Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Robert, Carlier"'
Autor:
Nicholas Heming, Robert Carlier, Helene Prigent, Ahmed Mekki, Camille Jousset, Frederic Lofaso, Xavier Ambrosi, Rania Bounab, Virginie Maxime, Arnaud Mansart, Pascal Crenn, Pierre Moine, Fabien Foltzer, Bernard Cuenoud, Tobias Konz, John Corthesy, Maurice Beaumont, Mickaël Hartweg, Claudia Roessle, Jean-Charles Preiser, Denis Breuillé, Djillali Annane
Publikováno v:
Critical Care, Vol 26, Iss 1, Pp 1-14 (2022)
Abstract Background A defining feature of prolonged critical illness is muscle wasting, leading to impaired recovery. Supplementation with a tailored blend of amino acids may bolster the innate gut defence, promote intestinal mucosa repair and limit
Externí odkaz:
https://doaj.org/article/60d1a1313e5f4b1db84d5a7ef95c2a4c
Autor:
Thomas Le Tat, Robert Carlier, Mostafa El Hajjam, Guillaume-Marie Sarrot, Ilan Obadia, Mickael Tordjman, Jeffery Zhou
Publikováno v:
CVIR Endovascular, Vol 5, Iss 1, Pp 1-3 (2022)
Abstract Background Pancreatic microcystic serous cystadenoma are rare benign pancreatic tumors. No treatment is needed in most cases as this lesion is often discovered incidentally. Surgery is not required except in symptomatic cases. Case presentat
Externí odkaz:
https://doaj.org/article/95dd9eab5c8544489f55ad65aef0bb41
Autor:
Malika Foy, Corinne Métay, Michael Frank, Nicolas Denarié, Salma Adham, Clarisse Billon, Anne Legrand, Xavier Jeunemaitre, Fabrice Gillas, Karen Gaudon, Philippe De Mazancourt, Ahmed Mekki, Robert Carlier, Karelle Benistan
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Kyphoscoliotic Ehlers–Danlos syndrome (kEDS) is a rare genetic disorder combining congenital hypotonia, congenital/early onset and progressive kyphoscoliosis, and generalized joint hypermobility. Vascular fragility is another characteristi
Externí odkaz:
https://doaj.org/article/45807d7cf6fb4df093eb632eb220d642
Autor:
Abdallah FAYSSOIL, MD, Robert CARLIER, MD, Nicolas MANSENCAL, MD, Frédéric LOFASO, MD, Djillali ANNANE, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 3, Pp 843-846 (2022)
Acute hypoxemic respiratory failure (AHRF) is a major complication of COVID-19 pneumonia and parasternal intercostal muscle thickening may be used as a biomarker to assess inspiratory effort. We report the case of a high utilization of parasternal in
Externí odkaz:
https://doaj.org/article/2428e6e4fe5847d08677eb2ebf3f3fe1
Autor:
Malika Foy, Philippe deMazancourt, Dominique Bremond Gignac, Fabrice Gillas, Nawel Trigui, Ahmed Mekki, Robert Carlier, Karelle Benistan
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract We described a novel de novo missense variant of the gene encoding Collagen alpha‐2(V) chain, associated with the classical Ehlers–Danlos syndrome (cEDS) (OMIM#130010), in a 14‐year‐old patient who presented with congenital and sever
Externí odkaz:
https://doaj.org/article/55177b8865a34caf8d28f756301e46df
Publikováno v:
European Medical Journal, Pp 54-62 (2021)
Objective: The main purpose of this study was to evaluate the prevalence, form, and severity of scoliosis in a population of adults meeting the 2017 criteria for hypermobile Ehlers-Danlos syndrome (hEDS). The second objective was to compare the preva
Externí odkaz:
https://doaj.org/article/3473ad32ae444b5d90459393cced82a6
Autor:
Andreas Marg, Helena Escobar, Nikos Karaiskos, Stefanie A. Grunwald, Eric Metzler, Janine Kieshauer, Sascha Sauer, Diana Pasemann, Edoardo Malfatti, Dominique Mompoint, Susanna Quijano-Roy, Anastasiya Boltengagen, Joanna Schneider, Markus Schülke, Séverine Kunz, Robert Carlier, Carmen Birchmeier, Helge Amthor, Andreas Spuler, Christine Kocks, Nikolaus Rajewsky, Simone Spuler
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Skeletal muscle stem cells express the transcription factor Pax7. Here, the authors isolate, from human muscle, cells that are positive for the endothelial marker CLEC14A and show that despite not expressing pax7, these cells regenerate muscle and co
Externí odkaz:
https://doaj.org/article/ce96cb57dae14384b0b97d2a3e6fda84
Autor:
Quentin Cosnefroy, François Marchal, Laurence Bellaiche, Robert Carlier, Cyrille Cazeau, Antoine Perrier, Jean-Christophe Theil, Gilles Berillon
Publikováno v:
Bulletins et Mémoires de la Société d’Anthropologie de Paris, Vol 34 (2021)
Externí odkaz:
https://doaj.org/article/8ae8e01987b840c9937394004ad292bb
Autor:
Malika Foy, Philippe De Mazancourt, Corinne Métay, Robert Carlier, Valérie Allamand, Corine Gartioux, Fabrice Gillas, Nawel Miri, Valérie Jobic, Ahmed Mekki, Pascale Richard, Caroline Michot, Karelle Benistan
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract COL1‐related overlap disorder is a condition, which is not yet considered as part of the 2017 EDS classification. However, it should be investigated as an alternative diagnosis for any patient with hypermobile EDS. This could allow providi
Externí odkaz:
https://doaj.org/article/bc9b9c0659c04f07a950e25423c47d42
Autor:
Simon Bessis, Latifa Noussair, Veronica Rodriguez-Nava, Camille Jousset, Clara Duran, Alina Beresteanu, Morgan Matt, Benjamin Davido, Robert Carlier, Emmanuelle Bergeron, Pierre-Edouard Fournier, Jean Louis Herrmann, Aurélien Dinh
Publikováno v:
Emerging Infectious Diseases, Vol 26, Iss 2, Pp 376-378 (2020)
Mycetoma is a chronic infection that is slow to develop and heal. It can be caused by fungi (eumycetoma) or bacteria (actinomycetoma). We describe a case of actinomycetoma caused by Actinomadura mexicana in the Caribbean region.
Externí odkaz:
https://doaj.org/article/96b30b0fe0844a1fafe3882a3bb08328