Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Djibrilla Almoustapha A"'
Autor:
Ousseini Fanta, Inouss A, Djibrilla Almoustapha A, Housseini Malam-Laminou Y, Mouusa Saley S, Abdou N, Malam-Abdou B
Publikováno v:
Saudi Journal of Medical and Pharmaceutical Sciences. 8:780-782
Polycystic liver disease is an autosomal dominant disorder, rare and benign in the majority of cases [1]. It is frequently associated with polycystic kidney disease, but can also be isolated in rare cases. Liver cysts result from abnormal growth of t
Autor:
Dr. Ousseini Fanta, Inouss Ali, Djibrilla Almoustapha Amadou, Housseini Malam-Laminou, Youhanizou Youhanizou, Moussa Saley Sahada, Abdou Nafissa, Malam-Abdou Badé
Publikováno v:
Saudi Journal of Medicine. 7:607-609
The hemorrhagic syndrome in its clinical, cutaneous and ocular diversity most often constitutes the circumstances in which acute leukemia is discovered. Digestive mucosal involvement is rarely indicative of serious bone marrow failure, thus posing a
Autor:
Amadou Djibrilla-Almoustapha, Moustapha Mamane-Brah, Moustapha Elhadj-Chefou, Maman Rabiou Badé, Faiza Abba-Ousmane, Fanta Ousseini, Oumoulkairou Abdoulaye-Soumana, Badé Malam-Abdou
Publikováno v:
Open Journal of Blood Diseases. 12:103-109
Autor:
Youssoufa Seydou-Moussa, Amadou Djibrilla-Almoustapha, Maman Rabiou Badé, Moustapha Elhadji-Chefou, M Daou, Maman Aminou Mahamane Sani, B Malam-Abdou, Amal Al-Azhari, Souleymane Brah, Moustapha Maman-Brah
Publikováno v:
Open Journal of Blood Diseases. 11:1-5
Von Willebrand’s disease was first described in 1926 by Erik Von Willebrand. It is a genetic, constitutional defect of hemostasis that is different from hemophilia. It is classified among the rare diseases whose clinical manifestations are dominate
Autor:
Amadou Djibrilla-Almoustapha, Chaibou-Yacouba Maimouna, Moctar Abdoulaye-Maliki, Hamidou Soumana-Diaouga, Madeleine Garba-Rah, Idi Nafiou, Madi Nayama, Mansour Sidi-Mahamane
Publikováno v:
Open Journal of Blood Diseases. 11:25-30
Pregnancy in a sickle cell patient is a source of maternal and perinatal morbidities. Thromboembolic diseases of which Deep Vein Thrombosis (DVT) is one of the complications. The frequency of the latter is poorly assessed. Very few studies have been
Autor:
Mahamane Sani Ma, Kabaou S Malam-Abdou B, Maman Brah M, Djibrilla Almoustapha A, Daou M, M Chefou, Hamissou M. R, Eric Adehossi, Brah S
Publikováno v:
Saudi Journal of Medical and Pharmaceutical Sciences. :311-314
Publikováno v:
Saudi Journal of Pathology and Microbiology. :190-192
Autor:
MA Mahamane Sani, Souleymane Brah, B Malam-Abdou, M. Maman Brah, M Chefou, M. R. Badé, M Daou, Eric Adehossi, F. Abba Ousmane, A. Djibrilla Almoustapha
Publikováno v:
Open Journal of Blood Diseases. 10:71-76
Plasma cell leukemia is a rare malignant hemopathy, characterized by a peripheral plasma cell proliferation of more than 20% of the leukocyte formula. A few rare cases have been described. From which we report a case of plasma cell leukemia in a 52-y