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Research 871–900 of 881
- An overview about Therapeutic uses, clinical efficacy, safety and classes of Retinoids and its efficacy for Treatment of skin aging
- Dermatologic manifestations of thyroid disease: a literature review
- A Series of Clinical Cases of Psychocutaneous Disorders in a Dermatology Unit in Albania
- Neuropathic Pruritus: An Underrecognized and Often Misdiagnosed and Difficult to Treat Medical Condition
- Referee report. For: Case Report: Tuberculosis lymphadenitis with systemic lupus erythematosus in a young woman: a case report [version 2; peer review: 1 approved, 1 approved with reservations, 1 not approved]
- Recurrent pruritic polymorphic lesions associated with weight loss
- Hair loss in women
- Prominent Cutaneous Manifestation of COVID-19: A Case Report
- Assessment of Dysregulation of HERC6 and Essential Biological Processes in Response to Laser Therapy of Human Arm Skin
- Skin Disease in Korean Human Immunodeficiency Virus Patient
- Viva questions from the IJDVL
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Pigmentary mosaicism: An update
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Hypopigmented Mycosis Fungoides Treated with 308 nm Excimer Laser
- Fibromodulin reduces scar formation in adult cutaneous wounds by eliciting a fetal-like phenotype
- 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
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Hyperpigmented Upper Eyelid: A Clue to the Diagnosis of Facial Lichen Planus Pigmentosus in a Patient with Frontal Fibrosing Alopecia
- The effects of gamma rays on the regeneration of hair follicles are carried over to later hair cycles
- Obstetric and Gynecologic Dermatology
- LITERATURE REVIEW
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women