Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Ricardo Laurini"'
Publikováno v:
Cellular Oncology, Vol 26, Iss 1-2, Pp 21-29 (2004)
This analysis of DNA‐ploidy heterogeneity in advanced gastric carcinomas is consistent with the hypothesis of the emergence of a single aneuploid cell clone as a crucial mechanism in the progression from early gastric carcinoma to advanced gastric
Externí odkaz:
https://doaj.org/article/9fb1e4255bde4c0a9dc3a3ac1eaab536
Publikováno v:
Pediatric Surgery International, vol. 19, no. 9-10, pp. 662-8
Surgery for Hirschsprung's disease is often complicated by post-operative bowel motility disorders. The impact of intestinal neural histology on the surgical outcome has been previously studied, but no information is available concerning the influenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f4a2a93dad979c9df5c522a155435a0
http://doc.rero.ch/record/319854/files/383_2003_Article_1026.pdf
http://doc.rero.ch/record/319854/files/383_2003_Article_1026.pdf
Autor:
Ricardo Laurini, Blaise J. Meyrat
Publikováno v:
Pediatric Surgery International, vol. 19, no. 11, pp. 715-20
Intestinal neuronal dysplasia is a controversial form of dysganglionosis that has been described both as an isolated disorder and in association with Hirschsprung's disease. It has been blamed for the bad outcome of bowel function in patients operate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba2f87f08c8544ca2ff1e18f54dfc23d
http://doc.rero.ch/record/316308/files/383_2003_Article_1035.pdf
http://doc.rero.ch/record/316308/files/383_2003_Article_1035.pdf
Autor:
Ann Hellström, Gerd Holmström, Vineta Fellman, Lena Hellström-Westas, Hugo Lagercrantz, Ricardo Laurini, Karin Källén, Marija Simic, Uwe Ewald, Annika Jeppsson, Ingrid Oestlund, Lennart Stigson, Dordi Austeng, Solveig Nordén-Lindeberg, Gunnar Sjörs, Peter Jakobsson, Thomas Fritz, Elisabeth Olhager, Kristina Tornqvist, Eva Lindberg, Fredrik Serenius, Mikael Norman, Agneta Wallin, Kent Johansson, Bo Strömberg, M Wennergren, Tore Nilstun, Karel Marsal, Anita Lundqvist, Mats Blennow, Karin Stjernqvist, Magnus Westgren, Per Holmgren
Publikováno v:
Acta Paediatrica. 99:978-992
Aims: The aim of this study was to determine the incidence of neonatal morbidity in extremely preterm infants and to identify associated risk factors. Methods: Population based study of infants born before 27 gestational weeks and admitted for neonat
Publikováno v:
Tidsskrift for Den norske legeforening. 129:1000-1003
A 61-year-old man was admitted to our department with radicular back-pain and progressive gait-difficulties. On examination he had flaccid paraparesis and bladder-retention. He subsequently developed palsy of n. oculomotorius, dysarthria, right-sided
Autor:
Claudio De Felice, Gabriele Tonni, Ricardo Laurini, Giuseppe Latini, Daniele Costantini, Paolo Toti, Carla Martufi, Bruno De Capua, Annalisa Giannuzzi
Publikováno v:
Early Human Development. 84:667-671
Recurrent otitis media with effusion (OME) is a leading cause of acquired hearing loss in childhood. Histological chorioamnionitis (HCA) is an important cause of preterm delivery and neonatal morbidity and mortality. Here, we tested the hypothesis of
Publikováno v:
International Journal of Gynecological Cancer. 16:1679-1684
Matrix metalloproteinases (MMPs) are group of enzymes thought to play an important role in trophoblastic and tumor invasion. The aim of our study was to investigate the trophoblastic expression of MMPs and p53 in normal trophoblast and hydatidiform m
Publikováno v:
Journal of International Medical Research. 34:247-255
This study evaluated the relationship between the activity of the inflammatory indicator adenosine deaminase (ADA) in placental tissue and maternal and fetal (umbilical cord) plasma and the severity of pre-eclampsia. Maternal and umbilical vein whole
Publikováno v:
Fetal Diagnosis and Therapy. 21:8-12
A 34-year-old healthy gravida 2 para 1 presented after an uncomplicated pregnancy at term with a 2-day history of diminished fetal movements. Fetal anemia was suspected by fetal heart rate monitoring and Doppler estimation of the fetal peak blood flo
Autor:
Ricardo Laurini, Giuseppe Latini, Giorgio Bianciardi, K Shirriff, Stefano Parrini, C De Felice, G. Di Maggio
Publikováno v:
Fractals. 13:73-82
Approximately 90% of achondroplasia (ACH) cases are the result of a de novo mutation, with no phenotypical markers for the unaffected ACH parents being known to date. Here, the hypothesis of the presence of an oral mucosal microvascular abnormality i