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Research 91–120 of 189
- Caffeine Induces Autophagy and Apoptosis in Auditory Hair Cells via the SGK1/HIF-1α Pathway
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Aplasia cutis congenita on lumbosacral area
- Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial
- Insulin-like Growth Factor 1 (IGF-1) in Hair Regeneration: Mechanistic Pathways and Therapeutic Potential
- E-Poster
- Risk of Safety Events in Vitiligo Patients: A Retrospective Real‐World Data Study in the US
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments
- Multifunctional Self-Assembled Peptide Hydrogels for Biomedical Applications
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Fresh Umbilical Cord Blood—A Source of Multipotent Stem Cells, Collection, Banking, Cryopreservation, and Ethical Concerns
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Episodic Neuropathic-Like Musculoskeletal Pain Associated With Ritlecitinib Therapy in Alopecia Universalis: A Case Report
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Epidemiology and burden of alopecia areata in Taiwan: a systematic review
- Use of Platelet Rich Plasma in Otolaryngology-Review Article
- Comorbidities in alopecia areata: A systematic review and meta-analysis
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ
- ONKOLOGIA OKULISTYCZNA WCZORAJ I DZIŚ
- AUTOLOGOUS FAT GRAFTING UPDATE. PRESENTATION OF OWN RESULTS IN FACIAL REGENERATION
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Syndromes of Severe Insulin Resistance (SSIRs)