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Research 871–900 of 1000+
- British Society for Dermatopathology: Summaries of Papers
- A Case of Hair Structure Abnormality Associated with Iron Deficiency Anaemia
- Poster session
- Eye and skin disease
- National scientific medical meeting 1996 abstracts
- Antiulcer drugs
- Cutaneous signals of immune system disease
- Cytostatics and immunosuppressive drugs
- Self-medication by Jockeys
- 187 Protective Effect of DA-9401 on Acute use of Finasteride on Sprague–Dawley Rats
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Skin precancer.
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Therapeutic effects of minoxidil high extra combination therapy in patients with androgenetic alopecia.
- [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Abstract 10845: Spontaneous Coronary Artery Dissection as the Primary Presentation of Ana-Negative Lupus
- [Treatment of androgenic alopecia with minoxidil].
- Adult bone-marrow-derived mesenchymal stem cells contribute to wound healing of skin appendages
- Trichoscopy in genetic hair shaft abnormalities
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Analysis of breast health outcomes in women on oral 5-alpha reductase inhibitors: A single-center retrospective cohort study
- [The Netherton syndrome with alopecia and prolinuria].
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia