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Research 151–180 of 1000+
- Transitional Changes in Fatigue-Related Symptoms Due to Long COVID: A Single-Center Retrospective Observational Study in Japan
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- 567 Acute generalized exanthematous pustulosis (AGEP) induced by plaquenil
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Dermatological diseases from a genetic perspective
- Onychomatricoma in the Light of the Microanatomy of the Normal Nail Unit
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- A 61-year-old Filipino man with lichen planus concomitant with cicatricial alopecia, mimicking discoid lupus erythematosus
- Increased Risk of Local Recurrence in Cutaneous Squamous Cell Carcinoma Arising in Sun-Exposed Skin: A Retrospective Cohort Study
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- SARS-CoV-2 Non-Structural Proteins and Their Roles in Host Immune Evasion
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Clinical and demographic characteristics associated with nail involvement in alopecia areata: A cross‐sectional study of 197 patients
- Treatment Strategies for Cutaneous and Oral Mucosal Side Effects of Oncological Treatment in Breast Cancer: A Comprehensive Review
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- COVID-19 pandemic and teledermatology in low-income regions
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Peripheral neuropathy associated with tofacitinib use in alopecia universalis
- Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Spotlight commentary: Navigating the cutaneous side effects of chemotherapy