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Research 661–690 of 1000+
- Skin grafting for the treatment of chronic leg ulcers – a systematic review in evidence‐based medicine
- Inborn Errors of Biotin Metabolism
- Treatment of Alopecia Areata With Squaric Acid Dibutylester
- Subacute cutaneous lupus erythematosus presenting as erythroderma
- Congenital ptosis: Long-term outcome of frontalis suspension using autogenous temporal fascia or fascia lata in children
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Pollen Allergies in Humans and their Dogs, Cats and Horses: Differences and Similarities
- Diagnosis of sports‐related dermatoses
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Dermoscopic evaluation of therapeutic response to an intralesional corticosteroid in the treatment of alopecia areata
- Acrodermatitis Enteropathica
- Key targets of hormonal treatment of prostate cancer. Part 2: the androgen receptor and 5α-reductase
- Wolf's isotopic response: Trichophyton rubrum folliculitis appearing on a herpes zoster scar
- Trichotillomania in children and adolescents: Review of the literature and case report
- Photobiomodulation: A Systematic Review of the Oncologic Safety of Low-Level Light Therapy for Aesthetic Skin Rejuvenation
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Liposomes in cancer therapy
- The molecular pathogenesis of Trichilemmal carcinoma
- An unusual case report of rapunzel syndrome trichobezoar in a 3-year-old boy
- The role of metabolism in cellular quiescence
- Follicular dysplasia in five Weimaraners
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- The treatment of alopecia areata
- Lupus Panniculitis as an Initial Manifestation of Systemic Lupus Erythematosus
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Erosive pustular dermatosis of the scalp: challenges and solutions