Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Polichronis, A."'
Publikováno v:
In Clinical Nutrition ESPEN December 2022 52:395-420
Autor:
Wehner, Elizabeth H., Gallagher, John S., Papaderos, Polichronis, Alvensleben, Uta Fritze-von, Westfall, Kyle B.
Publikováno v:
Mon.Not.Roy.Astron.Soc.371:1047-1056,2006
NGC 3310 is a local galaxy with an intense, ongoing starburst thought to result from a merger with a companion galaxy. It has several known tidal features in the northwest and southern regions around the main galactic disc, as well as a closed, tidal
Externí odkaz:
http://arxiv.org/abs/astro-ph/0607088
Publikováno v:
Clinical Nutrition ESPEN. 52:395-420
The micronutrient status of those receiving long-term enteral nutrition (EN) is poorly characterised. This systematic review was undertaken to determine prevalence of micronutrient deficiency in those receiving EN; the impact of the route of feeding;
Autor:
Karakasi, Maria-Valeria, Vasilikos, Epameinondas, Voultsos, Polichronis, Vlachaki, Aikaterini, Pavlidis, Pavlos
Publikováno v:
In Journal of Forensic and Legal Medicine February 2017 46:1-10
Autor:
Bousios, Polichronis
Αυτή η διατριβή φιλοδοξεί να απαντήσει στο ερώτημα της σχέσης ανάμεσα στη φιλοσοφία και τη μη φιλοσοφία στο έργο του Gabriel Marcel. Με άλλα λόγ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::5c81b6847718360e2b57f653114b2281
https://olympias.lib.uoi.gr/jspui/handle/123456789/32410
https://olympias.lib.uoi.gr/jspui/handle/123456789/32410
Akademický článek
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Autor:
Christos Paliouras, Georgios Aperis, Foteini Lamprianou, Giorgos Ntetskas, Konstantinos Roufas, Polichronis Alivanis
Publikováno v:
Nefrología, Vol 35, Iss 6, Pp 578-581 (2015)
Fabry disease is a rare X-linked lysosomal storage disorder of glycosphingolipids, caused by the partial or complete deficiency of the lysosomal enzyme alpha-galactosidase A (a-Gal A). The missense mutation pN215S usually causes a milder form of the
Externí odkaz:
https://doaj.org/article/23d80a9068c64a5d93e04258fe67731b
Autor:
Despina Hadjipanagi, Gregory Papagregoriou, Constantina Koutsofti, Christiana Polydorou, Polichronis Alivanis, Aimilios Andrikos, Stalo Christodoulidou, Manthos Dardamanis, Athanasios A. Diamantopoulos, Anastasios Fountoglou, Eleni Frangou, Eleni Georgaki, Ioannis Giannikouris, Velissarios Gkinis, Pavlos C. Goudas, Rigas G. Kalaitzidis, Nikolaos Kaperonis, Georgios Koutroumpas, George Makrydimas, Grigorios Myserlis, Andromachi Mitsioni, Christos Paliouras, Fotios Papachristou, Dorothea Papadopoulou, Nikolaos Papagalanis, Aikaterini Papagianni, Garyfalia Perysinaki, Ekaterini Siomou, Konstantinos Sombolos, Ioannis Tzanakis, Georgios V. Vergoulas, Nicoletta Printza, Constantinos Deltas
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2203
Alport syndrome (AS) is the most frequent monogenic inherited glomerulopathy and is also genetically and clinically heterogeneous. It is caused by semi-dominant pathogenic variants in the X-linked COL4A5 (NM_000495.5) gene or recessive variants in th
Autor:
Sánchez Goñi, María Fernanda, Desprat, Stéphanie, Daniau, Anne-Laure, Bassinot, Frank C., Polanco-Martínez, Josué M., Harrison, Sandy P., Allen, Judy R. M., Anderson, R. Scott, Behling, Hermann, Bonnefille, Raymonde, Burjachs, Francesc, Carrión, José S., Cheddadi, Rachid, Clark, James S., Combourieu-Nebout, Nathalie, Mustaphi, Colin. J. Courtney, Debusk, Georg H., Dupont, Lydie M., Finch, Jemma M., Fletcher, William J., Giardini, Marco, González, Catalina, Gosling, William D., Grigg, Laurie D., Grimm, Eric C., Hayashi, Ryoma, Helmens, Karin, Heusser, Linda E., Hill, Trevor, Hope, Geoffrey, Huntley, Brian, Igarashi, Yaeko, Irino, Tomohisa, Jacobs, Bonnie, Jiménez-Moreno, Gonzalo, Kawai, Sayuri, Kershaw, A. Peter, Kumon, Fujio, Lawson, Ian T., Ledru, Marie-Pierre, Lézine, Anne-Marie, Liew, Ping Mei, Magri, Donatella, Marchant, Robert, Margari, Vasiliki, Mayle, Francis E., McKenzie, G. Merna, Moss, Patrick, Müller, Stefanie, Müller, Ulrich C., Naughton, Filipa, Newnham, Rewi M., Oba, Tadamichi, Pérez-Obiol, Ramón, Pini, Roberta, Ravazzi, Cesare, Roucoux, Katy H., Rucina, Stephen M., Scott, Louis, Takahara, Hikaru, Tzedakis, Polichronis C., Urrego, Dunia H., van Geel, Bas, Valencia, B. Guido, Vandergoes, Marcus J., Vincens, Annie, Whitlock, Cathy L., Willard, Debra A., Yamamoto, Masanobu
Quaternary records provide an opportunity to examine the nature of the vegetation and fire responses to rapid past climate changes comparable in velocity and magnitude to those expected in the 21st-century. The best documented examples of rapid clima
Externí odkaz:
http://hdl.handle.net/10150/625837
http://arizona.openrepository.com/arizona/handle/10150/625837
http://arizona.openrepository.com/arizona/handle/10150/625837
Publikováno v:
Clinical Nutrition ESPEN. 54:460