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Research 151–180 of 1000+
- Cutaneous drug reactions
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- Cutaneous Granular Cell Tumor with Overlying Hypertrichosis in an Adult: A Rare Case Report
- Hipertricose generalizada exuberante em um lactente: relato de caso
- Evaluación de la seguridad de minoxidil oral a dosis bajas en el tratamiento de la alopecia
- Hirsutism and Hypertrichosis
- Genital Dermatology
- A child with generalized hypertrichosis due to secondary topical minoxidil exposure
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- 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
- Phosphodiesterase inhibitors and prostaglandin analogues in dermatology: A comprehensive review
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- The eyelash comes to the fore
- Familial congenital generalized hypertrichosis
- Bioactive Proteolytic Enzymes Chymotrypsin and Papain as Adjuvants to Laser Hair Removal: Reducing the Risk of Paradoxical Hypertrichosis in Women with Facial Hirsutism
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- The human hair: from anatomy to physiology
- Calcineurin-based immunosuppression in renal transplantation : focus on efficacy, the role of steroids, and the cardiovascular risk
- Coat Problems
- News & Notes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis