• A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report
• Age-based disparities in statin use for primary prevention in US adults: National Health and Nutrition Examination Surveys 2013-2020
• Anti-lubricin monoclonal antibodies created using lubricin-knockout mice immunodetect lubricin in several species and in patients with healthy and diseased joints
• Assessment and management of chronic kidney disease in people living with obesity
• Axial involvement with facet joint arthropathy and bony ankylosis in a case of camptodactyly, arthropathy, coxa vara, pericarditis (CACP) syndrome
• Botulism mimicking Guillain-Barre syndrome: The question of plasma exchange in an unusual case of acute paralysis
• Brothers with constrictive pericarditis - A novel mutation in a rare disease
• Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
• Camptodactyly-arthropathy-coxa vara-pericarditis syndrome and an unusual association with mitral stenosis
• Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome with Shoulder Joint Involvement: A Case Report with Literature Review
• Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene
• Case report: Coexistence of Jacobs syndrome, congenital adrenal hyperplasia, and ambiguous genitalia in a male infant
• Clinical Presentation and Management of Malignant Psoas Syndrome: A Scoping Review of Case Reports and Case Series
• Diagnosis and treatment of cardiovascular manifestations of COVID-19: a narrative review
• Double Aneuploidy of Down Syndrome (Trisomy 21) and Jacobs Syndrome (Trisomy XYY) with Complete Tracheal Rings Deformity: Case Report and Literature Review
• Electrical Impedance Tomography Identifies Evolution of Regional Perfusion in a Porcine Model of Acute Respiratory Distress Syndrome
• Evidence for the <em>DRD2</em> Gene as a Determinant of Reward Deficiency Syndrome (RDS)
• Fetal Muse-based therapy prevents lethal radio-induced gastrointestinal syndrome by intestinal regeneration
• Gender differences in the associations between childhood adversity and psychopathology in the general population
• Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
• Ileal Dysbiosis Is Associated with Increased Acoustic Startle in the 22q11.2 Microdeletion Mouse Model of Schizophrenia
• Jacobs Syndrome
• Jacobs Syndrome
• Joint manifestations revealing inborn metabolic diseases in adults: a narrative review
• Klinefelter Syndrome
• Klinefelter Syndrome
• Metformin
• Morbidity, mortality, and socioeconomics in Klinefelter syndrome and 47,XYY syndrome: a comparative review
• Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
• Pathognomonic acetabular cysts in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
• Patient-specific distractors for customized mandibular distraction osteogenesis to relieve upper airway obstruction in infants with Pierre Robin sequence
• Prenatal Intravenous Magnesium at 30-34 Weeks' Gestation and Neurodevelopmental Outcomes in Offspring: The MAGENTA Randomized Clinical Trial
• Presentation and Treatment of a Patient With Jacobs Syndrome and Metopic Craniosynostosis
• Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
• Quadruped Gait and Regulation of Apoptotic Factors in Tibiofemoral Joints following Intra-Articular rhPRG4 Injection in <em>Prg4</em> Null Mice
• Quality analysis of publicly available information about hypoplastic left heart syndrome
• Susac syndrome: neurological update (clinical features, long-term observational follow-up and management of sixteen patients)
• Syndrome of progressive deforming non-inflammatory arthritis of childhood: two patients of camptodactyly-arthropathy-coxa vara-pericarditis syndrome
• Viral anti-inflammatory serpin reduces immuno-coagulopathic pathology in SARS-CoV-2 mouse models of infection