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Research 301–330 of 1000+
- A case of unilateral congenital triangular alopecia
- Congenital adrenal hyperplasia with polycystic ovarian disease: A rare cause of hirsutism
- Hair loss and its Unani concept and management
- Molecular Genetics of Alopecias
- Acquired scalp alopecia. Part I: A review
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Histopathology of non-scarring alopecia
- Targetoid Hair Regrowth Pattern in Alopecia Areata: A Case Series
- Facial Hair Transplantation
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Polycystic ovary syndrome and the differential diagnosis of hyperandrogenism
- Androgen excess and post-reproductive health
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Hair Anomalies in a 6-Year-Old Girl
- Putting the Human Hair Follicle Cycle on the Map
- Le gène<i>hairless</i>de la souris
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- The Molecular Basis of Blood Diseases
- Balding man.
- The Requirement to Monitor Low-dose Oral Minoxidil in the Management of Hair Loss
- Learning from nudity: lessons from the nude phenotype
- Alopecia in Children: The Most Common Causes
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Westwood Carolina Conference on Clinical Dermatology
- Dermatoses of pregnancy
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Androgens in women