Search
for
Sort by
Research 30 of 1000+
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Hair: more than just an appendage
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Hypertrichosis lanuginosa acquisita following cytotoxic chemotherapy
- Hair and scalp disorders
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Genetics of Structural Hair Disorders
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Inherited Disorders of the Hair
- Hair Changes due to Drugs
- Female Adolescent Hair Disorders
- Two females with hair loss
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Marie-unna hereditary hypotrichosis
- Disorders of hair in children