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Research 181–210 of 1000+
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- The Hairdex Quality of Life Instrument—A Translation and Psychometric Validation in Patients with Alopecia Areata
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Fibroblast bioelectric signaling drives hair growth
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Case report: Dermatosis neglecta mimicking pemphigus foliaceus in association with obsessive–compulsive disorder
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- A Rare Case of Cutis Verticis Gyrata with Underlying Cerebriform Intradermal Nevus
- A guide to diagnosis and management of hypertrichosis
- Dermatologic care of patients with differences of sex development
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Using the Mechanisms of Action Involved in the Pathogenesis of Androgenetic Alopecia to Treat Hair Loss
- Importance of alexithymia on anxiety and depression in alopecia areata: a cohort study
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Linc-PINT downregulation of TGF-β signaling pathway in heart arrhythmia: an in silico analysis
- Pemilihan Obat Anti-Epilepsi (OAE) untuk Penyandang Epilepsi Wanita Usia Subur
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Joint Public Review: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Author Response: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report