Publications by authors named "Matteo Marini"

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Role of F-FDG PET/CT Radiomics Features in the Differential Diagnosis of Solitary Pulmonary Nodules: Diagnostic Accuracy and Comparison between Two Different PET/CT Scanners.
Domenico Albano, Roberto Gatta, Matteo Marini, Carlo Rodella, Luca Camoni

J Clin Med· October 2021

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Relapsing-remitting painful masses of the skeletal muscle.
Gaetano Vattemi, Valeria Guglielmi, Matteo Marini, Giuliano Tomelleri

J Clin Pathol· July 2020

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Acute Sarcomeric M-Line Disease Associated With ATP Synthase Subunit α Autoantibodies in Ankylosing Spondylitis.
Valeria Guglielmi, Gaetano Vattemi, Daniela Cecconi, Giulio Fracasso, Matteo Marini

J Neuropathol Exp Neurol· November 2018

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Bortezomib-Induced Muscle Toxicity in Multiple Myeloma.
Valeria Guglielmi, Dominika Nowis, Martina Tinelli, Manuela Malatesta, Laura Paoli, Matteo Marini

J Neuropathol Exp Neurol· July 2017

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Evidence for caspase-dependent programmed cell death along with repair processes in affected skeletal muscle fibres in patients with mitochondrial disorders.
Valeria Guglielmi, Gaetano Vattemi, Roberto Chignola, Anna Chiarini, Matteo Marini

Clin Sci (Lond)· February 2016

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Abnormal expression of RNA polymerase II-associated proteins in muscle of patients with myofibrillar myopathies.
Valeria Guglielmi, Matteo Marini, Émilie Fiola Masson, Manuela Malatesta, Diane Forget

Histopathology· December 2015

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Immunoblot as a potential diagnostic tool for myofibrillar myopathies.
Matteo Marini, Valeria Guglielmi, Georgine Faulkner, Silvio Piffer, Giuliano Tomelleri

Electrophoresis· December 2015

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Differential regulation of TNF receptors in maternal leukocytes is associated with severe preterm preeclampsia.
Pietro Minuz, Cristiano Fava, Shoujin Hao, Paulina Pedraza, Gabriella Amen, Matteo Marini

J Matern Fetal Neonatal Med· May 2015

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Polymyositis in solid organ transplant recipients receiving tacrolimus.
Gaetano Vattemi, Matteo Marini, Marzia Di Chio, Maria Colpani, Valeria Guglielmi

J Neurol Sci· October 2014

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SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers.
Valeria Guglielmi, Gaetano Vattemi, Francesca Gualandi, Nicol C Voermans, Matteo Marini

Mol Genet Metab· March 2014

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Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria.
Gaetano Vattemi, Matteo Marini, Nicholas R Ferreri, Shoujin Hao, Manuela Malatesta

Free Radic Biol Med· October 2013

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Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency.
Gaetano Vattemi, Marcella Neri, Matteo Marini, Francesca Gualandi, Paola Tonin

Neurologist· September 2012

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A metabolic shift induced by a PPAR panagonist markedly reduces the effects of pathogenic mitochondrial tRNA mutations.
Tina Wenz, Xiao Wang, Matteo Marini, Carlos T Moraes

J Cell Mol Med· November 2011

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Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement.
Gaetano Vattemi, Yehia Mechref, Matteo Marini, Paola Tonin, Pietro Minuz

Mol Cell Proteomics· April 2011

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Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation.
Gaetano Vattemi, Francesca Gualandi, Arie Oosterhof, Matteo Marini, Paola Tonin

J Neuropathol Exp Neurol· March 2010

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SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy.
Giuliano Tomelleri, Laura Palmucci, Paola Tonin, Tiziana Mongini, Matteo Marini

Brain· August 2006

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Circulating monocyte chemoattractant protein-1 and early development of nephropathy in type 1 diabetes.
Francesco Chiarelli, Francesco Cipollone, Angelika Mohn, Matteo Marini, Annalisa Iezzi

Diabetes Care· October 2002

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