Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Maria Ammendola"'
Autor:
Edoardo Rosato, Gregorino Paone, Alessandro Maria Ferrazza, Maria Ludovica Gasperini, Antonietta Gigante, Rosa Maria Ammendola, Iacopo Carbone
Publikováno v:
Clinical Rheumatology. 39:1537-1542
Interstitial lung disease (ILD) remains a major cause of morbidity and mortality in systemic sclerosis (SSc). Study aim is to characterize and quantify SSc-ILD by using Computer-Aided Lung Informatics for Pathology Evaluation and Rating (CALIPER). Se
Publikováno v:
European Journal of Radiology Open, Vol 2, Iss C, Pp 1-2 (2015)
A 75-year-old female underwent a High Resolution Computed Tomography (HRCT) scan for recurrent bronchitis and cough. HRCT images showed an anomalous supernumerary bronchus to the right upper lobe directly arising from the right side of distal trachea
Externí odkaz:
https://doaj.org/article/f0e07642a92a47ffbfbbe8e206c73049
Autor:
Rosa Maria Ammendola, Carlo Catalano, Marco Francone, Gian Marco Dacquino, Francesco Fedele, Iacopo Carbone, Luciano Agati, Laura De Luca, Simona Coco, Nicola Galea
Publikováno v:
European radiology. 29(5)
To investigate the prognostic role of early post-infarction cardiac magnetic resonance (CMR) on long-term risk stratification of ST segment elevation myocardial infarction (STEMI) patients with preserved left ventricular ejection fraction (LVEF). Sev
Autor:
Patrizia Saccucci, Egidio Bottini, Adalgisa Pietropolli, Maria Ammendola, Fulvia Gloria-Bottini
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 185:96-98
Objective It has been suggested that the development of uterine leiomyomas is positively influenced by an immune system in a chronically inflammatory state and that a lower level of regulating T cell (Treg cells) would play a central role. Since it h
A 14-year-old female patient affected by ataxia telangiectasia (AT) syndrome presented with mild dyspnoea and chest discomfort of a few days duration. After a short course of antibiotic therapy, which yielded no significant clinical improvement, a ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a11ef8df71a4968cb01d3cc59f8f479
http://hdl.handle.net/11573/909575
http://hdl.handle.net/11573/909575
Autor:
Egidio Bottini, Fulvia Gloria-Bottini, Patrizia Saccucci, Maria Ammendola, Anna Neri, Andrea Magrini
Publikováno v:
Archives of gynecology and obstetrics. 293(2)
Association between p53 codon 72 and endometriosis has been observed in populations of East Asia but not in those of European descent. Genetic polymorphisms could interact with p53 codon 72 influencing its association with endometriosis, thus explain
Autor:
Maria Ammendola, Egidio Bottini, Andrea Magrini, Anna Neri, Fulvia Gloria-Bottini, Patrizia Saccucci
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 199:108-109
Objective The recent observation of an association of colon cancer with two polymorphic sites within the Adenosine Deaminase (ADA) gene suggests an involvement of these polymorphisms in the development of solid tumors. This prompted us to search for
Publikováno v:
Fertility and Sterility. 90:406-408
Objective To study the association of endometriosis with p53 codon 72 polymorphism in the population of central Italy and to search for possible interaction with the PTPN22 polymorphism. Design Study of p53 and PTPN22 polymorphisms in women with endo
Publikováno v:
European Journal of Radiology Open, Vol 2, Iss C, Pp 1-2 (2015)
European Journal of Radiology Open
European Journal of Radiology Open
A 75-year-old female underwent a High Resolution Computed Tomography (HRCT) scan for recurrent bronchitis and cough. HRCT images showed an anomalous supernumerary bronchus to the right upper lobe directly arising from the right side of distal trachea
Autor:
Patrizia Saccucci, Fulvia Gloria-Bottini, Andrea Magrini, Adalgisa Pietropolli, Maria Ammendola, Egidio Bottini
Objective To investigate the possible effect of clinical and genetic variables on the association between PTPN22 and endometriosis. Methods PTPN22, ACP1 and p53 codon 72 genetic polymorphisms and duration of previous pharmacological treatment were st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d049c2aec8bf94d277b980080b9b146d
http://hdl.handle.net/2108/79053
http://hdl.handle.net/2108/79053