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Research 241–270 of 1000+
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Unruly hair
- Short anagen syndrome: Case series and literature review
- Hair loss
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Evaluating 5 alpha reductase inhibitors for the treatment of male androgenic alopecia
- Current understanding and treatment of sex hormone-related hair diseases
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Female Pattern Hair Loss and its Relationship to Permanent/Cicatricial Alopecia: A New Perspective
- Clinical biochemistry of dihydrotestosterone
- Hair Shaft Dysplasias
- Alopecia
- Profile of Female Hyperandrogenism at the Medical Clinic II: About 19 Cases
- Alopecia in general medicine
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A rare hair loss in children: Monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Hair
- Ichthyosis
- Trichoscopy in genetic hair shaft abnormalities
- Substance P in keratosis follicularis spinulosa decalvans
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Importancia de la pseudopelada de Brocq en la práctica de la medicina estética capilar
- Itchy Black Hair Bristles on Back