Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Youlouza, Coulibaly"'
Autor:
Lassana Cissé, Abdoulaye Yalcouyé, Kadidia Oumar Touré, Youlouza Coulibaly, Alassane Baneye Maiga, Salia Bamba, Dramane Diallo, Salimata Diarra, Abdoulaye Taméga, Oumou Traoré, Mahamadou Kotioumbé, Moussa Aly Sangaré, Hamidou Oumar Ba, Assiatou Simaga, Fatogoma Issa Koné, Oumar Samassekou, Amadou Koné, Cheick Oumar Guinto, Guida Landouré, the H3Africa consortium
Publikováno v:
Clinical Case Reports, Vol 12, Iss 2, Pp n/a-n/a (2024)
Key Clinical Message Cleidocranial dysplasia (CCD) is a rare genetic skeletal disorder with only few cases reported in Africa, mostly based on clinical and radiological findings. We report the first case in Mali, caused by a novel de novo variant in
Externí odkaz:
https://doaj.org/article/3d1bcdfff01a4e70b7d6c92ffddb67c7
Autor:
Abdoulaye, Koné, Sylvain, Coulibaly, Moussa, Konaté, Youssouf, Koné, Youlouza, Coulibaly, Adama D, Keita, Siaka, Sidibé
Publikováno v:
Journal Africain d’Imagerie Médicale; Vol. 12 No. 2 (2020); 74-79
Objectif : Evaluer la concordance de la classification BI-RADS échographique mammographique dans la prédiction de la malignité des masses mammaires en comparaison à l’histologie.Méthodologie: Etude transversale descriptive réalisée au servic
Autor:
Modibo Sangare, Ilo Dicko, Cheick Oumar Guinto, Adama Sissoko, Kekouta Dembele, Youlouza Coulibaly, Siaka Y. Coulibaly, Guida Landoure, Abdallah Diallo, Mamadou Dolo, Housseini Dolo, Boubacar Maiga, Moussa Traore, Mamadou Karembe, Kadiatou Traore, Amadou Toure, Mariam Sylla, Arouna Togora, Souleymane Coulibaly, Sékou Fantamady Traore, Brant Hendrickson, Katherine Bricceno, Alice B. Schindler, Angela Kokkinis, Katherine G. Meilleur, Hammadoun Ali Sangho, Brehima Diakite, Yaya Kassogue, Yaya Ibrahim Coulibaly, Barrington Burnett, Youssoufa Maiga, Seydou Doumbia, Kenneth H. Fischbeck
Publikováno v:
eNeurologicalSci, Vol 3, Iss C, Pp 17-20 (2016)
Introduction: Spinal muscular atrophy (SMA) and sporadic amyotrophic lateral sclerosis (SALS) are both motor neuron disorders. SMA results from the deletion of the survival motor neuron (SMN) 1 gene. High or low SMN1 copy number and the absence of SM
Externí odkaz:
https://doaj.org/article/398cea98f58a47b7bc911dd309ab2e9b
Autor:
Lassana Cissé, Salimata Diarra, Abdoulaye Yalcouyé, Youlouza Coulibaly, Abdoulaye Tamega, Alassane Baneye Maiga, Oumou Traoré, Mahamadou Kotioumbé, Moussa Sangaré, Seybou Hassane Diallo, Salimata Diallo, Hamidou O Bah, Assiatou Simaga, Koné Fatogoma Issa, Thomas Coulibaly, Oumar Samassékou, Cheick Guinto, Guida Landouré
Acalvaria is a rare and lethal congenital malformation characterized by the absence of the cranial vault bones, dura mater and associated muscles with complete cranial content. We report a 5-year-old Malian girl seen at 20 months old for facial dysmo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b30371b6fe9e6fc15dfc13cd077ce0d1
https://doi.org/10.22541/au.163577941.11511652/v1
https://doi.org/10.22541/au.163577941.11511652/v1
Autor:
Youlouza Coulibaly, Bréhima Coulibaly, Adama Seriba Diarra, Abdoulaye Kanté, Nouhoum Ongoïba, Mariam Daou, Babou Ba, Abdoulaye Koné, Bréhima Bengaly, Oncoumba Diarra, Drissa Traoré
Publikováno v:
Forensic Medicine and Anatomy Research. :44-49
Aim: The aim of this work is to determine the dimensions and the capacity of the gall-bladder by ultrasound. Methodology: We realized a descriptive study over 2 years (from January, 2015 till December, 2017). It concerned an ultrasound exploration of
Autor:
K. Dembele, Abdoulaye Yalcouyé, Salimata Diarra, C.O. Guinto, Samba Djimdé, Guida Landouré, Lassana Cissé, B Maiga, Youlouza Coulibaly
Publikováno v:
eNeurologicalSci
Autor:
Abdallah A. Diallo, K. Dembele, Guida Landouré, Ilo Dicko, Moussa Traoré, Arouna Togora, Souleymane Coulibaly, Mariam Sylla, Seydou Doumbia, K Traoré, Alice B. Schindler, Barrington G. Burnett, Mamadou Dolo, Mamadou karembe, Amadou Toure, Brant C. Hendrickson, B Maiga, Modibo Sangare, Kenneth H. Fischbeck, Sekou F. Traore, C.O. Guinto, Youlouza Coulibaly, Katherine V. Bricceno, Katherine G. Meilleur, Angela Kokkinis, Housseini Dolo, Adama Sissoko, Siaka Y. Coulibaly, Yaya Ibrahim Coulibaly, Youssoufa Maiga, Brehima Diakite, Yaya Kassogue, Hammadoun Ali Sangho
Publikováno v:
eNeurologicalSci
eNeurologicalSci, Vol 3, Iss C, Pp 17-20 (2016)
eNeurologicalSci, Vol 3, Iss C, Pp 17-20 (2016)
Introduction: Spinal muscular atrophy (SMA) and sporadic amyotrophic lateral sclerosis (SALS) are both motor neuron disorders. SMA results from the deletion of the survival motor neuron (SMN) 1 gene. High or low SMN1 copy number and the absence of SM