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Your search keyword '"Mirri G."' showing total 4 results
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4 results on '"Mirri G."'

2. 'Sotto l'ombra di Cicerone'. Vico oltre la mathesis universalis

Author

Giuseppe Moro, M. Adinolfi, A. Bellantone, S. Benso, G. Bensussan, M. Cacciari, G. Cantillo, G. Carillo, J.-F. Courtine, B. de Giovanni, D. Di Cesare, G. Di Tommaso, M. Donà, F. Duque, R. Esposito, A. Fabris, F. Ferrari, E. Forcellino, B. Forte, R. Gasparotti, G. Giorello, G. Goria, E. Lisciani-Petrini, N. Magliulo, E. Mazzarella, E. Mirri, G. Moro, G. Petrarca, G. Rametta, E. Redaelli, V. Rocco Lozano, R. Ronchi, E. Severino, C. Sini, A. Tagliapietra, L. V. Tarca, F. Tessitore, F. Tomatis, A. Trione, F. Valagussa, C. Invernizzi., Massimo Adinolfi Massimo Donà, and Moro, Giuseppe

Subjects
Vico Cicerone Vitiello eloquenza linguaggio
Published
2017

3. [Molecular biology as a diagnostic tool in the newborn Emergency department: a rare case of idiopathic infantile arterial calcification].

Author

Borromini A, Rossi G, Maggi P, Speciale D, Mirri G, Cogliardi A, Addis C, Dainese E, Bonoldi E, and Marando A

Subjects
Arteries pathology, Biomarkers blood, Fatal Outcome, Female, Humans, Infant, Rare Diseases, Vascular Calcification genetics, Cardiopulmonary Resuscitation adverse effects, Emergency Service, Hospital, Heart Arrest etiology, Mutation, Phosphoric Diester Hydrolases genetics, Pyrophosphatases genetics, Vascular Calcification complications, Vascular Calcification diagnosis
Abstract

A Turkish female infant of 96 days was admitted to the pediatric emergency room because of inconsolable crying, persistent cough, and difficulty in feeding during the previous day. She was conscious and did not show any signs or symptoms of multiorgan failure. A few minutes afterwards, the child experienced cardiac arrest with an initial cardiac rhythm of asystole and died 75 minutes later following cardiopulmonary resuscitation maneuvers. As the pathological cause of death, autopsy findings revealed a rare type of idiopathic infantile arterial calcification resulting from a mutation in the gene encoding for the ENPP1 enzyme.

Published
2016
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