Search
for
Sort by
Research 721–750 of 1000+
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Hyperandrogenism: Acne and Hirsutism
- Scalp melanoma after antihair loss mesotherapy
- Androgenic alopecia in a postmenopausal Sicilian baroness
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Follicular ichthyosis
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Endo&Art why Diana is depicted with mild androgenic alopecia?
- Clinical report of a Holstein's calf with ichthyosis.
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Endocrinology of Hirsutism: From Androgens to Androgen Excess Disorders
- Hair Shaft Dysplasias
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- A Review on-Types and Treatment of Alopecia
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Temporal triangular alopecia and a review of 52 past cases
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- A rare case of woolly hair with unusual associations
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Finasteride in the Treatment of Hirsutism
- Generalized Congenital Hypotrichosis in a Female Rottweiler