Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Mathioudakis, J"'
Publikováno v:
Breathe (Sheffield, England) [Breathe (Sheff)] 2024 Nov 12; Vol. 20 (3), pp. 245081. Date of Electronic Publication: 2024 Nov 12 (Print Publication: 2024).
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
In Clinical Microbiology and Infection October 2003 9(10):1006-1010
Autor:
Michelakakis, H, Skardoutsou, A, Mathioudakis, J, Moraitou, M, Dimitriou, E, Voudris, C, Karpathios, Th
Publikováno v:
In Blood Cells, Molecules and Diseases January 2002 28(1):1-4
Autor:
Najimi, Nouhaila1,2,3 (AUTHOR) Nouhaila.najimi@um5r.ac.ma, Kadi, Chaimae2,3,4 (AUTHOR), Elmtili, Noureddine4 (AUTHOR), Seghrouchni, Fouad2,3 (AUTHOR), Bakri, Youssef1 (AUTHOR)
Publikováno v:
Human Antibodies. 2024, Vol. 32 Issue 3, p85-106. 22p.
The clinical efficacy, safety and bacteriological eradication of Group A p-haemolytic streptococci (GABHS) from the throat was studied after treatment of streptococcal tonsillopharyngitis with three commonly used oral antibiotics in a prospective, op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::92f2df8b431f4da4470b67d991920fb4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084993
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084993
Objective To document, over two consecutive respiratory syncytial virus (RSV) seasons, the occurrence of acute otitis media (AOM) and recurrence of respiratory distress in children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::b5356f418e3d65f2da13913c41982e15
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084397
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084397
Autor:
Michelakakis, H Skardoutsou, A Mathioudakis, J Moraitou, M and Dimitriou, E Voudris, C Karpathios, T
Gaucher disease, in most cases, is the result of mutations in the beta-glucocerebrosidase gene. More than 150 such mutations have been identified so far. Mutation D409H is the second most frequent in Greek patients, accounting for 15.5% of all identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::10b54ae1a1081ca889e9ea7613f5de6a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081124
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081124
Visceral focal lesions are rarely encountered in patients with leishmaniasis despite the fact that splenomegaly, and to a lesser extent hepatomegaly, predominate among the clinical features of the disease. We present, using high resolution ultrasonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8ec0809042007be17ea10d31182ede61
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3004863
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3004863
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare hamartomatous polyposis syndrome with features of macrocephaly, intestinal juvenile polyposis, visceral lipomas and developmental delay. An autosomal dominant pattern of inheritance exists in some fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::4615dbb726f52d0667fb1f3af8df634b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2986914
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2986914