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Research 61–90 of 95
- Importance of a multi-tiered treatment approach for intellectually and developmentally disabled patients with hidradenitis suppurativa
- Importance of a multi-tiered treatment approach for intellectually and developmentally disabled patients with hidradenitis suppurativa
- COLLAB: A Global Survey of Clinical and Laboratory Assessment in Alopecia Areata by Hair Specialists
- Acne Syndromes and Mosaicism
- TONGUE, RED
- Androgen Treatment in Adolescent Males With Hypogonadism
- Pigmentary mosaicism: An update
- Case Report: Penile Strangulation Secondary to Hair Tourniquet
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- TRANSMEDCON 2022: E-Poster Abstracts
- Analogs of human genetic skin disease in domesticated animals
- Congenital Trichomegaly of the Eyelashes
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Dermatoscopy of hair shaft disorders
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Dynamic expression of Runx1 in skin affects hair structure
- The Genetics of Human Skin Disease
- Epigenetic age estimation in saliva and in buccal cells
- Hair shaft disorders in children – An update
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Outcomes of paediatric patients with chronic liver disease in early adulthood: A heterogeneous, but representative, regional cohort study
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Biomedical applications of organoids in genetic diseases
- Diagnosis and Management of Alopecia Areata: A Saudi Expert Consensus Statement (2023)
- Association of Acne Tarda with Endocrinological Disorders
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes