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Research 481–510 of 1000+
- A study of endocrine profile in premenopausal women with hirsutism
- Telogen Effluvium
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Keratins: the hair shaft's backbone revealed
- Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games
- Drug-Induced Hair Changes
- Persistent hair growth during treatment with the EGFR inhibitor erlotinib
- Ichthyosis with confetti: clinics, molecular genetics and management
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- IMPORTANCE OF HAIR GROWTH IN HISUTISM: DIAGNOSIS AND TREATMENT
- From male PCOS to male endocrine-metabolic syndrome: a gender-neutral hypothesis
- Astragalus membranaceus and Cinnamomum cassia Stimulate the Hair Follicle Differentiation-Related Growth Factor by the Wnt/β-Catenin Signaling Pathway
- Alopecia and Thyroid Disease
- Telogen Effluvium: A Review
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Effect of Oral Minoxidil on Monilethrix
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- Molecular Genetics of Human Hair Diseases
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Medical and Professional Ethics: Spotlight on Cosmetic vs Non-Cosmetic Hair Transplant Surgery
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis