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Research 901–930 of 1000+
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Hair and cord blood element levels and their relationship with air pollution, dietary intake, gestational diabetes mellitus, and infant neurodevelopment
- BBS7–SHH Signaling Activity Regulates Primary Cilia for Periodontal Homeostasis
- Safety of skin care products during pregnancy.
- Advancements in Dermatological Imaging Modalities
- The PI3K-Akt-mTOR and Associated Signaling Pathways as Molecular Drivers of Immune-Mediated Inflammatory Skin Diseases: Update on Therapeutic Strategy Using Natural and Synthetic Compounds
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Sex Differences in Animal Models of Sodium-Valproate-Induced Autism in Postnatal BALB/c Mice: Whole-Brain Histoarchitecture and 5-HT2A Receptor Biomarker Evidence
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Characterization of DNA Methylation and Screening of Epigenetic Markers in Polycystic Ovary Syndrome
- Towards the Development of AgoKirs: New Pharmacological Activators to Study Kir2.x Channel and Target Cardiac Disease
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Biologics and Small Molecule Targeted Therapies for Pediatric Alopecia Areata, Psoriasis, Atopic Dermatitis, and Hidradenitis Suppurativa in the US: A Narrative Review
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Limb amputations; etiopathogenesis, diagnosis and the multidisciplinary therapeutic approach
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Efficacy and safety of anti-androgens in the management of polycystic ovary syndrome: a systematic review and meta-analysis of randomised controlled trials
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Recommendations from the 2023 international evidence-based guideline for the assessment and management of polycystic ovary syndrome
- Quercetin and polycystic ovary syndrome
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Monilethrix in three generations