Associated Papers
Vanishing Bones and Stubborn Joints: Unravelling the Enigma of Multicentric Osteolysis, Nodulosis, and Arthropathy Syndrome.
Sahu RK et al.
Cureus, 2025
A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome.
Ahmad S et al.
Bone Reports, 2024
Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy.
Ishaq T et al.
Bmc Musculoskeletal Disorders, 2023
Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.
Elsebaie H et al.
Bone Reports, 2021
Comparative Serum Analyses Identify Cytokines and Hormones Commonly Dysregulated as Well as Implicated in Promoting Osteolysis in MMP-2-Deficient Mice and Children.
Sarker H et al.
Frontiers in Physiology, 2020
Bisphosphonates in multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder - an alternative therapeutic approach.
Pichler K et al.
Scientific Reports, 2016
Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy.
Bhavani GS et al.
American Journal of Medical Genetics. Part A, 2016
Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy.
Azzollini J et al.
Journal of Human Genetics, 2014
Multicentric osteolysis with nodulosis and arthropathy (MONA) with cardiac malformation, mimicking polyarticular juvenile idiopathic arthritis: case report and literature review.
Castberg FC et al.
European Journal of Pediatrics, 2013
Matrix metalloproteinase-2 promoter variability in psoriasis.
Vasku V et al.
Archives of Dermatological Research, 2009
Matrix Metallopeptidase 2 Gene Polymorphism is Associated with Obesity in Korean Population.
Han DH et al.
The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology, 2008
Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome.
Zankl A et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2007
A novel homozygous MMP2 mutation in a family with Winchester syndrome.
Rouzier C et al.
Clinical Genetics, 2006
Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2.
Zankl A et al.
Clinical Genetics, 2005
Al-Aqeel Sewairi syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy. The first genetic defect of matrix metalloproteinase 2 gene.
Al-Aqeel AI
Saudi Medical Journal, 2005
Linked common polymorphisms in the gelatinase a promoter are associated with diminished transcriptional response to estrogen and genetic fitness.
Harendza S et al.
The Journal of Biological Chemistry, 2003
Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome.
Martignetti JA et al.
Nature Genetics, 2001