Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Kaba, Condé"'
Autor:
Ham, Andrew Siyoon, Traore, Mohamed, Othon, Guelngar Carlos, Conde, Mohamed Lamine, Lamine, Toure Mohamed, Djigué, Barry Souleymane, Kaba, Condé, Karinka, Diawara, Idrissa, Doumbouya, Idrissa, Camara, Diallo, Djenabou, Duan, Rui, Rice, Dylan R., Cisse, Fode Abass, Mateen, Farrah J.
Publikováno v:
In Seizure: European Journal of Epilepsy October 2023 111:30-35
Autor:
Kaba Condé, Carlos Othon Guelngar, Mamadou Ciré Barry, Hugues Ghislain Atakla, Awada Mohamed, Fodé Abass Cissé
Publikováno v:
European Journal of Medical Research, Vol 26, Iss 1, Pp 1-3 (2021)
Abstract Objectives Sjögren’s syndrome is rare in children and most often secondary. It frequently affects girls and is characterized by dry eye syndrome, mouth and sometimes systemic involvement. Its diagnosis is difficult to establish in childre
Externí odkaz:
https://doaj.org/article/fce2d2f9686f4d2cb5f51f8f951f3fda
Autor:
Abdoulaye Barry, Oumar Diouhé Bah, Adama Bah, Mamadou Lamine Diallo, Kaba Condé, Samba Frein Condé, Aly Badra Kamissoko
Publikováno v:
Open Journal of Rheumatology and Autoimmune Diseases. 13:8-16
Autor:
Dr. Adama Bah, Sidiki Charifah, Abandazegoue Andjembe Laetitia Cynthia, Abdoulaye Barry, Harine Abdel Aziz Garba, Ramadhane Bouchrane, Kaba Condé, Aly Badra Kamissoko
Publikováno v:
SAS Journal of Medicine. 8:764-769
Introduction: Ankylosing spondylitis (AS) is an inflammatory rheumatic disease characterized by predominant axial and peripheral (enthesitis, sacroiliitis) involvement affecting young subjects aged 30 to 40 years, 80 to 98% of cases are associated wi
Autor:
Kaba Condé, Guelngar Carlos-Othon, Souleymane-Djigué Barry, Mohamed-Lamine Touré, Mohamed-Tafsir Diallo, Mamadou-Lamarana Diallo, Karinka Diawara, Idrissa Doumbouya, Mamady Konaté, Amara Cissé, Fodé-Abass Cissé
Publikováno v:
Médecine des Maladies Métaboliques. 16:558-563
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 385 (2020)
X-linked agammaglobulinemia (XLA) is a rare genetic disease caused by a mutation in the Bruton tyrosine kinase (BTK) gene. It is characterized by a profound deficiency of B cells and a decrease in all classes of immunoglobulins (Ig). We report one ca
Externí odkaz:
https://doaj.org/article/f8fdba032c9a45d7adde24c22666827b
Autor:
Kaba Condé, Garba Mahaman Salissou
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 332 (2020)
Nous rapportons le cas d´un patient de 48 ans sans antécédent particulier suivi pour une spondylarthrite ankylosante depuis 2012 en accord avec les critères d´ASAS (Assessment of SpondyloArthritis International Society). Il présente une lombalg
Externí odkaz:
https://doaj.org/article/c2fcd01d3fa642b1b9d000082dfb2d2a
Autor:
Kaba Condé, Guelngar Carlos Othon, Abdoulaye Barry, Moriba Touré, Alybadara Kamissoko, FodéAbass Cissé
Introduction- Spondyloarthritis is classically considered rare in sub-Saharan Africa where the majority of the population is considered HLA-B27 negative.The objective of this study was to describe the profile of spondyloarthritis in the rheumatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62126e68079032810ac7c98d98b5d63b
https://doi.org/10.21203/rs.3.rs-2497462/v1
https://doi.org/10.21203/rs.3.rs-2497462/v1
Autor:
Barry Abdoulaye, Touré Moriba, Kaba Condé, Kamissoko AB., Baldé Alpha Boubacar, Niass Moustapha, Diallo Saidou
Publikováno v:
European Scientific Journal ESJ. 9
Objectif : Déterminer le profil épidémiologique des cas d’arthropathies microcristallines dans le service de rhumatologie du CHU Aristide Le Dantec. Matériel et méthodes : Il s’agit d’une étude rétrospective menée entre janvier 2002 et
Autor:
Kaba Condé, Mamadou Ciré Barry, Carlos Othon Guelngar, Igue Kadidjatou, Mamadou Hady, Karinka Diawara, Konaté Mamady, Touré Moriba, D. Granga D, Awada Mohamed, Fodé Abass Cissé
Publikováno v:
Open Journal of Rheumatology and Autoimmune Diseases. 11:1-8
Introduction: Juvenile Idiopathic Arthritis (JIA) is the most common rheumatoid disease in children. In Sub-Saharan Africa, little data is available on the prevalence of JIA. The objective of our study was to determine the frequency and describe the