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Research 661–690 of 1000+
- Ichthyosis hystrix
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Congenital atrichia associated with situs inversus and mesocardia
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- [The Netherton syndrome with alopecia and prolinuria].
- Sexual, physical, and overall adverse effects in patients treated with 5α-reductase inhibitors: a systematic review and meta-analysis
- Pediatric Dermatopathology
- Kelulut Honey Regulates Sex Steroid Receptors in a Polycystic Ovary Syndrome Rat Model
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Successful treatment of a scalp arteriovenous malformation with ulcerative hemorrhage and localized alopecia.
- Fetal gender: preferences, predictions, and its impact on women's sexuality, physical activity, and well-being during pregnancy
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Hair Growth Promoting Potential of Consciousness Energy Healing Treatment in Human Dermal Papilla Cells
- Transient treatment response of platelet-rich plasma injection for temporal triangular alopecia: A case report with dermoscopic examination follow-up
- Structure and biochemistry of mammalian hard keratin
- Expression of μ-Opiate Receptor in Human Epidermis and Keratinocytes
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Disorders of Sex Development
- Hair That Is Difficult to Manage in a Hispanic Girl
- Biochemical predictor for polycystic ovary syndrome
- Exploring the Gut Microbiome and Metabolome in Individuals with Alopecia Areata Disease
- TONGUE, RED
- Stem Cells Applications in Regenerative Medicine and Disease Therapeutics
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair