Zobrazeno 1 - 10
of 891
pro vyhledávání: '"Nassogne"'
Autor:
Paquay Stephanie, Barrea Catherine, Sluysmans Thierry, Vachiery Jean-Luc, Loeckx Isabelle, Seneca Sara, Vô Christophe, Nassogne Marie-Cecile
Publikováno v:
Annals of Pediatric Cardiology, Vol 12, Iss 3, Pp 325-328 (2019)
NFU1 deficiency is a rare metabolic disorder affecting iron–sulfur cluster synthesis, an essential pathway for lipoic acid-dependent enzymatic activities and mitochondrial respiratory chain complexes. It is a little-known cause of pulmonary arteria
Externí odkaz:
https://doaj.org/article/513184f52510492c9780762e0393c5ea
Publikováno v:
Endocrine Regulations, Vol 51, Iss 4, Pp 216-219 (2017)
Cerebral germinoma is rare. Although the imaging of the germinoma is very evocative, it’s very polymorphic clinical expression is at the origin of misguided diagnosis, as illustrated in our case. We report the case of a 10-year-old girl with diabet
Externí odkaz:
https://doaj.org/article/4f9d10013b2547f494ca5dfbc5891922
Autor:
Grünert, Sarah C., Gautschi, Matthias, Baker, Joshua, Boyer, Monica, Burlina, Alberto, Casswall, Thomas, Corpeleijn, Willemijn, Çıki, Kismet, Cotter, Melanie, Crushell, Ellen, Derks, Terry G.J., Haas, Dorothea, Kilavuz, Sebile, Kingma, Sandra D.K., Korman, Stanley H., Kozek, Anne, de Laet, Corinne, Mundy, Helen, Nassogne, Marie Cecile, Quintero, Victor, Rossi, Alessandro, Spenger, Johannes, Spiegel, Ronen, Stephenne, Xavier, Stojkov, Darko, Tal, Galit, Veiga-da Cunha, Maria, Wortmann, Saskia B.
Publikováno v:
In Molecular Genetics and Metabolism June 2024 142(2)
Autor:
Everard, Emilie, Laeremans, Hilde, Boemer, François, Marie, Sandrine, Vincent, Marie-Françoise, Dewulf, Joseph P., Debray, François-Guillaume, De Laet, Corinne, Nassogne, Marie-Cécile
Publikováno v:
In European Journal of Paediatric Neurology March 2024 49:60-65
Publikováno v:
In European Journal of Paediatric Neurology January 2024 48:69-77
Autor:
Yeboah Kofi Gyening, Keren Boris, Mignot Cyril, Richard S. Brush, Marie-Cécile Nassogne, Martin-Paul Agbaga
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-10 (2023)
Abstract Spinocerebellar ataxia 34 (SCA34) is an autosomal dominant inherited disease characterized by age-related cerebellar degeneration and ataxia caused by mutations in the Elongation of Very Long Chain Fatty Acid-4 (ELOVL4) gene. The ELOVL4 enzy
Externí odkaz:
https://doaj.org/article/56bf065f1de443278b312bf8792439b0
Autor:
Blumental Sophie, Huisman Elisabeth, Cornet Marie-Coralie, Ferreiro Christine, De Schutter Iris, Reynders Marijke, Wybo Ingrid, Kabamba-Mukadi Benoît, Armano Ruth, Hermans Dominique, Nassogne Marie-Cécile, Mahadeb Bhavna, Fonteyne Christine, Van Berlaer Gerlant, Levy Jack, Moulin Didier, Vergison Anne, Malfroot Anne, Lepage Philippe
Publikováno v:
BMC Infectious Diseases, Vol 11, Iss 1, p 313 (2011)
Abstract Background During the 2009 influenza A/H1N1v pandemic, children were identified as a specific "at risk" group. We conducted a multicentric study to describe pattern of influenza A/H1N1v infection among hospitalized children in Brussels, Belg
Externí odkaz:
https://doaj.org/article/0d3bc712d4574a4a8b1c25fdc909e705
Autor:
von Wintzingerode, Lydia, Ben-Zeev, Bruria, Cesario, Claudia, Chan, Katie M., Depienne, Christel, Elpeleg, Orly, Iascone, Maria, Kelley, Whitley V., Nassogne, Marie-Cécile, Niceta, Marcello, Pezzani, Lidia, Rahner, Nils, Revencu, Nicole, Bekheirnia, Mir Reza, Santiago-Sim, Teresa, Tartaglia, Marco, Thompson, Michelle L., Trivisano, Marina, Hentschel, Julia, Sticht, Heinrich, Abou Jamra, Rami, Oppermann, Henry
Publikováno v:
In Genetics in Medicine July 2023 25(7)
Publikováno v:
In European Journal of Medical Genetics February 2023 66(2)
Publikováno v:
In Molecular Genetics and Metabolism July 2022 136(3):190-198