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Research 481–510 of 1000+
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- hKAP1.6 and hKAP1.7, Two Novel Human High Sulfur Keratin-Associated Proteins are Expressed in the Hair Follicle Cortex
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Genetics of Structural Hair Disorders
- Characterization of Human Keratin-Associated Protein 1 Family Members
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Androgenetic alopecia in adolescents.
- AN UPDATE OF HAIR SHAFT DISORDERS
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- Congenital atrichia and hypotrichosis
- Algorithm of Hair Restoration Surgery in Children
- Focal and Generalized Alopecia
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Nutritive Beeinflussung des Haarwachstums
- Androgenetic Alopecia: Stress of Discovery
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Diseases of the skin. Treatment of scalp disorders.
- PLCD1 and Pilar Cysts
- Diffuse hair loss in women.
- Analogs of human genetic skin disease in domesticated animals
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Inherited Disorders of the Hair
- Assessing the Impact of Alopecia on Quality of Life, Depression, and Self-Esteem in Saudi Arabia
- Treatment of cutaneous leiomyomas with botulinum toxin. Case report and review of literature
- Trichodystrophies: A hair-raising differential diagnosis
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Disorders of the hair and scalp.
- Knowledge, Beliefs, and Perceptions among Alopecia Areata Patients: A Cross-Sectional Study in CMH Kharian