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Research 121–150 of 1000+
- The Role of MicroRNA, Long Non-Coding RNA and Circular RNA in the Pathogenesis of Polycystic Ovary Syndrome: A Literature Review
- Cases Report the Cronkhite-Canada Syndrome
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Bachmann–Bupp syndrome and treatment
- The emerging roles of N6-methyladenosine (m6A) deregulation in polycystic ovary syndrome
- Harnessing Microbiome, Bacterial Extracellular Vesicle, and Artificial Intelligence for Polycystic Ovary Syndrome Diagnosis and Management
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- The guidelines issued by the European Society for Human Reproduction and Embryology and the American Society for Reproductive Medicine regarding the induction of ovulation with metformin in patients with the polycystic ovary syndrome potentially require reconsideration
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Minoxidil ameliorates myelodysplastic syndrome by targeting Wnt4 while sparing normal hematopoiesis
- Cushings syndrome complicating pemphigoid gestationis
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Dermoscopy Update: Review of its Extradiagnostic and Expanding Indications and Future Prospects
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Approach to Alopecia in Dogs in Clinical Practice