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Gaetano Vattemi

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Clinical Neurology and Neurosurgery|October 2, 2019
A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae ruptureElia Pancheri, Silvia Bozzetti, Paola Rimessi, et al.
International Journal of Molecular Sciences|January 23, 2024
Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal OrganoidsCristina Bombieri, Andrea Corsi, Elisabetta Trabetti, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 15, 2020
Chronic Graft-Versus-Host-Disease-Related Polymyositis: a 17-Months-Old Child with a Rare and Late Complication of Haematopoietic Stem Cell TransplantationMatteo Chinello, Rita Balter, Massimiliano De Bortoli, et al.
Free Radical Biology & Medicine|April 27, 2013
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondriaGaetano Vattemi, Matteo Marini, Nicholas R Ferreri, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 19, 2014
Differential regulation of TNF receptors in maternal leukocytes is associated with severe preterm preeclampsiaPietro Minuz, Cristiano Fava, Shoujin Hao, et al.
Clinical Science (London, England : 1979)|October 6, 2011
Endothelial dysfunction and increased oxidative stress in mitochondrial diseasesPietro Minuz, Cristiano Fava, Gaetano Vattemi, et al.
Plos One|November 4, 2014
Autophagy, inflammation and innate immunity in inflammatory myopathiesCristina Cappelletti, Barbara Galbardi, Dimos Kapetis, et al.
Neuromuscular Disorders : NMD|March 18, 2008
Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotypeMassimiliano Filosto, Paola Tonin, Mauro Scarpelli, et al.
The Neurologist|August 31, 2012
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiencyGaetano Vattemi, Marcella Neri, Matteo Marini, et al.
Clinical Science (London, England : 1979)|November 4, 2015
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disordersValeria Guglielmi, Gaetano Vattemi, Roberto Chignola, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Clinical Neurology and Neurosurgery|October 2, 2019
A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae ruptureElia Pancheri, Silvia Bozzetti, Paola Rimessi, et al.
International Journal of Molecular Sciences|January 23, 2024
Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal OrganoidsCristina Bombieri, Andrea Corsi, Elisabetta Trabetti, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 15, 2020
Chronic Graft-Versus-Host-Disease-Related Polymyositis: a 17-Months-Old Child with a Rare and Late Complication of Haematopoietic Stem Cell TransplantationMatteo Chinello, Rita Balter, Massimiliano De Bortoli, et al.
Free Radical Biology & Medicine|April 27, 2013
Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondriaGaetano Vattemi, Matteo Marini, Nicholas R Ferreri, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 19, 2014
Differential regulation of TNF receptors in maternal leukocytes is associated with severe preterm preeclampsiaPietro Minuz, Cristiano Fava, Shoujin Hao, et al.
Clinical Science (London, England : 1979)|October 6, 2011
Endothelial dysfunction and increased oxidative stress in mitochondrial diseasesPietro Minuz, Cristiano Fava, Gaetano Vattemi, et al.
Plos One|November 4, 2014
Autophagy, inflammation and innate immunity in inflammatory myopathiesCristina Cappelletti, Barbara Galbardi, Dimos Kapetis, et al.
Neuromuscular Disorders : NMD|March 18, 2008
Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotypeMassimiliano Filosto, Paola Tonin, Mauro Scarpelli, et al.
The Neurologist|August 31, 2012
Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiencyGaetano Vattemi, Marcella Neri, Matteo Marini, et al.
Clinical Science (London, England : 1979)|November 4, 2015
Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disordersValeria Guglielmi, Gaetano Vattemi, Roberto Chignola, et al.
Pageof 6