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Research 151–180 of 1000+
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Androgenetic alopecia.
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- A Reappraisal of Surgical Techniques and Efficacy in Forehead Rejuvenation
- Sjogren-Larsson syndrome
- Frontal Fibrosing Alopecia and Increased Scalp Sweating: Is Neurogenic Inflammation the Common Link
- Correcting problems in hair restoration surgery: an update
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- 4 Vitamin D resistance
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Scalp Advancement and the Pretrichial Brow Lift
- Frontal fibrosing alopecia – review of recent case reports and case series in PubMed
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hairline Restoration: Difference in Men and Woman—Length and Shape
- Congenital atrichia with papular lesions
- Nomenclature Proposal for the Zones and Landmarks of the Balding Scalp
- Siberian cats help in solving part of the mystery surrounding golden cats
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Refining hair restoration technique
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Correcting hairline deformities after facial rejuvenation
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Alopezien und Hypotrichosen im Kindesalter
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- At the crossroads of 2 alopecias: Androgenetic alopecia pattern of hair regrowth in patients with alopecia areata treated with oral Janus kinase inhibitors
- Congenital atrichia with papular lesions