Multicentric osteolysis with nodulosis and arthropathy (MONA) with cardiac malformation, mimicking polyarticular juvenile idiopathic arthritis: case report and literature review

Mutation of Membrane Type-1 Metalloproteinase, MT1-MMP, Causes the Multicentric Osteolysis and Arthritis Disease Winchester Syndrome

(2012) Brad R. Evans et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Nosology and classification of genetic skeletal disorders: 2010 revision

(2011) Matthew L. Warman et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A novel homozygous MMP2 mutation in a patient with Torg–Winchester syndrome

(2010) Seon-Yong Jeong et al.   JOURNAL OF HUMAN GENETICS

Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene

(2009) Faysal Gok et al.   EUROPEAN JOURNAL OF PEDIATRICS

A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects

(2008) Beyhan Tuysuz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Cinética de la metaloproteasa 9: importancia del ritmo luz-oscuridad de la metaloproteasa 9 en el síndrome coronario agudo

(2008) Alberto Domínguez-Rodríguez et al.   REVISTA ESPANOLA DE CARDIOLOGIA