Search
for
Sort by
Research 541–570 of 1000+
- Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Association of Sensorineural Hearing Loss in Patients With Alopecia Areata
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Clinical Hair Loss: Diagnosis and Treatment
- Hair India 2010
- Alopecia areata: The disease of hairless patches on the scalp and any area of face
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Polycystic ovarian syndrome: an updated review of pathophysiology, clinical features, biomarkers, and management
- Upadacitinib in dermatologic therapy: Emerging evidence and expanding indications
- A Survey of Women Polycystic Ovarian Disease (PCOD)
- A Survey of Women Polycystic Ovarian Disease (PCOD)
- Polycystic Ovary Syndrome: Pathophysiology, Clinical Manifestations and Emerging Therapeutic Approaches
- A Comprehensive Review On: Polycystic Ovarian Disease and It’s Impact on Health Care of Female
- Alopecia Areata Treatment: Past, Present, and Future
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Clinical Snippets
- 원저 : 유전성 안드로겐탈모증의 임상적 고찰(제6보)
- Book review
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- The Rotterdam Study: 2018 update on objectives, design and main results
- The Rotterdam Study: 2016 objectives and design update
- The Rotterdam Study: 2012 objectives and design update
- Epidemiology and burden of alopecia areata: a systematic review
- Obesity and the skin
- Autoimmune Disease Induction in a Healthy Human Organ: A Humanized Mouse Model of Alopecia Areata
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature