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Research 241–270 of 1000+
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Postsclerotherapy Hyperpigmentation: A Histologic Evaluation
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Sensitive scalp: does this condition exist? An epidemiological study
- The clinical evaluation of hirsutism
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- An overview on congenital alopecia in domestic animals
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Severe steroid-dependent idiopathic angioedema with response to rituximab
- BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS
- The diagnosis and treatment of mange in the guinea‐pig caused by <i>Trixacarus (Caviacoptes) caviae</i> (Fain, Hovell & Hyatt, 1972)*
- BLACK DOT TINEA CAPITIS IN A MAN
- Eruptive Vellus Hair Cyst
- Madarosis from mitochondriopathy
- 'The Cry of the Children' : The Edwardian Medical Campaign Against Maternal Drinking
- Problems in pattern alopecia
- Viewpoint 6
- A novel method for visualizing hair lipids at the cell membrane complex: Argon sputter etching/scanning electron microscopy<sup>1</sup>
- Androgenetic alopecia in men: the scale of the problem and prospects for treatment.
- Treatment of Alopecia Areata
- 368 The Unanticipated Costs, Deficits, and Other Unexpected Burdens in a Diagnosis of Alopecia Areata
- A Retrospective Case-Control Study Evaluating Medications Associated with Inpatient Falls in a Single Veterans Affairs Medical Center
- Androgens in postmenopausal women
- 'The Cry of the Children': The Edwardian Medical Campaign Against Maternal Drinking
- LGR5 is a Marker of Poor Prognosis in Glioblastoma and is Required for Survival of Brain Cancer Stem‐Like Cells
- Skin Manifestations in Primary Immunodeficient Children
- Male fertility and skin diseases
- Connexin mutations in human disease
- Mitochondrial dysfunction as a cause of ageing
- The pathophysiology of polycystic ovary syndrome