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Research 91–120 of 675
- A Clinical Study To Evaluate The Efficacy Of Selected Traditional Hair Pack For Dandruff
- A Review of the Most Common Dermatologic Conditions and their Debilitating Psychosocial Impacts
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- HX01 Avicenna: an influence on modern dermatology
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Skin Development and Disease: A Molecular Perspective
- Novel Technologies for Exploring the Skin–Brain Axis
- A Decade With Sheehan's Syndrome: A Case Report and Personal Experience.
- Dermatoses in Postmenopausal Women in a Tertiary Health Care Center of Bihar: A Prospective Cross-Sectional Study
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- COVID-19 pandemic and teledermatology in low-income regions
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Dermatologic Problems of Older Women
- Skin diseases and conditions among students of a medical college in southern India
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Endocrine-skin interactions
- Psychodermatology
- The Role of Medical Language in Changing Public Perceptions of Illness
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Topical use of systemic drugs in dermatology: A comprehensive review
- The Impact of Bariatric Surgery on the Development and Progression of Dermatologic Diseases: A Narrative Review
- Pathologies of the skin and its appendages in endocrine diseases
- Congenital Atrichia: A Case Report
- Comparison of Complications after Coronavirus Disease and Seasonal Influenza, South Korea
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Dermatological drugs and topical agents
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome