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Research 691–720 of 1000+
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- PA31 Traction alopecia in the paediatric Sikh population
- Exosomes derived stem cells as a modern therapeutic approach for skin rejuvenation and hair regrowth
- The Frontal Fibrosing Alopecia Treatment Dilemma
- Upadacitinib for Alopecia Areata in Different Backgrounds: A Case Series
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Introductory Chapter: Alopecia Management – An Update
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- iPSC-based approach for human hair follicle regeneration
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Commentary on: Hair Transplantation in Burn Scar Alopecia After Combined Non-Ablative Fractional Laser and Microfat Graft Treatment
- Essential syphilitic alopecia: Non-scarring alopecia in 21-year-old man
- Hypotrichosis in a child with olmsted syndrome
- Lichen Planopilaris: Retrospective Study and Stepwise Therapeutic Approach
- Amyloid-Associated Alopecia: A Reappraisal Including Its Pathophysiology
- Comparative Efficacy Study Combination of Oral Methotrexate and Prednisolone versus Oral Methotrexate in Patients with Lichen Planopilaris
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Diffuse hair loss in a patient with systemic lupus erythematosus
- Trichobezoar: An Uncommon Cause of Upper GI Bleeding
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata