Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Giovanni Cannataro"'
Autor:
MARIA G. CHIARILLI, ANDREA DELLI PIZZI, PIERO CHIACCHIARETTA, ANDREA PRATTICHIZZO, ANTONIETTA CIFARATTI, GIOVANNI CANNATARO, MASSIMO CAULO
Publikováno v:
In Vivo
Aim: The present study aimed to examine meniscal morphology in an adult population in vivo through computed tomographic images, including research into morphological differences related to osteoarthritis, ageing and the meniscal location within the k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8aafe62a7b590c934beb6336ee4343e
https://europepmc.org/articles/PMC9087097/
https://europepmc.org/articles/PMC9087097/
Autor:
Emma Altobelli, Giovanni Farello, Giuseppe Lapergola, Giovanni Cannataro, Reimondo Petrocelli, Luciana Breda, Paolo Matteo Angeletti
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 4861, p 4861 (2021)
Journal of Clinical Medicine, Vol 10, Iss 4861, p 4861 (2021)
Juvenile idiopathic arthritis (JIA) is the most common inflammatory chronic disease affecting children and adolescents. Today, there are no specific biomarkers of inflammation. Therefore, it is important to identify new markers as predictors of disea
Autor:
Giovanni Cannataro, Antonietta Cifaratti, Michela Pontolillo, Fabrizio Fascione, Massimo Caulo, Andrea Delli Pizzi, Maria Pia Febo, Bruno Consorte, Emanuela Di Ilio, Maria Grazia Chiarilli
Publikováno v:
Minerva Orthopedics. 72
Autor:
Bruno Consorte, Giovanni Cannataro, Massimo Caulo, Valentina Panara, Domenico Mastrodicasa, Beatrice Cardinali, Maria Pia Febo, Antonietta Cifaratti, Maria Grazia Chiarilli, Andrea Delli Pizzi
Publikováno v:
La Radiologia medica. 126(2)
Magnetic resonance imaging (MRI) plays a leading role in the non-invasive evaluation of bone marrow (BM). Normal BM pattern depends on the ratio and distribution of yellow and red marrow, which are subject to changes with age, pathologies, and treatm
Autor:
Valentina Chiavaroli, Chiara Palka, Massimo Savastano, Antonio Raffaele Cotroneo, Angelika Mohn, Liborio Stuppia, Valentina Gatta, Sara Franchi, Giovanni Cannataro, Francesco Chiarelli
Publikováno v:
BMC Medical Genetics
Background SHOX alterations have been reported in 67% of patients affected by Léri-Weill dyschondrosteosis (LWD), with a larger prevalence of gene deletions than point mutations. It has been recently demonstrated that these deletions can involve the