physiology of Hair
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Management of Skin Toxicities in Cancer Treatment: An Australian/New Zealand Perspective
- Comparative study between mesotherapy and topical 5% minoxidil by dermoscopic evaluation for androgenic alopecia in male: A randomized controlled trial
- Overview of Nanocosmetics with Emphasis on those Incorporating Natural Extracts
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Baricitinib Safety for Events of Special Interest in Populations at Risk: Analysis from Randomised Trial Data Across Rheumatologic and Dermatologic Indications
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Inter-species differences in wound-healing rate: a comparative study involving primates and rodents
- Beyond cancer treatment: dermo-aesthetic and other wellness recommendations for breast cancer patients
- Expert recommendations on supportive skin care for non‐surgical and surgical procedures
- Nanomaterials in hair care and treatment
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Clinical recognition and management of alopecia in women of color,
- Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review