Trichomycosis Axillaris: A Clinicoetiological Study. [PDF]
Kalimuthu A +3 more
europepmc +1 more source
Desmosomal-Type Acantholysis-A New Histologic Pattern Related to Mutations of Genes for Desmosomal Proteins. [PDF]
Metze D +4 more
europepmc +1 more source
Increased Interest in Oral Minoxidil for Hair Loss Treatment Following Publication of August 2022 New York Times Article: A Google Trends Analysis. [PDF]
Desir N, Desai AD, Lipner SR.
europepmc +1 more source
Circ 0020938 inhibits hair follicle stem cells proliferation via the miR-142-5p/DSG4 axis in cashmere goats. [PDF]
Du J +5 more
europepmc +1 more source
Gene detection in a family with monilethrix and treatment with 5% topical minoxidil [PDF]
Abstract Objective To determine the causative gene mutation in a family with monilethrix and observe the therapeutic effect of 5% topical minoxidil. Method Clinical data from a family with monilethrix were collected. Peripheral blood samples were taken from the proband, the parents, and 100 unrelated healthy controls. Genomic DNA was extracted.
Pengqiang Du
exaly +3 more sources
This case report describes sparse, unruly, fragile, and easily breakable hair, with patchy alopecia with diffuse follicular papules throughout the scalp as well as short hair with an alternation of darker elliptical nodes, with paler nonmedullated paler internodes giving a necklace appearance.
Piccolo V., Argenziano G.
openaire +3 more sources
Monilethrix and Pseudo-Monilethrix
The name is derived from monile (Lat.) = necklace and thrix (Gk.) = hair to indicate a resemblance to a string of beads or a necklace (Fig. 1).
B. Bentley-Phillips
openaire +2 more sources
Monilethrix Treated with Minoxidil [PDF]
In literature many different therapies are proposed to treat Monilethrix, but a definitive therapy still doe not exist. We decided to treat four patients affected by Monilethrix, with topical minoxidil 2%, 1 ml night and day for 1 year.
Alessandra Iorio +2 more
exaly +2 more sources
Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype [PDF]
Monilethrix is an hereditary hair dystrophy recently shown to be due to mutations in the helix termination motif of two type II (basic) human hair keratin genes, hHb1 and hHb6. It has been suggested that mutation in hHb1 produces a less severe phenotype.
Eugene Healy +2 more
exaly +8 more sources

