Search
for
Sort by
Research 31–60 of 466
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Clinical risk factors associated with intraoperative floppy iris syndrome: a prospective study
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Intraoperative Floppy Iris Syndrome: Updated Perspectives
- Intraoperative Floppy Iris Syndrome: Updated Perspectives
- A study of risk factors and predictive factors in intraoperative floppy iris syndrome during phacoemulsification
- Intraoperative floppy iris syndrome
- Risk factors for intraoperative floppy iris syndrome: a retrospective study
- Risk factors for intraoperative floppy iris syndrome: One year prospective study
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs
- Myotonic Dystrophy—A Progeroid Disease?
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Cellular Senescence and Aging in Myotonic Dystrophy
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Clinical Pearls in Men's Health
- 8242 A Case of Ayme Gripp Syndrome
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Effect of minoxidil on rabbit lens epithelial cell behavior in vitro and in situ
- Bioactive Compounds Isolated from Pinus densiflora and koraiensis and their Applications
- Floppy Iris Syndrome
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Long-Term Administration of Triterpenoids From Ganoderma lucidum Mitigates Age-Associated Brain Physiological Decline via Regulating Sphingolipid Metabolism and Enhancing Autophagy in Mice
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Madarosis from mitochondriopathy
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome