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Research 271–300 of 1000+
- Enhanced ex vivo skin retention of bicalutamide using a nano-in-micro composite: Drug-loaded lipid vesicles in a dissolving microarray patch
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Successfully Nonsurgical Epidermoid Cyst Management with Recombinant Hydrolytic Enzymes: A Case Report
- Association of Acne Tarda with Endocrinological Disorders
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- Overweight and Obesity in Children and Adolescents
- Do men’s faces really signal heritable immunocompetence?
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Skin signs in anorexia nervosa
- Neuroimmunoregulation of Androgens in the Adrenal Gland and the Skin
- Complementary and Alternative Treatments for Alopecia: A Comprehensive Review
- Hormonal Treatment of Transgender Women with Oral Estradiol
- Current evaluation of amenorrhea
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Is Satoyoshi syndrome an autoimmune disease? A systematic review
- Assessment of Heavy Metal and Trace Element Levels in Patients with Telogen Effluvium.
- Simultaneous Determination of Selected Steroids with Neuroactive Effects in Human Serum by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Co-expression of PADI isoforms during progenitor differentiation enables functional diversity
- Endocrine and metabolic comorbidities in juvenile-onset systemic lupus erythematosus
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Pharmacological Strategies for Mitigating Cytarabine-Induced Multi-Organ Toxicity: A Scoping Review on Mechanisms, Efficacy and Clinical Implications
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes