Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Moustapha Niasse"'
Autor:
Baïdy Sy Kane, Ahmadou Bamba Mbodji, Mouhamed Dieng, Christelle Sabrina Yando Longo, Biram Codou Fall, Awa Cheikh Ndao, Moustapha Niasse, Adama Berthe, Maimouna Sow, Fatimata Ly, Souhaibou Ndongo, Abdoulaye Pouye
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 35, Iss 1, Pp 1-6 (2023)
Externí odkaz:
https://doaj.org/article/08fc58a53bf74667b2fd13cfef6a143d
Publikováno v:
SAS Journal of Medicine. 9:144-147
Introduction: Gougerot-Sjögren’s syndrome (GSS) is a systemic autoimmune disease with malignant transformation to non-Hodgkin’s lymphoma (NHL) as its most formidable complication. There are few associations described in the literature with other
Autor:
Harine Abdel Aziz Garba, Dr. Adama Bah, Ramadhane Bouchrane, Vanessa Lienou Tagne, Sariette Carolne Ndoumbe Moukala Douala, Anne Stephanie Doun Fouda Elodie, Moustapha Niasse, Saïdou Diallo
Publikováno v:
SAS Journal of Medicine. 8:843-846
Cervical Pott's disease is an uncommon spinal location. Spinal cord compression and epidural abscesses are serious complications that can be life threatening. We report a case of cervical Pott's disease revealed by dysphagia due to a minimal retropha
Autor:
Fatimata Keita, Boubacar Ahy Diatta, Seynabou Fall, Boundia Djiba, Moustapha Niasse, Moussa Diallo
Publikováno v:
Our Dermatology Online. 13:54-57
Leukocytoclastic vasculitis is a rare cutaneous manifestation in multiple myeloma and only twenty cases have been described to date. We report an unusual case with kappa IgA multiple myeloma in a 63 years old woman presented with leukocytoclastic vas
Autor:
Dr. Adama Bah, Harine Abdel Aziz Garba, Ramadhane Bouchrane, Laurine Marlyse Adogle, Vanessa Lienou Tagne, Aissata Tata Kante, Sira Tall, Moustapha Niasse, Saïdou Diallo
Publikováno v:
SAS Journal of Medicine. 6:624-627
Introduction: SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) is autoinflammatory rheumatism of the spondyloarthritis group. It is rare, it prevalence is 1/10000 inhabitants. The average age at diagnosis is 38 years, with no gender pr
Autor:
Adama BAH, Harine Abdoul Aziz GARBA, Ramadhane BOUCHRANE, Mondukpe Joanne Immanuelle HOUANSOU, Moustapha NIASSE, Saïdou DIALLO
Publikováno v:
SAS Journal of Medicine. 8:597-600
Introduction: Rhupus is the combination of manifestations of RA and SLE, meeting the respective classification criteria of these two pathologies. This uncommon clinical entity with a prevalence of about 0.09% was described by Toone in 1960. Objective
Autor:
Harine Abdel Aziz Garba, Dr. Adama Bah, Ramadhane Bouchrane, Vanessa Lienou Tagne, Adamou Saoudatou Hamidou, Moustapha Niasse, Saïdou Diallo
Publikováno v:
SAS Journal of Medicine. 8:847-849
Gout is a microcrystalline arthropathy resulting from the deposition of sodium urate microcrystals in the articular and periarticular tissues, and even in the extra-articular tissues. It affects mainly men and its mechanism is at the origin of a dela
Autor:
Adama BAH, Ramadhane BOUCHRANE, Harine Abdoul Aziz GARBA, Moussa TRAORE, Mamadou Diouldé KANTE, Aïssatou N’diaye, Chekh Ahamad Bamba DIAO, Moustapha NIASSE, Saïdou DIALLO
Publikováno v:
SAS Journal of Medicine. 8:594-596
Introduction: Systemic lupus erythematosus (SLE) is a non- organ specific auto-immune disease of multifactorial origin (genetic, immunological, and environmental) acting in concert. The one with juvenile-onset is rare, renal involvement is the most f
Autor:
Moustapha Niasse, Awa Cheikh Ndao, Ramadhane Bouchrane, Siddiki Charifah, Adama Bah, Saïdou Diallo
Publikováno v:
Journal of Rare Diseases Research & Treatment. 6:1-4
Publikováno v:
La Tunisie medicale. 99(10)
Very few studies have focused on spondyloarthritis (SpA) in sub-Saharan Africa. The majority of these studies have focused on series of HLA B27-negative SpA.To determine the epidemiological, diagnostic, therapeutic and evolutionary aspects of SpA in