Search
for
Sort by
Research 31–60 of 1000+
- Early onset androgenetic alopecia in men and associated risk factors: a hospital based study
- Androgenetic alopecia: Update on etiology
- Alopecia Areata in a Pediatric Patient with Delayed Maternal Manifestation: A Case Report
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Androgenetic Alopecia in Men: An Update On Genetics
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Przewidywanie cech wyglądu człowieka na podstawie markerów DNA do celów medyczno-sądowych i kryminalistycznych
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair.
- Cosmeceutical Treatments for Androgenetic Alopecia
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- A Mutation of the Androgen Receptor Associated with Partial Androgen Resistance, Familial Gynecomastia, and Fertility*
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Congenital hypotrichosis due to short anagen
- Atrichia With Papular Lesions
- Familial Nonmembranous Aplasia Cutis of the Scalp
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Keratosis follicularis spinulosa decalvans in a female
- Short anagen hair syndrome
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Eruptive Vellus Hair Cyst