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Research 871–900 of 1000+
- A case of severe hyperandrogenism, acanthosis nigricans and overt diabetes: the use of non-invasive methods for diagnosis, pathogenesis and management
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Integrative insights into polycystic ovarian syndrome (PCOS): A comparative review of unani and modern medical perspective
- Hirsutism due to polycystic ovarian syndrome: An integrative review of pathophysiology and management
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Swastyayanam of Bhela indriya Sthana - an explorative study
- Síndrome de ovario poliquístico: la distancia anogenital como marcador del entorno androgénico prenatal y revisión y comparación de los criterios diagnósticos
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- 5α- Reductase Inhibitors in Prostate Cancer: An Overview
- Cycle pilaire et alopécie X chez le chien
- Androgenetic Alopecia
- A patient with combined polycystic ovary syndrome and autoimmune polyglandular syndrome type 2
- Contents
- Photothermal hydrogels for infection control and tissue regeneration
- Nanobiotechnology: Applications in Chronic Wound Healing
- Treatment of Alopecia in Children
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Hair in the Wrong Place
- Clinical Applications of Punch-Based Techniques in Dermatologic Surgery
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Myotonic Dystrophy—A Progeroid Disease?
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata
- Zebrafish Model of Hereditary Pigmentary Disorders
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia