Search
for
Sort by
Research 31–60 of 1000+
- The Role of Medical Language in Changing Public Perceptions of Illness
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- The eyelash comes to the fore
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Minoxidil induced hypertrichosis in a 2 year-old child
- Genital Dermatology
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Genital Rejuvenation: The Next Frontier in Medical and Cosmetic Dermatology
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The human hair: from anatomy to physiology
- Drug Reactions Affecting Hair: Diagnosis
- Drug-Induced Hair Disorders
- Understanding and Management of Female Pattern Alopecia
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Familial congenital generalized hypertrichosis
- Hair Disorders
- A guide to diagnosis and management of hypertrichosis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Biology and Genetics of Hair
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- HAIR AND SYSTEMATIC DISEASE
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Diseases of Periocular Hair
- Hair Changes due to Drugs