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Research 571–600 of 1000+
- Diagnostic dilemma: Multiple Autoimmune Syndrome versus incomplete Graham-Little-Piccardi-Lassueur Syndrome overlap mixed connective tissue disease
- Management of Pediatric Alopecia Universalis through Ayurveda: An experience
- Endocrine evaluation of hirsutism
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- From Bald to Bold: Reversal of Alopecia Totalis in an Adolescent Using Dupilumab Monotherapy
- Randomised controlled study for comparing the efficacy of tretinoin 0.05% cream alone versus tretinoin combined with microdermabrasion in adult patients of alopecia areata
- Real-life effectiveness and safety of baricitinib in 17 Japanese patients with alopecia areata: a 60-week single center study
- A falling out following minoxidil: Telogen effluvium
- An Updated in the Management of Alopecia Areata
- Guidelines for the management of alopecia areata
- The Role of Diet as an Adjuvant Treatment in Scarring and Nonscarring Alopecia
- A Case of Inflammatory Nonscarring Alopecia Associated With the Tyrosine Kinase Inhibitor Nilotinib
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Rejuvenation of the Male Brow
- An evidence based case report of alopecia areata treated with individualised homoeopathic medicine
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- An excellent response to tofacitinib in a Brazilian adolescent patient with alopecia areata: A case report and a review of the literature
- Phosphodiesterase inhibitors and prostaglandin analogues in dermatology: A comprehensive review
- Management of congenital ichthyoses: European guidelines of care, part two
- Hirsutism: diagnosis and treatment
- Drugs and Androgenetic Alopecia: What to look out for
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Diffuse face and ear hypertrichosis caused by 5% topical minoxidil in an adult woman with spontaneous resolution
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Therapeutic Response of Alopecia Areata‐Associated Nail Changes to Baricitinib
- Management of Alopecia and Onychomycosis in a Lupus Patient
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- Metastatic Embryonal Cell Carcinoma with High Testosterone and Absence of Secondary Sexual Characteristics
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation