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Research 31–60 of 1000+
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Generalized hypertrichosis associated with the use of interleukin 17 blockers in 2 patients with psoriasis
- PRIDE syndrome with lumbosacral hypertrichosis
- Generalized Hypertrichosis Due to Topical Minoxidil
- Androgenetic alopecia, hirsutism and hypertrichosis
- Congenital atrichia and hypotrichosis
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Infantile generalized hypertrichosis caused by topical minoxidil
- Hypertrichosis of the pinnae in a patient using panitumumab
- Hypertrichosis of vellus hairs of the malar region after unilateral treatment with bimatoprost
- Hypertrichosis of vellus hairs of the malar region after unilateral treatment with bimatoprost
- Omeprazole-induced hypertrichosis in two children
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Marie-unna hereditary hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Diffuse Hair Loss
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- Madarosis
- Disorders of hair in children
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- In That Issue: Proceedings From the Third Intercontinental Meeting of Hair Research Societies
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CHRONIC TELOGEN EFFLUVIUM