Disease: Osteolysis hereditary multicentric
- A CARE-compliant article: A case report of scoliosis complicated with multicentric carpotarsal osteolysis
- A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome
- A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy
- A report of three patients with MMP2 associated hereditary osteolysis
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Art, the visual imagination and neuroscience: The Chauvet Cave, Mona Lisa's smile and Michelangelo's terribilitá
- Carpo-tarsal osteolysis. Case report and review of the literature
- Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy
- Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy
- Familial vanishing limbs: four generations of idiopathic multicentric osteolysis
- Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy
- Hereditary multicentric osteolysis
- Hereditary multicentric osteolysis with recessive transmission: a new syndrome
- Identification of a novel mutation in the MAFB gene in a pediatric patient with multicentric carpotarsal osteolysis syndrome using next-generation sequencing
- Mice harboring an MCTO mutation exhibit renal failure resembling nephropathy in human patients
- Multicentric carpal-tarsal osteolysis
- Multicentric carpotarsal osteolysis in a rheumatologist's practice
- Multicentric Carpotarsal Osteolysis Syndrome Associated Nephropathy: Novel Variants of <em>MAFB</em> Gene and Literature Review
- Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis
- Multicentric carpotarsal osteolysis syndrome: long-term follow-up of three patients
- Occlusal rehabilitation of a patient with hereditary multicentric osteolysis
- Patient with mutation in the matrix metalloproteinase 2 (MMP2) gene - a case report and review of the literature
- Regulatory mechanisms of anthrax toxin receptor 1-dependent vascular and connective tissue homeostasis
- The diagnosis and management of patients with idiopathic osteolysis
- THE ENIGMA of the Mona Lisa smile
- The genesis of Mona Lisa
- Three cases of multicentric carpotarsal osteolysis syndrome: a case series
- What surprises the Mona Lisa? The relative importance of the eyes and eyebrows for detecting surprise in briefly presented face stimuli