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Research 181–210 of 1000+
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- 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
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- A clinician’s guide to pediatric and adolescent alopecia areata treatments
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Premature Graying of Hair: A Comprehensive Review and Recent Insights
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Surgical approach of ectropion in lamellar ichthyosis
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Congenital Adrenal Hyperplasia
- Androgenetic alopecia: An update
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Alopecia areata: An update
- The impact of SARS-CoV-2 and COVID-19 on male reproduction and men’s health
- Recent therapeutic developments for acne
- Hair loss and its management in children
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Optimizing clinical monitoring and management guidelines for capivasertib in HR-positive/HER2-negative advanced breast cancer: expert opinion
- Polycystic Ovarian Disease (PCOD): Epidemiological Perspectives and Preventive Strategies through Healthy Lifestyle and Alternative Approaches
- Areata progressing to totalis: A 24-month journey of hair regrowth at Dr. Batra’s