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Research 331–360 of 1000+
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Biostimulatory Action of a Plant-Derived Protein Hydrolysate on Morphological Traits, Photosynthetic Parameters, and Mineral Composition of Two Basil Cultivars Grown Hydroponically under Variable Electrical Conductivity
- Case number 19th of perforating necrobiosis lipoidica worldwide
- The photosensitive patient: could it be pellagra?
- Delayed diagnosis of Kearns-Sayre syndrome in a 38-year-old male patient: a case report.
- Patchy presentation of central centrifugal cicatricial alopecia
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- 66-Year-Old Female with Itchy Scalp and Hair Loss
- Lateral Leg Pain in a 26-Year-Old Woman
- Dermoscopy in General Dermatology: A Practical Overview
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Liposomal systems as drug delivery vehicles for dermal and transdermal applications
- Congenital Adrenal Hyperplasia
- Kenogen
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Frontiers in alopecia areata pathobiology research
- Frequent downregulation of DMBT1 and galectin‐3 in epithelial skin cancer
- The cultural and philosophical concepts of cosmetics in beauty and art through the medical history of mankind
- A discourse on human hair fibers and reflections on the conservation of drug molecules
- The nocebo effect: A clinicians guide
- A study of etretinate alopecia
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- New steps forward in the neuroactive steroid field
- Diagnostic approach to low‐renin hypertension
- The role of androgen therapy
- Exploring the combination and modular characteristics of herbs for alopecia treatment in traditional Chinese medicine: an association rule mining and network analysis study
- Alopecia areata incognita
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Congenital adrenal hyperplasia
- Nonclassic 21-hydroxylase deficiency