Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Dimitrios, Zafeiriou"'
Autor:
Vasiliki Sgouropoulou, Efthymia Vargiami, Maria Kyriazi, Sofia Kafterani, Stella Stabouli, Georgios Tsigaras, Athanasia Anastasiou, Maria Trachana, Dimitrios Zafeiriou
Publikováno v:
Prague Medical Report, Vol 125, Iss 1, Pp 62-68 (2024)
Takayasu arteritis is a large vessel vasculitis, characterized by granulomatous inflammation of arterial vessels, that typically affects the aorta, its main branches and pulmonary arteries. Disease diagnosis is a challenge and requires awareness of t
Externí odkaz:
https://doaj.org/article/64351338c71b43b29629ab7d712a9705
Autor:
Eleni Gavriilaki, Stefanos A. Tsiftsoglou, Tasoula Touloumenidou, Evangelia Farmaki, Paraskevi Panagopoulou, Elissavet Michailidou, Evaggelia-Evdoxia Koravou, Ioulia Mavrikou, Elias Iosifidis, Olga Tsiatsiou, Eleni Papadimitriou, Efimia Papadopoulou-Alataki, Penelope Georgia Papayanni, Christos Varelas, Styliani Kokkoris, Apostolia Papalexandri, Maria Fotoulaki, Assimina Galli-Tsinopoulou, Dimitrios Zafeiriou, Emmanuel Roilides, Ioanna Sakellari, Achilles Anagnostopoulos, Athanasios Tragiannidis
Publikováno v:
Current Issues in Molecular Biology, Vol 44, Iss 7, Pp 2811-2824 (2022)
Complement dysregulation has been documented in adults with COVID-19 and implicated in relevant pediatric inflammatory responses against SARS-CoV-2. We propose that signatures of complement missense coding SNPs associated with dysregulation could als
Externí odkaz:
https://doaj.org/article/026382604f88499ab0ee29b1303b5891
Autor:
Martin Magner, Zsuzsanna Almássy, Zoran Gucev, Beata Kieć-Wilk, Vasilica Plaiasu, Anna Tylki-Szymańska, Dimitrios Zafeiriou, Ioannis Zaganas, Christina Lampe
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022)
Abstract Background Mucopolysaccharidosis IVA (MPS IVA), or Morquio A syndrome, is a rare inherited metabolic disorder caused by deficiency of the lysosomal enzyme N-acetylgalactosamine-6-sulfatase. A progressive systemic skeletal chondrodysplasia, l
Externí odkaz:
https://doaj.org/article/3835f3c99fe74eb6b71668d6e1fb2966
Autor:
Anna Tylki-Szymańska, Zsuzsanna Almássy, Violetta Christophidou-Anastasiadou, Daniela Avdjieva-Tzavella, Ingeborg Barisic, Rimante Cerkauskiene, Goran Cuturilo, Maja Djiordjevic, Zoran Gucev, Anna Hlavata, Beata Kieć-Wilk, Martin Magner, Ivan Pecin, Vasilica Plaiasu, Mira Samardzic, Dimitrios Zafeiriou, Ioannis Zaganas, Christina Lampe
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-16 (2022)
Abstract Background Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by defects in genes coding for different lysosomal enzymes which degrade glycosaminoglycans. Impaired lysosomal degradation causes cell dysfunction lead
Externí odkaz:
https://doaj.org/article/c70c1cc31551430c8564d28031134aef
Autor:
Stella Stabouli, Vasilios Kotsis, Olga Maliachova, Nikoleta Printza, Athanasia Chainoglou, Athanasios Christoforidis, Anna Taparkou, John Dotis, Evangelia Farmaki, Dimitrios Zafeiriou
Publikováno v:
International Journal of Cardiology. Hypertension, Vol 4, Iss , Pp 100025- (2020)
Background and aims: Matrix metalloproteinases (MMPs) may contribute to the pathogenesis of arterial stiffness inducing extracellular matrix remodeling. We aimed to compare MMP-2 and -9 levels in children with chronic kidney disease (CKD), type 1 dia
Externí odkaz:
https://doaj.org/article/a08350046d344f9994d49934a6a252c7
Autor:
Lauren A. Beslow, Shannon C. Agner, Jonathan D. Santoro, Dipak Ram, Jenny L. Wilson, Dana Harrar, Brian Appavu, Stuart M. Fraser, Thomas Rossor, Marcela D. Torres, Manoëlle Kossorotoff, Yenny C. Zuñiga Zambrano, Marta Hernández-Chávez, Sahar M.A. Hassanein, Dimitrios Zafeiriou, Michael M. Dowling, Ilona Kopyta, Nicholas V. Stence, Timothy J. Bernard, Nomazulu Dlamini, Ahmed Abd El-Hamid Rihan, Maha Mohammed, Moustafa Farid, Wessam S.S. Guergues, Mohamed O.E. Babiker, Oded Hochberg, Paola Saracco, Thomas Main, Andrew Mallick, Selina Kala, Bryan L. Philbrook, Kartik Reddy, Rebecca N. Ichord, Evelyn K. Shih, Rachel P. Pearson, Mubeen F. Rafay, Mukta Sharma, Mary Allen Staat, Sudhakar Vadivelu, Marvid Duarte, Mary Suzanne Whitworth, Manish Parakh, Kevin Meesters, Charles-Joris Roud, Marianne Leruez- Ville, Vijeya Ganesan, Laura L. Lehman, Michael Rivkin, Zulma Hernandez, Fernanda Balut, Maria Celeste Buompadre, Heidy J. Gómez Naranjo, Veronica Gonzalez Alvarez, Nihal Bakeer, Stephanie Garrison, Christopher Belcher, Lorie Miller, Maria Whitmore, Giulia Amico, Mariasavina Severino, Marta Bertamino, Sara Signa, Lisa R. Sun, Ryan J. Felling, Pawan Kashyape, Lucia Gerstl, Gordana Kovacevic, Anna Basu, Yusri Taha, Warren D. Lo, Maggie L.Y. Yau, Deirdre Peake, Kim Stevenson, Samson Gwer, Andrea Andrade, Catherine Amlie- Lefond, Jacqueline Lee-Eng, Sarah Lee, Janette Mailo, Moran Hausman- Kedem, Kamna Jaiswal, Kellie Brown, Belinda Stojanovski, Mark T Mackay, Adriana Carolina Vargas Nino, Daune McGregor, Gabrielle deVeber, Ishvinder Bhathal, NP Liza Pulcine, Mahendra Moharir, Bruce Bjornson, Danny H.C. Kim, Adam Kirton, Amalia Floer, Christine K. Fox, Christiana Smith- Anderson, Kelly Wilt, Vivian Thompson, Michael L. Chang, Marilyn Tan, Lori C Jordan, Annette E. Grefe, Kristin Guilliams, Michael J. Noetzel
Publikováno v:
Stroke. 53:2497-2503
Background: Data from the early pandemic revealed that 0.62% of children hospitalized with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had an acute arterial ischemic stroke (AIS). In a larger cohort from June 2020 to December 2020, w
Neuromuscular diseases and their cardiac manifestations under the spectrum of cardiovascular imaging
Autor:
Georgios M. Alexandridis, Efstathios D. Pagourelias, Nikolaos Fragakis, Maria Kyriazi, Efthymia Vargiami, Dimitrios Zafeiriou, Vassilios P. Vassilikos
Publikováno v:
Heart Failure Reviews. 27:2045-2058
Autor:
Maria Kyriazi, Efrosini Kalyva, Efthymia Vargiami, Konstantinos Krikonis, Dimitrios Zafeiriou
Publikováno v:
Frontiers in Psychiatry, Vol 10 (2019)
Tics wax and wane regarding their severity, while their expression is affected by non-motor sensory or cognitive elements that are mostly known as “premonitory urges.” Since premonitory urges are often used in non-pharmacological interventions to
Externí odkaz:
https://doaj.org/article/f70549aba3a94725bd56bbb5a74e9bbe
Autor:
Vasiliki Karava, Antonia Kondou, John Dotis, Georgia Sotiriou, Spyridon Gerou, Helen Michelakakis, Euthymia Vargiami, Marina Economou, Dimitrios Zafeiriou, Nikoleta Printza
Publikováno v:
Children, Vol 8, Iss 2, p 112 (2021)
Methylmalonic acidemia and homocystinuria cobalamin C (cblC) type is the most common inborn error of the intracellular cobalamin metabolism, associated with multisystem involvement and high mortality rates, especially in the early-onset form of the d
Externí odkaz:
https://doaj.org/article/9143bdbdfe004d12a7863baf602d7f84
Autor:
Stella Stabouli, Euthymia Vargiami, Olga Maliachova, Nikoleta Printza, John Dotis, Maria Kyriazi, Konstantinos O. Papazoglou, Dimitrios Zafeiriou
Publikováno v:
Case Reports in Pediatrics, Vol 2018 (2018)
Arterial hypertension is a common finding in patients with neurofibromatosis (NF) type 1. Renovascular hypertension due to renal artery stenosis or midaortic syndrome could be the underlying cause. We report the case of a 4-year-old girl with NF type
Externí odkaz:
https://doaj.org/article/8a97ccaebb80476da3ecaaa2509b0f58