Zobrazeno 1 - 10
of 213
pro vyhledávání: '"A. Xaidara"'
Autor:
Emilia Papakonstantinou, Marina Xaidara, Vassiliki Siopi, Marianna Giannoglou, George Katsaros, Georgios Theodorou, Eirini Maratou, Kalliopi-Anna Poulia, George D. Dimitriadis, Panagiotis N. Skandamis
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 5; Pages: 3001
This randomized, single blind, cross-over study investigated the glycemic responses to three spaghetti No 7 types differing in dietary protein and soluble fiber content. Fourteen clinically and metabolically healthy, fasting individuals (25 ± 1 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::749e9c7784a118cbf2abb7ae45a079e4
https://pubmed.ncbi.nlm.nih.gov/35270698
https://pubmed.ncbi.nlm.nih.gov/35270698
This randomized, single blind, cross-over study investigated the glycemic responses to three spaghetti No 7 types differing in dietary protein and soluble fiber content. Fourteen clinically and metabolically healthy, fasting individuals (25 ± 1 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::159e3773655071bbb8628f1d07c14d09
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3057325
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3057325
Akademický článek
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Publikováno v:
Pediatric Pulmonology. 50:E13-E16
Summary Postinfectious bronchiolitis obliterans is a chronic incapacitating disease with persistent airway inflammation. However, the efficacy of systemic corticosteroids has never been studied systematically. In the presented case, serial spirometry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0cb4697002c8552b21387e89583ae89
https://doi.org/10.1002/ppul.23157
https://doi.org/10.1002/ppul.23157
Autor:
E. Karavitakis, P. Krallis, A. Xaidara, Artemis Doulgeraki, Helen Athanasopoulou, Alice Costantini, Outi Mäkitie, Nina Jäntti, Anders Kämpe
Publikováno v:
Bone Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83c7fbd310c911e4fb895ad8fb4092ad
https://doi.org/10.1530/boneabs.6.p107
https://doi.org/10.1530/boneabs.6.p107
Niemann-Pick type C disease (NPC) is a neurovisceral lysosomal storage disease caused by mutations in either the NPC1 or the NPC2 gene. It is a cellular lipid trafficking disorder characterized by the accumulation of unesterified cholesterol and vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8c90da242ccb3feedc9563448cc5d524
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086762
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086762
Autor:
Dimitrios I. Zafeiriou, Irene Mavridou, Lilia Lycopoulou, Helen Michelakakis, Philippe Latour, Daniel Grinberg, Lluïsa Vilageliu, E. Dimitriou, Marie T. Vanier, Athina Xaidara, Sevasti Bostantjopoulou
Publikováno v:
JIMD Reports ISBN: 9783662561379
Niemann-Pick type C disease (NPC) is a neurovisceral lysosomal storage disease caused by mutations in either the NPC1 or the NPC2 gene. It is a cellular lipid trafficking disorder characterized by the accumulation of unesterified cholesterol and vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9930c24fad1938a2c3ee266e045a046
https://doi.org/10.1007/8904_2016_41
https://doi.org/10.1007/8904_2016_41
Autor:
Emmanouil Karavitakis, Maria Tzetis, Periklis Makrythanasis, Eleni Apazidou, Emmanuel Kanavakis, Athena Xaidara, Konstantina Kosma, Sofia Kitsiou-Tzeli
Publikováno v:
American Journal of Medical Genetics Part A. 164:666-670
Constitutional microdeletions affecting 3q13.2q13.31 are rare and attempts for genotype–phenotype correlations have only recently been made in a cohort of 28 patients. The major phenotypic features of this rare syndrome are hypotonia, developmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e3913a9418bd16d87752d0c85f92cd
https://doi.org/10.1002/ajmg.a.36346
https://doi.org/10.1002/ajmg.a.36346
Publikováno v:
Pediatric Dermatology. 31:125-130
A growing number of dermatologists dispute the existence of infantile seborrheic dermatitis (ISD) as an independent clinical entity. Therefore the aim of the present study was to estimate the epidemiologic features of ISD in a defined population of G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ec01b08dbb2f92cc549ded882604b09
https://doi.org/10.1111/pde.12216
https://doi.org/10.1111/pde.12216
Autor:
Helen Michelakakis, Daniel Grinberg, S. Douzgou, E. Dimitriou, Marie T. Vanier, Irene Mavridou, Athina Xaidara, Lluïsa Vilageliu, Mónica Cozar, D. Lianou
Publikováno v:
Clinical Genetics. 85:543-547
Niemann–Pick type C (NPC) disease is a rare autosomal recessive lysosomal storage disease, exhibiting an extremely heterogeneous clinical phenotype. It is a cellular lipid trafficking disorder characterized by the accumulation in the lysosomal/late
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0949738c296b083dba4ad4479ff599c
https://doi.org/10.1111/cge.12200
https://doi.org/10.1111/cge.12200