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Research 91–120 of 1000+
- Microscopic Study concerning Hair Form of One Family in the Mixed Blood between European and Ponapean
- Treatment of monilethrix with oral minoxidil
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Trichodystrophies: A hair-raising differential diagnosis
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia
- Understanding and Management of Female Pattern Alopecia
- Drug eruptions in dermatology
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- TRICHOPATHOPHOBIA.
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Diseases of Periocular Hair
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- HAIR AND SYSTEMATIC DISEASE
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Hair and scalp disorders
- Causes and Management of Hypertrichosis
- Hirsutism: diagnosis and treatment
- Hair Disorders
- Calcineurin-based immunosuppression in renal transplantation : focus on efficacy, the role of steroids, and the cardiovascular risk