Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Abdourahim Chamouine"'
Autor:
Issifou Yaya, Adrien Pourageaud, Benjamin Derbez, Marie-Hélène Odièvre, Damien Oudin Doglioni, Marieke Podevin, Gaëlle Thomas, Lisa Yombo-Kokule, Christian Godart, Maryannick Lepetit, Tania Cassubie-Mercier, Frederic Galacteros, Olivier Chassany, DREPAtient study group, Frédéric Galactéros, Odièvre-Montanié Marie-Hélène, Sonia Pavan, Patricia Aguilar-Martinez, Jean-Benoït Arlet, Giovanna Cannas, Abdourahim Chamouine, Maryse Etienne-Julan, Corinne Guitton, Sylvain Le Jeune, Gylna Loko, Corinne Pondarre
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundSickle cell disease (SCD) is an inherited autosomal recessive disorder exhibiting a range of symptoms and acute and/or chronic complications that affect the quality of life. This study aimed to assess health-related quality of life (HRQoL)
Externí odkaz:
https://doaj.org/article/a284d4e29c9e4cdea9cf3d21b8684a57
Autor:
Mathilde Veneziano Broccia, Julia Vergier, Audrey Benoit, Yoann Huguenin, Anne Lambilliotte, Marie Pierre Castex, Stephanie Gourdon, Ghislaine Ithier, Kamila Kebaili, Pierre Rohrlich, Corinne Pondarre, Abdourahim Chamouine, Pauline Simon, Kokou Placide Agbo Kpati, Slimane Allali, Sandrine Baron-Joly, Sophie Bayart, Nicolas Billaud, Valentine Brousse, Cecile Dumesnil, Nathalie Garnier, Isabelle Guichard, Laure Joseph, Annie Kamdem, Julie Maitre, Catherine Mathey, Catherine Paillard, Aurelie Phulpin, Cecile Renard, Cecile Stoven, Mohamed Touati, Capucine Trochu, Suzanne Mathieu Nafissi, Catherine Badens, Sarah Szepetowski, Isabelle Thuret
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/c9cd9bf063f14502a2b276034138b71d
Autor:
Mathilde Veneziano, Audrey Benoit, Yoann Huguenin, Anne Lambilliotte, Marie-Pierre Castex, Stephanie Gourdon, Ghislaine Ithier, Kamila Kebaili, Pierre-Simon Rohrlich, Corinne Pondarre, Abdourahim Chamouine, Pauline Simon, Placide Agbo-Kpati-Kokou, Slimane Allali, Sandrine Baron-Joly, Sophie Bayart, Nicolas Billaud, Valentine Brousse, Cecile Dumesnil, Nathalie Garnier, Isabelle Guichard, Laure Joseph, Annie Kamdem, Julie Maitre, Catherine Mathey, Catherine Paillard, Aurélie Phulpin, Cécile Renard, Cecile Stoven, Mohamed Touati, Capucine Trochu, Suzanne Mathieu, Julia Vergier, Catherine Badens, Szepetowski Sarah, Isabelle Thuret
Publikováno v:
HemaSphere, Vol 7, p e77759aa (2023)
Externí odkaz:
https://doaj.org/article/697a6df9113e4fdd9ea248e91b76280f
Autor:
Abdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, Juliette Larmaraud, Laurent Lambrecht, Jean Poisson, Julien Balicchi, Serge Pissard, Narcisse Elenga
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-13 (2020)
Abstract Background Understanding the genetics underlying the heritable subphenotypes of sickle cell anemia, specific to each population, would be prognostically useful and could inform personalized therapeutics.The objective of this study was to des
Externí odkaz:
https://doaj.org/article/ef222bf6d85c4d13b62f6497c576fff9
Autor:
Loïc Epelboin, Renaud Blondé, Abdourahim Chamouine, Alexandra Chrisment, Laure Diancourt, Nicolas Villemant, Agnès Atale, Claire Cadix, Valérie Caro, Denis Malvy, Louis Collet
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 10, Iss 5, p e0004635 (2016)
INTRODUCTION:Human angiostrongyliasis (HA) is a neurological helminthic disease caused by the lung worm Angiostrongylus cantonensis. It is suspected in the combination of travel or a residence in an endemic area and eosinophilic meningitis. In Mayott
