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pro vyhledávání: '"Skardoutsou, Angeliki"'
BACKGROUND: In the present study we investigated the levels of proapoptotic caspase-9 and antiapoptotic Bcl-2 proteins in the sera of children and adolescents with idiopathic epilepsy and tried to relate the findings to the patients' clinical paramet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::873f4d84344244663bc1dc7c51a7db50
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3214319
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3214319
Akademický článek
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Autor:
Neilson, Derek E., Adams, Mark D., Orr, Caitlin M.D., Schelling, Deborah K., Eiben, Robert M., Kerr, Douglas S., Anderson, Jane, Bassuk, Alexander G., Bye, Ann M., Childs, Anne-Marie, Clarke, Antonia, Crow, Yanick J., Di Rocco, Maja, Dohna-Schwake, Christian, Dueckers, Gregor, Fasano, Alfonso E., Gika, Artemis D., Gionnis, Dimitris, Gorman, Mark P., Grattan-Smith, Padraic J., Hackenberg, Annette, Kuster, Alice, Lentschig, Markus G., Lopez-Laso, Eduardo, Marco, Elysa J., Mastroyianni, Sotiria, Perrier, Julie, Schmitt-Mechelke, Thomas, Servidei, Serenella, Skardoutsou, Angeliki, Uldall, Peter, van der Knaap, Marjo S., Goglin, Karrie C., Tefft, David L., Aubin, Cristin, de Jager, Philip, Hafler, David, Warman, Matthew L.
Publikováno v:
In The American Journal of Human Genetics 9 January 2009 84(1):44-51
Autor:
Voudris, Konstantinos A., Attilakos, Achilleas, Katsarou, Eustathia, Drakatos, Antonios, Dimou, Stamatia, Mastroyianni, Sotiria, Skardoutsou, Angeliki, Prassouli, Alexia, Garoufi, Anastasia
Publikováno v:
In Epilepsy Research 2006 70(2):211-217
Autor:
Voudris, Konstantinos A. *, Attilakos, Achilleas, Dimou, Stamatia, Mastroyianni, Sotiria, Katsarou, Eustathia, Skardoutsou, Angeliki, Garoufi, Anastasia
Publikováno v:
In Clinica Chimica Acta 2004 350(1):175-180
Publikováno v:
In Seizure: European Journal of Epilepsy 2003 12(8):599-601
Autor:
Voudris, Konstantinos 11Correspondence to: K. Voudris, MD, Department of Neurology, “P&A Kyriakou" Children’s Hospital, Thibon and Levadias St, Athens 115-27, Greece. march193@hol.gr, Moustaki, Maria, Zeis, Petros M., Dimou, Stamatia, Vagiakou, Eleni, Tsagris, Basilios, Skardoutsou, Angeliki
Publikováno v:
In Seizure: European Journal of Epilepsy September 2002 11(6):377-380
Autor:
Skardoutsou, Angeliki1,2 ppk@otenet.gr, Voudris, Konstantinos A.1,2, Tsagris, Vassilis1,2, Mathioudakis, John1,2, Karpathios, Themistoklis1,2
Publikováno v:
International Journal on Disability & Human Development (De Gruyter). Oct2000, Vol. 1 Issue 4, p243-246. 4p.
A 13-year-old Greek girl with pyruvate kinase deficiency and moya moya angiographic pattern is reported. She also had raised serum lipoprotein (a) concentration and was homozygous for the C677T mutation of the methylenetetrahydrofolate reductase gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6b3f97baaaf73b456bc4175dcd38fc3a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3116635
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3116635
Congenital cataracts-facial dysmorphism-neuropathy syndrome (CCFDN, MIM: 604168), is a recently delineated neurogenetic disease causing recurrent episodes of rhabdomyolysis; prevention and early diagnosis of rhabdomyolysis should be part of the clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f7701b41a21f32d6d06c74b1e83b7358
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3117388
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3117388