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Research 61–90 of 1000+
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Diseases of Hair
- Diseases of Hair
- Madarosis: A marker of many Maladies
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Congenital erythropoietic porphyria five years observation with standard treatment: a case report
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Becker's Nevus Syndrome
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Síndrome do nevo de Becker
- Congenital Triangular Alopecia (Brauer Nevus)
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Off-Label Use of Topical Minoxidil in Alopecia: A Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Hair Disorders
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- Short anagen syndrome: Case series and literature review
- Skin Development and Disease: A Molecular Perspective
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles