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Research 421–450 of 1000+
- Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome
- Anthropometric Indices and Clinical Manifestations After Gluten Free Diet Therapy and Nutritional Education in Pediatric Patients with Celiac Disease
- Frontal fibrosing alopecia, clinical and histopathological characteristics of mexican patients: an original research study and review of literature
- Polycystic Ovarian Syndrome - A Pain for Young Women? An Autobiographical Case Studies
- Modeling the pharmacodynamics of nandrolone doping drug and implications for anti‐doping testing
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- Poster Abstracts
- Plasmaproteinbindung endogener Glucocorticosteroide und deren Einfluss auf Haar- und Speichelkonzentrationen
- Genetic Defects of Female Sexual Differentiation
- 217 The adenosine-generating ecto-enzyme CD73 regulates human hair growth
- 14 Rhytidectomy
- 皮膚組織の再生に向けた皮膚由来幹細胞に関する研究
- Immunopathogenesis of Primary Cicatricial Alopecia
- Teriflunomide efficacy, safety and tolerability in patients with relapsing forms of multiple sclerosis
- Wound healing
- Surgical Management of Leukotrichia
- Abstracts Pt.30
- Syndromes of Severe Insulin Resistance (SSIRs)
- National scientific medical meeting 1996 abstracts
- The Angiosome Theory, Flap Delay, and Scalp Surgery
- Cutaneous signals of immune system disease
- AMERICAN SOCIETY FOR DERMATOLOGIC SURGERY, INC.
- The role of integrin alphavbeta6 in impaired wound healing and hair follicle regeneration
- Tumour regression predicts higher risk of sentinel node involvement in thin cutaneous melanomas
- Sex steroid synthesis in human skin in situ: The roles of aromatase and steroidogenic acute regulatory protein in the homeostasis of human skin
- Insight into Reepithelialization: How Do Mesenchymal Stem Cells Perform?
- The effects of extended photoperiod and warmth on hair growth in ponies and horses at different times of year
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Donor Site Preservation and Long-Term Management in Follicular Unit Extraction (FUE): A Structured Clinical Framework for Surgical Planning and Complication Prevention