Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alain Saga Ouermi"'
Autor:
Nogognan Ignace Lengane, Milckisédek Judicaël Marouruana Some, Mohamed Tall, Alain Saga Ouermi, John Pepin Nikiema, Joséphine Wendemy Ouoba, Moussa Kadyogo, Moustapha Sereme
Publikováno v:
The Pan African Medical Journal, Vol 37, Iss 370 (2020)
Le fibromatosis colli ou pseudotumeur infantile du muscle sternocléidomastoïdien est une cause rare de masse cervicale bénigne du nouveau-né et du nourrisson. L´étude a concerné tous les patients admis pour une tuméfaction cervicale et chez q
Externí odkaz:
https://doaj.org/article/ad4531f4b2594f8ab390f4724843eb0c
Autor:
Bintou Sanogo, Alain Saga Ouermi, Makoura Barro, Anselme Millogo, Ad Bafa Ibrahim Ouattara, Ouédraogo Abdoul Salam, Boubacar Nacro
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0241789 (2020)
ObjectiveEvaluate the performance of QuantiFERON ® -TB Gold In-Tube test (QFT-GIT), to improve the diagnosis of active tuberculosis (TB) in Human Immuno-Deficiency Virus (HIV)-infected children.MethodSensitivity, specificity, Positive Predictive Val
Externí odkaz:
https://doaj.org/article/3957f80f476d436299ffaffe6b46c45c
Autor:
Fla Kouéta, Sonia Kaboret, Aïssata Kaboré, Issa Tondé, Diarra Yé, Hamidou Savadogo, Laure Tamini, Alain Saga Ouermi, Arzouma Idrissa Ouédraogo, Lassina Dao, Toguyeni
Publikováno v:
Néphrologie & Thérapeutique. 17:532-537
Resume Introduction L’infection urinaire figure au second rang des infections bacteriennes de l’enfant, apres celle des voies respiratoires. L’objectif du present travail etait d’etudier l’ecologie bacterienne et la sensibilite aux antibiot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab2560bfff3074474c9fa1ea8a652c84
https://doi.org/10.1016/j.nephro.2021.04.003
https://doi.org/10.1016/j.nephro.2021.04.003
Autor:
Mohamed Tall, Moussa Kadyogo, Alain Saga Ouermi, Nogognan Ignace Lengane, Joséphine Wendemy Ouoba, Milckisédek Judicaël Marouruana Some, John Pepin Nikiema, Moustapha Sereme
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol. 37 No. 1 (2020)
Pan African Medical Journal; Vol. 37 No. 1 (2020)
Le fibromatosis colli ou pseudotumeur infantile du muscle sternocléidomastoïdien est une cause rare de masse cervicale bénigne du nouveau-né et du nourrisson. L´étude a concerné tous les patients admis pour une tuméfaction cervicale et chez q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc87733f37e5bc851dda63a8dbc139d
http://europepmc.org/articles/PMC7992433
http://europepmc.org/articles/PMC7992433
Autor:
Hamidou, Savadogo, Lassina, Dao, Issa, Tondé, Laure, Tamini/Toguyeni, Arzouma Idrissa, Ouédraogo, Alain Saga, Ouermi, Sonia, Kaboret, Aïssata, Kaboré, Fla, Kouéta, Diarra, Yé
Publikováno v:
Nephrologietherapeutique. 17(7)
Urinary tract infection is the second most common bacterial infection in children, after respiratory tract infection. The objective of this work was to study the bacterial ecology and antibiotic susceptibility of germs isolated during childhood urina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6885dfc5a703ef80253eda750e4720c7
https://pubmed.ncbi.nlm.nih.gov/34103257
https://pubmed.ncbi.nlm.nih.gov/34103257
Autor:
Alain Saga Ouermi, Boubacar Nacro, Ouédraogo Abdoul Salam, Ad Bafa Ibrahim Ouattara, Bintou Sanogo, Anselme Millogo, Makoura Barro
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0241789 (2020)
PLoS ONE
PLoS ONE
Objective Evaluate the performance of QuantiFERON ® -TB Gold In-Tube test (QFT-GIT), to improve the diagnosis of active tuberculosis (TB) in Human Immuno-Deficiency Virus (HIV)-infected children. Method Sensitivity, specificity, Positive Predictive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa252aaee5b6ce8350b7e021a18bd09b
https://doaj.org/article/3957f80f476d436299ffaffe6b46c45c
https://doaj.org/article/3957f80f476d436299ffaffe6b46c45c
Autor:
Boubacar Nacro, Fatimata Sahoura Nacro, Alain Saga Ouermi, Hassane Tamboura, Bintou Sanogo, Raymond K. Cessouma, Solange O. Kombasséré, Yahaya S. Ouedraogo, Makoura Barro
Publikováno v:
Pediatric Reports, Vol 11, Iss 4 (2019)
Pediatric Reports
Volume 11
Issue 4
Pediatric Reports
Volume 11
Issue 4
Apert syndrome or acrocephalosyndactyly is a rare genetic disease characterized by craniofacial dysmorphism and syndactyly of the hands and feet. We report an observation in a 4-month-old female infant, whose father was 65 years old. The infant was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2afd3ca6136bd97003d7e72b4b7690fa
https://www.pagepress.org/journals/index.php/pr/article/view/8224
https://www.pagepress.org/journals/index.php/pr/article/view/8224