Search
for
Sort by
Research 31–60 of 1000+
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Congenital atrichia associated with situs inversus and mesocardia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Morphological Approach to Hair Disorders
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital hair loss disorders: Rare, but not too rare
- Dermatopathology and molecular genetics
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Disorders of hair in children
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Hairless is a nuclear receptor corepressor essential for skin function
- Hair follicles and their role in skin health
- Le gène<i>hairless</i>de la souris
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetics of Structural Hair Disorders
- Hair loss in infancy and childhood
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Hair loss and its management in children
- Diseases of Periocular Hair
- Madarosis
- The Role of Histone Demethylases in Disease
- Footprints of the EADV: a meeting report from the 17th Congress of the European Academy of Dermatology and Venereology
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Reply
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Utility of trichoscopy