Search Results - "Delpino, M.V."

Bone marrow adipocytes alteration in an in vitro model of Gaucher Disease by Crivaro, A., Mucci, J.M., Bondar, C., Ormazabal, M., Vaena, E., Delpino, M.V., Rozenfeld, P.A.

“…Gaucher disease (GD) is caused by biallelic pathogenic variants in GBA1 gene that encodes the lysosomal enzyme glucocerebrosidase. Up to now, specific…”
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Use of enrofloxacin in the treatment of canine brucellosis in a dog kennel (clinical trial) by Wanke, M.M., Delpino, M.V., Baldi, P.C.

“…To date, no totally effective antibiotic for the eradication of canine brucellosis has been found. The purpose of this study was to evaluate the efficacy of…”
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Unraveling the mystery of Gaucher bone density pathophysiology by Rozenfeld, P.A., Crivaro, A.N., Ormazabal, M., Mucci, J.M., Bondar, C., Delpino, M.V.

“…Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal enzyme β-glucocerebrosidase. Despite the existence of a…”
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Gaucher disease-associated alterations in mesenchymal stem cells reduce osteogenesis and favour adipogenesis processes with concomitant increased osteoclastogenesis by Crivaro, A., Bondar, C., Mucci, J.M., Ormazabal, M., Feldman, R.A., Delpino, M.V., Rozenfeld, P.A.

“…Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal enzyme β-glucocerebrosidase. Until now, treatments for GD…”
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Corrigendum to “Gaucher disease-associated alterations in mesenchymal stem cells reduce osteogenesis and favour adipogenesis processes with concomitant increased osteoclastogenesis” [Molecular Genetics Metabolism 130 (2020) 274-282] by Crivaro, A., Bondar, C., Mucci, J.M., Ormazabal, M., Feldman, R.A., Delpino, M.V., Rozenfeld, P.A.

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Proinflammatory and proosteoclastogenic potential of peripheral blood mononuclear cells from Gaucher patients: Implication for bone pathology by Mucci, J.M., Cuello, M.F., Kisinovsky, I., Larroude, M., Delpino, M.V., Rozenfeld, P.A.

“…Gaucher disease (GD) is caused by mutations in the GBA gene that confer a deficient level of activity of glucocerebrosidase (GCase). This deficiency leads to…”
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