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Research 331–360 of 1000+
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Actinic Keratosis: Risk Factors, Clinical, Diagnosis and Therapeutics Aspects. Part I
- Flares of systemic lupus erythematosus during pregnancy and the puerperium: prevention, diagnosis and management
- Safety and efficacy of tavaborole (AN2690), a novel boron-based molecule, in 3 phase II trials for the topical treatment of toenail onychomycosis
- Analysis of Gene Expression in Isolated Single Hair Follicles: An Approach Using Semiquantitative Reverse-Transcriptase—Polymerase Chain Reaction
- Hydrogels: current biomedical applications and future directions
- The Diagnostic Value of Serum Ferritin in Telogen Effluvium
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Epidermal cyst of temporal bone as a delayed complication of myringoplasty
- Molecular Insight of Active Plant-Based Drug Molecules for the Treatment of PCOS
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- Alopecias
- Diagnosis, treatment, and long‐term outcomes of pediatric pemphigus: a retrospective study at tertiary medical centers
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Emerging Diagnostic and Therapeutic Potentials of Human Hair Proteomics
- Nanocarrier Systems for Transdermal Drug Delivery
- Psychophysiological Mechanisms of Stress Impact on Hair Loss Processes
- Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- Metabolomic and lipidomic atlas of human hair across its length
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- Delayed Diagnosis of Ectopic Thyroid Due to Ignored Borderline Result of Newborn Screening for Congenital Hypothyroidism
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Diagnostic Modalities in Trichology - An Update
- Molecular basis of androgen insensitivity
- Molecular basis of hair cell loss
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Biological Determinants of Hair Quality: An Integrated Review of Nutritional, Molecular, and Environmental Factors Supporting Hair Longevity
- 414 A fitst-in-human study of BLZ-100 (tozuleristide) demonstrates tolerability and fluorescence contrast in skin cancer
- Preliminaries