Carmela Preziuso

Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure.

Authors:

Annalinda Pisano Bruna Cerbelli Elena Perli Maria Pelullo Valentina Bargelli Carmela Preziuso Massimiliano Mancini Langping He Matthew G D Bates Joaquin R Lucena Paola Lilla Della Monica Giuseppe Familiari Vincenzo Petrozza Chiara Nediani Robert W Taylor Giulia d'Amati Carla Giordano

Cardiovasc Pathol 2016 Mar-Apr;25(2):103-12. Epub 2015 Sep 30.

Department of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome, Policlinico Umberto I, Viale Regina Elena 324, 00161, Rome, Italy. Electronic address:

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December 2016

Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations.

Authors:

Elena Perli Annarita Fiorillo Carla Giordano Annalinda Pisano Arianna Montanari Paola Grazioli Antonio F Campese Patrizio Di Micco Helen A Tuppen Ilaria Genovese Elena Poser Carmela Preziuso Robert W Taylor Veronica Morea Gianni Colotti Giulia d'Amati

Hum Mol Genet 2016 Mar 31;25(5):903-15. Epub 2015 Dec 31.

Department of Radiology, Oncology and Pathology, Pasteur Institute-Cenci Bolognetti Foundation, Rome 00161, Italy,

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March 2016

Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration.

EMBO Mol Med 2016 Mar;8(3):176-90

Department of Neurology, Haukeland University Hospital, Bergen, Norway Department of Clinical Medicine (K1), University of Bergen, Bergen, Norway

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March 2016

Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

Authors:

Annalinda Pisano Carmela Preziuso Luisa Iommarini Elena Perli Paola Grazioli Antonio F Campese Alessandra Maresca Monica Montopoli Laura Masuelli Alfredo A Sadun Giulia d'Amati Valerio Carelli Anna Ghelli Carla Giordano

Hum Mol Genet 2015 Dec 26;24(24):6921-31. Epub 2015 Sep 26.

Department of Radiological, Oncological and Pathological Sciences,

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December 2015

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

EMBO Mol Med 2015 Jun;7(6):848-58

U.O. Genetica Medica, Policlinico Sant'Orsola-Malpighi, Bologna, Italy Dipartimento di Scienze Mediche Chirurgiche (DIMEC), University of Bologna, Bologna, Italy

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June 2015

Publications by authors named "Carmela Preziuso"

Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure.

Authors:

Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations.

Authors:

Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration.

Authors:

Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

Authors:

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

Authors: