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Research 31–60 of 1000+
- Cetuximab-induced hypertrichosis of the scalp and eyelashes
- Marie-unna hereditary hypotrichosis
- Diseases of Periocular Hair
- Dermatological Manifestations of Pegylated Interferon alfa2a and Ribavirin Combination Therapy in Chronic HCV Patients
- Corrective Hyaluronic Acid Fillers and Combination Cosmetic Treatments for Facial Cutaneous Defects Due to Autoimmune Connective Tissue Diseases: A Retrospective Review
- Topical minoxidil effectiveness in enhancing facial aesthetics: A systematic review and meta-analysis
- Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment
- Periocular Manifestations of Afatinib Therapy
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Congenital hypotrichosis due to short anagen
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Loose anagen hair syndrome presenting as patchy hypotrichosis – clinico-trichoscopic correlation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Lack of efficacy of topical latanoprost in the treatment of eyebrow alopecia areata
- Development of Clinician-Reported Outcome (ClinRO) and Patient-Reported Outcome (PRO) Measures for Eyebrow, Eyelash and Nail Assessment in Alopecia Areata
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- PRIDE syndrome with lumbosacral hypertrichosis
- Hypertrichosis of the pinnae in a patient using panitumumab
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Congenital atrichia and hypotrichosis
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities