Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Somaschini, M"'
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 6, Iss 1, Pp e060134-e060134 (2017)
Mutations in genes encoding surfactant protein B (SP-B), ATP-binding cassette transporter A3 (ABCA3) and surfactant protein C (SP-C) can result in neonatal and pediatric lung disease. We retrospectively reviewed 391 molecular analyses of genes encodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e920df5cfa114104b97e0c9d73f00f0a
http://www.jpnim.com/index.php/jpnim/article/download/060134/425
http://www.jpnim.com/index.php/jpnim/article/download/060134/425
Autor:
Brenner, BM, Charlton, J, Luyckx, V, Manfellotto, D, Perico, N, Remuzzi, G, Somaschini, M, Valensise, H, Adu, D, Allegaert, Karel, Benedetto, C, Cetin, I, Chevalier, R, Cortinovis, M, D'Anna, R, Duvekot, J.J., Escribano, J, Fanos, V, Ferrazzi, E, Frusca, T, Glassock, RJ, Gyselaers, W, Mecacci, F, Montini, G, Osmond, C, Ramenghi, L, Romagnani, P, Santoro, A, Simeoni, U, Steegers, Eric, Vikse, BE
Publikováno v:
Nephron, 136(1), 3-49. Karger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::801a6bb65f04f9580236659ce54f9ce0
https://pure.eur.nl/en/publications/05e82919-78e2-4777-bf88-11ff4e3178b6
https://pure.eur.nl/en/publications/05e82919-78e2-4777-bf88-11ff4e3178b6
Publikováno v:
European Journal of Pediatrics. 1999, Vol. 158 Issue 10, p780-784. 5p.
Autor:
Mattia Glauber, P. Ferrazzi, Fiocchi R, Somaschini M, Mamprin F, Szefner J, Michele Senni, Amando Gamba
Publikováno v:
The International Journal of Artificial Organs. 18:649-655
Two different anticoagulation protocols were used in 49 consecutive patients mechanically supported either for bridge to transplantation (11) or for recovery of myocardial function after cardiac surgery (35). In 46 patients a Biomedicus centrifugal p
Autor:
Somaschini, M., Castiglioni, E., Volonteri, C., Cursi, M., Ferrari, M., Carrera, P., Nobile, Stefano
Publikováno v:
Scopus-Elsevier
Bronchopulmonary dysplasia (BPD) is the most frequent chronic lung disease in preterm newborn infants. It is a multifactorial disease caused by the interaction between environmental and genetic factors. The aim of this study is to identify genetic va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0a86e45ec60d57999ba5e054d71e200
Publikováno v:
In European Urology Supplements October 2019 18(7):e2952-e2952
Autor:
Salvatore, Silvia, Finazzi, Sergio, Radaelli, Giovanni, Lotzniker, Milvia, Zuccotti, Gian Vincenzo, Agosti, M., Avanzini, A., Besana, R., Biasucci, G., Bonabitacola, T., Busti, G., Calzi, P., Colombo, M., Cucchi, G., Dilillo, D., Elsi, B., Galluzzo, C., Gibelli, A., Guidali, P., Lazzati, A., Luini, C., Meneghin, F., Milone, V., Morandi, F., Nespoli, L., Pacati, I., Pigni, S., Podestà, A., Rondanini, G. F., Rottoli, A., Santucci, S., Scotta, M. S., Somaschini, M., Sterpa, A., Taveggia, A., Varisco, T.
Publikováno v:
The American journal of gastroenterology. 102(1)
The aim of this study was to estimate the prevalence of undiagnosed celiac disease (CD) in the parents of preterm and/or small for gestational age (SGA) infants.A sample of 1,714 parents (868 women, 846 men) of 905 preterm (37 wk of gestational age)