Externí odkaz:
https://doaj.org/article/fff480b6e0b04b2389fbfa529b971382
Publikováno v:
Child's Nervous System. 39:17-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e01895e6e951a134fcad28efc7efde79
https://doi.org/10.1007/s00381-022-05721-2
https://doi.org/10.1007/s00381-022-05721-2
Autor:
Marion, Subiros, Charlotte, Robert De Latour, Fanny, Parenton, Ibtissame, Soulaimana, Youssouf, Hassani, Renaud, Blondé, François, Pousset, Yvonnick, Boué, Camille, Estagnasie, Gonzague, Martin-Lecamp, Abdoulahy, Diallo, Lucas, Balloy, Mohamadou, Niang, Christophe, Caralp, Aurélie, Cann, Abdourahim, Chamouine, Alice, Miquel, Geneviève, Dennetière, Julie, Durand, Maxime, Jean, Sophie, Olivier, Louis, Collet, Nicole, Tayeb, Patrice, Combe
Publikováno v:
Eurosurveillance. 27
Background During the COVID-19 pandemic, national and local measures were implemented on the island of Mayotte, a French overseas department in the Indian Ocean with critical socioeconomic and health indicators. Aim We aimed to describe the COVID-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98973709d224e418b42b04f787a5e488
https://doi.org/10.2807/1560-7917.es.2022.27.34.2100953
https://doi.org/10.2807/1560-7917.es.2022.27.34.2100953
Autor:
Philippe Connes, Céline Renoux, Abdourahim Chamouine, Yves Bertrand, Françoise Bernaudin, Nathalie Bonello-Palot, Catherine Badens, Philippe Joly, Serge Pissard
Publikováno v:
Clinical Hemorheology and Microcirculation
Clinical Hemorheology and Microcirculation, IOS Press, 2021, 77 (3), pp.267-272. ⟨10.3233/CH-200951⟩
Clinical Hemorheology and Microcirculation, 2021, 77 (3), pp.267-272. ⟨10.3233/CH-200951⟩
Clinical Hemorheology and Microcirculation, IOS Press, 2021, 77 (3), pp.267-272. ⟨10.3233/CH-200951⟩
Clinical Hemorheology and Microcirculation, 2021, 77 (3), pp.267-272. ⟨10.3233/CH-200951⟩
International audience; Sickle cell anemia (SCA) is a disease characterized by abnormal red blood cell rheology. Because of their effects on HbS polymerization and red blood cell deformability, alpha-thalassemia and the residual HbF level are known g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd26c9c0bc089d9bd57e7ff46c8eb1cd
https://doi.org/10.3233/ch-200951
https://doi.org/10.3233/ch-200951
Autor:
Chiara Cattaneo, Abdourahim Chamouine, Thomas Simon, Maureen Drean, Soumeth Abasse, Marion Subiros, Patrice Combe
Publikováno v:
Journal of the Pediatric Infectious Diseases Society
During the COVID-19 outbreak in the French overseas department Mayotte, 11 children developed multisystem inflammatory syndrome (MIS-C). They all had a fever and gastrointestinal symptoms. Six patients were admitted to intensive care unit; management
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76562acb2ca42df8e9b0c645fd573f2b
https://doi.org/10.1093/jpids/piab011
https://doi.org/10.1093/jpids/piab011
Autor:
Marie Boyadjian, Emilie Follenfant, Abdourahim Chamouine, Olivier Maillard, Philippe Durasnel, Louis Collet, Renaud Blondé
Publikováno v:
Journal of pediatric hematology/oncology. 44(7)
Severe hemolytic anemia is a rare complication of glucose-6-phosphate dehydrogenase (G6PD) deficiency. It occurs with the Mediterranean (Med) variant corresponding to a class 2 deficiency according to the World Health Organization (WHO) classificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcffcec64775727a16e4ad6991d2f5f2
https://pubmed.ncbi.nlm.nih.gov/34966093
https://pubmed.ncbi.nlm.nih.gov/34966093