• A child with Winchester syndrome responding to oral betamethasone and methotrexate
• A novel gene mutation for multicentric osteolysis nodulosis and arthropathy: Case report and review of literature
• A report of three patients with MMP2 associated hereditary osteolysis
• Adolescence exposure to China's great famine period and the association of metabolic syndrome in adulthood: a retrospective study
• Anaesthesia management for Winchester syndrome
• Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy
• Eat, Sleep, Console Approach or Usual Care for Neonatal Opioid Withdrawal
• Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype
• Identification of drug-target interaction from interactome network with 'guilt-by-association' principle and topology features
• Integration of multimodal data in the developing tooth reveals candidate regulatory loci driving human odontogenic phenotypes
• International Analgesia and Sedation Weaning and Withdrawal Practices in Critically Ill Adults: The Adult Iatrogenic Withdrawal Study in the ICU
• International Validation of a Methicillin-Resistant Staphylococcus aureus Risk Assessment Tool for Skin and Soft Tissue Infections
• Japanese siblings with multicentric osteolysis nodulosis and arthropathy
• Langerhans Cell Histiocytosis Involving Both Jaws in an Adult
• Machine-learning based prediction of in-hospital death for patients with takotsubo syndrome: the InterTAK-ML model
• Management of chronic musculoskeletal pain in an adult with Down syndrome using a modified pain neuroscience approach: a case report
• Multicentric Osteolysis Nodulosis and Arthropathy
• Multicentric Osteolysis Nodulosis Arthropathy Syndrome Simulating Juvenile Idiopathic Arthritis in an Adult Female: A Case Report and a Literature Review
• Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations
• Multicentric osteolytic syndromes represent a phenotypic spectrum defined by defective collagen remodeling
• Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome
• Patient with mutation in the matrix metalloproteinase 2 (MMP2) gene - a case report and review of the literature
• Perceptions of exercise and restless legs syndrome: Results from a nationwide survey
• Protection against SARS-CoV-2 after Covid-19 Vaccination and Previous Infection
• Protection Conferred by Delta and BA.1/BA.2 Infection Against BA.4/BA.5 Infection and Hospitalization: A Retrospective Cohort Study
• SLN124, a GalNAc conjugated 19-mer siRNA targeting tmprss6, reduces plasma iron and increases hepcidin levels of healthy volunteers
• Taurodontism in dental genetics
• The diagnosis and management of patients with idiopathic osteolysis
• The importance for wellbeing of having views of nature from and in the home during the COVID-19 pandemic. Results from the GreenCOVID study
• Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report
• World Allergy Organization (WAO) Diagnosis and Rationale for Action against Cow's Milk Allergy (DRACMA) Guideline update - VII - Milk elimination and reintroduction in the diagnostic process of cow's milk allergy