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- Sjogren-Larsson syndrome
- Levetiracetam in the Treatment of Idiopathic Generalized Epilepsies
- Skin manifestations of Bardet–Biedl syndrome
- Emerging smart microneedle technologies in psoriasis: convergence of nanocarriers, machine learning, and personalized delivery
- Predicting Polycystic Ovary Syndrome among Reproductive-Aged Women in Bangladesh Using Machine Learning Algorithms: Development of a Hospital-Based Predictive Model
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Learning to Read in Multilingual Malaysia: A Focus on Bahasa Melayu, Tamil and Chinese
- KRDQN: An Interpretable Prediction Framework for Adverse Drug Reactions via Knowledge–Graph Reinforced Deep Q-Learning
- Global, Regional, and National Burden of Alopecia Areata in Children and Adolescents Aged 0-19 years from 1990 to 2021 and Projection to 2040
- Trichothiodystrophy in a child with occult learning disorder
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Regenerative Strategies for Androgenetic Alopecia: Evidence, Mechanisms, and Translational Pathways
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Predictive Modeling of Hair Fall using Random Forest Algorithms
- Clinical and macrophotographic study of the percutaneous implantation of synthetic hair (Nido SHI)
- The Rotterdam Study: 2012 objectives and design update
- Management of the psychological comorbidities of dermatological conditions: practitioners' guidelines
- Performance exploration of multi-gene panels of alopecia areata susceptibility and drug-binding targets
- Grand challenges in dermatologic drug discovery: four priorities to transform skin disease treatment
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Suicidality Risks Associated with Finasteride, a 5-Alpha Reductase Inhibitor: An Evaluation of Real-World Data from the FDA Adverse Event Reports
- A Quantitative Measurement Method for Nuclear-Pleomorphism Scoring in Breast Cancer
- The 3D Bioprinted Scaffolds for Wound Healing
- Alopecia: Association with Resistance to Thyroid Hormones
- Delayed Puberty
- Scalp, Skull, Orbit, and Maxilla Reconstruction and Hair Transplantation