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Research 31–60 of 1000+
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Alopecia in Children: The Most Common Causes
- The histopathology of alopecia areata in vertical and horizontal sections
- Bridging psychoneuroimmunology and homeopathy: Modulating the cellular and emotional cascades in refractory alopecia
- Multiple Autoimmune Syndrome With Alopecia Universalis and Immune Thrombocytopenic Purpura
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- “Case Report : Early Congenital Syphilis”
- Molecular basis of congenital atrichia in humans and mice.
- Dermatopathology and molecular genetics
- Hair Loss in Children
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Le gène<i>hairless</i>de la souris
- British Hair and Nail Society
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Disorders of hair in children
- Hairless is a nuclear receptor corepressor essential for skin function
- Congenital atrichia with papular lesions
- Hair Loss in Children
- Hair loss in elderly women
- Hair Disorders
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- An Excellent Response to Tofacitinib in a Pediatric Alopecia Patient: A Case Report and Review.
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- British Association of Dermatologists living guideline for managing people with alopecia areata 2024
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Polarized microscopy in genetic hair disorders: case series
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita