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Research 121–150 of 1000+
- KOMPLEKSOWE LECZENIE GŁUCHOTY ODBIORCZEJ W PRZYPADKU URAZU WYBUCHOWEGO
- Les nouvelles stratégies thérapeutiques du traumatisme sonore par bruit d'arme chez le cobaye
- Control of testosterone 5alpha-reductase activity in the human hyperplastic prostate
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Severe Hypertrichosis of the External Ear Canal During Minoxidil Therapy
- Melatonin protects cochlear hair cells from nicotine‐induced injury through inhibiting apoptosis, inflammation, oxidative stress and endoplasmic reticulum stress
- Connexin mutations in human disease
- Author response: Generation of inner ear hair cells by direct lineage conversion of primary somatic cells
- Is There a Role for Sodium Fluoride in Otosclerosis Treatment?
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Three-row stereocilia model predicts mammalian hair bundle behavior
- Influence of Myosin Regulatory Light Chain and Myosin Light Chain Kinase on the Physiological Function of Inner Ear Hair Cells
- Melanocytes in regenerative medicine applications and disease modeling
- BRAIN HEALTH SERVICES – A NEW APPROACH TO PREVENTING ALZHEIMER’S DISEASE
- Schimmelpenning Syndrome: A Neuro-Oculo-Cutaneous Disorder
- Assessing Auditory and Cochlear Function in Alopecia Areata Patients: Exploring the Link to Cochlear Melanocyte Damage
- Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects
- A rare case of complete Vogt-Koyanagi-Harada disease presenting to a tertiary care hospital in late stage: Clinical features, diagnosis, and management
- News in brief
- Natural Bizbenzoquinoline Derivatives Protect Zebrafish Lateral Line Sensory Hair Cells from Aminoglycoside Toxicity
- A 26-year-old man presenting with loss of vision, skin lesions and wasting
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Proceedings of the RAMI Intern Section Meeting, 18th January 2014
- Citrate Anticoagulation in Hemodialysis
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Late presentation of biotinidase deficiency with acute visual loss and gait disturbance
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia