Zobrazeno 1 - 10
of 79
pro vyhledávání: '"M Papadimas"'
Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are part of the same pathophysiological spectrum and have common genetic and cerebrospinal fluid (CSF) biomarkers. Our aim here was to identify causative gene variants in a cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::16efcbfdfe0d59ae1b72913be5a8e14d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997050
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997050
The congenital disorders of glycosylation (CDG) are inborn errors of metabolism with a great genetic heterogeneity. Most CDG are caused by defects in the N-glycan biosynthesis, leading to multisystem phenotypes. However, the occurrence of tissue-rest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::fcaeb25187629c7b16fe45627d34e55a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078415
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078415
Autor:
Tavares, Ailton M.1,2,3 (AUTHOR) acmt@uevora.pt, Conceição, Ricardo4 (AUTHOR) ricardo.conceicao@imdea.org, Lopes, Francisco M.5,6 (AUTHOR) francisco.lopes@ipma.pt, Silva, Hugo G.3,7,8 (AUTHOR) hgsilva@uevora.pt
Publikováno v:
Energies (19961073). Nov2024, Vol. 17 Issue 21, p5490. 18p.
Autor:
Agah, Elmira1,2 (AUTHOR), Mojtabavi, Helia2,3 (AUTHOR), Behkar, Atefeh4 (AUTHOR), Heidari, Arash5,6 (AUTHOR), Ajdari, Atra2 (AUTHOR), Shaka, Zoha2 (AUTHOR), Mousavi, Seyed Vahid1 (AUTHOR), Firoozeh, Negar7 (AUTHOR), Tafakhori, Abbas1 (AUTHOR) abbas.tafakhori@gmail.com, Rezaei, Nima2 (AUTHOR) rezaei_nima@yahoo.com
Publikováno v:
Journal of Translational Medicine. 10/21/2024, Vol. 22 Issue 1, p1-15. 15p.
Autor:
Meher, Jitendra Kumar1 (AUTHOR) jitendra.meher@solarad.ai, Rizvi, Syed Haider Abbas1,2 (AUTHOR) bhramar@solarad.ai, Choudhary, Bhramar1 (AUTHOR) ravi@solarad.ai, Choudhary, Ravi1 (AUTHOR), Thakre, Yash1 (AUTHOR), Kumar, Ritesh1 (AUTHOR), Singh, Vikram2 (AUTHOR)
Publikováno v:
Energies (19961073). Jun2024, Vol. 17 Issue 12, p2913. 22p.
Publikováno v:
Pediatric Research. 58:390-390
Neonatal sepsis continues to speculate neonatologists all over the world, while it remains the prime cause of mortality and morbility of neonates, and especialy the preterms. Aim: Was to enrole sepsis, the pathogenic microbes and their sensitivities
Autor:
Conte, Federica1,2 (AUTHOR), Sam, Juda-El1 (AUTHOR), Lefeber, Dirk J.1,3 (AUTHOR) dirk.lefeber@radboudumc.nl, Passier, Robert2,4 (AUTHOR) dirk.lefeber@radboudumc.nl
Publikováno v:
International Journal of Molecular Sciences. May2023, Vol. 24 Issue 10, p8632. 60p.
Autor:
Natera‐de Benito, Daniel1,2 (AUTHOR), Olival, Jonathan3 (AUTHOR), Garcia‐Cabau, Carla4 (AUTHOR), Jou, Cristina2,5 (AUTHOR), Roldan, Mònica6,7 (AUTHOR), Codina, Anna2 (AUTHOR), Expósito‐Escudero, Jessica1,2 (AUTHOR), Batlle, Cristina3 (AUTHOR), Carrera‐García, Laura1,2 (AUTHOR), Ortez, Carlos1,2,8 (AUTHOR), Salvatella, Xavier4,9 (AUTHOR), Palau, Francesc3,7,8,10,11 (AUTHOR), Nascimento, Andrés1,2,8 (AUTHOR), Hoenicka, Janet3,8 (AUTHOR) janet.hoenicka@sjd.es
Publikováno v:
Annals of Clinical & Translational Neurology. Mar2023, Vol. 10 Issue 3, p408-425. 18p.
Autor:
Barnard, Jodi1 (AUTHOR), Hunt, Rachel1 (AUTHOR), Yucel, Mert1 (AUTHOR), Mazaud, David1 (AUTHOR), Smith, Bradley N.1,2 (AUTHOR), Fanto, Manolis1 (AUTHOR) manolis.fanto@kcl.ac.uk
Publikováno v:
Biomedical Reports. Nov2024, Vol. 21 Issue 5, pN.PAG-N.PAG. 1p.