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Research 61–90 of 1000+
- Genetic Hair Disorders: A Review
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Congenital Atrichia: A Case Report
- Hirsutism: diagnosis and treatment
- Urticariform plaques: delayed hypersensitivity reaction type IV to enoxaparin
- Eczema-like, erythematous, infiltrated plaques: A common side effect of subcutaneous heparin therapy
- Diagnostic, Therapeutic, and Theranostic Multifunctional Microneedles
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- A guide to diagnosis and management of hypertrichosis
- DERMATOLOGICAL AND SYSTEMIC REACTIONS TO HAIR DYES: CURRENT EVIDENCE AND MANAGEMENT
- Editorial: Exploring innovative therapies for rare inflammatory skin diseases
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Venous thromboembolism and women's health
- Allergens and Irritants
- Tracking research trends and hotspots in sperm DNA fragmentation testing for the evaluation of male infertility: a scientometric analysis
- Specificity of anti-SSB as a diagnostic marker for the classification of systemic lupus erythematosus
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- An in silico approach to the identification of potential proteomic and genomic diagnostic biomarkers for primary cicatricial alopecia
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- First Symposium of Ichthyosis Experts
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case