Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mamadou Ciré, Barry"'
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:
Emmanuel Camara, Ibrahima koolo Barry, Fatoumata Binta Diallo, Mohamed Lamine Diallo, Mamadou Moustapha Diop, Mahamoud Sama Cherif, Ibrahima Sory Diallo, Moustapha Kouyaté, Mmah Aminata Bangoura, Aissata Barry, Mamadou Ciré Barry, Ipolithe Honde Ngadande, Oumar Kaba, Ouo Ouo Kolié, Diarra Doura Camara, Saliou Bella Diallo, Hasmiou Dia
Publikováno v:
The Pan African Medical Journal, Vol 37, Iss 363 (2020)
La COVID-19 est due au virus SRAS-CoV-2 génétiquement semblable au virus du syndrome respiratoire aigu sévère (SRAS). En pédiatrie, les formes cliniques ont un caractère bénin. En Guinée, suite à la pandémie du COVID-19 dont l´épicentre
Externí odkaz:
https://doaj.org/article/afa639546cb04cfe88e584591a14b85f
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, 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c443d5ba3e981c7f4f43c4fdde1ed645
https://doi.org/10.4236/ojra.2021.111001
https://doi.org/10.4236/ojra.2021.111001
Autor:
Mamadou Hady, Touré Moriba, Fode Abass Cisse, Konaté Mamady, Carlos Othon Guelngar, Mamadou Ciré Barry, Kaba Condé, Karinka Diawara, Igué Kadidjatou, Awada Mohamed, D. D. Granga
Publikováno v:
Open Journal of Rheumatology and Autoimmune Diseases. 11:48-52
Tuberculous sacroiliitis secondary to a psoas abscess is rare, only a few sporadic cases were reported in the literature. Tuberculous sacroiliitis is rare, usually unilateral, its symptomatology is misleading, its diagnosis is often delayed or even c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fdd73101f99adfb361fcd64503db0ba
https://doi.org/10.4236/ojra.2021.112006
https://doi.org/10.4236/ojra.2021.112006
Autor:
Karinka Diawara, Douna Granga Daouya, Touré Moriba, Awada Mohamed, Kaba Condé, Konaté Mamady, M. Diallo, Mamadou Ciré Barry, Igué Kadidjatou, Carlos Othon Guelngar, Fode Abass Cisse
Publikováno v:
Open Journal of Rheumatology and Autoimmune Diseases. 11:73-78
Secondary hypertrophic osteoarthropathy, or Pierre-Marie Bamberger syndrome, is characterized by the association of digital clubbing, polyarthritis and periostitis affecting the long bones. Most commonly it is a paraneoplastic syndrome associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78578405692e183d43f7f3c4e0870ea0
https://doi.org/10.4236/ojra.2021.112009
https://doi.org/10.4236/ojra.2021.112009
Autor:
Mamadou Pathé Diallo, Mamadou Moustapha Diop, Mamadou Aliou Doukoure, Saliou Bella Diallo, Ibrahima Koolo Barry, Hasmiou Dia, Emmanuel Camara, Mohamed Lamine Diallo, Mamadou Ciré Barry, N. V. Gateu Tadjom, Aissata Barry
Publikováno v:
Open Journal of Pediatrics. 10:688-694
Introduction: Acute thoracic syndrome is the appearance of a new pulmonary infiltrate on radiology associated with fever, desaturation or respiratory signs. It is the second leading cause of hospitalization and the first cause of death in sickle cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58248196cd83ab4b636da1369d819fd7
https://doi.org/10.4236/ojped.2020.104071
https://doi.org/10.4236/ojped.2020.104071
Autor:
Mahamoud Sama Cherif, Aissata Barry, Hasmiou Dia, Mamadou Moustapha Diop, Diarra Doura Camara, Fatoumata Binta Diallo, Ipolithe Honde Ngadande, Mamadou Ciré Barry, Ouo Ouo Kolié, Ibrahima Koolo Barry, Mohamed Lamine Diallo, Ibrahima Sory Diallo, Mmah Aminata Bangoura, Oumar Kaba, Emmanuel Camara, Moustapha Kouyate, Saliou Bella Diallo
Publikováno v:
Pan African Medical Journal; Vol. 37 No. 1 (2020)
The Pan African Medical Journal
The Pan African Medical Journal
La COVID-19 est due au virus SARS-CoV-2 génétiquement semblable au virus du syndrome respiratoire aigu sévère (SARS). En pédiatrie, les formes cliniques ont un caractère bénin. En Guinée, suite à la pandémie du COVID-19 dont l´épicentre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fb782e2a5223caff48187e4b3cf4923
https://www.ajol.info/index.php/pamj/article/view/232320
https://www.ajol.info/index.php/pamj/article/view/232320
Autor:
Hugues Ghislain Atakla, Mahugnon Maurel Ulrich Dénis Noudohounsi, Aichat Yabo Salami, Hélène Sacca, Axel Gaël Houinato, Mamadou Ciré Barry, Guelngar Carlos Othon, Ayeratou Abèbi Adjadi, Dismand Stephan Houinato
Publikováno v:
The Pan African Medical Journal
The aim of this study was to evaluate the main clinical and evolutionary features of SARS-CoV-2 infection in children aged 0-18 years who were suspected and diagnosed for COVID-19 during routine consultations in the pediatric ward of the Ignace Deen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eca21d1b2c821826f8e631a26272bb3e
https://pubmed.ncbi.nlm.nih.gov/33552370
https://pubmed.ncbi.nlm.nih.gov/33552370
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol. 36 No. 1 (2020)
Pan African Medical Journal; Vol. 36 No. 1 (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://explore.openaire.eu/search/publication?articleId=doi_dedup___::348b49847c574c315962098a959b2aeb
http://europepmc.org/articles/PMC7666687
http://europepmc.org/articles/PMC7666687