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Research 91–120 of 1000+
- The switch from patented medicine to the generic one: an option or a necessity?
- ChatGPT in medicine: Evaluating psoriasis patient concerns
- The reasons and solutions for lipsotrichia and pelada phenomenon
- The autoimmune basis of alopecia areata: A comprehensive review
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- An unusual presentation of X-linked adrenoleukodystrophy
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- Alopecia Areata with Renal Dysgenesis
- [Androgenetic alopecia].
- Hair Sciences: An interview with Dr. Rodney Sinclair on female pattern hair loss
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Hypotrichosis with juvenile macular dystrophy
- Proteomic Analysis of Single Hairs
- The Association Between Polycystic Ovary Syndrome and Its Dermatological Manifestations
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- 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
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology
- A Cross-Sectional Study on the Prevalence of Premature Canities Among University Students in the Eastern Province, Kingdom of Saudi Arabia