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Research 721–750 of 1000+
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Werner's syndrome: incidental finding during pregnancy
- Physiology of Skin, Hair, and Nails as Differentiated by Sex and Age
- Alopecia Areata
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- Serum Levels of Transforming Growth Factor Beta1 (TGF β1) in Patients with Alopecia Areata.
- THE EFFECT OF AUTOLOGOUS PLATELET RICH PLASMA (PRP) ON PATIENTS WITH ALOPECIA AREATA
- Monilethrix – Case report of a rare disease
- In the quest to stymie time, will laboratory data stand up in man?
- Structural features and sites of expression of a new murine 65 kD and 48 kD hair-related keratin pair, associated with a special type of parakeratotic epithelial differentiation
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Common causes of paediatric alopecia
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Serenoa repens: Does it have any role in the management of androgenetic alopecia?
- A randomized controlled, single-observer blinded study to determine the efficacy of topical minoxidil plus microneedling versus topical minoxidil alone in the treatment of androgenetic alopecia
- A comparative study of efficacy of 5% minoxidil and 5% minoxidil plus platelet-rich plasma in same patient for treatment of androgenetic alopecia
- Role of low-level light therapy (LLLT) in androgenetic alopecia
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Trichotillomania: Neurobiology and treatment
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Alopecia and Associated Toxic Agents: A Systematic Review
- Involucrin: A Constituent of Cross-Linked Envelopes and Marker of Squamous Maturation
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms