Search
for
Sort by
Research 61–90 of 1000+
- Inherited Hair Disorders
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the <i>LIPH</i> gene at c.742C > A and c.614A > G: The first Japanese case
- Review of Keratin Disorders
- Hair Manifestations of Systemic Disease
- The possibilities of correction of premature greying of hair and involutive hair changes
- Female Pattern Hair Loss: Clinical features
- A Comprehensive Overview on Alopecia Areata with Review on Advances in Genetics and Treatment
- Hair shaft disorders
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Premature greying of hair in children: A comprehensive review for pediatricians and primary care physicians
- Premature greying of hair in children: A comprehensive review for pediatricians and primary care physicians
- Premature greying of hair in children: A comprehensive review for pediatricians and primary care physicians
- Proceedings of the 7thworld congress of hair research
- EXPLORATION OF THE MAHIYAT-E- MARAḌI (ETIOPATHOGENESIS) OF AMRĀḌ-E-SHA’R (HAIR DISORDERS) IN UNANI MEDICINE: A SYSTEMATIC LITERATURE REVIEW
- Inherited Disorders of the Hair
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Inherited Disorders of the Hair
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Disorders of Hair Pigmentation
- Pigmentary and Hair Disorders
- The Successful Treatment of Alopecia Areata with Platelet Rich Plasma in a Case of Twins with Genetic Risk for Autoimmune Disorders
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- Masquerading of trichotillomania in a family with monilethrix
- A human prenatal skin cell atlas reveals immune cell regulation of skin morphogenesis
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Report from the Cicatricial Alopecia Colloquium
- Claves diagnósticas en displasias pilosas II